drugset / Trial / NCT06198712

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

NCT06198712

Phase 2 Recruiting 95 enrolled Forma Therapeutics, Inc. Novo Nordisk A/S · collab
NaSingle-groupOpen-labelTreatment

Summary

This study is being done to learn about etavopivat, a once a day medicine taken by mouth in adolescents with sickle cell disease. The main goals are to study safety and how long etavopivat stays in the bloodstream, while also studying if there are benefits from taking etavopivat. Eligible participants who enter the study will start a 96-week treatment period. At the end of the 96 weeks, participants will have an end of study visit that occurs 4 weeks later. The participants will receive etavopivat every day throughout the treatment period.

Timeline

Start
2023-01-12
Primary completion
2028-02-23
Completion
2029-08-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Etavopivat Small molecule Oral

Indications