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
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
- lead INDUSTRY
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
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