NCT05878704

Study of GBT021601 in Participants With Renal Impairment

A Phase I, Open-Label, Single-Dose, Non-Randomized, Parallel Group Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of GBT021601, an Oral Hemoglobin S Polymerization Inhibitor, in Adult Participants With Renal Impairment
Pfizer·Phase 1·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Renal Impairment
Drug/Device/Intervention
GBT021601
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Pfizer
Location
Tustin,Miami, United States of America
Timeline & enrollment
Phase
Phase 1
Start date
Jun 29, 2023
End date
Jul 09, 2024
Enrollment
56 participants
Primary outcome

Concentration of GBT021601 in whole blood and plasma,Single-dose PK parameters

Summary

Renal Impairment study of GBT021601.

ICD-10 classifications
Renal failureDisorders resulting from impaired renal tubular functionDisorder resulting from impaired renal tubular function, unspecifiedOther disorders resulting from impaired renal tubular functionAcute renal failure
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05878704
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05878704 through Pure Global AI's free database. This Phase 1 trial is sponsored by Pfizer and is currently Recruiting. The study focuses on Renal Impairment. Target enrollment is 56 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.