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Phase 2 Completed N=78 Randomized Quadruple-blind Treatment

Safety, Pharmacokinetics and Efficacy of Bimagrumab in Overweight and Obese Patients With Type 2 Diabetes

Source: ClinicalTrials.gov NCT03005288 ↗
Enrolled (actual)
78
Serious AEs
8.0%
Results posted
Jun 2020
Primary outcomePrimary: Change From Baseline in Total Body Fat Mass by Dual Energy X-ray Absorptiometry (DXA) at Week 48 — -7.49; -0.18 kg — p=<0.001

Summary

This study assessed the safety, pharmacokinetics and efficacy of bimagrumab when administered in overweight and obese patients with type 2 diabetes

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Total Body Fat Mass by Dual Energy X-ray Absorptiometry (DXA) at Week 48
-7.49; -0.18 <0.001 sig
SECONDARY
Change From Baseline in Total Body Fat Mass by Dual Energy X-ray Absorptiometry (DXA) at Week 24
-5.37; -0.18 <0.001 sig
SECONDARY
Change From Baseline in HbA1c at Week 24 and 48
-0.85; 0.28; -0.76; 0.04 <0.001 sig
SECONDARY
The Trough Observed Analyte Concentration (Ctrough) of Repeat Doses of BYM338 10 mg/kg on Day 84, 168, 252, 308 and 336
25.3; 27.5; 31.0; 29.9; 27.8
SECONDARY
Maximum Observed Serum Concentration(Cmax) Derived on Day 1, 168 and 308
283; 292; 271
SECONDARY
Time to Reach the Maximum Concentration After Drug Administration (Tmax) Derived on Day 168 and 308
0.750; 0.750; 0.750
SECONDARY
Change From Baseline in Body Mass Index (BMI)
-1.50; -0.17; -2.19; -0.28 <0.001 sig
SECONDARY
Change From Baseline in Weight
-3.99; -0.57; -5.90; -0.79 <0.001 sig
SECONDARY
Change From Baseline in Lean Body Mass (LBM) Measured by DXA
1.72; 0.23; 1.70; -0.44 0.003 sig
SECONDARY
Change From Baseline in Waist Circumference
-5.04; -0.95; -9.00; 0.45 <0.001 sig
SECONDARY
Change From Baseline in Waist to Hip Ratio
-0.02; -0.01; -0.05; 0.01 0.062
SECONDARY
Change From Baseline in Insulin Resistance (HOMA2-IR)
0.10; 0.76; -0.09; 0.57 0.028 sig
SECONDARY
Immunogenicity Assessed by the Number of Participants Developing Anti-BYM338 Antibodies During the Trial
2; 4

Eligibility Criteria

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];
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03005288). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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