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
- Diseases
- Acute myeloid leukemia
- 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
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hematology department / Necker Children's Hospital Coordinator of this site? Confirm its status | Paris | France | Recruiting |
| Hopital Saint Louis Coordinator of this site? Confirm its status | Paris | France | Recruiting |
| Service d'Hématologie et thérapie cellulaire / CHU of Bordeaux Coordinator of this site? Confirm its status | Pessac | France | Recruiting |
| IUCT Oncopole Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Recruiting |
| Institut Gustave Roussy Coordinator of this site? Confirm its status | Villejuif | France | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.