drugset / Trial / NCT06389955

Assessment of Relative Bioavailability and Effect of Food on Capsule and Tablet Formulations of TP-3654

NCT06389955

Phase 1 Completed 12 enrolled Sumitomo Pharma America, Inc.
RandomizedCrossoverOpen-labelOther

Summary

This study comprised of 2 parts, Part A and Part B. Part B will only be conducted if the relative bioavailability of the tablet formulation was at least 70% of the capsule formulation.

Timeline

Start
2023-05-22
Primary completion
2023-08-01
Completion
2023-08-24

Drugs

EvaluationDrugModalityDoseRoute
Subject NUVISERTIB Small molecule 480 mg Oral

Indications

No indication recorded.