Asenapine monotherapy in the acute treatment of both schizophrenia and bipolar I disorder.

Asenapine is a new atypical antipsychotic agent currently under development for the treatment of schizophrenia and bipolar disorder. It has high affinity for various receptors including antagonism at 5HT(2A), 5HT(2B), 5HT(2C), 5HT(6) and 5HT(7) serotonergic receptor subtypes, alpha(1A), alpha(2A), alpha(2B) and alpha(2C) adrenergic and D(3) and D(4) dopaminergic receptors. As with other atypicals, asenapine exhibits a high 5HT(2A):D(2) affinity ratio. Although similar to clozapine in its multi-target profile, it shows no appreciable affinity for muscarinic receptors. Asenapine has shown efficacy in alleviating both positive and negative symptoms of schizophrenia compared with placebo. Although promising, further studies are required in order to determine whether it has advantages over placebo and other antipsychotics in alleviating cognitive impairment associated with schizophrenia. It has also shown long-term efficacy comparable with olanzapine in bipolar I disorder. Asenapine is generally well tolerated and appears to be metabolically neutral. It has low propensity to cause weight gain and prolactin elevation. There were no concerns in the studies about its effects on the cardiovascular system and QTc prolongation. The incidence of extrapyramidal symptoms with asenapine however has been found to be higher than that with olanzapine. It may be a useful alternative to aripiprazole in schizophrenia and bipolar disorder in patients who are at high risk of metabolic abnormalities.

Introduction

Schizophrenia

The symptoms of schizophrenia are thought to result from the dysfunction of several neurotransmitters mainly dopamine1 and serotonin2 although noradrenaline, acetylcholine and glutamate have also been implicated.3 The multidimensional facet of the disorder means that life-long therapeutic intervention with psychotropic agents and principally antipsychotics is often warranted. Although the specific mechanism of action of antipsychotics is still not fully understood, the antagonism of dopamine transmission is likely to play a major role. The dopamine system affects the mesolimbic, striatal and cortical areas of the brain. Neurones in the midbrain release dopamine which interacts with dopamine receptors. Antipsychotics block dopaminergic transmission by binding to these dopamine receptors, in particular D2 receptors, the affinity for which correlates with the clinical dose in many cases.4

The history of antipsychotic drug development has been haphazard. In 1952, the accidental use of chlorpromazine revolutionized the treatment of schizophrenia. In the following years, several other first-generation or typical antipsychotics were launched and although this group of antipsychotic agents were effective in managing the positive symptoms of schizophrenia, they demonstrated relatively poor efficacy for negative symptoms and associated cognitive impairment. Typical antipsychotics have also been associated with severe and devastating extrapyramidal symptoms (EPS)5 and tardive dyskinesia,6 thus limiting their long-term use. In addition, adverse effects relating to elevation in serum prolactin7 also made their use problematic. It is thought that the blockade of dopamine D2 receptors is responsible for the antipsychotic-induced movement disorders and rise in prolactin.4

The introduction of second generation, or atypical antipsychotics, over the last 20 years has contributed considerably to the advancement in the treatment of schizophrenia, both in terms of scope of efficacy and more favorable tolerability in some respects. Atypical antipsychotics have demonstrated clinical effectiveness comparable to that with typical antipsychotics with regards to positive symptoms8 and are argued to be more effective in the management of negative symptoms9,10 and cognitive impairment.11,12 Moreover, they are associated with a significantly lower incidence of EPS.13 As a result, atypicals quickly replaced the older typical antipsychotics and for many years they were considered the treatment of choice in the management of schizophrenia.14

The atypical antipsychotic clozapine which was actually synthesized shortly after chlorpromazine in the 1950s, has a unique pharmacological profile in view of its affinity for a diverse range of receptors. These include D1, D2 and D4 dopaminergic, α1 and α2 adrenergic, H1 histaminergic and muscarinic receptors as well as various serotonin receptor subtypes.15 Consequently, clozapine has unique properties in the prevention of suicide16 and treatment-refractory schizophrenia (TRS),17 although there has been some suggestion that other antipsychotics such as olanzapine may also be effective in TRS at higher than typically prescribed doses.18 In addition to clozapine’s superior efficacy profile, it has a more favorable motor system side effect profile, with minimal risk of causing EPS or tardive dyskinesia.19 Its use however is somewhat limited by its potential to cause neutropenia and agranulocytosis,20 of possibly fatal consequence if it were not for the strict haematological monitoring requirements which are obligatory with the use of clozapine.

Several hypotheses have been put forward to explain the differences in clinical and adverse effect profiles between typical and atypical antipsychotic drugs. It has been suggested that atypical drugs have a stronger 5HT2A receptor affinity compared with that for the D2 receptor21 leading to their lower propensity to cause EPS and prolactin elevation. This hypothesis, however, has been challenged with the suggestion that the “atypicality” of atypical agents is actually due to the fast dissociation from the D2 receptor, resulting in transient and easily reversible occupancy of this receptor.22 In addition, the fact that atypicals have a moderate D2 receptor occupancy23 compared with typicals has also been proposed as an explanation for their different profiles.

However, despite atypicals having shown more favorable tolerability for movement disorders and prolactin-related adverse effects, other serious safety concerns have surfaced over the years with certain agents in this class. Metabolic24 and cardiovascular disease25 including weight gain, increased plasma lipids, new onset diabetes, prolongation of QTc interval and sudden death are the most concerning adverse effects of atypical agents, which were once considered relatively safe.

In the last decade, drug development in the field of schizophrenia has slowed somewhat, with the only advancement having been the introduction of the dopamine partial agonist, aripiprazole. Dopamine partial agonists are thought to exert their effects by acting as dopamine antagonists in the mesolimbic system where there is a high concentration of dopamine, however, in the mesocortical system where reduced dopamine activity is thought to produce negative symptoms and cognitive impairment, they act as dopamine agonists, thus the concept of dopamine system stabilization.26,27 Since the launch of aripiprazole in 2004, no new antipsychotics have emerged on the market.

Bipolar disorder

The complexities of managing bipolar disorder are numerous. Firstly, the diagnostic criteria used for diagnosing bipolar disorder by psychiatrists in different parts of the world varies, resulting in a lack of clear distinction between schizophrenia and bipolar disorder thus influencing the management of the condition worldwide. Secondly, different treatments need to be considered separately for the specific manic, hypomanic, mixed and depressive episodes in addition to whether control of the acute state or maintenance of therapy is required. Furthermore, the pathogenesis and neurochemistry of bipolar disorder remains unclear, although serotonergic, noradrenergic and dopaminergic transmitter systems appear to be targeted during therapy.

For over 50 years, traditional mood stabilizers such as lithium have been the mainstay of therapy in bipolar disorder. However, increasingly atypical antipsychotics are also establishing themselves, with several agents having received regulatory approval for use in both bipolar depression and mania.

Of the atypicals, olanzapine28 and quetiapine29 have shown significantly greater efficacy than placebo in the treatment of bipolar depression. Both agents are known to antagonize 5HT2A receptors as well as D2 receptor blockade. Their antagonistic effects on 5HT2A receptors, which are present on presynaptic dopamine neurons, are thought to lead to an increase in dopamine levels in the prefrontal cortex. It would appear therefore that a selective balance between dopamine and serotonin in specific regions of the brain is necessary in order to stabilize mood. In addition, quetiapine’s metabolite N-desalkylquetiapine, has been shown to be a potent noradrenaline re-uptake inhibitor and partial 5HT1A agonist, also contributing to its antidepressant activity.30 Furthermore, olanzapine also exhibits potent antagonistic activity at α1 adrenergic receptors leading to substantial increases in the firing neurons in the locus ceruleus with resulting increase in noradrenaline release in the prefrontal cortex.31

Atypicals are generally thought to owe their antimanic properties to their antagonism at dopamine receptors, although it is believed that antagonism at α1 adrenergic, H1 histaminergic and serotonergic receptors may also play a role. However, unlike with bipolar depression, the importance of blocking 5HT2A serotonergic receptors in the treatment of mania is still unclear.32

Asenapine

Pharmacology and mode of action

Asenapine is novel pharmacological agent currently under clinical development for the treatment of schizophrenia and bipolar disorder. This new antipsychotic has high affinity for a number of receptors including antagonism at 5HT2A, 5HT2B, 5HT2C, 5HT6 and 5HT7 serotonergic receptor subtypes, α1A, α2A, α2B and α2C adrenergic and D3 and D4 dopaminergic receptors. As with atypical antipsychotics, asenapine also exhibits an appreciable affinity for D2 receptors with a high 5HT2A: D2 affinity ratio. Although similar to clozapine in its high affinity for a variety of different receptors, it has no appreciable affinity for muscarinic receptors, with the highest ratio of separation existing for its affinity for D2: M1, M2, M3 and M4 receptors.33

The multi-target nature of this new atypical antipsychotic agent has led to certain expectations for both its efficacy and tolerability. The higher affinity of asenapine for 5HT2A receptors relative to D2 receptors gives it its “atypicality” as it is an important mechanism thought to be responsible for enhanced efficacy of antipsychotics and reduced potential to cause EPS.34,35 In addition, antagonism at 5HT2A receptors, leading to an increase in dopamine activity in the prefrontal cortex, has also been suggested as a possible mechanism for alleviating negative symptoms2,35 and enhancing cognition36 in schizophrenia and other disorders. Findings from rat studies deduced that asenapine causes a dose-dependent increase in cortical37 and hippocampal dopamine37, noradrenaline38 and acetylcholine38 comparable to previous reports with clozapine and quetiapine. Similarly, the 5HT2C receptor may also have a similar role as 5HT2A and its antagonism has been linked to improvement in negative symptoms.39 Therefore, the combined antagonism at 5HT2A and 5HT2C which occurs with asenapine may prove promising for the management of negative symptoms.

The resulting clinical effects of a high affinity for other serotonin receptor subtypes such as 5HT6 and 5HT7 are still unclear. Emerging evidence however suggests that 5HT6 antagonism may afford benefits for cognition40 and that 5HT7 antagonism may confer benefits for anxiety management and mood regulation as well as cognition.41 Such claims with asenapine however remain to be explored further.33 Similarly, activity at α-adrenergic receptors has also been suggested to improve negative and cognitive symptoms by antagonism of α2 receptors, whereas improvement in positive symptoms is via α1 receptor antagonism.42 Since asenapine appears to have relatively high affinity for adrenergic receptors, and more specifically α2 receptors43, it may potentially offer these therapeutic benefits.

Data from preclinical studies also suggests that antagonism at D3 receptors may help ameliorate negative and cognitive symptoms,44 although again the clinical evidence with asenapine for this is still lacking. Indeed, in animal models, asenapine did not improve cognition in rats, but rather, at doses greater than those required for antipsychotic activity, it impaired cognitive performance due to disturbance of motor function.45 This effect has also been observed with both olanzapine and risperidone. In contrast, in studies with monkeys, asenapine produced substantial improvement in executive functions which were maintained across a period of long-term dosing.46 Further studies in rat brain have indicated that chronic treatment with asenapine exerts regional and dose-dependent effects on inotropic glutamate receptors,47 thus another potential mechanism for its effectiveness in schizophrenia.

Since olanzapine and clozapine’s high muscarinic receptor binding affinity is thought to be responsible for contributing to their anticholinergic adverse effects and potentially causing metabolic syndrome (via M3 antagonism),48 asenapine’s minimal antimuscarinic activity means that it may therefore be less likely to cause these effects.33 In the animal models, asenapine induced a marked increase in dopamine in the nucleus accumbens compared to the core region, sharing a similar profile to other atypical antipsychotics. In addition, results from microdialysis and electrophysiological techniques found that asenapine potentiates prefrontal dopaminergic as well as glutaminergic transmission, indicating a highly potent antipsychotic activity with very low propensity for EPS.49 Whether this receptor binding profile and related pharmacology of asenapine will actually translate into such clinical benefits in practice still remains to be ascertained by ongoing studies in the management of schizophrenia and bipolar disorder.

Pharmacokinetics

Results from separate phase I studies assessing the pharmacokinetic interactions between asenapine and several cytochrome P450 (CYP) modulators and the glucuronyl transferase (UGT) inhibitor valproate found that asenapine exposure was increased by fluvoxamine but was otherwise minimally affected. Asenapine was found to have a maximum plasma concentration occurring at 0.5 to 1.5 hours after oral administration and an elimination half life of approximately 24 hours, following single dosing. In addition, there were no significant correlations between creatinine clearance and asenapine exposure in renal impairment. However, although mild or moderate hepatic impairment did not affect asenapine exposure, severe hepatic impairment increased exposure 7-fold. Furthermore, smoking was found not to affect exposure to asenapine therapy.50

Efficacy and safety studies in schizophrenia

In a 6-week, double-blind study investigating the efficacy and tolerability of asenapine in acute schizophrenia,51 patients were randomly assigned to receive twice daily doses of sublingual asenapine 5 mg, placebo or oral risperidone 3 mg. Results for the primary efficacy outcome measure, the Positive and Negative Syndrome Scale (PANSS) total score52 for the intention to treat population comprising 174 patients found mean changes at end point from baseline were −15.9 with asenapine, vs −5.3 with placebo (P < 0.005); the change with risperidone (−10.9) compared with placebo however was non-significant. Asenapine produced significantly greater decreases in PANSS total scores compared with placebo from week 2 onward.51

Secondary efficacy measures included the PANSS positive subscale, which showed mean changes at endpoint from baseline of −5.5 for asenapine vs −2.5 for placebo (P = 0.01) and −5.1 for risperidone (P < 0.05). Asenapine produced significant reductions in PANSS positive subscale scores from week 3 onward. PANSS negative score results showed mean changes at endpoint from baseline of −3.2 for asenapine vs −0.6 for placebo (P = 0.01) and a non-significant change of −1.05 with risperidone compared with placebo. Significant decreases in PANSS negative subscale scores were again seen with asenapine from week 3 onward. For Clinical Global Impression-Severity (CGI-S) scores,53 both active treatments were associated with significantly greater decreases in CGI-S scores from week 4 onward. At endpoint, mean changes from baseline were −0.74 for asenapine and −0.75 for risperidone vs −0.28 for placebo (P < 0.01 and P < 0.005 respectively). Overall, the main efficacy findings from this study suggest that asenapine 5 mg twice daily is superior to placebo in treating positive and negative symptoms of schizophrenia. Risperidone 3 mg twice daily, however, was superior to placebo in alleviating the positive symptoms but its effects on negative symptoms were non-significant compared with placebo,51 in contrast to previous studies showing significant improvements in negative symptoms with risperidone.10,54

In the same study,51 investigations into the safety and tolerability of asenapine found that 83% of patients assigned to the drug experienced at least 1 adverse event compared with 79% of patients assigned to placebo and 90% assigned to risperidone. The most frequently reported adverse events in the asenapine group were insomnia (11%), somnolence (11%), nausea (11%) and anxiety (10%).51

The incidence of clinically significant weight gain with asenapine was equivalent to that seen with placebo, whereas the incidence with risperidone was higher, in accordance with previous reports. Similarly, asenapine had minimal effects on prolactin and metabolic parameters. The proportion of patients with normal baseline prolactin levels but with post-baseline levels of ≥2 times the laboratory upper limit of normal (ULN) were 9%, 2% and 79% for asenapine, placebo and risperidone groups respectively. Similarly, post-baseline fasting glucose levels ≥20% above ULN were observed in 14%, 12% and 20% of patients assigned asenapine, placebo and risperidone respectively. Moreover, mean changes from baseline in total cholesterol were −0.4, −1.7 and +2.3 mmol/L and mean changes in fasting triglycerides were 0, −0.1 and 0 mmol/L for asenapine, placebo and risperidone groups respectively.51

Cardiovascular assessments found no clinically important differences between the groups with respect to blood pressure, heart rate and ECG changes.51

A further study examined the long-term safety of asenapine in patients with schizophrenia.55 The phase III, double-blind, 1-year-long trial included 1219 patients, randomly assigned (3:1 ratio) to asenapine 10 to 20 mg and olanzapine 20 to 40 mg a day. The 2 groups were comparable in terms of frequency of adverse events experienced (60% and 61% in asenapine and olanzapine groups respectively) and withdrawals due to serious adverse events (6.3% and 6.8% respectively).55

In contrast, differences were apparent with regards to incidence of EPS (18% vs 8%), mean weight gain (1.6 kg vs 5.6 kg) and significant weight gain of ≥7% of original body weight (14.7% vs 36.1%) for asenapine and olanzapine groups respectively. Cardiovascular assessments found that the incidence of QTcF (Fridericia’s correction formula) >500 ms or prolongation >60 ms was 0% and 0.3% for asenapine and olanzapine respectively. In addition, both groups showed small mean declines in prolactin levels and small mean changes were noted for fasting glucose, cholesterol and triglycerides.55

The effects of asenapine on cardiovascular parameters were compared with those for quetiapine and placebo in a 16-day multicenter, randomized, double-blind, parallel-group study of 148 patients with schizophrenia or schizoaffective disorder.56 Patients were randomized to one of the 4 following groups: asenapine 5 mg twice daily for 10 days then asenapine 10 mg twice daily for 6 days; asenapine 15 mg twice daily for 10 days then asenapine 20 mg twice daily for 6 days; quetiapine 375 mg twice daily for 16 days and placebo twice daily for 16 days.

Results showed no statistically significant differences between asenapine and quetiapine and no reports of QTc interval >500 ms in any patient in any group. In addition, there were no reports of QTc increase from baseline >60 ms with asenapine, although there was 1 with quetiapine 375 mg twice daily and 2 with placebo. Furthermore, exposure-response modeling depicted a small positive relationship between QTc and plasma levels of both asenapine and quetiapine. In summary, although doses of asenapine 30 mg and 40 mg a day (but not 10 mg) showed a significant QTc prolongation compared with placebo, this was comparable to the increase seen with quetiapine.56

The effects of asenapine on cognitive function were assessed in a 6-week randomized, double-blind placebo-and risperidone-controlled study of 180 patients with acute exacerbation of schizophrenia.57 Patients were assigned to fixed doses of asenapine 5 mg twice daily, risperidone 3 mg twice daily or placebo. Patients treated with asenapine demonstrated improvement on all cognitive tests related to verbal learning and memory which are important domains of cognitive function in schizophrenia. Overall, the effects size compared with placebo on most cognitive function measures, was greater with asenapine than with risperidone, although the authors concluded that further investigations were needed in order to confirm these results.57

Efficacy and safety studies in bipolar disorder

The efficacy of asenapine in bipolar I disorder was evaluated in two 3-week multinational, randomized, double-blind, placebo- and olanzapine-controlled trials in patients with manic or mixed episodes associated with bipolar I disorder.58 A total of 976 patients was randomly assigned in a 2:2:1 ratio to flexible-dosing of asenapine 10 mg twice daily (adjustable to 5 mg twice daily), olanzapine 15 mg daily (adjustable to 5 to 20 mg daily) or placebo treatment. Results from these 2 studies found that the lean squares (LS) mean change in Young Mania Rating Scale (YMRS)59 score from baseline to day 21 were significantly greater (all P < 0.05) with asenapine (−14.2 and −13.1) and olanzapine (−16.1 and −13.9) than placebo (−10.8 and −7.4) in the 2 studies respectively. The active agents demonstrated superiority as early as day 2 of treatment.58

Asenapine was well tolerated in both studies and caused low incidence of weight gain. In the all-treated population, the incidence of clinically significant weight gain was reported as 7% and 6% for asenapine, 19% and 13% for olanzapine and 1.2% and 0% for placebo in the 2 studies respectively.58

Following these 2 trials, a subsequent 9-week double-blind extension study60 was carried out comprising patients who had completed the initial 3-week phase. In addition, those who completed the 9-week extension period were also screened for an additional 40-week extension, focusing on safety of asenapine, thus bestowing a total treatment period of 1 year. Flexible doses of asenapine 5 to 10 mg twice daily or olanzapine 5 to 10 mg daily were initiated at the maintenance dosages used in the initial 3-week phase. The efficacy of asenapine was assessed using the mean change from baseline in YMRS total score which was −24.4 with asenapine vs −23.9 with olanzapine. Inferential analysis indicated that asenapine was not inferior to olanzapine (P < 0.0001). This comparable efficacy was maintained throughout the 40 week extension phase. In addition, more than 90% of patients showed response (YMRS total score reduced by ≥50%) or remission (total score ≤12) in both groups, and rates for completion and discontinuation were similar between the groups.60

In terms of safety, incidence rates of treatment-related adverse events were 65.7% for asenapine and 61.7% for olanzapine. Although prolactin elevation, weight gain and metabolic syndrome were more common in the olanzapine group, EPS were more common with asenapine.60

For a comparison of asenapine’s adverse effects with other antipsychotics, see Table 1.

Table 1

Adverse effects of asenapine compared with other antipsychotics

Drug	QTc prolongation	Sedation	Weight gain	Diabetes	Extrapyramidal effects	Anti-cholinergic effects	Prolactin elevation
Amisulpride	+	−	+	+	+	−	+++
Aripiprazole	−	−	+/−	−	+	−	−
Asenapine	+	+	+/−	−	+	−	+/−
Chlorpromazine	++	+++	++	++	++	++	++
Clozapine	+	+++	+++	+++	−	+++	−
Haloperidol	+	+	+	+	+++	−	+++
Olanzapine	+	++	+++	+++	+/−	+	+
Quetiapine	++	++	++	++	−	−	−
Risperidone	+	+	++	++	+	+	+++
Sulpiride	+	−	+	+	+	−	+++
Ziprasidone	++	+	+/−	−	+/−	−	+/−

Abbreviations:+++, high incidence/severity; ++, moderate incidence/severity; +, low incidence/severity; −, very low incidence/severity. Adapted from The Maudsley Prescribing Guidelines 10th Edition.61

Conclusions and place in therapy

Whilst there are a variety of antipsychotics currently available on the market, there are clearly still certain needs in the treatment of schizophrenia and bipolar disorder that have not yet been met. Available antipsychotics have shown to be effective against the positive symptoms of schizophrenia however they do little to alleviate the negative symptoms and the cognitive impairment often associated with the illness.

In addition, many of the available typical antipsychotics can cause movement disorders and atypical antipsychotics can cause considerable weight gain and serious metabolic abnormalities including diabetes. Hence, a drug that can potentially provide improvement in negative and cognitive symptoms as well as the positive symptoms of schizophrenia and which is metabolically neutral and has low rate of EPS is clearly warranted. Aripiprazole already meets some of these criteria; however, an alternative would be helpful.

Furthermore, the pharmaceutical industry has spent many years trying to develop a new drug that mimics the effectiveness of clozapine but with a much improved toxicity profile. A safer alternative to clozapine is also clearly needed, although for over 50 years now no drug has been shown to match its efficacy.

Asenapine has a high affinity for a number of receptors including antagonism at serotonergic, dopaminergic and adrenergic receptors but, unlike clozapine, it has no discernible affinity for muscarinic receptors. Studies showed that asenapine caused a significant reduction in PANSS positive and negative scores compared with placebo. Thus it may not only be effective in treating positive symptoms but also has a statistically significant advantage over placebo in treating negative symptoms, although the later may not be clinically significant. Further evidence is required in order to determine whether asenapine has advantages over placebo or other antipsychotics in terms of improving functional impairment. In bipolar disorder, asenapine showed comparable efficacy with olanzapine (which was maintained throughout a 40-week period), in patients with manic, mixed episodes or bipolar I disorder.

Asenapine appears to be well tolerated and has minimal effects on prolactin and metabolic parameters. Cardiovascular assessments found no cause for concern and asenapine’s effects on QTc prolongation were comparable to quetiapine, at the higher dose range of asenapine. The incidence of EPS was higher with asenapine than olanzapine in one study.

Overall, asenapine appears to have advantages over other antipsychotics for negative symptoms of schizophrenia and possibly cognitive function, although further research is required in order to assess whether this is of clinical importance and could improve the functional ability of patients. It may have a place in therapy as an atypical antipsychotic with neutral metabolic effects. There is no evidence as yet to show that it may be useful in treatment-resistant schizophrenia, as an alternative to clozapine.