Evaluation of the Pharmacokinetics and Safety of Inaxaplin in Participants With Mild or Moderate Hepatic Impairment

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

August 2, 2024

Primary Completion Date

December 20, 2024

Study Completion Date

December 20, 2024

Conditions
Focal Segmental Glomerulosclerosis (FSGS)
Interventions
DRUG

IXP

Tablet for oral administration.

Trial Locations (3)

33136

Division of Clinical Pharmacology, University of Miami, Miami

33705

GCP Research, St. Petersburg

78215

Texas Liver Institute, San Antonio

All Listed Sponsors
lead

Vertex Pharmaceuticals Incorporated

INDUSTRY

NCT06529796 - Evaluation of the Pharmacokinetics and Safety of Inaxaplin in Participants With Mild or Moderate Hepatic Impairment | Biotech Hunter | Biotech Hunter