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Jardiance(empagliflozin filmcoated tablets)

2014-11-06 01:08:34  作者:新特药房  来源:互联网  浏览次数:597  文字大小:【】【】【
简介: 2014年8月3日,勃林格殷格翰-礼来糖尿病新药Jardiance(empagliflozin)获欧盟委员会(EC)批准,用于饮食结合运动未能取得充分血糖控制的2型糖尿病成人患者的治疗,以改善血糖控制。Jardiance的获批, ...

2014年5月24日,糖尿病新药Jardiance(empagliflozin)获欧盟委员会(EC)批准,用于饮食结合运动未能取得充分血糖控制的2型糖尿病成人患者的治疗,以改善血糖控制。
Jardiance的获批,也标志着勃林格殷格翰-礼来糖尿病联盟获批的第3个糖尿病产品。
Jardiance为每日一次的片剂,获批剂量为10mg和25mg。Jardiance可单独用药,也可与其他降糖药联合用药,包括胰岛素,二甲双胍。
Jardiance的获批,是基于一项涵括超过10个跨国III期试验的大型临床项目的数据,涉及超过1.3万例2型糖尿病患者。该项目数据表明,Jardiance 10mg和25mg剂量作为单药疗法或与广泛的背景疗法(包括二甲双胍,磺酰脲,胰岛素,pioglitazone等)联合用药,均显著降低了患者的糖化血红蛋白(HA1c)水平,同时也显著降低了体重、血压。
Jardiance属于钠-葡萄糖协同转运蛋白-2(SGLT-2)抑制剂类药物。新兴的SGLT-2抑制剂类药物,已被证实能够阻断肾脏中葡萄糖的再吸收作用,将过多的葡萄糖排泄到体外,从而达到降低血糖水平的效果,而且该降糖效果不依赖于β细胞功能和胰岛素抵抗。


Jardiance 10 mg and 25 mg film-coated tablets
1. Name of the medicinal product
Jardiance 10 mg film-coated tablets
Jardiance 25 mg film-coated tablets
2. Qualitative and quantitative composition
Jardiance 10 mg film-coated tablets
Each tablet contains 10 mg empagliflozin.
Excipient with known effect
Each tablet contains lactose monohydrate equivalent to 154.3 mg lactose anhydrous.
Jardiance 25 mg film-coated tablets
Each tablet contains 25 mg empagliflozin.
Excipient with known effect
Each tablet contains lactose monohydrate equivalent to 107.4 mg lactose anhydrous.
For the full list of excipients, see section 6.1.
3. Pharmaceutical form
Film-coated tablet (tablet).
Jardiance 10 mg film-coated tablets
Round, pale yellow, biconvex, bevel-edged film-coated tablet debossed with “S10” on one side and the Boehringer Ingelheim logo on the other (tablet diameter: 9.1 mm).
Jardiance 25 mg film-coated tablets
Oval, pale yellow, biconvex film-coated tablet debossed with “S25” on one side and the Boehringer Ingelheim logo on the other (tablet length: 11.1 mm, tablet width: 5.6 mm).
4. Clinical particulars
4.1 Therapeutic indications
Jardiance is indicated in the treatment of type 2 diabetes mellitus to improve glycaemic control in adults as:
Monotherapy
When diet and exercise alone do not provide adequate glycaemic control in patients for whom use of metformin is considered inappropriate due to intolerance.
Add-on combination therapy
In combination with other glucose–lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control (see sections 4.4, 4.5 and 5.1 for available data on different combinations).
4.2 Posology and method of administration
Posology
Monotherapy and add-on combination
The recommended starting dose is 10 mg empagliflozin once daily for monotherapy and add-on combination therapy with other glucose-lowering medicinal products including insulin. In patients tolerating empagliflozin 10 mg once daily who have an eGFR ≥60 ml/min/1.73 m2 and need tighter glycaemic control, the dose can be increased to 25 mg once daily. The maximum daily dose is 25 mg (see below and section 4.4).
When empagliflozin is used in combination with a sulphonylurea or with insulin, a lower dose of the sulphonylurea or insulin may be considered to reduce the risk of hypoglycaemia (see sections 4.5 and 4.8).
Special populations
Renal impairment
Due to the mechanism of action, the efficacy of empagliflozin is dependent on renal function. No dose adjustment is required for patients with an eGFR ≥60 ml/min/1.73 m2 or CrCl ≥60 ml/min.
Empagliflozin should not be initiated in patients with an eGFR <60 ml/min/1.73 m2 or CrCl <60 ml/min. In patients tolerating empagliflozin whose eGFR falls persistently below 60 ml/min/1.73 m2 or CrCl below 60 ml/min, the dose of empagliflozin should be adjusted to or maintained at 10 mg once daily. Empagliflozin should be discontinued when eGFR is persistently below 45 ml/min/1.73 m2 or CrCl persistently below 45 ml/min (see sections 4.4, 4.8, 5.1, and 5.2).
Empagliflozin should not be used in patients with end stage renal disease (ESRD) or in patients on dialysis as it is not expected to be effective in these patients (see sections 4.4 and 5.2).
Hepatic impairment
No dose adjustment is required for patients with hepatic impairment. Empagliflozin exposure is increased in patients with severe hepatic impairment. Therapeutic experience in patients with severe hepatic impairment is limited and therefore not recommended for use in this population (see section 5.2).
Elderly
No dose adjustment is recommended based on age. In patients 75 years and older, an increased risk for volume depletion should be taken into account (see sections 4.4 and 4.8). In patients aged 85 years and older, initiation of empagliflozin therapy is not recommended due to the limited therapeutic experience (see section 4.4).
Paediatric population
The safety and efficacy of empagliflozin in children and adolescents has not yet been established. No data are available.
Method of administration
The tablets can be taken with or without food, swallowed whole with water. If a dose is missed, it should be taken as soon as the patient remembers. A double dose should not be taken on the same day.
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
4.4 Special warnings and precautions for use
General
Jardiance should not be used in patients with type 1 diabetes or for the treatment of diabetic ketoacidosis.
Renal impairment
Jardiance should not be initiated in patients with an eGFR below 60 ml/min/1.73 m2 or CrCl <60 ml/min. In patients tolerating empagliflozin whose eGFR is persistently below 60 ml/min/1.73 m2 or CrCl <60 ml/min, the dose of empagliflozin should be adjusted to or maintained at 10 mg once daily. Empagliflozin should be discontinued when eGFR is persistently below 45 ml/min/1.73 m2 or CrCl persistently below 45 ml/min. Empagliflozin should not be used in patients with ESRD or in patients on dialysis as it is not expected to be effective in these patients (see sections 4.2 and 5.2).
Monitoring of renal function
Due to the mechanism of action, the efficacy of empagliflozin is dependent on renal function. Therefore assessment of renal function is recommended as follows:
- Prior to empagliflozin initiation and periodically during treatment, i.e. at least yearly (see sections 4.2, 5.1 and 5.2).
- Prior to initiation of any concomitant medicinal product that may have a negative impact on renal function.
Hepatic injury
Cases of hepatic injury have been reported with empagliflozin in clinical trials. A causal relationship between empagliflozin and hepatic injury has not been established.
Elderly
The effect of empagliflozin on urinary glucose excretion is associated with osmotic diuresis, which could affect the hydration status. Patients aged 75 years and older may be at an increased risk of volume depletion. A higher number of these patients treated with empagliflozin had adverse reactions related to volume depletion as compared to placebo (see section 4.8).
Therapeutic experience in patients aged 85 years and older is limited. Initiation of empagliflozin therapy in this population is not recommended (see section 4.2).
Risk for volume depletion
Based on the mode of action of SGLT-2 inhibitors, osmotic diuresis accompanying therapeutic glucosuria may lead to a modest decrease in blood pressure (see section 5.1). Therefore, caution should be exercised in patients for whom an empagliflozin-induced drop in blood pressure could pose a risk, such as patients with known cardiovascular disease, patients on anti-hypertensive therapy with a history of hypotension or patients aged 75 years and older.
In case of conditions that may lead to fluid loss (e.g. gastrointestinal illness), careful monitoring of volume status (e.g. physical examination, blood pressure measurements, laboratory tests including haematocrit) and electrolytes is recommended for patients receiving empagliflozin. Temporary interruption of treatment with empagliflozin should be considered until the fluid loss is corrected.
Urinary tract infections
The overall frequency of urinary tract infection reported as adverse event was similar in patients treated with empagliflozin 25 mg and placebo and higher in patients treated with empagliflozin 10 mg (see section 4.8). Complicated urinary tract infection (e.g. pyelonephritis or urosepsis) occurred at a similar frequency in patients treated with empagliflozin compared to placebo. However, temporary interruption of empagliflozin should be considered in patients with complicated urinary tract infections.
Cardiac failure
Experience in New York Heart Association (NYHA) class I-II is limited, and there is no experience in clinical studies with empagliflozin in NYHA class III-IV.
Urine laboratory assessments
Due to its mechanism of action, patients taking Jardiance will test positive for glucose in their urine.
Lactose
The tablets contain lactose. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency, or glucose-galactose malabsorption should not take this medicinal product.
4.5 Interaction with other medicinal products and other forms of interaction
Pharmacodynamic interactions
Diuretics
Empagliflozin may add to the diuretic effect of thiazide and loop diuretics and may increase the risk of dehydration and hypotension (see section 4.4).
Insulin and insulin secretagogues
Insulin and insulin secretagogues, such as sulphonylureas, may increase the risk of hypoglycaemia. Therefore, a lower dose of insulin or an insulin secretagogue may be required to reduce the risk of hypoglycaemia when used in combination with empagliflozin (see sections 4.2 and 4.8).
Pharmacokinetic interactions
Effects of other medicinal products on empagliflozin
In vitro data suggest that the primary route of metabolism of empagliflozin in humans is glucuronidation by uridine 5'-diphosphoglucuronosyltransferases UGT1A3, UGT1A8, UGT1A9, and UGT2B7. Empagliflozin is a substrate of the human uptake transporters OAT3, OATP1B1, and OATP1B3, but not OAT1 and OCT2. Empagliflozin is a substrate of P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP).
Co-administration of empagliflozin with probenecid, an inhibitor of UGT enzymes and OAT3, resulted in a 26% increase in peak empagliflozin plasma concentrations (Cmax) and a 53% increase in area under the concentration-time curve (AUC). These changes were not considered to be clinically meaningful.
The effect of UGT induction on empagliflozin has not been studied. Co-medication with known inducers of UGT enzymes should be avoided due to a potential risk of decreased efficacy.
An interaction study with gemfibrozil, an in vitro inhibitor of OAT3 and OATP1B1/1B3 transporters, showed that empagliflozin Cmax increased by 15% and AUC increased by 59% following co-administration. These changes were not considered to be clinically meaningful.
Inhibition of OATP1B1/1B3 transporters by co-administration with rifampicin resulted in a 75% increase in Cmax and a 35% increase in AUC of empagliflozin. These changes were not considered to be clinically meaningful.
Empagliflozin exposure was similar with and without co-administration with verapamil, a P-gp inhibitor, indicating that inhibition of P-gp does not have any clinically relevant effect on empagliflozin.
Interaction studies conducted in healthy volunteers suggest that the pharmacokinetics of empagliflozin were not influenced by co-administration with metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, warfarin, verapamil, ramipril, simvastatin, torasemide and hydrochlorothiazide.
Effects of empagliflozin on other medicinal products
Based on in vitro studies, empagliflozin does not inhibit, inactivate, or induce CYP450 isoforms. Empagliflozin does not inhibit UGT1A1, UGT1A3, UGT1A8, UGT1A9, or UGT2B7. Drug-drug interactions involving the major CYP450 and UGT isoforms with empagliflozin and concomitantly administered substrates of these enzymes are therefore considered unlikely.
Empagliflozin does not inhibit P-gp at therapeutic doses. Based on in vitro studies, empagliflozin is considered unlikely to cause interactions with drugs that are P-gp substrates. Co-administration of digoxin, a P-gp substrate, with empagliflozin resulted in a 6% increase in AUC and 14% increase in Cmax of digoxin. These changes were not considered to be clinically meaningful.
Empagliflozin does not inhibit human uptake transporters such as OAT3, OATP1B1, and OATP1B3 in vitro at clinically relevant plasma concentrations and, as such, drug-drug interactions with substrates of these uptake transporters are considered unlikely.
Interaction studies conducted in healthy volunteers suggest that empagliflozin had no clinically relevant effect on the pharmacokinetics of metformin, glimepiride, pioglitazone, sitagliptin, linagliptin, simvastatin, warfarin, ramipril, digoxin, diuretics and oral contraceptives.
4.6 Fertility, pregnancy and lactation
Pregnancy
There are no data from the use of empagliflozin in pregnant women. Animal studies show that empagliflozin crosses the placenta during late gestation to a very limited extent but do not indicate direct or indirect harmful effects with respect to early embryonic development. However, animal studies have shown adverse effects on postnatal development (see section 5.3). As a precautionary measure, it is preferable to avoid the use of Jardiance during pregnancy.
Breast-feeding
No data in humans are available on excretion of empagliflozin into milk. Available toxicological data in animals have shown excretion of empagliflozin in milk. A risk to the newborns/infants cannot be excluded. Jardiance should not be used during breast-feeding.
Fertility
No studies on the effect on human fertility have been conducted for Jardiance. Animal studies do not indicate direct or indirect harmful effects with respect to fertility (see section 5.3).
4.7 Effects on ability to drive and use machines
Jardiance has minor influence on the ability to drive and use machines. Patients should be advised to take precautions to avoid hypoglycaemia while driving and using machines, in particular when Jardiance is used in combination with a sulphonylurea and/or insulin.
4.8 Undesirable effects
Summary of the safety profile
A total of 13,076 patients with type 2 diabetes were included in clinical studies to evaluate the safety of empagliflozin. 2856 patients received empagliflozin 10 mg and 3,738 patients received empagliflozin 25 mg for at least 24 weeks and 601 or 881 patients for at least 76 weeks, either alone or in combination with metformin, a sulphonylurea, pioglitazone, DPP-4 inhibitors, or insulin.
In 5 placebo-controlled trials of 18 to 24 weeks duration, 2,971 patients were included of which 995 were treated with placebo and 1,976 with empagliflozin. The overall incidence of adverse events in patients treated with empagliflozin was similar to placebo. The most frequently reported adverse reaction was hypoglycaemia when used with sulphonylurea or insulin (see description of selected adverse reactions).
Tabulated list of adverse reactions
Adverse reactions classified by system organ class and MedDRA preferred terms reported in patients who received empagliflozin in placebo-controlled studies are presented in the table below (Table 1).
The adverse reactions are listed by absolute frequency. Frequencies are defined as very common (≥1/10), common (≥1/100 to <1/10), uncommon (≥1/1,000 to <1/100), rare (≥1/10,000 to <1/1,000), or very rare (<1/10,000), and not known (cannot be estimated from the available data).
Table 1: Adverse reactions reported in placebo-controlled studies

System organ class

Very common

Common

Uncommon

Infections and infestations

 

Vaginal moniliasis, vulvovaginitis, balanitis and other genital infectiona

Urinary tract infectiona

 

Metabolism and nutrition disorders

Hypoglycaemia (when used with sulphonylurea or insulin)a

   

Skin and subcutaneous disorders

 

Pruritus (generalised)

 

Vascular disorders

   

Volume depletiona

Renal and urinary disorders

 

Increased urinationa

Dysuria

a see subsections below for additional information
Description of selected adverse reactions
Hypoglycaemia
The frequency of hypoglycaemia depended on the background therapy in the respective studies.
Minor hypoglycaemia
The frequency of patients with minor hypoglycaemia was similar for empagliflozin and placebo as monotherapy, add-on to metformin, and add-on to pioglitazone with or without metformin. An increased frequency was noted when given as add-on to metformin and a sulfonylurea (empagliflozin 10 mg: 16.1%, empagliflozin 25 mg: 11.5%, placebo: 8.4%), and as add-on to insulin with or without metformin and with or without a sulphonylurea (empagliflozin 10 mg: 19.5%, empagliflozin 25 mg: 27.1%, placebo: 20.6% during initial 18 weeks treatment when insulin could not be adjusted; empagliflozin 10 mg: 36.1%, empagliflozin 25 mg: 34.8%, placebo 35.3% over the 78-week trial).
Major hypoglycaemia (hypoglycaemia requiring assistance)
No increase in major hypoglycaemia was observed with empagliflozin compared to placebo as monotherapy, add-on to metformin, add-on to metformin and a sulfonylurea, and add-on to pioglitazone with or without metformin. An increased frequency was noted when given as add-on to insulin with or without metformin and with or without a sulfonylurea (empagliflozin 10 mg: 0%, empagliflozin 25 mg: 1.3%, placebo: 0% during initial 18 weeks treatment when insulin could not be adjusted; empagliflozin 10 mg: 0%, empagliflozin 25 mg: 1.3%, placebo 0% over the 78-week trial).
Vaginal moniliasis, vulvovaginitis, balanitis and other genital infection
Vaginal moniliasis, vulvovaginitis, balanitis and other genital infections were reported more frequently in patients treated with empagliflozin (empagliflozin 10 mg: 4.1%, empagliflozin 25 mg: 3.7%) compared to placebo (0.9%). These infections were reported more frequently in females treated with empagliflozin compared to placebo, and the difference in frequency was less pronounced in males. The genital tract infections were mild or moderate in intensity.
Increased urination
Increased urination (including the predefined terms pollakiuria, polyuria, and nocturia) was observed at higher frequencies in patients treated with empagliflozin (empagliflozin 10 mg: 3.4%, empagliflozin 25 mg: 3.2%) compared to placebo (1.0%). Increased urination was mostly mild or moderate in intensity. The frequency of reported nocturia was similar for placebo and empagliflozin (<1%).
Urinary tract infection
The overall frequency of urinary tract infection reported as adverse event was similar in patients treated with empagliflozin 25 mg and placebo (7.6%) and higher in empagliflozin 10 mg (9.3%). Similar to placebo, urinary tract infection was reported more frequently for empagliflozin in patients with a history of chronic or recurrent urinary tract infections. The intensity (mild, moderate, severe) of urinary tract infection was similar in patients treated with empagliflozin and placebo. Urinary tract infection was reported more frequently in females treated with empagliflozin compared to placebo; there was no difference in males.
Volume depletion
The overall frequency of volume depletion (including the predefined terms blood pressure (ambulatory) decreased, blood pressure systolic decreased, dehydration, hypotension, hypovolaemia, orthostatic hypotension, and syncope) was similar in patients treated with empagliflozin (empagliflozin 10 mg: 0.5%, empagliflozin 25 mg: 0.3%) and placebo (0.3%). The frequency of volume depletion events was increased in patients 75 years and older treated with empagliflozin 10 mg (2.3%) or empagliflozin 25 mg (4.4%) compared to placebo (2.1%).
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via:
United Kingdom
Yellow Card Scheme
Website: www.mhra.gov.uk/yellowcard
Ireland
HPRA Pharmacovigilance
Earlsfort Terrace
Ireland - Dublin 2
Tel: +353 1 6764971
Fax: +353 1 6762517
Website: www.hpra.ie
e-mail: medsafety@hpra.ie
Malta
ADR Reporting
Website: www.medicinesauthority.gov.mt/adrportal
4.9 Overdose
Symptoms
In controlled clinical studies single doses of up to 800 mg empagliflozin (equivalent to 32 times the highest recommended daily dose) in healthy volunteers and multiple daily doses of up to 100 mg empagliflozin (equivalent to 4 times the highest recommended daily dose) in patients with type 2 diabetes did not show any toxicity. Empagliflozin increased urine glucose excretion leading to an increase in urine volume. The observed increase in urine volume was not dose-dependent and is not clinically meaningful. There is no experience with doses above 800 mg in humans.
Therapy
In the event of an overdose, treatment should be initiated as appropriate to the patient's clinical status. The removal of empagliflozin by haemodialysis has not been studied.
5. Pharmacological properties
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Drugs used in diabetes, Other blood glucose lowering drugs, excl. insulins, ATC code: A10BX12
Mechanism of action
Empagliflozin is a reversible, highly potent (IC50 of 1.3 nmol) and selective competitive inhibitor of sodium-glucose co-transporter 2 (SGLT2). Empagliflozin does not inhibit other glucose transporters important for glucose transport into peripheral tissues and is 5000 times more selective for SGLT2 versus SGLT1, the major transporter responsible for glucose absorption in the gut. SGLT2 is highly expressed in the kidney, whereas expression in other tissues is absent or very low. It is responsible, as the predominant transporter, for the reabsorption of glucose from the glomerular filtrate back into the circulation. In patients with type 2 diabetes and hyperglycaemia a higher amount of glucose is filtered and reabsorbed.
Empagliflozin improves glycaemic control in patients with type 2 diabetes by reducing renal glucose reabsorption. The amount of glucose removed by the kidney through this glucuretic mechanism is dependent on blood glucose concentration and GFR. Inhibition of SGLT2 in patients with type 2 diabetes and hyperglycaemia leads to excess glucose excretion in the urine.
In patients with type 2 diabetes, urinary glucose excretion increased immediately following the first dose of empagliflozin and is continuous over the 24 hour dosing interval. Increased urinary glucose excretion was maintained at the end of the 4-week treatment period, averaging approximately 78 g/day. Increased urinary glucose excretion resulted in an immediate reduction in plasma glucose levels in patients with type 2 diabetes.
Empagliflozin improves both fasting and post-prandial plasma glucose levels. The mechanism of action of empagliflozin is independent of beta cell function and insulin pathway and this contributes to a low risk of hypoglycaemia. Improvement of surrogate markers of beta cell function including Homeostasis Model Assessment-β (HOMA-β) was noted. In addition, urinary glucose excretion triggers calorie loss, associated with body fat loss and body weight reduction. The glucosuria observed with empagliflozin is accompanied by mild diuresis which may contribute to sustained and moderate reduction of blood pressure.
Clinical efficacy and safety
A total of 11,250 patients with type 2 diabetes were treated in 10 double-blind, placebo- and active-controlled clinical studies, of which 7,015 received empagliflozin (empagliflozin 10 mg: 3021 patients; empagliflozin 25 mg: 3994 patients). Four studies had treatment durations of 24 weeks; extensions of those and other studies had patients exposed to empagliflozin for up to 102 weeks.
Treatment with empagliflozin as monotherapy and in combination with metformin, pioglitazone, a sulphonylurea, DPP-4 inhibitors, and insulin lead to clinically relevant improvements in HbA1c, fasting plasma glucose (FPG), body weight, and systolic and diastolic blood pressure. Administration of empagliflozin 25 mg resulted in a higher proportion of patients achieving HbA1c goal of less than 7% and fewer patients needing glycaemic rescue compared to empagliflozin 10 mg and placebo. Higher baseline HbA1c was associated with a greater reduction in HbA1c.
Monotherapy
The efficacy and safety of empagliflozin as monotherapy was evaluated in a double-blind, placebo- and active-controlled study of 24 weeks duration in treatment-naïve patients. Treatment with empagliflozin resulted in a statistically significant (p<0.0001) reduction in HbA1c compared to placebo (Table 2) and a clinically meaningful decrease in FPG.
In a prespecified analysis of patients (N=201) with a baseline HbA1c ≥8.5%, treatment resulted in a reduction in HbA1c from baseline of -1.44% for empagliflozin 10 mg, -1.43% for empagliflozin 25 mg, -1.04% for sitagliptin, and an increase of 0.01% for placebo.
In the double-blind placebo-controlled extension of this study, reductions of HbA1c, body weight and blood pressure were sustained up to Week 52.
Table 2: Efficacy results of a 24 week placebo-controlled study of empagliflozin as monotherapya

Placebo

Jardiance

Sitagliptin

10 mg

25 mg

100 mg

N

228

224

224

223

HbA1c (%)

Baseline (mean)

7.91

7.87

7.86

7.85

Change from baseline1

0.08

-0.66

-0.78

-0.66

Difference from placebo1 (97.5% CI)

 

-0.74*

(-0.90, -0.57)

-0.85*

(-1.01, -0.69)

-0.73

(-0.88, -0.59)3

N

208

204

202

200

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7%2

12.0

35.3

43.6

37.5

N

228

224

224

223

Body Weight (kg)

Baseline (mean)

78.23

78.35

77.80

79.31

Change from baseline1

-0.33

-2.26

-2.48

0.18

Difference from placebo1 (97.5% CI)

 

-1.93*

(-2.48, -1.38)

-2.15*

(-2.70,-1.60)

0.52

(-0.04, 1.00)3

N

228

224

224

223

SBP (mmHg)4

Baseline (mean)

130.4

133.0

129.9

132.5

Change from baseline1

-0.3

-2.9

-3.7

0.5

Difference from placebo1 (97.5% CI)

 

-2.6* (-5.2, -0.0)

-3.4* (-6.0, -0.9)

0.8 (-1.4, 3.1)3

a Full analysis set (FAS) using last observation carried forward (LOCF) prior to glycaemic rescue therapy
1 Mean adjusted for baseline value
2 Not evaluated for statistical significance as a result of the sequential confirmatory testing procedure
3 95% CI
4 LOCF, values after antihypertensive rescue censored
*p-value <0.0001
Combination therapy
Empagliflozin as add on to metformin, sulphonylurea, pioglitazone
Empagliflozin as add-on to metformin, metformin and a sulphonylurea, or pioglitazone with or without metformin resulted in statistically significant (p<0.0001) reductions in HbA1c and body weight compared to placebo (Table 3). In addition it resulted in a clinically meaningful reduction in FPG, systolic and diastolic blood pressure compared to placebo.
In the double-blind placebo-controlled extension of these studies, reduction of HbA1c, body weight and blood pressure were sustained up to Week 52.
Table 3: Efficacy results of 24 week placebo-controlled studiesa

Add-on to metformin therapy

 

Placebo

Jardiance

10 mg

25 mg

N

207

217

213

HbA1c (%)

Baseline (mean)

7.90

7.94

7.86

Change from baseline1

-0.13

-0.70

-0.77

Difference from placebo1 (97.5% CI)

 

-0.57*

(-0.72, -0.42)

-0.64*

(-0.79, -0.48)

N

184

199

191

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7%2

12.5

37.7

38.7

N

207

217

213

Body Weight (kg)

Baseline (mean)

79.73

81.59

82.21

Change from baseline1

-0.45

-2.08

-2.46

Difference from placebo1 (97.5% CI)

 

-1.63*

(-2.17, -1.08)

-2.01*

(-2.56, -1.46)

N

207

217

213

SBP (mmHg)2

Baseline (mean)

128.6

129.6

130.0

Change from baseline1

-0.4

-4.5

-5.2

Difference from placebo1 (95% CI)

 

-4.1*

(-6.2, -2.1)

-4.8*

(-6.9, -2.7)

Add-on to metformin and a sulphonylurea therapy

 

Placebo

Jardiance

10 mg

25 mg

N

225

225

216

HbA1c (%)

Baseline (mean)

8.15

8.07

8.10

Change from baseline1

-0.17

-0.82

-0.77

Difference from placebo1 (97.5% CI)

 

-0.64*

(-0.79, -0.49)

-0.59*

(-0.74, -0.44)

N

216

209

202

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7%2

9.3

26.3

32.2

N

225

225

216

Body Weight (kg)

Baseline (mean)

76.23

77.08

77.50

Change from baseline1

-0.39

-2.16

-2.39

Difference from placebo1 (97.5% CI)

 

-1.76*

(-2.25, -1.28)

-1.99*

(-2.48, -1.50)

N

225

225

216

SBP (mmHg)2

Baseline (mean)

128.8

128.7

129.3

Change from baseline1

-1.4

-4.1

-3.5

Difference from placebo1 (95% CI)

 

-2.7 (-4.6, -0.8)

-2.1 (-4.0, -0.2)

Add-on to pioglitazone +/- metformin therapy

 

Placebo

Jardiance

10 mg

25 mg

N

165

165

168

HbA1c (%)

Baseline (mean)

8.16

8.07

8.06

Change from baseline1

-0.11

-0.59

-0.72

Difference from placebo1 (97.5% CI)

 

-0.48*

(-0.69, -0.27)

-0.61*

(-0.82, -0.40)

N

155

151

160

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7%2

7.7

24

30

N

165

165

168

Body Weight (kg)

Baseline (mean)

78.1

77.97

78.93

Change from baseline1

0.34

-1.62

-1.47

Difference from placebo1 (97.5% CI)

 

-1.95*

(-2.64, -1.27)

-1.81*

(-2.49, -1.13)

N

165

165

168

SBP (mmHg)3

Baseline (mean)

125.7

126.5

126

Change from baseline1

0.7

-3.1

-4.0

Difference from placebo1 (95% CI)

 

-3.9

(-6.23, -1.50)

-4.7

(-7.08, -2.37)

a Full analysis set (FAS) using last observation carried forward (LOCF) prior to glycaemic rescue therapy
1 Mean adjusted for baseline value
2 Not evaluated for statistical significance as a result of the sequential confirmatory testing procedure
3 LOCF, values after antihypertensive rescue censored
* p-value <0.0001
Empagliflozin 24 months data, as add on to metformin in comparison to glimepiride
In a study comparing the efficacy and safety of empagliflozin 25 mg versus glimepiride (up to 4 mg per day) in patients with inadequate glycaemic control on metformin alone, treatment with empagliflozin daily resulted in superior reduction in HbA1c (Table 4), and a clinically meaningful reduction in FPG, compared to glimepiride. Empagliflozin daily resulted in a statistically significant reduction in body weight, systolic and diastolic blood pressure and a statistically significantly lower proportion of patients with hypoglycaemic events compared to glimepiride (2.5% for empagliflozin, 24.2% for glimepiride, p<0.0001).
Table 4: Efficacy results at 104 week in an active controlled study comparing empagliflozin to glimepiride as add on to metformina

Empagliflozin 25 mg

Glimepirideb

N

765

780

HbA1c (%)

Baseline (mean)

7.92

7.92

Change from baseline1

-0.66

-0.55

Difference from glimepiride1 (97.5% CI)

-0.11*

(-0.20, -0.01)

 

N

690

715

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7%2

33.6

30.9

N

765

780

Body Weight (kg)

Baseline (mean)

82.52

83.03

Change from baseline1

-3.12

1.34

Difference from glimepiride1 (97.5% CI)

-4.46**

(-4.87, -4.05)

 

N

765

780

SBP (mmHg)2

Baseline (mean)

133.4

133.5

Change from baseline1

-3.1

2.5

Difference from glimepiride1 (97.5% CI)

-5.6**

(-7.0,-4.2)

 
a Full analysis set (FAS) using last observation carried forward (LOCF) prior to glycaemic rescue therapy
b Up to 4 mg glimepiride
1 Mean adjusted for baseline value
2 LOCF, values after antihypertensive rescue censored
* p-value <0.0001 for non-inferiority, and p-value = 0.0153 for superiority
** p-value <0.0001
Add-on to insulin therapy
Empagliflozin as add on to multiple daily insulin
The efficacy and safety of empagliflozin as add-on to multiple daily insulin with or without concomitant metformin therapy was evaluated in a double-blind, placebo-controlled trial of 52 weeks duration. During the initial 18 weeks and the last 12 weeks, the insulin dose was kept stable, but was adjusted to achieve pre-prandial glucose levels <100 mg/dl [5.5 mmol/l], and post-prandial glucose levels <140 mg/dl [7.8 mmol/l] between Weeks 19 and 40.
At Week 18, empagliflozin provided statistically significant improvement in HbA1c compared with placebo (Table 5).
At Week 52, treatment with empagliflozin resulted in a statistically significant decrease in HbA1c and insulin sparing compared with placebo and a reduction in FPG and body weight.
Table 5: Efficacy results at 18 and 52 weeks in a placebo-controlled study of empagliflozin as add on to multiple daily doses of insulin with or without metformin

Placebo

Jardiance

10 mg

25 mg

N

188

186

189

HbA1c (%) at week 18

Baseline (mean)

8.33

8.39

8.29

Change from baseline1

-0.50

-0.94

-1.02

Difference from placebo1 (97.5% CI)

 

-0.44*

(-0.61, -0.27)

-0.52*

(-0.69, -0.35)

N

115

119

118

HbA1c (%) at week 522

     

Baseline (mean)

8.25

8.40

8.37

Change from baseline1

-0.81

-1.18

-1.27

Difference from placebo1 (97.5% CI)

 

-0.38***

(-0.62, -0.13)

-0.46*

(-0.70, -0.22)

N

113

118

118

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7% at week 52

26.5

39.8

45.8

N

115

118

117

Insulin dose (IU/day) at week 522

Baseline (mean)

89.94

88.57

90.38

Change from baseline1

10.16

1.33

-1.06

Difference from placebo1 (97.5% CI)

 

-8.83#

(-15.69, -1.97)

-11.22**

(-18.09, -4.36)

N

115

119

118

Body Weight (kg) at week 522

Baseline (mean)

96.34

96.47

95.37

Change from baseline1

0.44

-1.95

-2.04

Difference from placebo1 (97.5% CI)

 

-2.39*

(-3.54, -1.24)

-2.48*

(-3.63, -1.33)

1 Mean adjusted for baseline value
2 Week 19-40: treat-to-target regimen for insulin dose adjustment to achieve pre-defined glucose target levels (pre-prandial <100 mg/dl (5.5 mmol/l), post-prandial <140 mg/dl (7.8 mmol/l)
p-value <0.0001
p-value = 0.0003
p-value = 0.0005
p-value = 0.0040
Empagliflozin as add on to basal insulin
The efficacy and safety of empagliflozin as add on to basal insulin with or without metformin and/or a sulphonylurea was evaluated in a double-blind, placebo-controlled trial of 78 weeks duration. During the initial 18 weeks the insulin dose was kept stable, but was adjusted to achieve a FPG <110 mg/dl in the following 60 weeks.
At week 18, empagliflozin provided statistically significant improvement in HbA1c (Table 6).
At 78 weeks, empagliflozin resulted in a statistically significant decrease in HbA1c and insulin sparing compared to placebo. Furthermore, empagliflozin resulted in a reduction in FPG, body weight, and blood pressure.
Table 6 Efficacy results at 18 and 78 weeks in a placebo-controlled study of empagliflozin as add on to basal insulin with or without metformin or a sulphonylureaa

Placebo

Empagliflozin

10 mg

Empagliflozin

25 mg

N

125

132

117

HbA1c (%) at week 18

     

Baseline (mean)

8.10

8.26

8.34

Change from baseline1

-0.01

-0.57

-0.71

Difference from placebo1 (97.5% CI)

 

-0.56*

(-0.78, -0.33)

-0.70*

(-0.93, -0.47)

N

112

127

110

HbA1c (%) at week 78

     

Baseline (mean)

8.09

8.27

8.29

Change from baseline1

-0.02

-0.48

-0.64

Difference from placebo1 (97.5% CI)

 

-0.46*

(-0.73, -0.19)

-0.62*

(-0.90, -0.34)

N

112

127

110

Basal insulin dose (IU/day) at week 78

     

Baseline (mean)

47.84

45.13

48.43

Change from baseline1

5.45

-1.21

-0.47

Difference from placebo1 (97.5% CI)

 

-6.66**

(-11.56, -1.77)

-5.92**

(-11.00, -0.85)

a Full analysis set (FAS) - Completers using last observation carried forward (LOCF) prior to glycaemic rescue therapy
1 mean adjusted for baseline value
p-value <0.0001
p-value <0.025
Patients with renal impairment, 52 week placebo controlled data
The efficacy and safety of empagliflozin as add on to antidiabetic therapy was evaluated in patients with renal impairment in a double-blind, placebo-controlled study for 52 weeks. Treatment with empagliflozin led to a statistically significant reduction of HbA1c (Table 7) and clinically meaningful improvement in FPG compared to placebo at Week 24. The improvement in HbA1c, body weight, and blood pressure was sustained up to 52 weeks.
Table 7 Results at 24 week in a placebo-controlled study of empagliflozin in renally impaired type 2 diabetes patientsa

Placebo

Empagliflozin 10 mg

Empagliflozin 25 mg

Placebo

Empagliflozin 25 mg

eGFR ≥60 to <90 ml/min/1.73 m2

eGFR ≥45 to <60 ml/min/1.73 m2

N

95

98

97

89

91

HbA1c (%)

Baseline (mean)

8.09

8.02

7.96

8.08

8.12

Change from baseline1

0.06

-0.46

-0.63

-0.08

-0.54

Difference from placebo1 (95% CI)

 

-0.52*

(-0.72, -0.32)

-0.68*

(-0.88, -0.49)

 

-0.46

(-0.66, -0.27)

N

89

94

91

84

86

Patients (%) achieving HbA1c <7% with baseline HbA1c ≥7%2

6.7

17.0

24.2

10.7

15.1

N

95

98

97

89

91

Body Weight (kg)2

Baseline (mean)

86.00

92.05

88.06

83.20

84.90

Change from baseline1

-0.33

-1.76

-2.33

-0.25

-0.98

Difference from placebo1 (95% CI)

 

-1.43

(-2.09, -0.77)

-2.00

(-2.66, -1.34)

 

-0.74

(-1.50, -0.03)

N

95

98

97

89

91

SBP (mmHg)2

Baseline (mean)

134.69

137.37

133.68

137.29

135.04

Change from baseline1

0.65

-2.92

-4.47

0.37

-5.69

Difference from placebo1 (95% CI)

 

-3.57

(-6.86, -0.29)

-5.12

(-8.41, -1.82)

 

-6.07

(-9.79, -2.34)

a Full analysis set (FAS) using last observation carried forward (LOCF) prior to glycaemic rescue therapy
1 Mean adjusted for baseline value
2 Not evaluated for statistical significance as a result of the sequential confirmatory testing procedure
p<0.0001
Cardiovascular safety
In a prospective, pre-specified meta-analysis of independently adjudicated cardiovascular events from 12 phase 2 and 3 clinical studies involving 10,036 patients with type 2 diabetes, empagliflozin did not increase cardiovascular risk.
Fasting plasma glucose
In four placebo-controlled studies, treatment with empagliflozin as monotherapy or add-on therapy to metformin, pioglitazone, or metformin plus a sulfonylurea resulted in mean changes from baseline in FPG of -20.5 mg/dl [-1.14 mmol/l] for empagliflozin 10 mg and -23.2 mg/dl [-1.29 mmol/l] for empagliflozin 25 mg compared to placebo (7.4 mg/dl [0.41 mmol/l]). This effect was observed after 24 weeks and maintained for 76 weeks.
2-hour post-prandial glucose
Treatment with empagliflozin as add-on to metformin or metformin and a sulphonylurea resulted in a clinically meaningful reduction of 2-hour post-prandial glucose (meal tolerance test) at 24 weeks (add-on to metformin: placebo +5.9 mg/dl, empagliflozin 10 mg: -46.0 mg/dl, empagliflozin 25 mg: -44.6 mg/dl, add-on to metformin and a sulphonylurea: placebo -2.3 mg/dl, empagliflozin 10 mg: -35.7 mg/dl, empagliflozin 25 mg: -36.6 mg/dl).
Patients with high baseline HbA1c >10%
In a pre-specified pooled analysis of three phase 3 studies, treatment with open-label empagliflozin 25 mg in patients with severe hyperglycaemia (N=184, mean baseline HbA1c 11.15%) resulted in a clinically meaningful reduction in HbA1c from baseline of 3.27% at week 24; no placebo or empagliflozin 10 mg arms were included in these studies.
Body weight
In a pre-specified pooled analysis of 4 placebo controlled studies, treatment with empagliflozin resulted in body weight reduction (-0.24 kg for placebo, -2.04 kg for empagliflozin 10 mg and -2.26 kg for empagliflozin 25 mg) at week 24 that was maintained up to week 52 (-0.16 kg for placebo, -1.96 kg for empagliflozin 10 mg and -2.25 kg for empagliflozin 25 mg).
Blood pressure
The efficacy and safety of empagliflozin was evaluated in a double-blind, placebo controlled study of 12 weeks duration in patients with type 2 diabetes and high blood pressure on different antidiabetic and up to 2 antihypertensive therapies. Treatment with empagliflozin once daily resulted in statistically significant improvement in HbA1c, and 24 hour mean systolic and diastolic blood pressure as determined by ambulatory blood pressure monitoring (Table 8). Treatment with empagliflozin provided reductions in seated SBP and DBP.
Table 8 Efficacy results at 12 week in a placebo-controlled study of empagliflozin in patients with type 2 diabetes and uncontrolled blood pressurea

Placebo

Jardiance

10 mg

25 mg

N

271

276

276

HbA1c (%) at week 121

Baseline (mean)

7.90

7.87

7.92

Change from baseline2

0.03

-0.59

-0.62

Difference from placebo2 (95% CI)

 

-0.62*

(-0.72, -0.52)

-0.65*

(-0.75, -0.55)

24 hour SBP at week 123

Baseline (mean)

131.72

131.34

131.18

Change from baseline4

0.48

-2.95

-3.68

Difference from placebo4 (95% CI)

 

-3.44*

(-4.78, -2.09)

-4.16*

(-5.50, -2.83)

24 hour DBP at week 123

Baseline (mean)

75.16

75.13

74.64

Change from baseline5

0.32

-1.04

-1.40

Difference from placebo5 (95% CI)

 

-1.36**

(-2.15, -0.56)

-1.72*

(-2.51, -0.93)

a Full analysis set (FAS)
1 LOCF, values after taking antidiabetic rescue therapy censored
2 Mean adjusted for baseline HbA1c, baseline eGFR, geographical region and number of antihypertensive medicinal products
3 LOCF, values after taking antidiabetic rescue therapy or changing antihypertensive rescue therapy censored
4 Mean adjusted for baseline SBP, baseline HbA1c, baseline eGFR, geographical region and number of antihypertensive medicinal products
5 Mean adjusted for baseline DBP, baseline HbA1c, baseline eGFR, geographical region and number of antihypertensive medicinal products
p-value <0.0001
p-value <0.001
In a pre-specified pooled analysis of 4 placebo-controlled studies, treatment with empagliflozin resulted in a reduction in systolic blood pressure (empagliflozin 10 mg: -3.9 mmHg; empagliflozin 25 mg: -4.3 mmHg) compared with placebo (-0.5 mmHg) and in diastolic blood pressure (empagliflozin 10 mg: -1.8 mmHg; empagliflozin 25 mg: -2.0 mmHg) compared with placebo (-0.5 mmHg) at week 24 that were maintained up to week 52.
Paediatric population
The European Medicines Agency has deferred the obligation to submit the results of studies with Jardiance in one or more subsets of the paediatric population in type 2 diabetes mellitus (see section 4.2 for information on paediatric use).
5.2 Pharmacokinetic properties
Absorption
The pharmacokinetics of empagliflozin have been extensively characterised in healthy volunteers and patients with type 2 diabetes. After oral administration, empagliflozin was rapidly absorbed with peak plasma concentrations occurring at a median tmax of 1.5 hours post-dose. Thereafter, plasma concentrations declined in a biphasic manner with a rapid distribution phase and a relatively slow terminal phase. The steady state mean plasma AUC and Cmax were 1870 nmol.h and 259 nmol/l with empagliflozin 10 mg and 4740 nmol.h and 687 nmol/l with empagliflozin 25 mg once daily. Systemic exposure of empagliflozin increased in a dose-proportional manner. The single-dose and steady-state pharmacokinetic parameters of empagliflozin were similar suggesting linear pharmacokinetics with respect to time. There were no clinically relevant differences in empagliflozin pharmacokinetics between healthy volunteers and patients with type 2 diabetes.
Administration of empagliflozin 25 mg after intake of a high-fat and high calorie meal resulted in slightly lower exposure; AUC decreased by approximately 16% and Cmax by approximately 37% compared to fasted condition. The observed effect of food on empagliflozin pharmacokinetics was not considered clinically relevant and empagliflozin may be administered with or without food.
Distribution
The apparent steady-state volume of distribution was estimated to be 73.8 l based on the population pharmacokinetic analysis. Following administration of an oral [14C]-empagliflozin solution to healthy volunteers, the red blood cell partitioning was approximately 37% and plasma protein binding was 86%.
Biotransformation
No major metabolites of empagliflozin were detected in human plasma and the most abundant metabolites were three glucuronide conjugates (2-, 3-, and 6-O glucuronide). Systemic exposure of each metabolite was less than 10% of total drug-related material. In vitro studies suggested that the primary route of metabolism of empagliflozin in humans is glucuronidation by the uridine 5'-diphospho-glucuronosyltransferases UGT2B7, UGT1A3, UGT1A8, and UGT1A9.
Elimination
Based on the population pharmacokinetic analysis, the apparent terminal elimination half-life of empagliflozin was estimated to be 12.4 hours and apparent oral clearance was 10.6 l/hour. The inter-subject and residual variabilities for empagliflozin oral clearance were 39.1% and 35.8%, respectively. With once-daily dosing, steady-state plasma concentrations of empagliflozin were reached by the fifth dose. Consistent with the half-life, up to 22% accumulation, with respect to plasma AUC, was observed at steady-state. Following administration of an oral [14C]-empagliflozin solution to healthy volunteers, approximately 96% of the drug-related radioactivity was eliminated in faeces (41%) or urine (54%). The majority of drug-related radioactivity recovered in faeces was unchanged parent drug and approximately half of drug related radioactivity excreted in urine was unchanged parent drug.
Special populations
Renal impairment
In patients with mild, moderate or severe renal impairment (eGFR <30 - <90 ml/min/1.73 m2) and patients with kidney failure/end stage renal disease (ESRD), AUC of empagliflozin increased by approximately 18%, 20%, 66%, and 48%, respectively compared to subjects with normal renal function. Peak plasma levels of empagliflozin were similar in subjects with moderate renal impairment and kidney failure/ESRD compared to patients with normal renal function. Peak plasma levels of empagliflozin were roughly 20% higher in subjects with mild and severe renal impairment as compared to subjects with normal renal function. The population pharmacokinetic analysis showed that the apparent oral clearance of empagliflozin decreased with a decrease in eGFR leading to an increase in drug exposure.
Hepatic impairment
In subjects with mild, moderate, and severe hepatic impairment according to the Child-Pugh classification, AUC of empagliflozin increased approximately by 23%, 47%, and 75% and Cmax by approximately 4%, 23%, and 48%, respectively, compared to subjects with normal hepatic function.
Body Mass Index
Body mass index had no clinically relevant effect on the pharmacokinetics of empagliflozin based on the population pharmacokinetic analysis. In this analysis, AUC was estimated to be 5.82%, 10.4%, and 17.3% lower in subjects with BMI of 30, 35, and 45 kg/m2, respectively, compared to subjects with a body mass index of 25 kg/m2.
Gender
Gender had no clinically relevant effect on the pharmacokinetics of empagliflozin based on the population pharmacokinetic analysis.
Race
In the population pharmacokinetic analysis, AUC was estimated to be 13.5% higher in Asians with a body mass index of 25 kg/m2 compared to non-Asians with a body mass index of 25 kg/m2.
Elderly
Age did not have a clinically meaningful impact on the pharmacokinetics of empagliflozin based on the population pharmacokinetic analysis.
Paediatric population
Studies characterising the pharmacokinetics of empagliflozin in paediatric patients have not been performed.
5.3 Preclinical safety data
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, genotoxicity, fertility and early embryonic development.
In long term toxicity studies in rodents and dogs, signs of toxicity were observed at exposures greater than or equal to 10-times the clinical dose of empagliflozin. Most toxicity was consistent with secondary pharmacology related to urinary glucose loss and electrolyte imbalances including decreased body weight and body fat, increased food consumption, diarrhoea, dehydration, decreased serum glucose and increases in other serum parameters reflective of increased protein metabolism and gluconeogenesis, urinary changes such as polyuria and glucosuria, and microscopic changes including mineralisation in kidney and some soft and vascular tissues. Microscopic evidence of the effects of exaggerated pharmacology on the kidney observed in some species included tubular dilatation, and tubular and pelvic mineralisation at approximately 4-times the clinical AUC exposure of empagliflozin associated with the 25 mg dose.
Empagliflozin is not genotoxic.
In a 2 year carcinogenicity study, empagliflozin did not increase the incidence of tumours in female rats up to the highest dose of 700 mg/kg/day, which corresponds to approximately 72-times the maximal clinical AUC exposure to empagliflozin. In male rats, treatment-related benign vascular proliferative lesions (haemangiomas) of the mesenteric lymph node were observed at the highest dose, but not at 300 mg/kg/day, which corresponds to approximately 26-times the maximal clinical exposure to empagliflozin. Interstitial cell tumours in the testes were observed with a higher incidence in rats at 300 mg/kg/day and above, but not at 100 mg/kg/day which corresponds to approximately 18-times the maximal clinical exposure to empagliflozin. Both tumours are common in rats and are unlikely to be relevant to humans.
Empagliflozin did not increase the incidence of tumours in female mice at doses up to 1000 mg/kg/day, which corresponds to approximately 62-times the maximal clinical exposure to empagliflozin. Empagliflozin induced renal tumours in male mice at 1000 mg/kg/day, but not at 300 mg/kg/day, which corresponds to approximately 11-times the maximal clinical exposure to empagliflozin. The mode of action for these tumours is dependent on the natural predisposition of the male mouse to renal pathology and a metabolic pathway not reflective of humans. The male mouse renal tumours are considered not relevant to humans.
At exposures sufficiently in excess of exposure in humans after therapeutic doses, empagliflozin had no adverse effects on fertility or early embryonic development. Empagliflozin administered during the period of organogenesis was not teratogenic. Only at maternally toxic doses, empagliflozin also caused bent limb bones in the rat and increased embryofetal loss in the rabbit.
In pre- and postnatal toxicity studies in rats, reduced weight gain of offspring was observed at maternal exposures approximately 4-times the maximal clinical exposure to empagliflozin. No such effect was seen at systemic exposure equal to the maximal clinical exposure to empagliflozin. The relevance of this finding to humans is unclear.
In a juvenile toxicity study in the rat, when empagliflozin was administered from postnatal day 21 until postnatal day 90, non-adverse, minimal to mild renal tubular and pelvic dilation in juvenile rats was seen only at 100 mg/kg/day, which approximates 11-times the maximum clinical dose of 25 mg. These findings were absent after a 13 weeks drug-free recovery period.
6. Pharmaceutical particulars
6.1 List of excipients
Tablet core
Lactose monohydrate
Microcrystalline cellulose
Hydroxypropylcellulose
Croscarmellose sodium
Colloidal anhydrous silica
Magnesium stearate
Film coating
Hypromellose
Titanium dioxide (E171)
Talc
Macrogol (400)
Iron oxide yellow (E172)
6.2 Incompatibilities
Not applicable.
6.3 Shelf life
3 years
6.4 Special precautions for storage
This medicinal product does not require any special storage conditions.
6.5 Nature and contents of container
PVC/aluminium perforated unit dose blisters.
Pack sizes of 7 x 1, 10 x 1, 14 x 1, 28 x 1, 30 x 1, 60 x 1, 70 x 1, 90 x 1, and 100 x 1 film-coated tablets.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal and other handling
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7. Marketing authorisation holder
Boehringer Ingelheim International GmbH
Binger Str. 173
D-55216 Ingelheim am Rhein
Germany
8. Marketing authorisation number(s)
Jardiance 10 mg film-coated tablets
EU/1/14/930/010
EU/1/14/930/011
EU/1/14/930/012
EU/1/14/930/013
EU/1/14/930/014
EU/1/14/930/015
EU/1/14/930/016
EU/1/14/930/017
EU/1/14/930/018
Jardiance 25 mg film-coated tablets
EU/1/14/930/001
EU/1/14/930/002
EU/1/14/930/003
EU/1/14/930/004
EU/1/14/930/005
EU/1/14/930/006
EU/1/14/930/007
EU/1/14/930/008
EU/1/14/930/009
9. Date of first authorisation/renewal of the authorisation
Date of first authorisation: 22 May 2014
10. Date of revision of the text
October 2015
Detailed information on this medicinal product is available on the website of the European Medicines Agency http://www.ema.europa.eu.
Jardiance(empagliflozin 恩格列净)被证实可降低糖尿病患者心血管风险
2015年8月24日,勃林格殷格翰与礼来今日发布的EMPA-REG OUTCOME®初步阳性结果显示,在心血管事件风险较高的2型糖尿病成人患者中,标准治疗基础上加入 Jardiance®(恩格列净)在降低心血管风险上优效于安慰剂。由此,Jardiance®成为目前唯一在心血管终点试验中被证实可降低心血管风险的降糖药。
EMPA-REG OUTCOME®是一项长期临床试验,在超过7,000名心血管事件风险较高的2型糖尿病成人患者中研究 Jardiance® (恩格列净)治疗对于心血管事件的影响,试验达到其主要终点,主要终点定义为:至首次发生心血管死亡、或非致死性心肌梗死或非致死性脑卒中的时间。
勃林格殷格翰全球医学副总裁 Hans-Juergen Woerle教授指出:“Jardiance®在EMPA-REG OUTCOME®试验中表现出的降低心血管风险的影响令人兴奋,我们期盼分享所有的结果。全球2型糖尿病患者中约有一半的死亡事件由心血管疾病导致。降低心血管风险成为糖尿病管理的关键。”
Jardiance®的此项研究结果所显示的安全性特征和既往研究结果一致,将于9月17日在瑞典斯德哥尔摩举办的第51届欧洲糖尿病研究学会年会上报告详细研究结果。
关于这项研究
EMPA-REG OUTCOME 是一项多中心、随机化、双盲、安慰剂对照试验,涉及42个国家的逾7000例患者,其观察时间中值为3.1年。该研究旨在评估JARDIANCE(10mg或25mg,每天一次)加入到标准治疗相较于安慰剂加入标准治疗对于心血管事件高发风险且未获得最优血糖控制的2型糖尿病成年患者心血管事件的效应。该研究首先是为了检验非劣效性,其次是检验优越性。
标准治疗由降糖药物和心血管药物(包括降压药和降脂药物)组成。
关于JARDIANCE
JARDIANCE每天早晨服用一次,伴随进餐和运动服用,用于降低2型糖尿病成年患者的血糖(A1C)。JARDIANCE不得用于1型糖尿病患者或糖尿病酮症酸中毒(血液或尿液中酮体增加)的患者。

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