Canagliflozin: Efficacy and Safety in Combination with Metformin Alone or with Other Antihyperglycemic Agents in Type 2 Diabetes.

Metformin is typically the first pharmacologic treatment recommended for type 2 diabetes mellitus (T2DM), but many patients do not achieve glycemic control with metformin alone and eventually require combination therapy with other agents. Canagliflozin, a sodium glucose co-transporter 2 (SGLT2) inhibitor, was assessed in a comprehensive Phase 3 clinical development program consisting of ~10,000 participants, of which ~80% were on background therapy that consisted of metformin alone or in combination with other antihyperglycemic agents (AHAs; e.g., pioglitazone, sulfonylurea, and insulin). In addition, the efficacy and safety of canagliflozin and metformin as the initial combination therapy and canagliflozin monotherapy were assessed versus metformin in treatment-naïve patients with T2DM. Across studies in patients with T2DM who were on metformin alone or in combination with other AHAs, canagliflozin 100 and 300 mg provided improvements in glycated hemoglobin for up to 104 weeks. Canagliflozin was also associated with reductions in body weight and systolic blood pressure when added to background therapy consisting of metformin alone or with other AHAs. Canagliflozin was generally well tolerated, with increased incidence of adverse events (AEs) related to the mechanism of SGLT2 inhibition (i.e., genital mycotic infections, urinary tract infections, and osmotic diuresis-related AEs). Consistent with its insulin-independent mechanism of action, canagliflozin was associated with low rates of hypoglycemia when background therapy did not include sulfonylurea or insulin. Due to its favorable efficacy and safety profile, these results suggest that adding canagliflozin to a background regimen consisting of metformin or implementing treatment with a fixed-dose regimen of canagliflozin and metformin would provide an effective and safe treatment regimen for T2DM management. FUNDING: Janssen Global Services, LLC.

Introduction

Type 2 diabetes mellitus (T2DM) is characterized by chronic hyperglycemia and is closely associated with comorbidities, including obesity, hypertension, and dyslipidemia, and an increased risk of cardiovascular disease and mortality [1-4]. The interplay of these factors can complicate T2DM management; therefore, therapeutics that control weight and blood pressure (BP) in addition to blood glucose would be beneficial [2].

The first pharmacologic intervention typically recommended for the treatment of T2DM is metformin [5-7], which works primarily by decreasing hepatic glucose production [5, 8]. Metformin may also reduce endogenous glucose production by delaying intestinal glucose absorption [8], and recent evidence suggests that metformin’s action in the gut is responsible for its glucose-lowering effect [9]. Metformin has a well-established efficacy and safety profile, is not associated with hypoglycemia or weight gain, may reduce the risk of myocardial infarction and death, and is inexpensive [5, 6, 10]. Despite these advantages, many patients are unable to control their blood glucose levels with metformin alone and require combination therapy with other antihyperglycemic agents (AHAs) [5, 11, 12]. Some of the AHAs frequently used for combination therapy have undesirable effects, such as weight gain, hypoglycemia, and decreased efficacy over time [5, 11, 12].

Sodium glucose co-transporter 2 (SGLT2) inhibitors lower the renal threshold for glucose (RTG) in patients with T2DM, thus increasing urinary glucose excretion and leading to mild osmotic diuresis and a net caloric loss [5, 13]. This mechanism is independent of insulin and complementary to those of other classes of AHAs, including metformin [5, 13]. In addition to improving glycemic control, SGLT2 inhibitors have been associated with modest weight loss and BP reductions in patients with T2DM [14]. SGLT2 inhibitors are additionally associated with improvements in measures of beta-cell function, including glucose sensitivity and insulin secretion [15-17]. Along with potentially having favorable effects on components of T2DM, the benefits of this class may also improve cardiovascular outcomes in patients with T2DM [18, 19]. Due to their favorable efficacy and tolerability profile, the American Diabetes Association recommends adding an SGLT2 inhibitor in patients whose T2DM is inadequately controlled with metformin [6], and the American Association of Clinical Endocrinologists Glycemic Control Algorithm identifies SGLT2 inhibitors as the first choice of oral medications for add-on therapy in patients inadequately controlled on metformin [7].

Canagliflozin, an SGLT2 inhibitor, is approved in many countries for the treatment of adults with T2DM [20], and a fixed-dose combination of canagliflozin and metformin, is also available for the treatment of adults with T2DM [21]. When administered as an add-on treatment to metformin, canagliflozin was associated with reductions in glycated hemoglobin (HbA1c), weight loss, and BP lowering in a broad range of patients in Phase 2 [22, 23] and Phase 3 studies [24-26]. These effects were also observed in a Phase 3 study of the initial combination therapy with canagliflozin plus metformin [27]. The benefits noted in these studies were similar to those seen in other Phase 3 studies when canagliflozin was administered to patients on a background of metformin plus pioglitazone [28], metformin plus sulfonylurea [29, 30], or metformin plus insulin [31]. This review summarizes the efficacy and safety of canagliflozin when used in combination with metformin in Phase 3 studies in patients with T2DM.

Compliance with Ethics Guidelines

This article is based on previously conducted studies and does not involve any new studies of human or animal subjects performed by any of the authors.

Overview of Clinical Studies of Canagliflozin in Combination with Metformin

Table 1 provides an overview of the designs and patient populations of the Phase 3 studies, in which canagliflozin was administered with metformin alone or in combination with another AHA (i.e., pioglitazone, sulfonylurea, and insulin) in patients with T2DM. Key efficacy analyses in these studies included changes from baseline in HbA1c, body weight, and systolic BP. Safety was assessed based on adverse event (AE) reports.

Table 1

Study design and patient populations of Phase 3 studies of canagliflozin in combination with metformin in patients with T2DM

Study	Study design	Patients	Key inclusion criteria
Add-on to MET vs PBO/SITA [24]	PBO-controlled, 26-week core period; active-controlled (vs SITA), 26-week extension period	N = 1284; PBO/SITA, n = 183; SITA 100 mg, n = 366; CANA 100 mg, n = 368; CANA 300 mg, n = 367	≥18 and ≤80 years old; HbA1c ≥7.0% and ≤10.5%; Receiving stable MET dose (≥2000 mg/day [or ≥1500 mg/day if unable to tolerate a higher dose]) for ≥8 weeks; eGFR ≥55 mL/min/1.73 m2a
Add-on to MET vs GLIM [25, 26]	Active-controlled (vs GLIM) 52-week core period and 52-week extension	N = 1450; GLIM, n = 482; CANA 100 mg, n = 483; CANA 300 mg, n = 485	≥18 and ≤80 years old; HbA1c ≥7.0% and ≤9.5%; Receiving stable MET dose (≥2000 mg/day [or ≥1500 mg/day if unable to tolerate a higher dose]) for ≥10 weeks; eGFR ≥55 mL/min/1.73 m2a
Initial combination with CANA + MET [27]	Initial combination therapy with CANA + MET vs each component for 26 weeks	N = 1186; CANA 100 mg/MET, n = 237; CANA 300 mg/MET, n = 237; CANA 100 mg, n = 237; CANA 300 mg, n = 238; MET, n = 237	≥18 and <75 years old; HbA1c ≥7.5% and ≤12.0%; AHA-naïve (not on AHA therapy or off for ≥12 weeks before screening); eGFR ≥60 mL/min/1.73 m2
Add-on to MET + PIO vs PBO/SITA [28]	PBO-controlled, 26-week core period; active-controlled (vs SITA), 26-week extension period	N = 342; PBO/SITA, n = 115; CANA 100 mg, n = 113; CANA 300 mg, n = 114	≥18 and ≤80 years old; HbA1c ≥7.0% and ≤10.5%; Receiving stable MET dose (≥2000 mg/day [or ≥1500 mg/day if unable to tolerate a higher dose]) and PIO 30 or 45 mg/day for ≥8 weeks; eGFR ≥55 mL/min/1.73 m2a
Add-on to MET + SU vs PBO [29]	PBO-controlled, 26-week core period; PBO-controlled, 26-week extension period	N = 469; PBO, n = 156; CANA 100 mg, n = 157; CANA 300 mg, n = 156	≥18 and ≤80 years old; HbA1c ≥7.0% and ≤10.5%; Receiving stable MET dose (≥2000 mg/day [or ≥1500 mg/day if unable to tolerate a higher dose]) and SU (at least half of maximally labeled dose) for ≥8 weeks; eGFR ≥55 mL/min/1.73 m2a
Add-on to MET + SU vs SITA [30]	Active-controlled, 52-week treatment period	N = 756; CANA 300 mg, n = 377; SITA 100 mg, n = 378	≥18 years old; HbA1c ≥7.0% and ≤10.5%; Receiving stable MET dose (≥2000 mg/day [or ≥1500 mg/day if unable to tolerate a higher dose]) and SU (at least half of maximally labeled dose) for ≥8 weeks; eGFR ≥55 mL/min/1.73 m2a
Asian population: add-on to MET ± SU vs PBO [32]	PBO-controlled, 18-week treatment period	N = 676; PBO, n = 226; CANA 100 mg, n = 223; CANA 300 mg, n = 227	≥18 and ≤80 years old; HbA1c ≥7.0% and ≤10.5%; Receiving stable MET dose (≥1500 mg/day) with or without SU (at least half of maximally labeled dose) for ≥8 weeks; eGFR ≥60 mL/min/1.73 m2
Add-on to MET + insulin vs PBO [31]	Prespecified 18-week substudy in a subset of patients from the ongoing PBO-controlled, CANVAS trial	N = 432; PBO, n = 145; CANA 100 mg, n = 139; CANA 300 mg, n = 148	≥30 years old with documented, symptomatic, atherosclerotic cardiovascular disease, or ≥50 years old with ≥2 CV risk factors at screening; Receiving stable MET dose (≥2000 mg/day) and insulin ≥30 IU/day (basal and/or bolus); HbA1c ≥7.0% and ≤10.5%; eGFR ≥30 mL/min/1.73 m2

AHA antihyperglycemic agent, CANA canagliflozin, CANVAS CANagliflozin cardioVascular Assessment Study, CV cardiovascular, eGFR estimated glomerular filtration rate, GLIM glimepiride, MET metformin, PBO placebo, PIO pioglitazone, SITA sitagliptin, SU sulfonylurea, T2DM type 2 diabetes mellitus

aThe required eGFR was ≥60 mL/min/1.73 m2 if based on restriction of metformin use in the local label

Two randomized, double-blind, Phase 3 studies evaluated the efficacy and safety of canagliflozin 100 and 300 mg as add-on to metformin [24-26]. A 52-week study in 1284 participants evaluated the efficacy and safety of canagliflozin versus placebo at week 26 and versus sitagliptin 100 mg at week 52 (ClinicalTrials.gov Identifier, NCT01106677) [24]. Safety analyses included participants who received canagliflozin 100 or 300 mg or sitagliptin 100 mg over 52 weeks and those who switched from placebo to sitagliptin after 26 weeks (placebo/sitagliptin group). The second study (NCT00968812) evaluated canagliflozin 100 and 300 mg versus glimepiride in 1450 participants at 52 weeks [25] and 104 weeks [26]. A separate randomized, double-blind, Phase 3 study evaluated the efficacy and safety of the initial combination therapy with canagliflozin 100 or 300 mg plus metformin versus metformin alone in 1186 drug-naïve patients over 26 weeks (NCT01809327) [27]. This study also evaluated the efficacy and safety of canagliflozin 100 and 300 mg monotherapy versus metformin [27].

A randomized, double-blind, Phase 3 study evaluated canagliflozin 100 and 300 mg as add-on to metformin plus pioglitazone in 342 patients over 52 weeks (NCT01106690) [28]. Patients assigned to placebo were switched to sitagliptin 100 mg after 26 weeks. Efficacy comparisons were made versus placebo at week 26 and versus sitagliptin 100 mg at week 52. Safety data at week 52 included patients in the placebo group who were switched to sitagliptin at week 26.

Two randomized, double-blind, Phase 3 studies evaluated the efficacy and safety of canagliflozin as add-on to metformin plus sulfonylurea. A placebo-controlled study in 469 patients evaluated the efficacy and safety of canagliflozin 100 and 300 mg as add-on to metformin plus sulfonylurea over 52 weeks (NCT01106625) [29]. A separate head-to-head study evaluated the efficacy and safety of canagliflozin 300 mg versus sitagliptin 100 mg as add-on to metformin plus sulfonylurea over 52 weeks (NCT01137812) [30].

An 18-week, randomized, double-blind, placebo-controlled study of canagliflozin 100 and 300 mg as add-on therapy to metformin or metformin plus sulfonylurea was conducted in Asian patients with T2DM in China, Malaysia, and Vietnam (NCT01381900) [32]. Of 676 participants, 330 were receiving metformin monotherapy (metformin stratum) and 346 were receiving metformin plus sulfonylurea (metformin plus sulfonylurea stratum) at baseline.

An 18-week, prespecified substudy of the ongoing CANagliflozin cardioVascular Assessment Study (CANVAS; NCT01032629) evaluated the efficacy and safety of canagliflozin 100 and 300 mg compared with placebo in 432 patients with T2DM and a history or high risk of cardiovascular disease whose background therapy consisted of metformin plus insulin ≥30 IU/day (basal and/or bolus) [31].

Glycemic Efficacy

Combination with Metformin Alone

Figure 1 presents the least squares (LS) mean changes in HbA1c in the core periods of Phase 3 studies of canagliflozin added to metformin alone or in combination with other AHAs and in the initial combination therapy study. In the study of canagliflozin versus placebo/sitagliptin, canagliflozin 100 and 300 mg significantly lowered HbA1c versus placebo at week 26 (p < 0.001) [24]. At week 52, canagliflozin 100 mg demonstrated noninferiority and canagliflozin 300 mg demonstrated superiority in lowering HbA1c versus sitagliptin [24].

Fig. 1

Changes from baseline in HbA1c in Phase 3 studies of canagliflozin in combination with metformin ± other AHAs [24–32]. a p < 0.001 versus PBO; b p = 0.001 versus MET; c p = 0.001 versus CANA 100 mg; d p = 0.001 versus CANA 300 mg; e Noninferiority p = 0.001 versus MET. AHA antihyperglycemic agent, CANA canagliflozin, GLIM glimepiride, HbA1c glycated hemoglobin, LS least squares, MET metformin, PBO placebo, PIO pioglitazone, SE standard error, SITA sitagliptin, SU sulfonylurea

At week 52, canagliflozin 100 mg demonstrated noninferiority and canagliflozin 300 mg demonstrated superiority in lowering HbA1c in the head-to-head study versus glimepiride [25]. At week 104, HbA1c reductions were −0.65%, −0.74%, and −0.55% with canagliflozin 100 and 300 mg and glimepiride, respectively [26].

In the metformin stratum of the study in Asian patients, HbA1c reductions from baseline at week 18 were significantly larger with canagliflozin 100 and 300 mg compared with placebo (p < 0.001) [32].

In the initial combination therapy study, canagliflozin 100 mg/metformin and canagliflozin 300 mg/metformin significantly lowered HbA1c versus metformin monotherapy at week 26 (p = 0.001) [27].

Combination with Metformin Plus Other AHAs

In the placebo-controlled add-on to metformin plus pioglitazone study, significant reductions in HbA1c were seen with canagliflozin 100 and 300 mg versus placebo at week 26 (p < 0.001) [28]. At week 52, reductions in HbA1c with canagliflozin 100 and 300 mg were −0.92% and −1.03%, respectively.

In the placebo-controlled add-on to metformin plus sulfonylurea study, canagliflozin 100 and 300 mg significantly lowered HbA1c versus placebo over 26 weeks (p < 0.001) [29]. Reductions in HbA1c with canagliflozin 100 and 300 mg versus placebo were sustained over 52 weeks (−0.74%, −0.96%, and 0.01%, respectively). In the head-to-head study of canagliflozin as add-on to metformin plus sulfonylurea, canagliflozin 300 mg demonstrated superiority in HbA1c lowering versus sitagliptin 100 mg over 52 weeks [30]. Among patients in the metformin plus sulfonylurea stratum of the study in Asian patients, reductions in HbA1c were significantly larger with canagliflozin 100 and 300 mg compared with placebo at week 18 (p < 0.001) [32].

In the subset of CANVAS patients whose background therapy consisted of metformin plus insulin, canagliflozin 100 and 300 mg significantly lowered HbA1c compared with placebo over 18 weeks (p < 0.001) [31].

Body Weight Reductions

Figure 2 depicts LS mean percent changes in body weight in the core periods of Phase 3 studies of canagliflozin in combination with metformin. In the study versus placebo/sitagliptin, canagliflozin provided significant body weight reductions at week 26 compared with placebo (p < 0.001) [24]; reductions were sustained at week 52 (p < 0.001) [24].

Fig. 2

Changes from baseline in body weight in Phase 3 studies of canagliflozin in combination with metformin ± other AHAs [24–32]. a Absolute changes from baseline in kg are shown in parentheses; b p < 0.001 versus PBO; c p < 0.001 versus SITA 100 mg; d p < 0.0001 versus GLIM; e p = 0.001 versus MET; f p = 0.016 versus MET; g p = 0.002 versus MET. AHA antihyperglycemic agent, CANA canagliflozin, GLIM glimepiride, LS least squares, MET metformin, PBO placebo, PIO pioglitazone, SE standard error, SITA sitagliptin, SU sulfonylurea

In the active-controlled study versus glimepiride, significant body weight reductions were seen with canagliflozin 100 and 300 mg compared with an increase with glimepiride at week 52 (p < 0.0001) [25]. Body weight reductions with canagliflozin 100 and 300 mg versus glimepiride were sustained at week 104; changes from baseline were −4.1%, −4.2%, and 0.9% (−3.6, −3.6, and 0.8 kg), respectively [26].

In the metformin stratum of the study in Asian patients, greater reductions in body weight were seen with canagliflozin 100 and 300 mg compared with placebo at week 18 (p < 0.001) [32].

At week 26 in the initial combination therapy study, significantly greater weight loss was seen with canagliflozin 100 mg/metformin and canagliflozin 300 mg/metformin than with metformin alone (p = 0.001) [27].

Significant reductions in body weight were seen with canagliflozin 100 and 300 mg versus placebo as add-on to metformin plus pioglitazone at week 26 (p < 0.001) [28]. At week 52, body weight reductions with canagliflozin 100 and 300 mg were sustained (−2.7% and −3.7% [−2.5 and −3.6 kg], respectively).

In the placebo-controlled add-on to metformin plus sulfonylurea study, canagliflozin 100 and 300 mg significantly lowered body weight versus placebo over 26 weeks (p < 0.001) [29]. At week 52, reductions in body weight were −2.2%, −3.2%, −0.9% (−2.0, −3.1, and −1.0 kg) with canagliflozin 100 and 300 mg and placebo, respectively. In the head-to-head study of canagliflozin as add-on to metformin plus sulfonylurea, canagliflozin 300 mg significantly lowered body weight versus sitagliptin 100 mg over 52 weeks (p < 0.001) [30]. Among Asian patients in the metformin plus sulfonylurea stratum, significant reductions in body weight were seen with canagliflozin 100 and 300 mg compared with placebo at week 18 (p < 0.001) [32].

In the subset of CANVAS patients on metformin plus insulin, canagliflozin 100 and 300 mg significantly lowered body weight compared with placebo over 18 weeks (p < 0.001) [31].

Changes in Systolic BP

Figure 3 depicts LS mean changes in systolic BP in the core periods of Phase 3 studies of canagliflozin in combination with metformin. In the study of canagliflozin versus placebo/sitagliptin, significant reductions in systolic BP were seen with canagliflozin 100 and 300 mg versus placebo at week 26 (p < 0.001) [24]. Significant systolic BP reductions were also seen at week 52 with canagliflozin 100 and 300 mg compared with sitagliptin 100 mg (p < 0.001).

Fig. 3

Changes from baseline in systolic BP in Phase 3 studies of canagliflozin in combination with metformin ± other AHAs [24–32]. a p < 0.001 versus PBO; b p < 0.001 versus SITA 100 mg; c p = NS versus MET; d p < 0.01 versus PBO; e p < 0.025 versus PBO. AHA antihyperglycemic agent, BP blood pressure, CANA canagliflozin, GLIM glimepiride, LS least squares, MET metformin, NS not significant, PBO placebo, PIO pioglitazone, SE standard error, SITA sitagliptin, SU sulfonylurea

In the study of canagliflozin versus glimepiride, canagliflozin 100 and 300 mg were associated with reductions in systolic BP versus glimepiride at week 52 [25] and week 104 (−2.0, −3.1, and 1.7 mmHg, respectively) [26].

In Asian patients, reductions in systolic BP were numerically greater with canagliflozin 100 and 300 mg compared with placebo in the metformin stratum at week 18 [32].

At week 26 in the initial combination therapy study, canagliflozin 100 mg/metformin and canagliflozin 300 mg/metformin were associated with numerically larger reductions in systolic BP compared with metformin monotherapy [27].

Significant reductions in systolic BP were seen with canagliflozin 100 and 300 mg versus placebo as add-on to metformin plus pioglitazone at week 26 (p < 0.01 and p < 0.025, respectively) [28]. At week 52, reductions in systolic BP were −3.4 and −3.7 mmHg with canagliflozin 100 and 300 mg, respectively.

In the placebo-controlled add-on to metformin plus sulfonylurea study, canagliflozin 100 and 300 mg provided numerical reductions in systolic BP versus placebo over 26 weeks [29]. At week 52, changes in systolic BP were −3.7, −2.9, and 0.1 mmHg with canagliflozin 100 and 300 mg and placebo, respectively. In the head-to-head study of canagliflozin as add-on to metformin plus sulfonylurea, canagliflozin 300 mg significantly lowered systolic BP versus sitagliptin 100 mg over 52 weeks (p < 0.001) [30]. In the metformin plus sulfonylurea stratum of the study in Asian patients, larger changes in systolic BP were seen with canagliflozin 100 and 300 mg compared with placebo at week 18 [32].

In the subset of CANVAS patients on metformin plus insulin, reductions in systolic BP were seen with canagliflozin 100 and 300 mg compared with placebo at week 18 (p < 0.001 for canagliflozin 300 mg versus placebo) [31].

Efficacy of Canagliflozin Monotherapy Versus Metformin

The initial combination study also evaluated the efficacy and safety of canagliflozin 100 and 300 mg monotherapy versus metformin in treatment-naïve patients with T2DM [27]. Canagliflozin 100 and 300 mg demonstrated noninferiority in lowering HbA1c versus metformin at week 26 (noninferiority p = 0.001; Fig. 1). Body weight reductions were significantly greater with canagliflozin 100 and 300 mg versus metformin (p = 0.016 and p = 0.002, respectively; Fig. 2). Reductions in systolic BP were also observed with canagliflozin 100 and 300 mg compared with metformin (Fig. 3).

Safety of Canagliflozin in Combination with Metformin

Overall Safety and Selected AEs

Canagliflozin was generally well tolerated, with similar safety and tolerability profiles seen across studies in combination with metformin [24-32]. Table 2 summarizes safety data in Phase 3 studies of canagliflozin in combination with metformin alone, and Table 3 summarizes safety data in the studies of canagliflozin in combination with metformin and other AHAs. In addition to providing the overall incidence of AEs, the tables show the incidence of selected AEs related to SGLT2 inhibition, including urinary tract infections, genital mycotic infections, osmotic diuresis-related AEs, and volume depletion-related AEs. Overall, the frequency of AEs leading to discontinuation and serious AEs was generally low with canagliflozin versus comparators [24-32]. The incidence of genital mycotic infections and osmotic diuresis-related AEs was generally higher with canagliflozin versus comparators. Rates of volume depletion-related AEs, including postural dizziness and orthostatic hypotension, were low across groups in each study.

Table 2

Summary of overall safety and selected adverse events in Phase 3 studies of canagliflozin in combination with metformin [24–27, 32]

	Add-on to MET vs PBO/SITA (52 weeks)				Add-on to MET vs GLIM (104 weeks)
	PBO/SITA (n = 183)	SITA 100 mg (n = 366)	CANA 100 mg (n = 368)	CANA 300 mg (n = 367)	GLIM (n = 482)	CANA 100 mg (n = 483)	CANA 300 mg (n = 485)
Any AE	122 (66.7)	236 (64.5)	266 (72.3)	230 (62.7)	378 (78.4)	354 (73.3)	378 (77.9)
AEs leading to discontinuation	8 (4.4)	16 (4.4)	19 (5.2)	12 (3.3)	35 (7.3)	30 (6.2)	46 (9.5)
AEs related to study druga	23 (12.6)	72 (19.7)	97 (26.4)	73 (19.9)	134 (27.8)	138 (28.6)	159 (32.8)
Serious AEs	7 (3.8)	18 (4.9)	15 (4.1)	12 (3.3)	69 (14.3)	47 (9.7)	47 (9.7)
Deaths	1 (0.5)	1 (0.3)	0	1 (0.3)	2 (0.4)	3 (0.6)	3 (0.6)
Selected AEs
UTIs	12 (6.6)	23 (6.3)	29 (7.9)	18 (4.9)	33 (6.8)	51 (10.6)	42 (8.7)
Genital mycotic infections
Menb	1 (1.1)	2 (1.2)	9 (5.2)	4 (2.4)	5 (1.9)	24 (9.5)	22 (9.1)
Womenc	1 (1.1)	5 (2.6)	22 (11.3)	20 (9.9)	6 (2.7)	32 (13.9)	38 (15.6)
Osmotic diuresis-related AEsd	1 (0.5)	7 (1.9)	30 (8.2)	16 (4.4)	10 (2.1)	28 (5.8)	32 (6.6)
Volume depletion-related AEse	1 (0.5)	7 (1.9)	4 (1.1)	3 (0.8)	11 (2.3)	8 (1.7)	12 (2.5)
Hypoglycemia episodes
Documentedf	5 (2.7)	15 (4.1)	25 (6.8)	25 (6.8)	197 (40.9)	33 (6.8)	40 (8.2)
Severe	0	1 (0.3)	1 (0.3)	0	16 (3.3)	3 (0.6)	1 (0.2)

AE adverse event, CANA canagliflozin, GLIM glimepiride, MET metformin, PBO placebo, SITA sitagliptin, UTI urinary tract infection

aPossibly, probably, or very likely related to study drug, as assessed by investigators

bIncludes balanitis, balanitis candida, balanoposthitis, genital candidiasis, genital infection fungal, and posthitis

cIncludes genital infection female, genital infection fungal, vaginal discharge, vaginal infection, vaginal inflammation, vulvitis, vulvovaginal candidiasis, vulvovaginal mycotic infection, vulvovaginal pruritus, and vulvovaginitis

dIncludes dry mouth, micturition disorder and urgency, nocturia, pollakiuria, polydipsia, polyuria, thirst, and urine output increased

eIncludes blood pressure decreased, dehydration, postural dizziness, hypotension, orthostatic hypotension, presyncope, syncope, and urine output decreased

fIncluding biochemically documented episodes (fingerstick or plasma glucose ≤3.9 mmol/L) with or without symptoms and severe episodes (i.e., those requiring the assistance of another individual or resulting in seizure or loss of consciousness)

Table 3

Summary of overall safety and selected adverse events in Phase 3 studies of canagliflozin in combination with metformin and other antihyperglycemic agents [28–32]

	Add-on to MET + PIO vs PBO/SITA (52 weeks)			Add-on to MET + SU vs PBO (52 weeks)			Add-on to MET + SU vs SITA (52 weeks)
	PBO/SITA (n = 115)	CANA 100 mg (n = 113)	CANA 300 mg (n = 114)	PBO (n = 156)	CANA 100 mg (n = 157)	CANA 300 mg (n = 156)	SITA 100 mg (n = 378)	CANA 300 mg (n = 377)
Any AE	88 (76.5)	79 (69.9)	87 (76.3)	111 (71.2)	106 (67.5)	114 (73.1)	293 (77.5)	289 (76.7)
AEs leading to discontinuation	7 (6.1)	2 (1.8)	5 (4.4)	7 (4.5)	11 (7.0)	12 (7.7)	11 (2.9)	20 (5.3)
AEs related to study druga	27 (23.5)	22 (19.5)	33 (28.9)	24 (15.4)	41 (26.1)	57 (36.5)	105 (27.8)	128 (34.0)
Serious AEs	6 (5.2)	8 (7.1)	7 (6.1)	13 (8.3)	7 (4.5)	8 (5.1)	21 (5.6)	24 (6.4)
Deaths	0	0	0	0	0	0	0	2 (0.5)
Selected AEs
UTIs	9 (7.8)	6 (5.3)	9 (7.9)	12 (7.7)	13 (8.3)	13 (8.3)	21 (5.6)	15 (4.0)
Genital mycotic infections
Menb	0	3 (3.9)	3 (4.8)	1 (1.3)	6 (7.9)	5 (5.7)	1 (0.5)	19 (9.2)
Womenc	3 (7.7)	6 (16.7)	11 (21.6)	4 (5.0)	15 (18.5)	13 (18.8)	7 (4.3)	26 (15.3)
Osmotic diuresis-related AEsd	1 (0.9)	11 (9.7)	11 (9.6)	3 (1.9)	9 (5.7)	11 (7.1)	9 (2.4)	19 (5.0)
Volume depletion-related AEse	4 (3.5)	9 (8.0)	5 (4.4)	3 (1.9)	1 (0.6)	6 (3.8)	8 (2.1)	7 (1.9)
Hypoglycemia episodes
Documentedf	7 (6.1)	5 (4.4)	7 (6.1)	28 (17.9)	53 (33.8)	57 (36.5)	154 (40.7)	163 (43.2)
Severe	0	0	0	1 (0.6)	1 (0.6)	1 (0.6)	13 (3.4)	15 (4.0)

AE adverse event, CANA canagliflozin, GLIM glimepiride, MET metformin, PBO placebo, PIO pioglitazone, SITA sitagliptin, SU sulfonylurea, UTI urinary tract infection

aPossibly, probably, or very likely related to study drug, as assessed by investigators

bIncludes balanitis, balanitis candida, balanoposthitis, balanoposthitis infective, and genital infection fungal

cIncludes genital infection fungal, pruritus genital, vaginal infection, vulvitis, vulvovaginal candidiasis, vulvovaginal mycotic infection, and vulvovaginitis

dIncludes dry mouth, micturition urgency, nocturia, pollakiuria, polydipsia, polyuria, thirst, and urine output increased

eIncludes dehydration, dizziness postural, hypotension, orthostatic hypotension, and syncope

fIncluding biochemically documented episodes (fingerstick or plasma glucose ≤3.9 mmol/L) with or without symptoms and severe episodes (i.e., those requiring the assistance of another individual or resulting in seizure or loss of consciousness)

Gastrointestinal-related AEs, such as diarrhea, nausea, and vomiting, which are commonly associated with metformin, were generally similar across groups in each study [24-32]. At week 26 in the initial combination therapy study, the incidence of gastrointestinal-related AEs was 4.6%, 4.6%, and 4.2% with canagliflozin 100 mg/metformin, canagliflozin 300 mg/metformin, and metformin, respectively; rates were 1.7% with canagliflozin 100 mg and 2.9% with canagliflozin 300 mg [27].

Diabetic ketoacidosis was rare in the canagliflozin clinical development program [33]. No serious AEs of diabetic ketoacidosis were seen with canagliflozin when it was added to background therapy consisting of metformin alone or in combination with pioglitazone [33]. There was one serious AE of ketoacidosis with canagliflozin 300 mg in the initial combination therapy study [33]. This event occurred in a 62-year-old man on the 18th day of treatment. Confounding factors were: an abscessed boil of the anterior abdominal wall that required dissection and antibiotics; chronic pancreatitis, which was detected by abdominal ultrasound; and heart failure class II and treatment with indapamide. There was one serious AE of ketoacidosis with canagliflozin 100 mg in the placebo-controlled add-on to metformin plus sulfonylurea study [33]. The event occurred in a 47-year-old woman who had nearly 50-kg weight loss over 2 years and was subsequently diagnosed with type 1 diabetes. There were no serious AEs of diabetic ketoacidosis in the subset of patients from the CANVAS trial who were on metformin plus insulin during the 18-week treatment period.

An interim safety analysis of the overall CANVAS study identified an increased risk for lower limb amputation with canagliflozin (7.3, 5.4, and 3.0 per 1000 patient-years with canagliflozin 100 and 300 mg and placebo, respectively) [34]. This safety signal was not observed in a pooled analysis of 12 completed Phase 3 and Phase 4 studies representing a broad patient population on background metformin or other AHAs (data on file), or in an analysis of the CANVAS-R (renal outcomes; NCT01989754) study. In pooled Phase 3 studies, an increased risk for fracture, primarily in the upper and lower extremities, was observed with canagliflozin, which was driven by a higher incidence in patients from the CANVAS study [35]. Additional data regarding the risk for amputation and fracture with canagliflozin will be available upon completion of the CANVAS and CANVAS-R studies in 2017.

Hypoglycemia

As an SGLT2 inhibitor, canagliflozin reduces reabsorption of filtered glucose and lowers RTG, thereby increasing urinary glucose excretion and lowering elevated plasma glucose concentrations in patients with T2DM [20, 36]. The risk of hypoglycemia with canagliflozin is expected to be low because RTG typically remains above the threshold for hypoglycemia (~3.9 mmol/L) in patients with T2DM, and very little urinary glucose excretion occurs when plasma glucose levels are below RTG [20].

In Phase 3 studies of canagliflozin, documented hypoglycemia episodes were defined as biochemically documented episodes (concurrent fingerstick glucose or plasma glucose ≤3.9 mmol/L with or without symptoms) and severe episodes (requiring the assistance of another individual or resulting in seizure or loss of consciousness) [24-32]. In general, patients who were not on background therapy that included sulfonylurea had a low incidence of hypoglycemia with canagliflozin 100 and 300 mg that was generally slightly higher versus placebo and active comparators. The incidence of severe hypoglycemia episodes was low across groups in patients who were not on background sulfonylurea or insulin (Tables 2 and 3).

Of note, in the study of canagliflozin versus glimepiride, the incidence of documented hypoglycemia episodes at week 52 was significantly lower for canagliflozin 100 and 300 mg versus glimepiride (5.6%, 4.9%, and 34.2%, respectively; p < 0.0001) [25]. The frequency of severe hypoglycemia was also lower with canagliflozin 100 mg (two patients [0.4%]) and 300 mg (three patients [0.6%]) than with glimepiride (15 patients [3.1%]). At week 104, the proportion of patients with documented hypoglycemia episodes remained lower with canagliflozin 100 and 300 mg than with glimepiride (6.8%, 8.2%, and 40.9%, respectively) [26]. No additional severe hypoglycemia events with canagliflozin were reported after week 52.

As add-on to metformin versus placebo/sitagliptin, the incidence of documented hypoglycemia episodes at week 52 was higher with both canagliflozin doses compared with sitagliptin 100 mg and with placebo/sitagliptin [24]. The reason for the higher incidence of documented episodes of hypoglycemia with canagliflozin versus sitagliptin and placebo/sitagliptin in this study is unknown, although the greater HbA1c lowering seen with canagliflozin may have contributed to this difference. However, as add-on to metformin plus sulfonylurea, the incidence of hypoglycemia with canagliflozin 300 mg was similar to sitagliptin (43.2% and 40.7%, respectively), despite a nearly 0.4% larger reduction in HbA1c with canagliflozin [30].

Fasting Plasma Lipids and Laboratory Parameters

Across studies, canagliflozin was generally associated with reductions in triglycerides and increases in high-density lipoprotein cholesterol and low-density lipoprotein cholesterol [24-32]. In addition, no clinically meaningful changes in most laboratory parameters, including alanine aminotransferase, aspartate aminotransferase, bilirubin, blood urea nitrogen, creatinine, urate, and hemoglobin, were seen with canagliflozin across studies [24-32]. Treatment with canagliflozin in combination with metformin was associated with a transient reduction in estimated glomerular filtration rate (eGFR) that attenuated over time [24-32]. In the 104-week study as add-on to metformin versus glimepiride [26], canagliflozin was associated with a slower rate in decline in eGFR compared with glimepiride, suggesting a potential renoprotective effect for canagliflozin [37]. In addition, canagliflozin provided reductions in albumin-to-creatinine ratio (ACR) in the studies where ACR was assessed [25, 26, 37–40]. The ongoing Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation (CREDENCE; NCT02065791) study will provide further insight into the renal effects of canagliflozin in patients with T2DM and renal impairment.

Conclusion

Improving glycemic control is the cornerstone of diabetes management, as improvements in blood glucose levels can decrease the risk of diabetes-related complications. SGLT2 inhibitors may be suitable alternative therapeutic agents for combination therapy with metformin due to their favorable glycemic efficacy and added benefits of weight loss and BP reduction. Treatment with canagliflozin in combination with metformin was associated with reductions in HbA1c, body weight, and systolic BP versus placebo and active comparators across Phase 3 studies of up to 104 weeks in duration. Canagliflozin was generally well tolerated, with an increased incidence of AEs related to the mechanism of SGLT2 inhibition and low rates of hypoglycemia. As genital mycotic infections were more common in male and female patients with a prior history of infections and in uncircumcised males, awareness of these potential AEs with canagliflozin is important for these patient populations. Patients susceptible to the volume depletion effects of canagliflozin (i.e., older patients, patients with moderate renal impairment, and those taking loop diuretics) should be monitored while on canagliflozin treatment. The favorable efficacy and safety profile suggest that adding canagliflozin to a background treatment regimen consisting of metformin alone or in combination with other AHAs, or implementing treatment with a fixed-dose combination of canagliflozin and metformin would provide an effective and safe alternative treatment regimen for T2DM management.