U.S., Oct. 10 -- ClinicalTrials.gov registry received information related to the study (NCT07868926) titled 'Absorption, Distribution, Metabolism, and Excretion of 14C-VX-407 After a Single Oral Dose' on Oct. 05.
Brief Summary: The purpose of the study is to evaluate the pharmacokinetics, safety and tolerability of VX-407 following a single oral dose.
Study Start Date: Oct. 19
Study Type: INTERVENTIONAL
Condition:
Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Intervention:
DRUG: 14C-VX-407
Solution for Oral Administration.
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Vertex Pharmaceuticals Incorporated
Disclaimer: Curated by HT Syndication....