NIH-funded research U01 cooperative agreement

Hydroxyurea for children with sickle cell anemia in sub‑Saharan Africa

Official title: Realizing Effectiveness Across Continents with Hydroxyurea(REACH): A Phase I/II Pilot Study of Hyroxyurea for Children with Sickle Cell Anemia

Funded at Cincinnati Childrens Hosp Med Ctr · NIH-11399211 · Data updated 2026-11-12

This project gives hydroxyurea to young children with sickle cell anemia in sub‑Saharan Africa to find safe dosing and reduce sickle‑related complications.

More Anemia research and trials

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionCincinnati Childrens Hosp Med Ctr
NIH-funded
Lab location1 site (Cincinnati, United States)
Project startAugust 1, 2017
Project endJuly 31, 2027
Funding year2025
Award (this year)$282,506
NIH project number3U01HL133883-09S5
Project IDNIH-11399211 on NIH RePORTER

Who could benefit from this research

Could help

Young children (infants through about 11 years old) with confirmed sickle cell anemia who can attend regular clinic visits at a participating site are ideal candidates.

Less likely to help

Adults, people without sickle cell anemia, or children who cannot attend regular monitoring visits may not receive benefit from this program.

What this research studies

As a parent or young patient, you would get early diagnosis and daily hydroxyurea at a local clinic with doctors slowly increasing the dose to the highest safe level while checking blood tests and health events. The program ran at sites in Angola, the Democratic Republic of Congo, Kenya, and Uganda and collected thousands of patient‑years of follow‑up. Clinicians tracked safety, painful crises, hospital visits, and transfusion needs while adapting treatment to local health systems. The approach is open‑label and focused on making hydroxyurea practical, safe, and beneficial for children across African settings.

Why it matters

Potential benefit: If successful, this could lower painful crises, hospital visits, and early deaths for children with sickle cell anemia in Africa by making hydroxyurea safe and accessible.

How similar studies have gone: Hydroxyurea is already proven to reduce complications in children with sickle cell anemia in high‑income countries, and REACH provided large-scale data supporting its safety and benefit in African settings.

Where this research is happening

  • Cincinnati Childrens Hosp Med Ctr
    Cincinnati, United States
    Active

Researchers

  • Principal investigator: Ware, Russell E — Cincinnati Childrens Hosp Med Ctr
  • Study coordinator: Ware, Russell E

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.