A Phase 2 Study to Evaluate the Safety and Efficacy of CTP-499 in Type 2 Diabetic Nephropathy Patients
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Purpose
This study is being conducted to evaluate the safety and efficacy of treatment with CTP-499 for 24 weeks in patients with chronic kidney disease, Type 2 diabetic nephropathy and who are currently receiving treatment with an angiotensin converting enzyme inhibitor (ACEI) and/or angiotensin II receptor blocker (ARB).
| Condition | Intervention | Phase |
|---|---|---|
|
Type 2 Diabetes Mellitus Chronic Kidney Disease |
Drug: CTP-499 Drug: Placebo |
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 Phase 2, Randomized, Double Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of CTP-499 in Type 2 Diabetic Nephropathy Patients Currently Treated With ACEI and/or ARB Therapy |
- To assess the change in urinary albumin to creatinine ratio [ Time Frame: Weeks 16, 20, 24 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 170 |
| Study Start Date: | January 2012 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | July 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: Placebo
matching placebo tablets
|
Drug: Placebo
Matching placebo tablet
|
|
Active Comparator: CTP-499
600 mg tablet
|
Drug: CTP-499
600 mg tablet twice daily
|
Detailed Description:
There are two parts to this study, each part includes double-blind treatment with either CTP-499 or placebo. Part 1 will evaluate the safety and efficacy of treatment with CTP-499 twice daily for 24 weeks. Part 2 will evaluate the effects of longer term dosing for an additional 24 weeks. Following Part 2, patients will be allowed to participate in an Open Label extension with CTP-499 for a period of an additional 48 weeks.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Male or female 18 years or older
- Patient diagnosed with Type 2 diabetes mellitus and chronic kidney disease
- On a stable regimen of ACE inhibitors and/or ARB drugs for a minimum of 4 weeks
- Not expected to start dialysis for one year
- Patient has blood pressure less than or equal to 145/90 mm Hg
- Patient has UACR greater than or equal to 200 mg/g if male and 300 mg/g if female but not more than 5000 mg/g
- Patient has glycosylated hemoglobin A1c less than or equal to 10.5%
Exclusion Criteria:
- Patient has concurrent condition such as uncontrolled inflammatory disease, acute infection or other unstable illnesses
- Patient has a history of allergy or sensitivity to pentoxifylline or methylxanthines
- Patient has acute, active and/or unstable renal impairment or has been hospitalized for acute renal failure within the previous year
- Patient has active malignancy or history of neoplastic disease
- Patient has a QTc interval greater than 450 milliseconds
- Patient has ALT or AST greater than 3 times the upper limit of normal or a potassium greater than or equal to 5.5mEq/L at screening
- Patient is breast feeding or pregnant
Contacts and Locations
Hide Study Locations| United States, Arizona | |
| Agave Clinical Research | |
| Tempe, Arizona, United States, 85282 | |
| United States, Arkansas | |
| Harrisburg Family Medical Center | |
| Harrisburg, Arkansas, United States, 72432 | |
| Arkansas Primary Care Clinic | |
| Little Rock, Arkansas, United States, 72204 | |
| United States, California | |
| Providence Clinical Research | |
| Burbank, California, United States, 91505 | |
| California Institute of Renal Research | |
| Chula Vista, California, United States, 91910 | |
| SC Clinical Research | |
| Garden Grove, California, United States, 92844 | |
| Premiere Clinical Research | |
| Lakewood, California, United States, 90712 | |
| Long Beach Center for Clinical Research | |
| Long Beach, California, United States, 90806 | |
| Premiere Clinical Research | |
| Long Beach, California, United States, 90807 | |
| UCLA Kidney Transplant Research | |
| Los Angelas, California, United States, 90024 | |
| David Geffen School of Medicine Division of Nephrology | |
| Los Angelas, California, United States, 90095 | |
| Desert Oasis Healthcare Medical Group | |
| Palm Springs, California, United States, 92262 | |
| Apex Research of Riverside | |
| Riverside, California, United States, 92505 | |
| River City Clinical Research | |
| Sacramento, California, United States, 95816 | |
| California Institute of Renal Research | |
| San Diego, California, United States, 92123 | |
| Samsun Clinic | |
| Santa Barbara, California, United States, 93110 | |
| Orange County Research Center | |
| Tustin, California, United States, 92780 | |
| Infosphere Clinical Research | |
| West Hills, California, United States, 91307 | |
| United States, Colorado | |
| Creekside Endocrine Associates | |
| Denver, Colorado, United States, 80209 | |
| United States, Florida | |
| Palm Spring Research Institute | |
| Hialeah, Florida, United States, 33012 | |
| Advanced Pharma CR | |
| Miami, Florida, United States, 33136 | |
| San Marcus Research Clinic, Inc. | |
| Miami, Florida, United States, 33015 | |
| Ormond Medical Arts Pharmaceutical Research | |
| Ormond Beach, Florida, United States, 32174 | |
| Clincal Research of Central Florida | |
| Winter Haven, Florida, United States, 33880 | |
| United States, Georgia | |
| River Birch Research Alliance | |
| Blue Ridge, Georgia, United States, 30513 | |
| United States, Illinois | |
| Apex Medical Research | |
| Chicago, Illinois, United States, 60616 | |
| University of Chicago Medical Center | |
| Chicago, Illinois, United States, 60637 | |
| United States, Indiana | |
| American Health Network of IN | |
| Avon, Indiana, United States, 46123 | |
| American Healthcare Network of Indiana | |
| Greenfield, Indiana, United States, 46140 | |
| United States, Maryland | |
| Medstar Health Research Institute | |
| Hyattsville, Maryland, United States, 20782 | |
| United States, Massachusetts | |
| Brigham and Women's Hospital | |
| Boston, Massachusetts, United States, 02115 | |
| Harvard Medical School Beth Israel Deaconess Medical Center | |
| Boston, Massachusetts, United States, 02215 | |
| United States, Michigan | |
| Apex Medical Research MI | |
| Flint, Michigan, United States, 48504 | |
| United States, Missouri | |
| Clinical Research Consultants (MO) | |
| Kansas City, Missouri, United States, 64111 | |
| United States, New York | |
| The Rogosin Institute | |
| New York, New York, United States, 10021 | |
| Clinical Research Development Associates (NY) | |
| Rosedale, New York, United States, 11422 | |
| United States, North Carolina | |
| University of North Carolina School of Medicine | |
| Chapel Hill, North Carolina, United States, 27599 | |
| United States, Ohio | |
| Clinical Research Limited | |
| Canton, Ohio, United States, 44718 | |
| United States, Oklahoma | |
| Lynn Institute of Norman | |
| Norman, Oklahoma, United States, 73069 | |
| United States, South Carolina | |
| C.S.R.A. Renal Services | |
| Aiken, South Carolina, United States, 29801 | |
| Pharmacorp Clinical Trials | |
| Charleston, South Carolina, United States, 29412 | |
| Mountain View Clinical Research | |
| Greer, South Carolina, United States, 29651 | |
| United States, Tennessee | |
| Vanderbilt University Medical Center | |
| Nashville, Tennessee, United States, 37232 | |
| United States, Texas | |
| Research Across America | |
| Houston, Texas, United States, 77054 | |
| Millenium Clinical Research | |
| Houston, Texas, United States, 77054 | |
| Renal Associates | |
| San Antonio, Texas, United States, 78215 | |
| Cetero | |
| San Antonio, Texas, United States, 78229 | |
| Panacea Clinical Research | |
| San Antonio, Texas, United States, 78228 | |
| United States, Washington | |
| Multicare Research Institute (WA) | |
| Tacoma, Washington, United States, 98405 | |
| Study Director: | LuAnn Sabounjian | Concert Pharmaceuticals |
More Information
No publications provided
| Responsible Party: | Concert Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT01487109 History of Changes |
| Other Study ID Numbers: | CP505.2001 |
| Study First Received: | December 5, 2011 |
| Last Updated: | May 16, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Concert Pharmaceuticals:
|
Type 2 diabetes chronic kidney disease |
Additional relevant MeSH terms:
|
Diabetes Mellitus Diabetes Mellitus, Type 2 Diabetic Nephropathies Kidney Diseases Renal Insufficiency, Chronic Kidney Failure, Chronic |
Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Urologic Diseases Diabetes Complications Renal Insufficiency |
ClinicalTrials.gov processed this record on May 16, 2013