drugset / Trial / NCT05437419

A Study to Investigate Safety, Tolerability, and PK of Oral Doses of TCK-276 in Patients With Rheumatoid Arthritis

NCT05437419 ↗

Phase 1 Completed 32 enrolled Teijin America, Inc. Parexel · collab
RandomizedSequentialQuadruple-blindTreatment

Summary

The study is to evaluate the safety, tolerability, and pharmacokinetic (PK) of multiple orally administered TCK-276 in both males and females with Rheumatoid Arthritis (RA).

Timeline

Start
2022-08-10
Primary completion
2023-07-20
Completion
2023-07-27

Drugs

EvaluationDrugModalityDoseRoute
Subject TCK-276 Unknown 10 mg Oral
Subject TCK-276 Unknown 25 mg Oral
Subject TCK-276 Unknown 75 mg Oral
Subject TCK-276 Unknown 175 mg Oral

Indications