Study of RO6807952 in Patients With Diabetes Mellitus Type 2
This study has been terminated.
Sponsor:
Hoffmann-La Roche
Information provided by:
Hoffmann-La Roche
ClinicalTrials.gov Identifier:
NCT01516476
First received: January 12, 2012
Last updated: February 13, 2012
Last verified: February 2012
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Purpose
This randomized, double-blind, placebo-controlled, multi-center study will evaluate the efficacy and safety of RO6807952 in patients with diabetes mellitus type 2 inadequately controlled with metformin alone. Patients will be randomized to receive doses of RO6807952, placebo, or liraglutide. The anticipated time on study treatment is 12 weeks.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetes Mellitus, Type 2 |
Drug: RO6807952 Drug: Placebo Drug: liraglutide |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | A Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study to Assess the Efficacy and Safety of RO6807952 in Type 2 Diabetic Patients Inadequately Controlled With Metformin Alone |
Resource links provided by NLM:
Further study details as provided by Hoffmann-La Roche:
Primary Outcome Measures:
- Change in hemoglobin A1c (HA1c) [ Time Frame: Baseline and 12 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Change in fasting plasma glucose [ Time Frame: Baseline and 12 weeks ] [ Designated as safety issue: No ]
- Safety (incidence of adverse events) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
| Enrollment: | 2 |
| Study Start Date: | November 2011 |
| Estimated Study Completion Date: | February 2012 |
| Estimated Primary Completion Date: | February 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: RO6807952 Arm 1 |
Drug: RO6807952
multiple doses for 12 weeks
|
| Experimental: RO6807952 Arm 2 |
Drug: RO6807952
multiple doses for 12 weeks
|
| Placebo Comparator: Placebo Arm |
Drug: Placebo
Placebo for 12 weeks
|
| Experimental: Liraglutide Arm |
Drug: liraglutide
liraglutide for 12 weeks
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Adult patients >/= 18 and </=70 years of age
- Diagnosis of diabetes mellitus, type 2 for at least 3 months
- Treated with a stable dose of metformin
- Hemoglobin A1c >/=7.0% and </=10.5% at screening
- Fasting plasma glucose </=240 mg/dL at screening
- Body mass index >/=27 kg/m2 and </=42 kg/m2 at screening
- Willing and able to maintain existing diet and exercise habits throughout the study
- C-peptide >1.5 ng/mL at screening
Exclusion Criteria:
- History of significant liver or kidney disease
- History of uncontrolled hypertension
- History of significant cardiovascular disease
- History of significant diabetic complications
- History of significant gastrointestinal conditions
- History of weight loss surgery or procedures involving the gastrointestinal tract
- History of chronic or acute pancreatitis
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Disclosures Group, Hoffmann-La Roche |
| ClinicalTrials.gov Identifier: | NCT01516476 History of Changes |
| Other Study ID Numbers: | BP27804 |
| Study First Received: | January 12, 2012 |
| Last Updated: | February 13, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Diabetes Mellitus Diabetes Mellitus, Type 2 Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases |
ClinicalTrials.gov processed this record on May 19, 2013