Safety, Pharmacokinetics and Efficacy of Bimagrumab in Overweight and Obese Patients With Type 2 Diabetes
Status: | Active, not recruiting |
---|---|
Conditions: | Obesity Weight Loss, Diabetes, Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 10/4/2018 |
Start Date: | February 1, 2017 |
End Date: | May 8, 2019 |
A Randomized, Subject- and Investigator-blinded, Placebo Controlled Study to Assess the Safety, Pharmacokinetics and Efficacy of Intravenous Bimagrumab in Overweight and Obese Patients With Type 2 Diabetes
This study will assess the safety, pharmacokinetics and efficacy of bimagrumab when
administered in overweight and obese patients with type 2 diabetes
administered in overweight and obese patients with type 2 diabetes
Inclusion Criteria:
- Type 2 diabetes with HbA1c between 6.5% and 10% at screening with stable treatment for
3 months prior to randomization
- On one of the following anti-diabetes regimens with stable treatment for approximately
3 months prior to randomization: 1) metformin monotherapy; 2) DPP4 inhibitor agent
monotherapy; 3) combination therapy of metformin and DPP4 inhibitor agent; 4) no
anti-diabetes therapy.
- Body Mass Index of 28 to 40 kg/m2 at screening
- Body weight between 65 and 140 kg at screening
Exclusion Criteria:
- Women of child-bearing potential unless they are using highly effective methods of
contraception
- Diabetes other than Type 2 such as Type 1 diabetes, surgically induced diabetes,
"brittle" type 2 diabetes as per investigator judgement, history of severe
hypoglycemic episodes in the year preceding screening or hypoglycemic unawareness
- history of clinically significant arrythmias, heart failure, unstable angina,
myocardial infarction or stroke, coronary artery bypass graft surgery, or percutaneous
coronary intervention, deep vein thrombosis/pulmonary embolism, valve disorders or
defects, pulmonary hypertension within 6 months of screening or 1 year for
drug-eluting stents
- tachycardia
- use of anti-obesity medications, nutritional supplements or over the counter products
for weight loss within 3 months of screening
- use of medications known to induce weight gain such as some anti-convulsant and
psychotropic medications within 3 months of screening
- Any chronic active infection (e.g., HIV, Hepatitis B or C, tuberculosis, etc) or has
received anti-HCV treatments within the previous 6 months.
- uncontrolled thyroid disease. Stable euthyroid patients on stable thyroid replacement
therapy for at least 3 months of screening are allowed.
- Abnormal liver function tests such as SGOT, SGPT, alkaline phosphatase, or serum
bilirubin, or abnormal lipase and/or amylase.
- Known history or presence of severe active acute or chronic liver disease (e.g.,
cirrhosis).
- Uncontrolled depression
- Use of skeletal muscle anabolic agents in any form for 3 months prior to screening
- Chronic kidney disease [estimated glomerular filtration rate (GFR) < 30 mL/min];
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Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
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