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Study of RO6807952 in Patients With Diabetes Mellitus Type 2

This study has been terminated.
Information provided by (Responsible Party):
Hoffmann-La Roche Identifier:
First received: January 12, 2012
Last updated: November 1, 2016
Last verified: November 2016
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: Placebo
Drug: RO6807952
Drug: liraglutide
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Participant, 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 ]

Secondary Outcome Measures:
  • Change in fasting plasma glucose [ Time Frame: Baseline and 12 weeks ]
  • Safety (incidence of adverse events) [ Time Frame: 12 weeks ]

Enrollment: 2
Study Start Date: November 2011
Study Completion Date: January 2012
Primary Completion Date: January 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Liraglutide Arm Drug: liraglutide
liraglutide for 12 weeks
Placebo Comparator: Placebo Arm Drug: Placebo
Placebo for 12 weeks
Experimental: RO6807952 Arm 1 Drug: RO6807952
multiple doses for 12 weeks
Experimental: RO6807952 Arm 2 Drug: RO6807952
multiple doses for 12 weeks


Ages Eligible for Study:   18 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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
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Please refer to this study by its identifier: NCT01516476

United States, Ohio
Cincinnati, Ohio, United States, 45227
Sponsors and Collaborators
Hoffmann-La Roche
Study Director: Clinical Trials Hoffmann-La Roche
  More Information

Responsible Party: Hoffmann-La Roche Identifier: NCT01516476     History of Changes
Other Study ID Numbers: BP27804
Study First Received: January 12, 2012
Last Updated: November 1, 2016

Additional relevant MeSH terms:
Diabetes Mellitus
Diabetes Mellitus, Type 2
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Hypoglycemic Agents
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists processed this record on April 21, 2017