Phase 2 Sickle Cell Disease Trial, Recruiting NCT07252050 Sponsor: Arkansas Children's Hospital Research Institute Condition: Sickle Cell Disease
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Phase 2 Sickle Cell Disease Trial, Recruiting

NCT07252050
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
Arkansas Children's Hospital Research Institute
Registry
ClinicalTrials.gov
Start date
8 June 2026
Est. completion
19 November 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Event Free Survival

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov