Status:
TERMINATED
Study of Mana 312 (Multi Tumor-Associated Antigen T Cells) in Adults With AML/MDS After HSCT
Lead Sponsor:
Mana Therapeutics
Conditions:
AML/MDS
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
This is a Phase 1, open-label, non-randomized, single and multiple dose escalation study designed to evaluate the safety and preliminary efficacy of administering Mana 312 to subjects with AML/MDS aft...
Detailed Description
This is a Phase 1, open-label, non-randomized, single and multiple dose escalation study designed to evaluate the safety and preliminary efficacy (prevention of, or treatment of relapse) of administer...
Eligibility Criteria
Inclusion
- Select
- Subject is ≥18 years of age on the day Informed Consent is signed and dated.
- Subject must have received only one allogeneic HSCT from a related or unrelated donor prior to administration of Mana 312.
- Subject has a donor who has agreed to donate leukocytes for manufacture of Mana 312 and who is the same donor who provided cells for the subject's current HSCT.
- a. Prior to HSCT, for Escalation Cohort 1, subject has AML/MDS b. Prior to HSCT, for Escalation Cohorts after Cohort 1 and for the Expansion Cohort, a subject must have high risk of relapse AML/MDS
- Mana 312 product is available
- The following Inclusion Criteria apply only during the Pre-Infusion Screening Phase, prior to the time of the planned first infusion of Mana 312.
- Subject has Eastern Cooperative Oncology Group (ECOG) performance status ≤ 3 or Karnofsky/Lansky score of ≥ 50.
- Subjects in the Expansion Cohort must have a relapse of AML/MDS (MRD+ or morphologic relapse)
- Subject has adequate organ function
- Select
Exclusion
- Subject has received antibody that affects T-cell number or function
- Subject has received a donor lymphocyte infusion (DLI) for the current HSCT.
- Evidence of GVHD ≥ Grade 2 in any organ system, or active bronchiolitis obliterans syndrome, sclerotic GVHD, or symptomatic serositis.
- Subject has undergone major surgery (excluding minor procedures, eg, placement of vascular access, gastrointestinal/biliary stent, apheresis, or biopsy) \< 21 days prior to the first planned infusion of Mana 312.
- Subject has an active and clinically relevant infection
- Subject has symptomatic or uncontrolled brain metastases, leptomeningeal disease, or spinal cord compression (radiation therapy to local site for disease control is allowed if ≥ 14 days prior to Screening and all AE from radiation therapy have resolved to ≤ Grade 1 prior to the planned first Mana 312 infusion).
- Subject has any other medical condition not listed above or social condition that, in the opinion of the Investigator, might place the subject at increased risk, adversely affect compliance, or confound safety or other clinical study data interpretation.
Key Trial Info
Start Date :
December 8 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 28 2023
Estimated Enrollment :
11 Patients enrolled
Trial Details
Trial ID
NCT04679194
Start Date
December 8 2020
End Date
March 28 2023
Last Update
June 18 2023
Active Locations (8)
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1
Colorado Blood Cancer Institute
Denver, Colorado, United States, 80218
2
Northside Hospital - Atlanta
Atlanta, Georgia, United States, 30309
3
University of Kansas Cancer Center
Kansas City, Kansas, United States, 66103
4
Memorial Sloan Kettering Cancer Center
New York, New York, United States, 10065