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NCT04707300RecruitingPhase 1/2

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)

A Phase I/II 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

Source: ClinicalTrials.gov · Last updated 12 Aug 2026

Brief summary (registry, in English)

This is an open-labelled and non-controlled Phase I/II clinical trial, 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. The dose limiting toxicity of HTLP injection will be evaluated using a model-based design.

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
10 (estimated)
First submitted
30 Nov 2020
Start date
16 Feb 2022
Primary completion date
Jun 2027
Lead sponsor
Assistance Publique - Hôpitaux de Paris
NCT number
NCT04707300
EudraCT number
2019-004883-23

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 10
  • From 16 Feb 2022 to the primary completion date, Jun 2027
  • 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

  • Any of the standard contraindications to allogeneic transplant
  • Concomitant infectious disease: HTLV-I, HIV-I or HIV-II
  • Previous participation within one month before inclusion in another protocol in which drugs may influence immune reconstitution of bone marrow transplantation

Other illness

  • Patients with progressive hematologic malignancies

Lab values

  • Left ventricular ejection fraction \<50%
  • Abnormal biochemistry results (ALT/AST\>10xULN, total bilirubin\>2.5xULN, creatinin clearance \<60ml/min)

Other

  • Inability to understand and provide informed consent
  • Pregnancy or breastfeeding for women of childbearing potential

Who the study is looking for

  • Adult patients (≥ 18 years old and \<66 years old) at the time of inclusion and eligible for an allogeneic stem cells transplantation and fit to receive the specified conditioning regimen
  • Patients with hematologic malignancies
  • Absence of a matched - related sibling donor (MSD) or a matched unrelated donor (MUD) 10/10
  • Presence of two UCB units with the following criteria\*: HLA- matched 4/8, 5/8, 6/8, 7/8 or 8/8 for HLA- A, -B, -C and DRB1 loci
    • AND
  • Presence of at least one UCB unit with the following criteria\*: ≥ 3 x 10e7 TNC/kg or ≥ 1.5 10e5 CD34+/kg pre- freezing
    • \* For the UCB taken into HTLP culture, the CD34+ content does not need to meet the above cellularity criteria, as expansion during HTLP culture has been proven to ensure the appropriate number of CD7+ needed for each dose.
    • The non- cultured UCB will be chosen to have a higher CD34+ cell content in order to enable long- term hematopoietic engraftment
  • Absence of Donor Specific Antibodies (DSA) with a MFI \> 5000
  • Patient affiliated to social security
  • Written, informed consent of the patient

Age in the registry: 18 years to 66 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hematology department / Necker Children's Hospital
Coordinator of this site? Confirm its status
ParisFranceRecruiting
Hopital Saint Louis
Coordinator of this site? Confirm its status
ParisFranceRecruiting
Service d'Hématologie et thérapie cellulaire / CHU of Bordeaux
Coordinator of this site? Confirm its status
PessacFranceRecruiting
IUCT Oncopole Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceRecruiting
Institut Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.