drugset / Trial / NCT06886269

A Study to Evaluate How the Body Processes 14C-VX-993 After a Single Oral Dose

NCT06886269

Phase 1 Completed 8 enrolled Vertex Pharmaceuticals Incorporated
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the routes and rate of elimination and recovery of total radioactivity (TRA) and characterize the Pharmacokinetic (PK) of VX-993 after a single oral dose of 14C-VX-993.

Timeline

Start
2025-03-21
Primary completion
2025-05-17
Completion
2025-05-17

Drugs

EvaluationDrugModalityDoseRoute
Subject VX-993 Unknown Oral

Indications

No indication recorded.