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Clinical Trial Details

Trial ID: L3140
Source ID: NCT00675857
Associated Drug: Nc-503 (Eprodisate Disodium)
Title: A Phase IIa Proof-of-concept Study of NC-503 in Patients With Type II Diabetes
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes Mellitus, Type 2|Metabolic Syndrome X
Interventions: DRUG: NC-503 (eprodisate disodium)|OTHER: placebo
Outcome Measures: Primary: Change from baseline to Week 26 in HbA1c levels, 26 weeks | Secondary: Change in HbA1c levels, 26 weeks|The rate of achieving glycemic control, 26 weeks|Change in fasting serum glucose levels, 26 weeks
Sponsor/Collaborators: Sponsor: Bellus Health Inc. - a GSK company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 200
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2008-04
Completion Date: 2010-05
Results First Posted:
Last Update Posted: 2010-08-24
Locations: Calgary, Alberta, T3B 0M3, Canada|Winnipeg, Manitoba, R3E 3P4, Canada|Etobicoke, Ontario, M9R 4E1, Canada|London, Ontario, N6A 4V2, Canada|Oakville, Ontario, L6H 3P1, Canada|Ottawa, Ontario, K1H 1A2, Canada|Ottawa, Ontario, K1K 4L2, Canada|Thornhill, Ontario, L4J 8L7, Canada|Toronto, Ontario, M4R 2G4, Canada|Toronto, Ontario, M5C 2T2, Canada|Chicoutimi, Quebec, G7H 5H6, Canada|Greenfield Park, Quebec, J4V 2H1, Canada|Laval, Quebec, H7T 2P5, Canada|Montreal, Quebec, H1T 2M4, Canada|Montreal, Quebec, H2W 1T7, Canada|Montréal, Quebec, H3A 1A1, Canada|Montréal, Quebec, H3H 2L9, Canada|Montréal, Quebec, H3N 1S4, Canada|Québec, Quebec, G1V 4G5, Canada|Sherbrooke, Quebec, J1G 1B8, Canada|Sherbrooke, Quebec, J1H 5N4, Canada
URL: https://clinicaltrials.gov/show/NCT00675857