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DREPAMIR - A Phase 1/2 Open Label Cohort Comparative Study Evaluating the Efficacy and the safety of Gene Therapy of the Sickle Cell Disease by Transplantation of an Autologous CD34+ enriched cell fraction that contains autologous CD34+ cells transduced ex vivo by the bifunctional βAS3m/miR7m lentiviral vector expressing the βAS3m and a micro-RNA (miRNA) targeting specifically the endogenous βS-globin mRNA in Patients with Sickle Cell Disease (SCD)

Status
Not yet recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521257-17-00
Acronym
APHP241664
Enrollment
13
Registered
2026-01-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

SCD severe patients

Brief summary

Efficacy and safety after intravenous infusion of DREAM01 gene therapy with or without prior administration of Imatinib treatment.

Detailed description

Proportion of subjects with reduction in annualized rate of VOE at the time of analysis from baseline by at least 90% up to 24 months after DREAM01 infusion. The evaluation starts 60 days after the last RBC transfusion for post-transplant support or SCD disease management, Transfusion requirement and change in number of units of RBCs transfused for SCD-related indications over time, Percentage of HbAS3 and HbS over time, Vector copy number over time, Biologic parameters that reflect hemolysis and anemia over time (Total hemoglobin, Reticulocytes, lactate dehydrogenase LDH, circulating erythroblasts, haptoglobin, free plasmatic heme, no conjugated bilirubin, erythropoietin EPO), Biologic, functional and radiologic parameters reflecting organ function that may be affected by the disease or conditioning (evaluation of cerebral, ophthalmic, cardiac, renal, liver, pulmonary, bone, muscular), Evaluation of iron overload (ferritin, liver and cardiac MRI) and specific treatment (chelator, phlebotomy), Fertility evaluation: to be adapted according to sex: spermogram, hormone assays (estradiol, LH, FSH, testosterone, etc.), AMH, pelvic ultrasound for follicular count, Physical ability and capacity (6-minute walk-test, vertical jump test, physical ability questionnaire, cardiopulmonary exercise test), Quality of life Evaluation: SF-36 (Short Form-36 Health Survey), FACIT-Fatigue (Functional Assessment of Chronic Illness Therapy-Fatigue Scale), PROMIS (Patient-Reported Outcomes Measurement Information System) or PedsQL (Pediatric Quality of Life Inventory) Generic Core Scales

Interventions

DRUGIMATINIB
DRUGDream01

Sponsors

Assistance Publique Hopitaux De Paris
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Efficacy and safety after intravenous infusion of DREAM01 gene therapy with or without prior administration of Imatinib treatment.

Secondary

MeasureTime frame
Proportion of subjects with reduction in annualized rate of VOE at the time of analysis from baseline by at least 90% up to 24 months after DREAM01 infusion. The evaluation starts 60 days after the last RBC transfusion for post-transplant support or SCD disease management, Transfusion requirement and change in number of units of RBCs transfused for SCD-related indications over time, Percentage of HbAS3 and HbS over time, Vector copy number over time, Biologic parameters that reflect hemolysis and anemia over time (Total hemoglobin, Reticulocytes, lactate dehydrogenase LDH, circulating erythroblasts, haptoglobin, free plasmatic heme, no conjugated bilirubin, erythropoietin EPO), Biologic, functional and radiologic parameters reflecting organ function that may be affected by the disease or conditioning (evaluation of cerebral, ophthalmic, cardiac, renal, liver, pulmonary, bone, muscular), Evaluation of iron overload (ferritin, liver and cardiac MRI) and specific treatment (chelator, phle

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026