Hypervigilance, Allostatic Load, and Migraine Prevention: Antibodies to CGRP or Receptor.

Migraine involves brain hypersensitivity with episodic dysfunction triggered by behavioral or physiological stressors. During an acute migraine attack the trigeminal nerve is activated (peripheral sensitization). This leads to central sensitization with activation of the central pathways including the trigeminal nucleus caudalis, the trigemino-thalamic tract, and the thalamus. In episodic migraine the sensitization process ends with the individual act, but with chronic migraine central sensitization may continue interictally. Increased allostatic load, the consequence of chronic, repeated exposure to stressors, leads to central sensitization, lowering the threshold for future neuronal activation (hypervigilance). Ostensibly innocuous stressors are then sufficient to trigger an attack. Medications that reduce sensitization may help patients who are hypervigilant and help to balance allostatic load. Acute treatments and drugs for migraine prevention have traditionally been used to reduce attack duration and frequency. However, since many patients do not fully respond, an unmet treatment need remains. Calcitonin gene-related peptide (CGRP) is a vasoactive neuropeptide involved in nociception and in the sensitization of peripheral and central neurons of the trigeminovascular system, which is implicated in migraine pathophysiology. Elevated CGRP levels are associated with dysregulated signaling in the trigeminovascular system, leading to maladaptive responses to behavioral or physiological stressors. CGRP may, therefore, play a key role in the underlying pathophysiology of migraine. Increased understanding of the role of CGRP in migraine led to the development of small-molecule antagonists (gepants) and monoclonal antibodies (mAbs) that target either CGRP or the receptor (CGRP-R) to restore homeostasis, reducing the frequency, duration, and severity of attacks. In clinical trials, US Food and Drug Administration-approved anti-CGRP-R/CGRP mAbs were well tolerated and effective as preventive migraine treatments. Here, we explore the role of CGRP in migraine pathophysiology and the use of gepants or mAbs to suppress CGRP-R signaling via inhibition of the CGRP ligand or receptor.

Key Summary Points

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Introduction

Migraine is among the most disabling disorders globally; in 2016, an estimated 1 billion people were affected [1]. The global age-standardized prevalence was approximately 14%, with approximately twice as many women than men being affected [1]. Estimates in the USA indicate an annual cost of approximately $36 billion [2-4]. Prevalence increases between the ages of 12 and 40 years and accounts for at least 1 day of school or work lost every 3 months among up to one-third of individuals [2, 4]. Social perceptions of migraine mean that patients may be dismissed as not having a serious disease. This perception is shared by some physicians [5], which exacerbates the significant negative impact migraine has on patients’ quality of life and ability to work [6]. Migraine features include moderate-to-severe throbbing headache, nausea and/or vomiting, and hypersensitivity to light and noise [7]. There is an important and complex genetic component to the disorder, but it remains unclear which genes and loci are implicated in its pathogenesis [8]. Migraine may be triggered by stress [9], exposure to bright light [9], pungent or strong odors [10], and barometric pressure changes [11]. Prodromal symptoms (e.g., fatigue, irritability, difficulty concentrating, mood change, yawning, stiff neck, phonophobia, and nausea) and postdromal symptoms (e.g., tiredness, weakness, cognitive difficulties, and mood change) are characteristic [12]. Migraine is classified as either episodic migraine (EM; < 15 days of headache per month) or chronic migraine (CM; for > 3 months, headache for ≥ 15 days per month with features of a migraine headache on ≥ 8 days per month) [13, 14].

Acute migraine management aims to reduce pain and symptoms and to restore physical and psychosocial function [6]. Possibly owing to a lack of adequate preventive treatments, acute therapies are frequently overused, which can lead to medication-overuse headache. Therefore, attempts are made to limit use of these treatments to 2–3 days per week [15]. Preventive migraine therapies are used for patients who have frequent and/or debilitating attacks, in whom acute medication fails to provide relief, or in whom there is a risk of overuse of acute medication [15]. The goals of preventive therapies are to reduce migraine frequency, duration, and/or severity of attacks, to improve responsiveness to acute therapy, to decrease use of acute therapy, and to increase the patient’s functional ability [16].

Traditional preventive therapies for migraine are inadequate, with up to 86% of patients discontinuing treatment early [17-19]. A retrospective US claims analysis shows that persistence with oral migraine preventive medications decreases over time, with only 14% of patients remaining on initial preventive treatment at 12 months [18]. Additionally, in a US-based survey, 39% of patients with migraine reported that they had used preventive medication at some time, with only 12% indicating that they were current users [20]. Thus, there remains a considerable unmet need for efficacious, well-tolerated preventive therapies with low potential for side effects.

The neuropeptide calcitonin gene-related peptide (CGRP) is a vasodilator with multiple sites of action that is involved in nociception and sensitization of peripheral and central neurons in the trigeminovascular system, which is implicated in migraine pathophysiology [7, 21–24]. Levels of CGRP in jugular venous blood and cerebrospinal fluid are elevated in patients with CM or EM [25-27], and these levels fall as migraine pain subsides upon triptan treatment, supporting a relationship between CGRP and migraine [28]. In rodents, application of CGRP to the cranial meninges triggered migraine-like signs of allodynia and pain in females but not in males: this hypersensitivity may contribute to the higher prevalence of migraine in females [29]. The involvement of CGRP in migraine has been substantiated by preclinical and clinical trials of drugs that block the activity of CGRP [30-34]. Additionally, CGRP infusion can trigger an attack in susceptible patients who experience migraine [35]. This review explores the role of CGRP in migraine, including its involvement in allostatic overload (i.e., when the beneficial acute stress response to external stimuli becomes maladaptive owing to chronic exposure to stressors) [36] and the use of monoclonal antibodies (mAbs) that suppress CGRP receptor (CGRP-R) signaling, potentially rebalancing allostatic load (Fig. 1).

Fig. 1

Role of CGRP in migraine. Some individuals have a genetic predisposition to hypervigilance, thus having a heightened awareness of sensory stimuli, which may have provided an evolutionary advantage [151]. Association with too many risk factors leads to increased CGRP levels, which results in allostatic overload, making individuals more sensitive to sensory triggers that initiate a migraine attack [69]. mAbs targeting CGRP or the CGRP-R inhibit CGRP signaling, potentially rebalancing allostatic load and reducing the likelihood of a migraine attack. It remains to be seen if there is a direct effect of anti-CGRP therapeutics in helping to balance allostatic load. CGRP calcitonin gene-related peptide, CGRP-R CGRP receptor, mAb monoclonal antibody

This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Migraine Pathophysiology

Migraine consists of distinct phases; in ~ 30% of patients it may be associated with aura (visual, sensory, motor, and language or brain stem disturbances) [37, 38]. Phases include the prodromal phase, probably mediated by the hypothalamus with multiple neurotransmitters believed to be involved (e.g., serotonin, orexin) and a potential aura phase, associated with a slow wave of neural depolarization called cortical spreading depression (CSD) that may activate trigeminal afferents (although the precise mechanism is unknown) [9, 12]. These are followed by the headache phase, which is mediated by activation of the trigeminovascular system, and the postdromal phase, which is associated with hyperperfusion in patients with aura and with bilateral posterior cortical hypoperfusion that persists after treatment in patients without aura [12]. The final (interictal) phase is characterized by reduced activation of the spinal trigeminal nuclei (Fig. 2) [9].

Fig. 2

Migraine phases. Migraine consists of different phases characterized by physiological changes in the brain and trigeminovascular system. The headache phase is associated with activation of the trigeminovascular system and may last for ~ 4 to 72 h

CSD is associated with an increase in proinflammatory molecules and neuropeptides, including CGRP, and can activate the trigeminovascular system [39, 40]. The relationship between CSD and CGRP may be a contributory factor in migraine [39]. Drugs targeting CGRP-R signaling, including mAbs, reduce the activation of trigeminovascular neurons by CSD [41, 42].

Migraine is regarded as a neurovascular disease, driven by both neurovascular changes and modulation of nociceptive input [2]. Activation of the trigeminovascular system leads to an inflammatory cascade involving the meninges, meningeal blood vessels, and subsequent neural dysfunction (Fig. 3) [37]. The headache phase of migraine is thought to stem from activation of nociceptors that innervate the intracranial vasculature [21]. Nociceptive innervation of this vasculature consists of axons that originate in the trigeminal ganglion and release vasoactive neuropeptides such as CGRP and substance P [21]. Axonal projections of neurons in the trigeminovascular system transmit nociceptive signals via second-order neurons in the trigeminal nucleus caudalis and ascending fiber tracts to nuclei of the brain stem, hypothalamus, and basal ganglia and are thus potentially relevant to many symptoms of migraine (e.g., nausea, vomiting, fatigue, anxiety, and depression). Furthermore, relay trigeminovascular thalamic neurons projecting into various regions of the cortex could account for the location and intensity of migraine pain as well as transient symptoms such as clumsiness, loss of concentration and memory, photophobia, and phonophobia [40]. Perivascular CGRP in the periphery and central nervous system (CNS) may therefore act via the vessels innervated by the trigeminovascular system, the thalamus, and eventually the cortex to cause migraine symptoms [2].

Fig. 3

Components of the trigeminovascular system. The trigeminovascular system consists of sensory nerves with their cell bodies in the trigeminal ganglion that innervate the meningeal blood vessels. Activation of the trigeminovascular system leads to increased release of CGRP and vasodilation of the meningeal vessels. Pain in the face and head is primarily mediated by nociceptive afferents of the ophthalmic division of the trigeminal nerve. Activation of the meningeal afferents leads to activation of the trigeminal nucleus caudalis and subsequently rostral brain structures involved in pain perception. CGRP calcitonin gene-related peptide

CGRP

CGRP is a member of the calcitonin peptide family, which includes calcitonin, amylin, adrenomedullin, and adrenomedullin 2/intermedin [43, 44]. There are two human isoforms of CGRP, α and β, which differ by three amino acids and share similar biological activities, but are synthesized from two different genes on chromosome 11 [45]. CGRP is widely expressed [22, 33] and is best known for its vasodilatory effects. Most relevant to its role in the pathophysiology of migraine is its expression in peripheral components (sensory neurons of trigeminal and cervical dorsal root ganglia) and in central components (e.g., parabrachial nucleus, amygdala, and hypothalamus) [3, 45]. CGRP is primarily expressed in small, unmyelinated sensory C fibers and myelinated Aδ fibers in the peripheral nervous system [22]. In contrast to amino acid neurotransmitters, which act on ionotropic receptors to alter postsynaptic membrane potentials quickly, neuropeptides are slower-acting neuromodulators that act through G protein-coupled receptors (GPCRs) [46]. CGRP acts as a modulator of postsynaptic gain when released from trigeminal nociceptors [46] and indirectly increases vascular permeability by promoting the release of substance P [47]. CGRP is stored in axonal dense core vesicles and can be released from the axon terminal or along the length of the axon, unlike neurotransmitters, which are stored in clear vesicles and released only at the axon terminals. Neuropeptides such as CGRP also differ from neurotransmitters in that they can function locally or more distally via diffusion in the vasculature [48].

CGRP Receptors

The calcitonin receptor family comprises two GPCRs: the calcitonin receptor and the calcitonin-like receptor (CLR). Additional receptor diversity is provided by heterodimerization of each of these GPCRs with one of three receptor activity-modifying proteins (RAMPs), which modify receptor binding characteristics. The calcitonin receptor preferentially responds to calcitonin but also associates with one of the three RAMPs to form amylin receptors (AMY1–3) [43]. CLR binds to its ligands (CGRP, adrenomedullin, or adrenomedullin 2) only when associated with RAMPs [43]. Thus, the functional CGRP-R complex consists of two subunits: CLR and RAMP1. An additional protein, known as receptor component protein, can also enhance signaling by this receptor complex [49]. Although the RAMP1-CLR complex is the CGRP-R, recent studies have established that AMY1 acts as a second CGRP-R and is present in the trigeminovascular system (Fig. 4) [43, 50, 51].

Fig. 4

The calcitonin receptor family subunit composition. The histograms are indicative of relative ligand activity upon binding for human receptors. AM adrenomedullin, AM2 adrenomedullin 2, AMY amylin receptor, CGRP calcitonin gene-related peptide, CLR calcitonin-like receptor, CT calcitonin, CTR calcitonin receptor, RAMP receptor activity-modifying protein

CGRP-R is expressed on the trigeminal afferents that project into the meninges; cell bodies of trigeminal neurons, and satellite glial cells located in the ganglion; astrocytes and microglia within the CNS; and mast cells in the meninges [3, 24]. In cell-based assays, CGRP-R has high affinity for CGRP and lower affinity for other calcitonin family ligands [43]. This promiscuity in binding within the receptor family may have important consequences for therapies targeting CGRP-R signaling [43]. For example, AMY1 is equally well activated by both CGRP and amylin and may or may not be involved in migraine [26, 43]. Furthermore, in rat trigeminal neurons, CGRP has been shown to act at AMY1 in addition to CGRP-R, potentially implicating both receptors in CGRP ligand signal processing [50]. However, to date, a role for AMY1 in migraine has not been confirmed. The role of amylin in migraine is unclear, and an amylin and CGRP head-to-head provocation study is ongoing (NCT03598075) [52].

CGRP Receptor Signaling Pathway

GPCR signaling in the CGRP-R-mediated pathway is transduced via adenylate cyclase either to modulate vasodilation in cerebral and meningeal arteries or to transmit nociceptive signals centrally via the brain stem and midbrain to the thalamus and higher cortical regions [23]. Activation of CGRP-R may also trigger alternative signaling pathways dependent on the G proteins and other signaling proteins expressed [26, 53, 54]. Upon ligand binding to CGRP-R, the ligand-receptor complex is internalized into the cell [43, 55, 56]; however, the cell-type specificity and significance of CGRP-R internalization are not fully understood [43], and cell signaling may continue once the receptor is internalized [43, 57]. AMY1 signaling in response to CGRP and amylin is similar to that of the CGRP-R, but a recent study suggests that AMY1 regulation is distinct, because the receptor does not internalize in response to CGRP or amylin agonists [53, 55, 58, 59].

The action of a ligand can be subject to functional selectivity at a given receptor towards a specific signaling pathway (biased agonism) [60]. Receptor conformations are not binary; multiple subunit conformations can exist, and different ligands may stabilize different receptor conformations that interact with various cellular signaling pathways. Thus, different ligands acting at the same receptor (e.g., CGRP or adrenomedullin at the CGRP-R) could activate distinct downstream cellular responses, a phenomenon not related to their binding affinity or efficacy [43]. If other ligands prove to be involved in migraine pathophysiology, this may have implications for the importance of targeting the CGRP-R rather than the CGRP ligand.

CGRP in Migraine

CGRP-Rs are ubiquitous in the smooth muscle of the vasculature (human middle meningeal, middle cerebral, pial, and superficial temporal arteries) and in the trigeminal afferent terminals (Fig. 5a). CGRP initiates and maintains peripheral and central sensitization by modulating neurons, glia, and immune cells in the trigeminal pain signaling pathway (Fig. 5b) [3]. During migraine, CGRP is released at various sites in the trigeminovascular system, including trigeminal afferent terminals that innervate the meninges, trigeminal cell bodies in the ganglion, and trigeminal efferent fibers that terminate in the medulla and cervical spinal cord (Fig. 5c) [3, 24]. At synapses outside the CNS, CGRP causes vasodilation via receptors on smooth muscle cells, whereas, at synapses inside the CNS, CGRP acts on second-order neurons to transmit pain signals to higher cortical pain regions [7, 61].

Fig. 5

CGRP receptor and ligand expression sites in the trigeminovascular system. (a) Localization of the CGRP-R has been confirmed in the smooth muscle of the vasculature and in the trigeminal afferents. Some studies have suggested the CGRP-R may also be present in macrophages and fibroblasts. (b) CGRP released in the trigeminal ganglion acts on satellite glia triggering neurogenic inflammation. This initiates peripheral sensitization and, as a result, downstream central sensitization. (c) CGRP is released at various sites in the trigeminovascular system where it is involved in nociception and vasodilation. CGRP calcitonin gene-related peptide, CGRP-R CGRP receptor

In the dura, CGRP mediates neurogenic inflammation, immune cell recruitment (such as mast cells and macrophages), and activation of sensory neurons; it also activates neurons in the trigeminal ganglion and signals in a retrograde manner from the spinal cord to neurons and glia in the trigeminal ganglion, sensitizing peripheral nociceptors [24, 62–64]. Neuron activation activates second-order neurons and glia, which promote central sensitization in the dorsal horn and spinal trigeminal nucleus caudalis [2, 62].

In sensory neurons within the trigeminal ganglion, CGRP may increase its expression by a paracrine mechanism involving release of proinflammatory mediators from satellite cells [3, 22]. Although CGRP released in the trigeminal ganglion is unlikely to cross the blood-brain barrier (BBB), it may influence central expression of pro-nociceptive compounds and receptors [24]. Neurotrophic factors such as brain-derived neurotrophic factor are stimulated by CGRP, which may act to potentiate central nociceptive neurotransmission [24]. Neurons expressing CGRP project from the trigeminal ganglion to the trigeminal nucleus caudalis, where CGRP induces release of glutamate from trigeminal afferents, further facilitating nociception [24]. Together, these effects provide a mechanism by which drugs acting on CGRP-R signaling in the peripheral trigeminal ganglion may modulate both peripheral and central pain signaling through a peripheral site of action, highlighting the potential for the use of these drugs for migraine therapy. It is well established that when peripheral activation is switched off, central activation also decreases [65].

CGRP mediates neuron-glial signaling via gap junctions within the trigeminal ganglion [24, 61]. Regional nonsynaptic cross-excitation occurs within the trigeminal ganglion following neuronal and glial activation. This may allow for coordinated responses to noxious stimuli that may also, however, sensitize neighboring neurons [61]. Neuron-glial signaling probably contributes to peripheral sensitization, which drives central sensitization [40], facilitating a lower threshold for neuronal activation in patients with migraine. Peripheral and central sensitization in patients may therefore lead to hypersensitivity to sensory stimuli.

Hypervigilance, Anxiety-Like State, and Allostatic Overload

Anxiety-like states and a persistent state of hypervigilance are contributory risk factors for migraine [66]. Individuals affected by migraine have a hypervigilant or hyperexcitable nervous system that is characterized by a lower sensory activation threshold and hypersensitivity towards sensory stimuli [67]. The resulting sensitization and activation of trigeminal nerves and the nociceptive pathway are thought to play an important role in the pathology of migraine [67]. The increased sensitivity to sensory stimuli is caused by a state of sensory neuron hyperresponsiveness or hyperexcitability, which lowers pain threshold and tolerance levels [38, 67]. In essence, a state of hypervigilance is the same as a state of central sensitization, in which the sensory activation threshold is reduced.

The role of anxiety and hypervigilance in migraine may be potentiated by CGRP-R signaling. CGRP promotes sensitization of primary and secondary trigeminal nociceptive neurons, leading to an enhanced state of neuronal excitability [67]. CGRP has also been implicated in migraine-associated allodynia (a nociceptive response to normally non-painful stimuli, such as hair brushing) [67, 68]. Thus, it is possible that CGRP plays a role in hypervigilance. Cutaneous allodynia is considered to be a marker of central sensitization and can manifest both during and between attacks in CM. Brains of patients with CM remain hyperexcitable in the interictal phase [69].

Over 50% of people with migraine experience an anxiety disorder over their lifetime [66]. Infusion with CGRP has been demonstrated to cause anxiety-like behavior and to induce neuronal activation in the bed nucleus of the stria terminalis (BNST) [70]. Furthermore, it has been hypothesized that reciprocal connections between the BNST and CGRP-containing cells in the parabrachial nucleus may induce a persistent state of anxiety via positive feedback [71]. The BNST is continuous with the amygdala and integrates physiological and behavioral responses to stress and anxiety by acting as a relay between limbic structures and the hypothalamus [3, 72]. Neurons expressing CGRP in the parabrachial nucleus relay pain signals from the periphery to the amygdala, thus encoding the affective component of pain [73]. In rats, CGRP antagonism has been shown to suppress grooming and shaking behaviors induced by CSD, which could indicate that CGRP is implicated in anxiety and/or pain perception [74].

Migraine is a disorder of allostatic load [75], triggered by risk factors including stress, sleep deprivation, light, odors, and noise (Fig. 1). Allostasis is the body’s ability to respond to stressful events and it involves hormonal and neural mediator activation and behavior modification. When behavioral or physiological stressors become more severe or frequent, the prolonged exposure dysregulates allostasis, leading to allostatic overload [76]. Structural and functional brain networks are altered, and the responses to stressors become abnormal [69].

People with migraine have a high allostatic load, which is more prevalent in EM (50%) than CM (33%) [75]. Allostatic load is moderate or high in most patients, and higher than in people without migraine [75]. In migraine, four main processes are involved in allostatic overload: (1) repeated stress; (2) failure to habituate to repeated stressors; (3) inability to stop the stress response normally; and (4) altered stress response that ultimately leads to compensatory responses, such as photophobia [69]. Central sensitization and factors that trigger a migraine attack both contribute to an individual’s allostatic load and, as sensitization increases, the need for an attack trigger decreases. Over time, sensitization levels and exposure to triggers will vary within an individual and between individuals [40]. For migraine treatments to be effective, they need to inhibit or stop persistent central sensitization.

Migraine may provide an evolutionary mechanism that enforces a rebalancing of allostatic load in response to a hypersensitive/hypervigilant state, thus relieving hypothalamic and cortical overload [69]. According to this model, it may be that CNS-driven changes in descending inhibitory pain modulation pathways enable more peripheral sensory information to reach the brain via the trigeminal-thalamus ascending pain pathway, potentially improving survival prospects by increasing vigilance, but also increasing allostatic load. CGRP may play a key role in migraine by increasing allostatic load mediated by risk factors; therefore, rebalancing CGRP-mediated signaling may treat or prevent attacks (Fig. 1) [40, 77]. As a key player in migraine pathophysiology, CGRP-R signaling was recognized as a potential therapeutic target, leading to the development of small-molecule antagonists and mAbs that target either CGRP or CGRP-R [2, 23, 26]. By inhibiting the release of pro-inflammatory molecules within the trigeminal ganglion and/or the dura and, therefore, reducing peripheral sensitization, CGRP mAbs might indirectly diminish central sensitization, reducing allostatic load and contributing to migraine regression.

Development of CGRP Antagonists

Several therapeutics are used to treat migraine: acute treatment includes nonsteroidal anti-inflammatory drugs and oral serotonin (5-hydroxytryptamine receptor 1B/1D) agonists known as triptans [15], whereas drugs such as anticonvulsants, antidepressants, antihypertensives, and botulinum toxins are used for migraine prevention [78]. Many of these drugs, which were not designed specifically for migraine, can have multiple side effects [15] and have poorly understood mechanisms of action [79]. Furthermore, poor adherence and frequent treatment-switching limit the effective use of these medications [17-20].

Until recently, first-line treatment for migraine focused on the relief of acute pain with triptans [80]. Triptans may provide effective pain relief during acute migraine; however, a substantial proportion of patients remain unresponsive [26]. Triptans act to constrict cerebral blood vessels and to inhibit activation of peripheral nociceptors on trigeminal afferents to reduce CGRP release [80-82]. In clinical trials, it was shown that plasma CGRP levels were reduced in patients whose migraine pain subsided following treatment with sumatriptan, but not in those who did not experience pain relief [31]. CGRP levels also correlated positively with pain intensity [31].

Most migraine preventives inhibit fast synaptic transmission, whereas drugs targeting neuropeptide pathways such as CGRP modulate neuronal activity [46]. CGRP release may be initiated by a Ca2+-dependent process involving soluble N-ethylamide-sensitive factor attachment protein receptor (SNARE), which promotes vesicle docking and membrane fusion or, alternatively, by a Ca2+- and SNARE-independent process [83]. Although triptans may inhibit Ca2+ signaling and although botulinum toxin type A prevents vesicular fusion through cleavage of the SNARE protein SNAP-25, CGRP release at the proximal axon of sensory neurons independent of these mechanisms remains unaffected [83]. This may explain why some patients with migraine do not respond to these therapies and supports the use of agents that block CGRP-R signaling rather than CGRP release.

Consequently, the ‘gepants’ were developed; these are mostly oral, small-molecule CGRP-R antagonists [84], six of which have been studied clinically for the treatment of acute migraine: olcegepant, telcagepant, MK-3207, BI 44370 TA, rimegepant, and ubrogepant [85]. A seventh gepant, atogepant, is in development for EM prevention [85]. Gepants do not directly cause vasoconstriction [86, 87], lending further weight to the argument that migraine is not purely a vascular disorder [26]. In clinical trials, the first-generation gepant, telcagepant, demonstrated efficacy for the treatment of acute migraine compared with placebo and triptans [88, 89]. However, liver toxicity limited its use as a preventive treatment. Other first-generation gepants (olcegepant, MK-3207, and BI 44370 TA) also showed promising results in clinical trials [90-92], but were discontinued owing to liver toxicity and to difficulties in developing oral formulations [85]. Elevated aminotransferase levels were attributable to off-target effects by a toxic metabolite not produced by second-generation gepants [84, 93], unleashing the potential of these agents as preventive treatments for migraine. Ubrogepant has recently been approved in the USA for the acute treatment of migraine with or without aura in adults [94], based on positive results from Phase 3 studies, including a recent trial in which significantly more patients taking ubrogepant were symptom-free 2 h after taking the drug compared with patients taking placebo (21.2% vs. 11.8%, respectively, p < 0.001) [95]. The efficacy of rimegepant has been demonstrated in Phase 3 clinical trials in acute migraine, with patients experiencing freedom from pain at 2 h after dosing, sustained pain relief for up to 48 h, and a reduction in associated symptoms such as photophobia and nausea [84, 96]. A further Phase 3 trial reported results with a new formulation of rimegepant as an orally disintegrating tablet (ODT), which was superior to placebo when comparing proportions of patients free from pain and bothersome symptoms 2 h post dose (21% vs. 11%, respectively, p < 0.0001) [97]. Rimegepant ODT was recently approved by the US Food and Drug Administration (FDA) for the acute treatment of migraine with or without aura in adults [98].

Two gepants remain in development: atogepant and zavegepant (formerly known as vazegepant). Atogepant is the only gepant with positive Phase 3 trial data for migraine prevention, with statistically significant reductions in monthly headaches from baseline versus placebo (least squares mean differences: − 0.7 to − 1.4 days; p < 0.05) and no reported signal for hepatotoxicity [99, 100].

Positron emission tomography has shown central CGRP-R occupancy by gepants (telcagepant) is not required for their therapeutic effect in migraine, suggesting that large molecules such as mAbs, which cross the BBB very inefficiently, are a viable option [101]. Areas of the hypothalamus, pituitary, and circumventricular organs, such as the area postrema, are outside of the BBB, and so are accessible to mAbs. Despite their efficacy, early issues with tolerability of gepants drove the search for alternative agents with improved safety profiles, with a focus on mAbs [26].

Anti-CGRP and Anti-CGRP-R Monoclonal Antibodies

Therapeutic mAbs are highly selective for their target molecule, binding a single epitope with high affinity [26, 102] and not binding to other antibodies or targets. This largely overcomes the problem of off-target effects and toxicities associated with small-molecule drugs and their metabolites [26]. Therapeutic mAbs are used to treat several diseases, including cancer and autoimmune disorders [103]. They can trigger target cell destruction, as in some types of cancer treatment where the objective is to stimulate the patient’s immune system to attack the cancer cells [104]. Other types of mAb do not cause cell destruction, but instead bind to either a ligand or a receptor, modifying cell signaling pathways [104]; mAbs targeting CGRP-R signaling belong to this group. To reduce the likelihood of an immune reaction to therapeutic antibodies, which is characteristic of antibodies generated in mice, antibody engineering techniques have allowed the development of chimeric, humanized, or fully human mAbs [104].

mAbs targeting CGRP-R signaling are well suited for migraine prevention, not only because they target a pathway relevant to the disease, but also because they require infrequent administration relative to small-molecule drugs [26]. As only a small proportion of any circulating mAb will typically reach the CNS [105], targets within the CGRP-R signaling pathway are likely to be peripheral (vasculature, dura, or trigeminal ganglion) [106]. For CGRP-R signaling, one antibody reversibly targeting the CGRP-R, where it occupies the CGRP ligand-binding site (erenumab-aooe [26, 107]), and three targeting the CGRP ligand (fremanezumab-vfrm, galcanezumab-gnlm, and eptinezumab-jjmr) have been approved by the FDA for migraine prevention (Table 1, Fig. 6) [108]. Although many trials are ongoing, thus far the evidence for the clinical efficacy and tolerability profile of erenumab-aooe has been most comprehensively reported. Anti-CGRP-R signaling mAbs are efficacious in EM and CM in clinical trials of up to 6 months’ duration (Table 2) and are generally well tolerated. Erenumab-aooe has also been shown to be effective and well tolerated longer term in both EM and CM. In a 52-week open-label extension study in patients with CM who continued treatment after a 12-week double-blind period, treatment with erenumab-aooe (70 mg or 140 mg once monthly) was associated with changes in monthly migraine days (MMD; mean [95% confidence interval, CI]) from parent study baseline of − 9.3 [− 10.0 to − 8.6] at week 52; MMD were reduced to 8.8 from 18.1 at parent study baseline. At week 52, respective reductions in MMD of ≥ 50%, ≥ 75%, or 100% from parent-study baseline were observed in 59.0%, 33.2%, and 8.9% of patients still on study [109]. In an analysis of 5-year data from patients with EM who continued open-label treatment following a 12-week double-blind period, treatment with erenumab-aooe (70 mg or 140 mg once monthly) was associated, on average, with 5.3 fewer MMD at year 5, an average reduction of 62.3% from baseline. Moreover, reductions in MMD of ≥ 50%, ≥ 75%, or 100% at 5 years, based on the last 4-week period of assessment, were observed in 71.0%, 47.1%, and 35.5% of patients, respectively [110]. Notably, erenumab-aooe is efficacious in patients with EM in whom multiple preventive treatments have been unsuccessful (LIBERTY trial) [17], a patient population under investigation by others (FOCUS and CONQUER trials; patients with CM or EM). In the LIBERTY trial, which included patients with EM in whom two to four previous preventive treatments had been unsuccessful, 30% of patients treated with erenumab-aooe 140 mg had ≥ 50% reduction from baseline in mean number of MMD at week 12 compared with 14% of patients in the placebo group (odds ratio [OR] [95% CI]: 2.7 [1.4–5.2]; p = 0.002) [17]. Post hoc analyses of pivotal, double-blind, placebo-controlled trials of erenumab-aooe in patients with CM or EM are consistent with these findings. Thus, 41% of patients with CM in whom two or more prior preventive medications failed had ≥ 50% reduction from baseline in mean number of MMD at 12 weeks when treated with erenumab-aooe 140 mg compared with 14% of patients receiving placebo (OR [95% CI]: 4.2 [2.2–7.9]) [111]. Similarly, in patients with EM in whom two or more prior preventive medications failed, 36% of patients treated with erenumab-aooe 140 mg had ≥ 50% reduction from baseline in mean number of MMD (averaged over months 4 to 6) compared with 11% of patients in the placebo group (OR [95% CI]: 4.5 [1.7–12.4]) [112].

Table 1

FDA-approved anti-CGRP and anti-CGRP-R mAb characteristics

Feature	Erenumab-aooe [116]	Fremanezumab-vfrm [117]	Galcanezumab-gnlm [118]	Eptinezumab-jjmr [118]
Target	CGRP-R	CGRP ligand	CGRP ligand	CGRP ligand
Source	Fully human	Humanized	Humanized	Humanized
Isotype	IgG2	IgG2	IgG4	IgG1
Half-life	28 days [152]	31 days	25–30 days [152]	27 days
Glycosylation	Glycosylated	Both	No information available	No information available
Formulation	Tris buffer or acetate buffer, and sorbitol or a suitable substitute	L-histidine, sucrose, PS80, EDTA	L-histidine, hydrochloride monohydrate, NaCl, PS80, and water	L-histidine, L-histidine hydrochloride monohydrate, PS80, sorbitol, and water
Viscosity	No information available	High	No information available	No information available
Administration route	Subcutaneous	Subcutaneous	Subcutaneous	Intravenous
Administration dose and frequencya	70 mg, 140 mg QM	225 mg, QM 675 mg, Q3M	240 mg initial dose then 120 mg QM	100 mg Q3M; some patients may benefit from 300 mg Q3M
Adverse events	Injection-site reactions, hypersensitivity reactions (rash, swelling/edema, urticaria), constipation, cramps/muscle spasms, pruritus	Injection-site reactions (pain, induration, erythema, pruritus, rash)	Injection-site pain, injection-site reactions, vertigo, constipation, pruritus, hypersensitivity reactions (rash, urticaria, dyspnea)	Hypersensitivity reactions, (angioedema, urticaria, facial flushing, rash)

CGRP calcitonin gene-related peptide, CGRP-R CGRP receptor, EDTA ethylenediaminetetraacetic acid, FDA US Food and Drug Administration, IgG immunoglobulin G, mAb monoclonal antibody, PS polysorbate, Q3M every 3 months, QM monthly

aDoses and frequencies studied in registrational trials

Fig. 6

mAbs targeting CGRP or CGRP-R. CGRP-R signaling may be reduced by mAbs that target either CGRP or the CGRP-R. Although the CGRP-R is depicted as a CLR-RAMP1 complex, it is not known if all CGRP binding sites are formed by this complex. The CGRP-responsive receptor AMY1 has been found in the trigeminal ganglion and brainstem, although a role of AMY1 in migraine has not been confirmed [50]. AMY amylin receptor, CGRP calcitonin gene-related peptide, CGRP-R CGRP receptor, CLR calcitonin-like receptor, mAb monoclonal antibody, RAMP receptor activity-modifying protein

Table 2

Efficacy of FDA-approved mAbs in clinical trials for prevention of migraine

Name	Dose	Primary endpoint	Efficacy outcome, mean change
Erenumab-aooe
STRIVE [135] (EM)	70 mg SC QM for 24 weeks 140 mg SC QM for 24 weeks	Monthly migraine days (change from baseline to months 4 through 6)	Active (n = 312) − 3.2 (SE 0.2) days; p < 0.001 Active (n = 318) − 3.7 (SE 0.2) days; p < 0.001 Placebo (n = 316) − 1.8 (SE 0.2) days
ARISE [136] (EM)	70 mg SC QM for 12 weeks	Monthly migraine days (change from baseline in the last 4 weeks of the trial)	Active (n = 282) − 2.9 (SE 0.2) days; p < 0.001 Placebo (n = 288) − 1.8 (SE 0.2) days
Phase 2 in EM [153]	7 mg SC QM for 12 weeks 21 mg SC QM for 12 weeks 70 mg SC QM for 12 weeks	Monthly migraine days (change from baseline in the last 4 weeks of the trial)	Active 7 mg (n = 107) − 2.2 (SE 0.4) days; p = NS Active 21 mg (n = 102) − 2.4 (SE 0.4) days; p = NS Active 70 mg (n = 104) − 3.4 (SE 0.4) days; p = 0.021 Placebo (n = 153) − 2.3 (SE 0.3) days
Phase 2 in CM [154]	70 mg SC QM for 12 weeks 140 mg SC QM for 12 weeks	Monthly migraine days (change from baseline in the last 4 weeks of the trial)	Active 70 mg (n = 191) − 6.6 (SE 0.4) days; p < 0.0001 Active 140 mg (n = 190) − 6.6 (SE 0.4) days; p < 0.0001 Placebo (n = 286) − 4.2 (SE 0.4) days
Fremanezumab-vfrm
Phase 3 in EM [155]	225 mg SC QM for 12 weeks 675 mg SC Q3M for 12 weeks	Monthly migraine days (change during the 12-week trial period, after first dose)	Active (n = 287) − 3.7 (95% CI − 4.15 to − 3.18) days; p < 0.001 Active (n = 288) − 3.4 (95% CI − 3.94 to − 2.96) days; p < 0.001 Placebo (n = 290) − 2.2 (95% CI − 2.68 to − 1.71) days
Phase 3 in CM [156]	675 mg SC at baseline and 225 mg SC QM for 12 weeks 675 mg SC Q3M for 12 weeks	Monthly migraine days (change during the 12-week trial period, after first dose)	Active 675 mg + 225 mg (n = 375) − 4.6 (SE 0.3) days; p < 0.001 Active 675 mg (n = 375) − 4.3 (SE 0.3) days; p < 0.001 Placebo (n = 371) − 2.5 (SE 0.3) days
Galcanezumab-gnlm
EVOLVE-1 [157] (EM)	120 mg SC QM for 6 months	Monthly migraine days (change from baseline during the treatment period)	Active (n = 210) − 4.7 (error NR) days; p < 0.001 Placebo (n = 425) − 2.8 (error NR) days
EVOLVE-2 [158] (EM)	120 mg SC QM for 6 months	Monthly migraine days (change from baseline during the treatment period)	Active (n = 231) − 4.3 (SE 0.3) days; p < 0.001 Placebo (n = 461) − 2.3 (SE 0.2) days
REGAIN [159] (CM)	120 mg SC QM for 6 months	Monthly migraine days (change from baseline during the 3-month double-blind treatment period)	Active (n = 273) − 4.8 (SE 0.4) days; p < 0.001 Placebo (n = 538) − 2.7 (SE 0.4) days
Eptinezumab-jjmr
PROMISE-1 [142] (EM)	30 mg IV Q3M for up to four administrations 100 mg IV Q3M for up to four administrations 300 mg IV Q3M for up to four administrations	Monthly migraine days (change from baseline during weeks 1–12)	Active 30 mg (n = 223) − 4.0 (95% CI − 4.41 to − 3.61) days; p = 0.0046a Active 100 mg (n = 221) − 3.9 (95% CI − 4.28 to − 3.47) days; p = 0.0182 Active 300 mg (n = 222) − 4.3 (95% CI − 4.70 to − 3.90) days; p = 0.0001 Placebo (n = 222) − 3.2 (95% CI − 3.60 to − 2.79) days
PROMISE-2 [143] (CM)	100 mg IV Q3M for two administrations 300 mg IV Q3M for two administrations	Monthly migraine days (change from baseline during weeks 1–12)	Active 100 mg (n = 356) − 7.7 (error NR) days; p < 0.0001 Active 300 mg (n = 350) − 8.2 (error NR) days; p < 0.0001 Placebo (n = 366) − 5.6 (error NR) days

CI confidence interval, CM chronic migraine, EM episodic migraine, FDA US Food and Drug Administration, IV intravenous, mAb monoclonal antibody, NR not reported, NS nonsignificant, Q3M every 3 months, QM monthly, SC subcutaneous, SE standard error

aNot statistically significant per hierarchy testing

CM defined as ≥ 15 days/month in all trials; EM defined as 4–14 migraine days/month except in fremanezumab-vfrm trials in which it was defined as < 15 days/month

Results from a postmarketing study in 78 patients with EM and CM demonstrated erenumab-aooe (70 mg) to be highly effective and well tolerated. In the EM patient group, a reduction of 3.8 MMD was reported at 4 weeks compared with baseline; in the CM patient group, reductions of 12.2 and 15.0 MMD from baseline were reported at 4 and 8 weeks, respectively [113]. Furthermore, in a real-world cohort of 65 individuals with severe migraine, a reduction in MMD of ≥ 50% was commonly observed in 40–50% of individuals within different patient subgroups when treated with erenumab-aooe. The cohort included patients who would have been excluded from randomized controlled trials (i.e., those with more chronic, frequent, severe, and refractory migraine). For example, subgroups included patients with CM of duration > 10 years, patients in whom > 3 prophylactic medications had failed, and patients scoring > 60 on the six-item Headache Impact Test [114].

Initial results (6 months) from a 1-year open-label extension trial in 312 patients treated with fremanezumab have also been reported. Patients with EM taking monthly doses of fremanezumab experienced reductions in MMD from 8.9 at baseline to 5.3 at 12 weeks and 4.0 at 6 months; patients on quarterly doses reported decreases in MMD from 9.2 at baseline to 5.3 at 12 weeks and 4.2 at 6 months. Patients with CM taking monthly doses of fremanezumab reported a decrease in MMD from 16.2 at baseline to 11.4 at 12 weeks and 8.3 at 6 months; patients on quarterly doses experienced reductions in MMD from 16.4 at baseline to 11.9 at 12 weeks and 9.9 at 6 months [115].

Overall, mAbs have long elimination half-lives, approximately 27–31 days for the mAbs approved for the treatment of migraine [116-118]. Physiological antibody concentrations are maintained, at least in part, by the neonatal fragment crystallizable receptor, which protects mAbs and other immunoglobulin G molecules from lysosomal degradation, providing a salvage pathway that returns approximately two-thirds of immunoglobulin antibodies to the cell surface, the remainder being degraded [119].

Although the immunogenic potential of therapeutic antibodies is reduced by humanization, erenumab-aooe is the only fully human antibody [26]. Further differentiating erenumab-aooe from the ligand-targeted mAbs is the fact that those are CGRP-release dependent, whereas receptor-targeted strategies are release independent. It may be that, for migraine prevention, receptor-targeted strategies will provide a more sustained modulation of CGRP-R signaling than ‘waiting’ for ligand release to drive a feed-forward cycle.

CGRP expression is increased in RAMP1-deficient mice [120]. Conversely, CGRP-R expression is elevated in α-CGRP knockout mice [121]. Thus, upregulation of CGRP-R or AMY1 expression might be anticipated in response to chronic ligand depletion or receptor blockade in humans. If this occurs and receptor density increases, the observed efficacy of CGRP-R-targeted mAbs may increase over time because receptors remain saturated. The binding of antibodies to CGRP or to CGRP-R may result in the formation of distinct receptor conformations that signal through unique pathways (novel signaling bias), although this requires further investigation [122].

CGRP Receptor Signaling Monoclonal Antibody Safety

Given the widespread role of CGRP, it might be expected that CGRP-R signaling blockade could result in safety concerns; however, the clinical trial data for anti-CGRP and anti-CGRP-R mAbs showed only mild drug-related adverse events, including injection-site reactions, hypersensitivity reactions (such as erythema or pruritus), and constipation (Table 1) [116-118]. Analysis of 5-year data from patients with EM participating in an open-label extension after a 12-week double-blind phase showed no new safety signals and no increase in the incidence of adverse events or of serious adverse events with longer-term erenumab-aooe use compared with the double-blind treatment phase [110]. A pooled analysis of four double-blind randomized trials and their extension studies in 2375 patients who received at least one dose of erenumab-aooe (70 mg or 140 mg; cumulative exposure, 2641 patient-years) found that erenumab-aooe had a favorable and stable adverse event profile for over 3 years in patients with EM or CM. Exposure-adjusted adverse event rates with erenumab-aooe were similar to placebo during the double-blind phase, except injection site-reactions (17.1 vs. 10.8 per 100 patient-years), constipation (7.0 vs. 3.8 per 100 patient-years), and muscle spasm (2.3 vs. 1.2 per 100 patient-years). Adverse events reported during the long-term extensions were similar to those in the double-blind treatment phase, and rates of injection-site reactions, constipation, and muscle spasm were lower [123].

Furthermore, studies have explored any potential cardiovascular impact of erenumab-aooe. No differences between erenumab-aooe and placebo were observed for any endpoint during treadmill testing or the 12-week safety follow-up in a clinical trial of patients with ischemic cardiovascular disease [124], nor were any differences in arterial blood pressure observed in healthy volunteers in a placebo-controlled study of concomitant administration of erenumab-aooe and sumatriptan [125]. The cardiovascular, cerebrovascular, and peripheral vascular safety of erenumab-aooe in patients with CM or EM was investigated in a pooled analysis of four double-blind, placebo-controlled studies and their open-label extensions. A total of 2443 patients were included; of these, 1043 received placebo, 893 erenumab-aooe 70 mg, and 507 erenumab-aooe 140 mg. The incidence of vascular adverse events was similar between placebo and erenumab-aooe over 12 weeks, and the emergence of adverse events did not increase over time (up to 256 weeks) [126]. The lack of cardiovascular adverse effects associated with CGRP-R blockade suggests redundancy in the CGRP-R system (both CGRP and amylin bind to AMY1 with high affinity) or compensatory vasodilatory mechanisms [124, 127, 128]. However, the potential for cardiovascular adverse effects following CGRP ligand blockade cannot be ruled out based on results from these studies alone. Development of hypertension and worsening of pre-existing hypertension have been reported following the use of erenumab-aooe in the postmarketing setting. Many of these patients had pre-existing hypertension or risk factors for hypertension. In most cases, the onset or worsening of hypertension was reported after the first dose and were more frequently reported within seven days of dose administration although they could occur at any time during treatment. There were cases of hypertension requiring pharmacological treatment and, in some cases, hospitalization. Per the Aimovig (erenumab-aooe) US Prescribing Information, patients treated with erenumab-aooe should be monitored for new-onset or worsening of pre-existing hypertension and treatment discontinuation considered if an alternative etiology cannot be established [116].

Approved anti-CGRP-R signaling mAbs are administered by subcutaneous injection, via autoinjectors (erenumab-aooe and galcanezumab-gnlm), prefilled syringe (fremanezumab-vfrm), or intravenous infusion (eptinezumab-jjmr) [116–118, 129]. Injection-site reactions after subcutaneous administration are common, resulting in localized pain, pruritus, and erythema [130], and rates appear to be higher with fremanezumab-vfrm and galcanezumab-gnlm than with erenumab-aooe, with 26–30%, 6–21%, and 3–6% of patients, respectively, reporting injection-site pain in Phase 3 trials [116-118]. Fewer injection-site reactions with erenumab-aooe, together with the availability of an autoinjector, may have a positive effect on adherence, although this will need confirmation in dedicated studies. Reactions may be linked to the immunogenicity of the drug or excipients such as polysorbate-related activation of complement or reactive degradation products [131]. Additionally, drug volume, viscosity, sugar concentration, pH, and having L-histidine as an excipient may all contribute to the variability of injection-site reactions.

CGRP may have a role in regulating uteroplacental blood flow, other vascular adaptations during pregnancy, and relaxation of uterine smooth muscle, resulting in potential complications in pregnancy [132]. However, to date, no adverse effects have been observed on pregnancy in rats and rabbits (fremanezumab-vfrm, galcanezumab-gnlm, and eptinezumab-jjmr), or monkeys (erenumab-aooe) following anti-CGRP-R signaling mAb administration at doses higher than used clinically [116–118, 129].

The gastrointestinal tract is highly innervated by enteric neurons expressing CGRP, which is thought to affect intestinal blood flow, smooth muscle relaxation, and slow wave amplitude [133, 134]. Constipation was reported as an adverse event in erenumab-aooe clinical trials in 1–3% of patients [116, 135], and constipation rates did not increase with longer-term treatment (≤ 5 years) [110]. Suspected cases of constipation with serious complications have been observed in a postmarketing setting, although the incidence has not been reported [116]. For context, no cases of serious constipation were reported with erenumab-aooe during Phase 3 trials, which accumulated over 300 person-years [135, 136]. An incidence of serious constipation in people initiating migraine treatment of 0.63 per 100 person-years has been reported [137]. It is important to monitor and to manage patients receiving erenumab-aooe as clinically appropriate if cases of constipation with serious complications occur [116], although these cases are likely to be uncommon. Constipation is also now listed as a side effect of galcanezumab [138], implying that constipation may be a class effect. This side effect is consistent with preclinical studies showing that CGRP causes diarrhea in mice [139]. None of the approved CGRP-R and CGRP ligand mAbs are contraindicated in patients with impaired hepatic or renal function, and such impairment is not expected to alter the pharmacokinetics of the drugs [116-118]. The lack of any hepatotoxic effects in this drug class is in sharp contrast to those effects observed with repeated exposure to certain early gepants [23].

A known phenomenon of therapeutic antibodies is the development of neutralizing antibodies [140]. Pooled data from erenumab-aooe clinical trials showed that only a small proportion of patients developed anti-erenumab-aooe-binding antibodies (70 mg, 6.3% [56/884]; 140 mg, 2.6% [13/504]), only three of whom had neutralizing antibodies. By the end of the study, > 50% of patients who developed binding antibodies reverted to negative status and the mean change in MMD did not appreciably differ between patients who did or did not develop anti-erenumab-aooe-binding antibodies [141]. Furthermore, anti-erenumab-aooe-binding antibodies had no impact on safety, and the concentrations of erenumab-aooe overlapped with those of patients who were antibody negative [141]. In placebo-controlled studies of galcanezumab-gnlm, 4.8% of patients (33/688) developed anti-drug antibodies [118]; in a 12-month open-label trial, 12.5% of patients (16/128) developed anti-drug antibodies, most of which were neutralizing [118]. For fremanezumab-vfrm, placebo-controlled trials revealed that 0.4% of patients (6/1701) developed anti-drug antibodies, while in an ongoing open-label study, 1.6% of patients (30/1888) developed anti-drug antibodies [117]. In patients receiving eptinezumab 100 mg or 300 mg every 3 months in Phase 3 trials (PROMISE-1 and PROMISE-2), the incidence of anti-eptinezumab antibodies was 20.6% (92/447) in PROMISE-1 (up to 56 weeks) and 18.3% (129/706) in PROMISE-2 (up to 32 weeks) [129, 142, 143]. The impact of neutralizing antibody development on clinical efficacy has not been shown.

Drug-drug interactions are unlikely to occur between mAbs and other medications, because mAbs are degraded into peptides or amino acids, although the potential for issues arising with concomitant treatment with mAbs and other preventive therapies for migraine is not known. Additionally, it is unknown if there are issues with switching between receptor- and ligand-binding CGRP mAbs [140].

Future Directions for Monoclonal Antibodies for Migraine

Migraine presents with an abundance of non-pain signs and symptoms. Patients receiving anti-CGRP-R signaling treatments commonly experience improvements in other neurological abnormalities of migraine, including reduced sensory aura and improved cognition. However, no longitudinal data are available to indicate the long-term effects (e.g., rebound pain, disease modification) of anti-CGRP-R signaling mAbs [128]. Since the introduction of these agents, patients increasingly mention that the ‘brain fog’ associated with migraine has lifted, with many remarking that this change is more noticeable between than during attacks.

Anti-CGRP-R signaling mAbs are likely to be used effectively in combination with other migraine-preventive treatments, which have different molecular targets. Anti-CGRP-R signaling mAbs might be expected to decrease signaling between attacks, protecting against trigeminal nerve hypersensitivity, although longitudinal studies are required to demonstrate this. Additionally, although there is some evidence that the integration of anti-CGRP-R signaling mAbs may reduce the use of acute migraine treatments [144], further research is needed to evaluate the efficacy and safety of these mAbs in combination with other standard-of-care medications. Further to this, a post hoc analysis has been performed on erenumab-aooe Phase 2 trial data in patients with CM and medication overuse in whom preventive treatment had previously failed. Erenumab-aooe reduced the number of MMD and moderate-severe headache days, reduced the use of acute migraine medication, and increased the proportion of patients achieving nonmedication overuse status versus placebo [144]. Moreover, in a Phase 3 trial, fremanezumab-vfrm reduced the number of days of acute headache medication use over a 12-week period versus placebo in patients with medication overuse at baseline [145]. It will also be necessary to assess anti-CGRP-R signaling mAbs in children, adolescents, during pregnancy, and in similar headache conditions [146].

It has been shown that lower injection frequency and increased efficacy are key drivers of patient adherence [147]. Efficacious mAbs with relatively infrequent dosing may therefore be well received by some patients compared with small molecules or botulinum toxin type A, based on their frequency of administration or number of injections per dose (31–39 injections/dose for botulinum toxin type A) [148]. Further studies on adherence in a real-world setting are needed.

The involvement of other receptors and pathways (such as AMY1, the pituitary adenylate cyclase-activating peptide system, the serotonin-5-HT1F receptor, purinergic receptors, hyperpolarization-activated cyclic nucleotide-gated channels, adenosine triphosphate-sensitive potassium channels, and the glutaminergic system [149]) and the potential for treatments that work synergistically (such as concomitant small-molecule CGRP-R antagonists and CGRP-based mAbs [150]) could also be assessed. Approved anti-CGRP-R signaling mAbs are effective for approximately 50% of patients [116–118, 129] and may encourage future development of centrally and peripherally acting CGRP drugs. Combining medications that have peripheral effects with treatments that target central processes may be a good combination therapy approach for migraine control.

Conclusion

There is an unmet need for preventive migraine therapies, and targeting CGRP-R signaling offers much potential. Several mAbs that target the CGRP-R or ligand are approved by the FDA and have proven to be efficacious and well tolerated in pivotal clinical trials. These migraine-specific treatments may help patients who are hypervigilant and to reduce allostatic load. Further evidence is required to determine if there are any real-world differences between ligand- and receptor-targeted therapies and to optimize their use. It will be interesting to discover to what degree these therapies are disease-modifying and, if so, whether this results from an ability to modulate allostatic load.

Migraine is a common neurological disorder affecting approximately 14% of the population. There is an unmet need for new therapeutics because many patients do not respond to treatment.

Calcitonin gene-related peptide (CGRP) plays a key role in migraine pathogenesis, and recent therapeutic advances are based around targeting CGRP or its canonical receptor (CGRP-R).

Individuals affected by migraine have a reduced threshold for central sensitization: this is known as hypervigilance. The combination of central sensitization and migraine triggers (allostatic load) results in migraine attacks. Repeated migraine attacks, which involve the release of CGRP to facilitate peripheral and central sensitization, probably contribute to increased allostatic load.

In this review, the evidence supporting the role of CGRP in migraine is evaluated, including its role in the sensitization of peripheral and central neurons of the trigeminovascular system as well as its implication for hypervigilance and allostatic load.

By inhibiting the release of pro-inflammatory molecules within the trigeminal ganglion and/or the dura and, therefore, reducing peripheral sensitization, anti-CGRP monoclonal antibodies (mAbs) might indirectly diminish central sensitization, reduce allostatic load, and contribute to migraine regression.

Use of anti-CGRP and anti-CGRP-R mAbs for the treatment of migraine is promising. A summary of the latest mAb clinical trials and real-world data provides an overview of the therapeutic landscape, including erenumab-aooe, galcanezumab-gnlm, fremanezumab-vfrm, and eptinezumab-jjmr, which are approved by the US Food and Drug Administration (FDA) for the preventive treatment of migraine.

An update is also provided on clinical trials involving small-molecule CGRP receptor antagonists known as gepants, including ubrogepant and rimegepant, which were recently approved by the FDA for the acute treatment of migraine with or without aura in adults, and two additional therapeutic candidates (atogepant and zavegepant [formerly vazegepant]), which remain in development.