Condition: Healthy Volunteers · Sponsor: Teva Branded Pharmaceutical Products R&D LLC
The purpose of the trial is to evaluate the pharmacokinetics, safety, and tolerability of TEV-56286 at different doses. The main objective is to describe how TEV-56286 is absorbed, distributed, and removed from the body (the pharmacokinetics) following administration of TEV-56286 in single doses of increasing amounts and multiple doses in healthy participants. A secondary objective is to assess the safety of TEV-56286 and how well it is tolerated. The estimated duration for participants in Part 1 with Single Ascending Dose is approximately 58 days; including up to 45 days of screening, a 4-day in-clinic period, and follow-up 8+/-1 days post discharge from the clinical unit. The estimated duration for participants in Part 2 with Multiple Dose is approximately 64 days; including 45 days of screening, a 10-day in-clinic period, and follow-up 8+/-1 days post discharge from the clinical unit.
This description comes directly from the study's public registry record.
Teva U.S. Medical Information · 1-888-483-8279 · USMedInfo@tevapharm.com
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| Teva Investigational Site 12174 | Miramar, Florida, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07674940