Expanded Access of Omidubicel for Allogeneic Transplantation in Patients With Hematological Malignancies

  • STATUS
    Recruiting
  • End date
    Dec 31, 2024
  • participants needed
    60
  • sponsor
    Gamida Cell ltd
Updated on 19 February 2024
cancer
hematologic malignancy
allogeneic transplantation
investigational treatment

Summary

Omidubicel is an investigational therapy for patients with high-risk hematologic malignancies.

Description

Successful blood and marrow transplantation (BMT) requires the infusion of a sufficient number of hematopoietic stem/progenitor cells (HSPCs), capable of both homing to the bone marrow and regenerating a full array of hematopoietic cell lineages with early and late repopulating ability in a timely fashion.

Omidubicel is a stem/progenitor cell-based product composed of ex vivo expanded allogeneic cells from one entire unit of umbilical cord blood. Omidubicel utilizes the small molecule nicotinamide (NAM), as an epigenetic approach to inhibit differentiation and to increase the migration, bone marrow (BM) homing and engraftment efficiency of hematopoietic progenitor cells (HPC) expanded in ex vivo cultures.

The overall study objectives are to provide access to omidubicel for transplantation in patients with hematological malignancies and to collect additional safety and efficacy data.

Details
Condition Hematologic Malignancy, Blood disorder
Age 12-100 years
Treatment omidubicel
Clinical Study IdentifierNCT04260698
SponsorGamida Cell ltd
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients must be at least 12 years of age
Applicable disease criteria
Patients must have one or two partially HLA-matched CBUs
Back-up stem cell source
Sufficient physiological reserves
Females of childbearing potential agree to use appropriate method of contraception
Signed written informed consent

Exclusion Criteria

Extensive bone marrow fibrosis
Donor specific anti-HLA antibodies
Pregnancy
Medically unsuitable for transplant
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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