Phase 2 Sickle Cell Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 12 to 45 years who have any type of sickle cell disease (SCD), and who also have at least one of the following: a history of stroke or blood vessel problems (including silent brain changes in younger patients); repeated serious lung complications known as acute chest syndrome; repeated severe pain episodes that needed intravenous pain relief despite other treatments; a need for regular blood transfusions to prevent complications; or, for adult patients, a specific heart scan result showing abnormal blood flow through a valve (confirm with trial site for the exact measurement).
- People who have a close blood relative — a parent, brother, sister, or half-sibling — whose tissue type (HLA) is a half-match and who is willing and able to donate bone marrow.
- People who meet the institution's own health requirements for a bone marrow transplant procedure (confirm eligibility criteria with trial site).
Who may not be able to join:
- People who have a fully matched brother or sister who is willing and able to donate bone marrow.
- People with an uncontrolled infection, active tuberculosis, active Hepatitis B or C, or HIV.
- People who have previously had a bone marrow transplant or a solid organ transplant (such as a kidney or liver transplant).
- People who have had a brain surgery for blood vessel problems, a heart attack, a blood clot in the lungs, or a blood clot in a deep vein within the past 6 months.
- People currently taking medications that significantly affect how a drug called ruxolitinib is processed by the body.
- People with a known allergy or serious reaction to ruxolitinib or any other medication used in the treatment preparation process.
- People who are unable to swallow and keep down oral medication (note: feeding tubes may be permitted — confirm with trial site).
- People with a history of cancer, except for certain treated skin cancers or early-stage treated cancers (confirm with trial site).
- People who have participated in another clinical trial using an experimental or off-label drug or device in the past 3 months.
- People who are currently pregnant or breastfeeding.
- People with a significant autoimmune disease that is not well controlled.
- People with high levels of antibodies that could attack the donor's tissue type, unless reviewed and approved by the study's lead researcher.
- People, or in the case of younger participants their guardian, who are unwilling or unable to follow the study schedule, complete study assessments, sign the consent form, or use a highly effective form of contraception if applicable.
- People with any other condition that, in the treating doctor's judgement, could interfere with safe participation or with the study's results.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Laura McLaughlin, MD, Arkansas Children's Hospital Research Institute
Phone: 501-364-3908
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Event Free Survival
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.