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RECRUITING
NCT07708714
PHASE1/PHASE2

Optimizing Hydroxyurea Therapy in Children With Sickle Cell Anemia In Malaria Endemic Areas: The NOHARM Maximum Tolerated Dose (MTD) Study

Sponsor: Children's Hospital Medical Center, Cincinnati

View on ClinicalTrials.gov

Summary

NOHARM MTD is an extension of a previous study for children with Sickle Cell Anemia (SCA) who were enrolled in the NOHARM study. All children enrolled in NOHARM received hydroxyurea treatment at a fixed daily dose of 20 mg/kg/day. This dose was selected as a likely safe dose, but does not escalate hydroxyurea to maximum tolerated dose "MTD" as is commonly done in the US. Without this information, we cannot know whether hydroxyurea treatment at the MTD would be feasible (since it requires closer monitoring to avoid hematological toxicities), safe (since adverse events may be greater with MTD, risk of malaria may be altered by MTD, and risk of infections as a result of neutropenia could also be greater with MTD) or beneficial (MTD is associated with higher hemoglobin and fetal hemoglobin concentration).

Key Details

Gender

All

Age Range

11 Years - 18 Years

Study Type

INTERVENTIONAL

Enrollment

250

Start Date

2026-05-13

Completion Date

2032-11-30

Last Updated

2026-07-16

Healthy Volunteers

No

Interventions

DRUG

hydroxycarbamide

Hydroxyurea at optimized dose

Locations (1)

Mulago Hospital Sickle Cell Clinic

Kampala, Uganda