A Phase 2/3 Study in Adult and Adolescent Participants With SCD

NCT05431088 · Status: RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 389

Last updated 2026-03-20

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of osivelotor.

Conditions

Interventions

DRUG

Osivelotor

Tablets which contain drug substance

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-22
Primary Completion
2030-12-30
Completion
2032-12-31
FDA Drug
Yes

Countries

  • United States
  • Brazil
  • India
  • Kenya
  • Nigeria
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05431088 on ClinicalTrials.gov