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Clinical Trial Active — Not Recruiting Phase II NCT06924970

A Dose-Finding Study of Tebapivat to Assess Efficacy, and Safety in Participants With Sickle Cell Disease (SCD)

A Dose-Finding Study of Tebapivat to Assess Efficacy, and Safety in Participants With Sickle Cell Disease (SCD) — Active Not Recruiting • Phase II • NCT06924970.

📅 23 Apr 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase II
NCT ID
NCT06924970
Start
2025-05-01
Completion
2026-05
ClinicaliQ Trial Snapshot
  • A Dose-Finding Study of Tebapivat to Assess Efficacy, and Safety in Participants With Sickle Cell Disease (SCD) — Active Not Recruiting • Phase II • NCT06924970.
  • Trial testing tebapivat against placebo in sickle cell disease patients to find the best dose for improving hemoglobin levels.

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What This Trial Is Studying

The main purpose of this study is to compare the effect of tebapivat versus placebo on anemia and to detect a dose-response for hemoglobin (Hb) response in participants with SCD. Conditions: Sickle Cell Disease Interventions: Tebapivat, Tebapivat Matched Placebo Lead Sponsor: Agios Pharmaceuticals, Inc. Planned Enrollment: 59 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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