Safety Evaluation of Intramuscular Injections of PLX-R18 in Subjects With Incomplete Hematopoietic Recovery Following Hematopoietic Cell Transplantation

Completed · Phase 1

Conditions studied: Incomplete HCT (Hematopoietic Cell Transplantation)

In brief

This study aims to evaluate the safety of intramuscular (IM) administration of PLX-R18 in subjects with incomplete hematopoietic recovery following HCT.

Key facts

Study ID

NCT03002519

Run by

Pluristem Ltd.

People needed

21

Starts

2017-02-08

Expected to finish

2021-10-30

Last updated by the study team

2022-12-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥18 years.
• At least 3 months after HCT, either autologous or allogeneic (of any source, with any preparatory regimen, for any indication), prior to study treatment.
• Sustained platelet count ≤50,000/µL, and/or sustained Hb ≤8 g/dL and/or sustained ANC ≤1000/mm3, attributed to graft failure as a major contributor, as evident by hypocellular bone marrow.
• Cytopenia should be confirmed by at least 2 consecutive blood counts, at least one of them within 28 days prior to treatment (higher transient levels following occasional blood product transfusions are allowed).
• Stable donor cell chimerism in at least 3 consecutive tests prior to treatment (the most recent test should be within 28 days prior to treatment).
• If the subject had allogeneic HCT for a malignant disease, the subject should have complete donor chimerism.
• complete donor chimerism should be determined by the investigator per site's standards.
• General performance status evaluated by Eastern Cooperative Oncology Group 0-2 scale.
• Signed written informed consent.

You may not qualify if…

• INCLUSION AND EXCLUSION CRITERIA Inclusion Criteria
• Subjects must meet all of the inclusion criteria listed below to be eligible for the study:
• Age ≥18 years.
• At least 3 months after HCT, either autologous or allogeneic (of any source, with any preparatory regimen, for any indication), prior to study treatment.
• Sustained platelet count ≤50,000/µL, and/or sustained Hb ≤8 g/dL and/or sustained ANC ≤1000/mm3, attributed to graft failure as a major contributor, as evident by hypocellular bone marrow.
• Cytopenia should be confirmed by at least 2 consecutive blood counts, at least one of them within 28 days prior to treatment (higher transient levels following occasional blood product transfusions are allowed).
• Stable donor cell chimerism in at least 3 consecutive tests prior to treatment (the most recent test should be within 28 days prior to treatment).
• If the subject had allogeneic HCT for a malignant disease, the subject should have complete donor chimerism.
• complete donor chimerism should be determined by the investigator per site's standards.
• General performance status evaluated by Eastern Cooperative Oncology Group 0-2 scale.
• Signed written informed consent. Exclusion Criteria
• Evidence of developing malignancy since the HCT, or any evidence of malignancy at the time of screening.
• Current active infection requiring systemic treatment (if infection resolved but antibiotic coverage continues, patient may be included).
• Acute graft versus host disease (GvHD) Grade III or IV, or severe chronic GvHD at the time of screening.
• Subject has received prophylactic treatment with donor lymphocyte infusion (DLI) within 6 months prior to treatment, or any other cell therapy within 3 months prior to treatment.
• History of malignancy (other than the disease that required the HCT) within 2 years prior to screening (except for skin basal cell carcinoma or squamous cell carcinoma lesions that were fully resected with no need for further treatment, and not located at the injection site).
• History of significant transfusion reaction including: Transfusion related acute lung injury (pulmonary edema), shock, severe disturbances of liver function tests, renal dysfunction, or hemolytic anemia (as part of the transfusion reaction).
• Known allergies to any of the following: dimethyl sulfoxide (DMSO), human serum albumin, bovine serum albumin, gentamicin, or antihistamine.
• History of allergic/hypersensitivity reaction to any substance having required hospitalization and/or treatment with intra-venous steroids/epinephrine or in the opinion of the Investigator the subject is at high risk of developing severe allergic/hypersensitivity reactions (does not apply to transfusion reactions - see exclusion criterion 8).
• A known history of allergic/hypersensitivity reactions to 3 or more allergens.
• History of uncontrolled asthma (Global Initiative for Asthma Grade III IV).
• History of severe atopic disease (including but not limited to chronic urticaria, allergic reaction with respiratory symptoms requiring systemic steroids).
• Medical history of human immunodeficiency virus or syphilis infection.
• Known active hepatitis B or hepatitis C infection at the time of screening.
• A pregnant or lactating woman or a woman who plans to become pregnant during the study. In addition, any woman of childbearing potential (not sterile or postmenopausal), who is unwilling to adhere to the use of a highly effective contraception method for the duration of the study:

Where it is running

• The University of Chicago Medical Center — Chicago, Illinois, United States
• University of Kansas Cancer Center - The Richard and Annette Bloch Cancer Care Pavilion,2330 Shawnee Mission Parkway — Westwood, Kansas, United States
• University of Maryland Medical Center,22 South Greene Street — Baltimore, Maryland, United States
• Mayo Clinic Cancer Center (MCCC) - Rochester,200 1st Street SW — Rochester, Minnesota, United States
• Hackensack University Medical Center — Hackensack, New Jersey, United States
• University Hospitals Case Medical Center — Cleveland, Ohio, United States
• Baylor University Medical Center — Dallas, Texas, United States
• Rambam Medical Center — Haifa, Israel
• Hadassah Ein Karem Medical Center — Jerusalem, Israel
• Sheba Medical Center — Ramat Gan, Israel

Full record on ClinicalTrials.gov

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