RecruitingPhase 1Phase 2NCT07708714

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

Enrollment

250 participants

Start Date

May 13, 2026

Study Type

INTERVENTIONAL

Conditions

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).


Eligibility

Min Age: 11 YearsMax Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called hydroxycarbamide for people with sickle cell anemia in children and sickle cell disease. The study is currently recruiting participants at 1 location. People eligible for this study include aged 11 Years to 18 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGhydroxycarbamide

Hydroxyurea at optimized dose


Locations(1)

Mulago Hospital Sickle Cell Clinic

Kampala, Uganda

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NCT07708714


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