NCT06743113Not yet recruiting
Hypoxic Red Blood Cells in Sickle Cell Anemia
A Multi-Center, Randomized, Controlled, Cross-Over Study to Evaluate the Effectiveness of Hypoxic Red Blood Cells Processed With the Hemanext ONE® System Versus Conventional Red Blood Cells in Patients With Transfusion Dependent Sickle Cell Anemia
Source: ClinicalTrials.gov · Last updated 2 Nov 2026
Brief summary (registry, in English)
The overall objective of this study is to evaluate the effectiveness and safety of transfusing hypoxic red blood cells manufactured with the Hemanext ONE system in patients with sickle cell anemia. The Hemanext ONE device was cleared through the De Novo process in September 2023.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 48 (estimated)
- First submitted
- 12 Dec 2024
- Start date
- 30 Nov 2026
- Primary completion date
- 1 Apr 2029
- Lead sponsor
- Hemanext
- Diseases
- Sickle cell disease
- NCT number
- NCT06743113
What you commit to
- Study type: Interventional
- Planned participants: 48
- From 30 Nov 2026 to the primary completion date, 1 Apr 2029
- 5 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Are currently being evaluated for gene therapy;
- Have any clinically significant pulmonary, cardiovascular, endocrine, hepatic, gastrointestinal, renal, infectious, immunological (including significant allo- or auto-immunization) disease, considered not adequately controlled prior to the study;
Other illness
- Have a diagnosis of HbSC disease, HbSβ+ thalassemia or another SCD variant (excluding HbSS and HbSβ0 thalassemia)
- Have a history of allo-immunization that cannot be managed by the local blood bank;
Lab values
- Have received hemoglobin inducers (e.g. erythropoietin) in the 30 days prior to Screening;
Other
- Are not exclusively transfused at the site;
- Are routinely transfused with washed, packed RBC units;
- Are a female of child-bearing potential who is pregnant or planning to become pregnant in the next 14 months;
- Patients who, in the opinion of the Investigator, would not be able or willing to comply with the protocol;
- Is a ward of the state, prisoner, or transient
Who the study is looking for
- Male or female at least 7 years of age;
- Are able to provide informed consent, and assent as applicable, to participate in the study;
- Diagnosis of Sickle Cell Anemia (SCA) (HbSS, HbSβ0 thalassemia) with participation in a chronic transfusion program and have undergone regular transfusions during at least 6 months prior to Screening;
- Have had an average interval of at least 14 days between RBC transfusions over the past 6 months;
- If on iron chelation therapy, have been on a stable dose for ≥3 months prior to screening;
Age in the registry: 7 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Emory University School of Medicine Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| John Hopkins University School of Medicine Coordinator of this site? Confirm its status | Baltimore | United States | Unknown status |
| University of Illinois at Chicago Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| New England Sickle Cell Institute, University of Connecticut Coordinator of this site? Confirm its status | Farmington | United States | Unknown status |
| University of Pittsburgh Medical Center Coordinator of this site? Confirm its status | Pittsburgh | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.