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Clinical Trials in the USA / NCT06743113
Starting soon Not applicable

Hypoxic Red Blood Cells in Sickle Cell Anemia

NCT06743113 · tracked via the Priya Life Science USA tracker
Sponsor
Hemanext
Phase
Not applicable
Started
2026-09-01
Last updated
2026-08-17

Condition(s) studied

Sickle Cell AnaemiaSickle Cell Anemia CrisisSickle Cell Anemia in ChildrenSickle Cell Anemia (HbSS, or HbSβ-thalassemia0)

Investigational drug(s) / intervention(s)

Hemanext ONE SystemConventional RBCs

Hemanext ONE System: Hypoxic red blood cells

Conventional RBCs: Conventional red blood cells

Study summary

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.

Eligibility

Sex
ALL
Min age
7 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Male or female at least 7 years of age; 2. Are able to provide informed consent, and assent as applicable, to participate in the study; 3. 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; 4. Have had an average interval of at least 14 days between RBC transfusions over the past 6 months; 5. If on iron chelation therapy, have been on a stable dose for ≥3 months prior to screening; Exclusion Criteria: 1. Are not exclusively transfused at the site; 2. Have a diagnosis of HbSC disease, HbSβ+ thalassemia or another SCD variant (excluding HbSS and HbSβ0 thalassemia) 3. Are routinely transfused with washed, packed RBC units; 4. Have received hemoglobin inducers (e.g. erythropoietin) in the 30 days prior to Screening; 5. Are currently being evaluated for gene therapy; 6. 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; 7. Are a female of child-bearing potential who is pregnant or planning to become pregnant in the next 14 months; 8. Have a history of allo-immunization that cannot be managed by the local blood bank; 9. Patients who, in the opinion of the Investigator, would not be able or willing to comply with the protocol; 10. Is a ward of the state, prisoner, or transient

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
New England Sickle Cell Institute, University of Connecticut Farmington Connecticut
Emory University School of Medicine Atlanta Georgia
University of Illinois at Chicago Chicago Illinois
John Hopkins University School of Medicine Baltimore Maryland
University of Pittsburgh Medical Center Pittsburgh Pennsylvania

More Hemanext trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06743113 on ClinicalTrials.gov ↗ ← All trials in the USA