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Clinical Trial ● Currently Recruiting Phase II NCT06198712

A Study to Evaluate the Pharmacokinetics and Safety of Etavopivat in Pediatric Patients With Sickle Cell Disease

A Study to Evaluate the Pharmacokinetics and Safety of Etavopivat in Pediatric Patients With Sickle Cell Disease — Recruiting • Phase II • NCT06198712.

📅 12 Aug 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06198712
Start
2023-01-12
Completion
2028-02-23
ClinicaliQ Trial Snapshot
  • A Study to Evaluate the Pharmacokinetics and Safety of Etavopivat in Pediatric Patients With Sickle Cell Disease — Recruiting • Phase II • NCT06198712.
  • Trial testing a new sickle cell drug in children to check how the body processes it and whether it's safe over 96 weeks.

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What This Trial Is Studying

The purpose of this study is to evaluate the pharmacokinetics and safety of etavopivat in paediatric participants with sickle cell disease (SCD). Participants will receive etavopivat and will be enrolled in a staggered manner, starting with the oldest age group and followed sequentially by younger cohorts after review of pharmacokinetic and safety data from the preceding cohort. All participants will undergo a 24-week primary treatment period followed by a 72-week extension treatment period to further evaluate long-term safety and pharmacokinetics of etavopivat. The total duration of the study will be…

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