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

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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


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];
We found this trial at
8
sites
Baton Rouge, Louisiana 70808
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Anaheim, California 92801
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Anaheim, CA
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Berlin, New Jersey 08009
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Berlin, NJ
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Merthyr Tydfil, Mid Glamorgan
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Merthyr Tydfil,
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Miami, Florida 33136
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Miami, FL
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Miami Lakes, Florida 33014
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Miami Lakes, FL
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230 Park Avenue, 21st Floor
New York, New York 10169
1-888-669-6682)
Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
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New York, NY
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Orlando, Florida 32806
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Orlando, FL
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