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Clinical Trial Details

Trial ID: L5459
Source ID: NCT02762370
Associated Drug: Fx006 32 Mg
Title: Study to Assess the Effects of FX006 on Blood Glucose in Patients With OA of the Knee and Type 2 Diabetes
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT02762370/results
Conditions: Osteoarthritis of the Knee|Type 2 Diabetes Mellitus
Interventions: DRUG: FX006 32 mg|DRUG: TCA IR 40 mg
Outcome Measures: Primary: Change From Baseline for Average Blood Glucose (mg/dL), Average blood glucose was analyzed with a mixed model for repeated measures (MMRM), Baseline and 72 Hours post intra-articular (IA) injection | Secondary: Percent Time Blood Glucose Less Than 70 mg/dl, 70 - 180 mg/dl, 180.1 - 250.0 mg/dl, 250.1 - 350.0 mg/dl, and Greater Than 350.0 mg/dl, The glycemic variability was calculated as the coefficient of variation (CV) of the hourly averages in each of these time periods: Hour 1-24, Hour 1-48, Hour 1-72, Hour 1-168, and Hour 1-360. The % CV for each patient was derived using the formula: (SD/mean)\*100, using the values for each hourly average glucose measurement over the time period. Average % CV in the FX006 40 mg group was compared to the TCA IR 40 mg group using a linear model (ANCOVA) with fixed effects for treatment group. Model covariates were study center and baseline (72-hour) blood glucose average., Baseline to Days 1-3|Glycemic Variability Coeffecient of Variation (CV), The glycemic variability was calculated as the coefficient of variation (CV) of the hourly averages in each of these time periods: Hour 1-24, Hour 1-48, Hour 1-72, Hour 1-168, and Hour 1-360. The % CV for each patient was derived using the formula: (SD/mean)\*100, using the values for each hourly average glucose measurement over the time period. Average % CV in the FX006 40 mg group was compared to the TCA IR 40 mg group using a linear model (ANCOVA) with fixed effects for treatment group. Model covariates were study center and baseline (72-hour) blood glucose average., Baseline to 72 hours post injection (hourly average blood glucose measurement over the time period)|Area Under the Effect (AUE) Curves for Average Blood Glucose - FX006 Versus TCA IR, Baseline to 72 hours post injection (-72 hr, 0 hr, and 1, 2, 3, 7, and 15 days post-dose) | Other: Percent Time Blood Glucose Less Than 70 mg/dl, 70 - 180 mg/dl, 180.1 - 250.0 mg/dl, 250.1 - 350.0 mg/dl, and Greater Than 350.0 mg/dl, Baseline to Days 1-2|Change From Baseline for Maximum Blood Glucose: Baseline Average Blood Glucose (Hour -72 to Hour -1) to Maximum Blood Glucose (Hour 1 to Hour 72) for FX006 32 mg Relative to TCA IR 40 mg, Baseline (Hour -72 to Hour -1) to Hour 1 to Hour 72|Change in Average Blood Glucose From Baseline (Hour -48 to Hour -1) to Hour 1 to Hour 48 for FX006 32 mg Relative to TCA IR 40 mg., Baseline (Hour -48 to Hour -1) to Hour 1 to Hour 48
Sponsor/Collaborators: Sponsor: Pacira Pharmaceuticals, Inc
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 33
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2016-04
Completion Date: 2016-11
Results First Posted: 2018-01-26
Last Update Posted: 2024-01-24
Locations: Anaheim, California, 92801, United States|El Cajon, California, 92020, United States|North Hollywood, California, 91606, United States|Duncansville, Pennsylvania, 16635, United States|Mount Pleasant, South Carolina, 29464, United States|Knoxville, Tennessee, 37938, United States|Dallas, Texas, 75231, United States|San Antonio, Texas, 78258, United States
URL: https://clinicaltrials.gov/show/NCT02762370