RecruitingPHASE1, PHASE2NCT04707300
Study Evaluating the Safety and the Efficacy of Human T Lymphoid Progenitor (HTLP) Injection to Accelerate Immune Reconstitution After Umbilical Cord Blood (UCB) Transplantation in Adult Patients With Hematologic Malignancies (HTLP-ONCO)
Studying Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Principal Investigator
- Olivier HERMINE, PhD & MDAssistance Publique - Hôpitaux de Paris
- Intervention
- Human T Lymphoid Progenitor (HTLP) injection(drug)
- Enrollment
- 10 target
- Eligibility
- 18-66 years · All sexes
- Timeline
- 2022 – 2028
Study locations (5)
- Hôpital Saint Louis, Paris, France
- Service d'Hématologie et thérapie cellulaire / CHU of Bordeaux, Pessac, France
- IUCT Oncopole Toulouse, Toulouse, France
- Institut Gustave Roussy, Villejuif, France
- Hematology department / Necker Children's Hospital, Paris, Île-de-France Region, France
Collaborators
URC-CIC Paris Descartes Necker Cochin
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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