CTP-499
Drug3 X 200 mg tablets (QD for 2 weeks)
3 x 200 mg tablets (BID for 2 weeks)
NCT Number: NCT01460199
This study is being conducted to evaluate the safety and tolerability of treatment with CTP-499 in non-dialysis patients associated with moderate chronic kidney disease.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
West Coast Clinical Trials, Costa Mesa, California, United States
This study will evaluate the safety and tolerability of treatment with CTP-499 starting with 600 milligrams (mg) once a day (QD) for 2 weeks followed by 600 mg twice a day (BID) for 2 weeks in non-dialysis patients associated with moderate chronic kidney disease defined as an estimated Glomerular Filtration Rate or eGFR that is 30-59 mL/min/1.73m2
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
3 X 200 mg tablets (QD for 2 weeks)
3 x 200 mg tablets (BID for 2 weeks)
tablets
Time frame: 4 weeks
number of adverse events, vital signs, ECGs, clinical laboratory measures and physical exams
Time frame: 4 weeks
Time Frame: Predose, 0, 1, 2, 3, 4, 6, 8, 12, 18, 24 hours Cmax, Tmax, Area Under the Curve (AUC)
Concert Pharmaceuticals
Industry
A Multi Center, Double-Blind, Two-Arm,Placebo Controlled, Randomized Safety and Tolerability Study of CTP-499 in Non-Dialysis Patients With Stage 3 Chronic Kidney Disease
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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