CBM588 in Improving Clinical Outcomes in Patients Who Have Undergone Donor Hematopoietic Stem Cell Transplant

This is an interventional supportive care trial for Hematopoietic and Lymphoid Cell Neoplasm Read More

Inclusion Criteria:

• Documented informed consent of the participant and/or legally authorized representative.

  • Assent, when appropriate, will be obtained per institutional guidelines.
• Willingness to be followed for the planned duration of the trial (2 years).
• Karnofsky performance status must be >= 60%.
• Any hematologic disorders receiving allogeneic hematopoietic stem cell transplant with reduced intensity conditioning.
• Planned 8/8 or 7/8 (human leukocyte antigens [HLA]-A, B, C, DR) related or unrelated donor hematopoietic cell transplantation (HCT).
• Clinical Laboratory and Organ Function Criteria: Consistent with City of Hope (COH) standard operating procedure (SOP) for "patient evaluation for selection for hematopoietic cell transplantation.
• Patient is eligible to receive allogeneic hematopoietic cell transplantation with reduced intensity conditioning.

• Agreement by females and males of childbearing potential to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 3 months after the last dose of protocol therapy.

  • Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for > 1 year (women only).

Exclusion Criteria:

• Failure of research participant to understand the basic elements of the protocol and/or the risks/benefits of participating in this pilot study. A legal guardian may substitute for the research participant.
• Refusing to use contraception up to 90 days post-HCT.
• Pregnant and/or breast feeding if a female recipient.
• Patients with history of chronic intestinal disease (e.g., Crohn's disease, ulcerative colitis).
• In the opinion of the principal investigator (PI), the participant has a condition that will preclude them from complying with study treatment.
• Research participants receiving any other investigational agents.

• Known or documented history of hypersensitivity to all the listed antibiotics, used for severe infections related to CBM588:

  • Ampicillin.
  • Chloramphenicol.
  • Clindamycin.
  • Erythromycin.
  • Metronidazole.
  • Tetracycline.
  • Vancomycin.
• Research participants with presence of other active malignancy within 2 years of study entry. Participants with history of prior malignancy treated with curative intent who achieved complete response (CR) more than 2 years before study entry are eligible. This exclusion rule does not apply to non-melanoma skin tumors and in-situ cervical cancer.
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to study agent (i.e., research participants whom are severe lactose intolerance or intolerance to milk products).
• Research participants having any uncontrolled illness including ongoing or active infection. Research participants with known active hepatitis B or C infection; research participants who are human immunodeficiency virus (HIV) seropositive based on testing performed within 4 weeks of enrollment; research participants with any signs or symptoms of active infection, positive blood cultures, or radiological evidence of infections.
• Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures.
• Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics).