ApoGraft for the Prevention of Acute Graft Versus Host Disease in Haploidentical Hematopoietic Cell Transplant Recipients

• ClinicalTrials.gov Identifier: NCT04006652
• Recruitment Status: Recruiting
• First Posted: July 5, 2019
• Last Update Posted: July 13, 2022
• Sponsor: Washington University School of Medicine
• Collaborator: Cellect Biotechnology
• Information provided by (Responsible Party): Washington University School of Medicine

Study Description

Brief Summary:

Finding a donor remains a challenge for patients in need of an urgent hematopoietic stem cell transplantation (HSCT). The ability to obtain half matched stem cells from any family member represents a significant breakthrough in the field. Haploidentical haplo-HSCT is characterized by the nearly uniform and immediate availability of a donor and the availability of the donor for post-transplant cellular immunotherapy. However, haplo-HSCT has a high risk of Graft versus Host Disease (GvHD) and poor immune reconstitution when GvHD is prevented by all existing methods of vigorous ex vivo or in vivo T-cell depletion. Different treatment approaches are currently being explored to mitigate complications such as graft rejection, severe GvHD, and prolonged immune suppression. Novel experimental utilization of T regulatory cells, alloreactive natural killer (NK) cells, and other T cell subsets hold great promise. Cellect Biotherapeutics' platform technology, ApoGraft, is based on the findings that GvHD can be prevented by Fas receptor mediated selective depletion of T cell subsets, ex vivo. The investigators hypothesize that the use of ApoGrafts for haplo-HSCT will be safe, and reduce rates of GVHD without affecting Graft-versus-Leukemia (GvL).

Condition or disease	Intervention/treatment	Phase
Acute Graft Versus Host Disease; Haploidentical Hematopoietic Stem Cell Transplant	Drug: ApoGraft	Phase 1

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 36 participants
• Allocation: Non-Randomized
• Intervention Model: Parallel Assignment
• Intervention Model Description: The first three recipients will be treated in a sequential manner meaning that subjects will be transplanted with ApoGraft only after the engraftment of the previous subject has occurred.
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase I Study of ApoGraft for the Prevention of Acute Graft Versus Host Disease in Haploidentical Hematopoietic Cell Transplant Recipients
• Actual Study Start Date: December 16, 2020
• Estimated Primary Completion Date: June 30, 2024
• Estimated Study Completion Date: June 30, 2024

Arms and Interventions

Arm	Intervention/treatment
Experimental: Recipient; Will undergo institutionally standard myeloablative or reduced intensity chemotherapy or chemoradiotherapy which will be administered at the discretion of the treating physician; Recipients will undergo a single fresh ApoGraft transplant as per standard clinical site guidelines	Drug: ApoGraft; ApoGraft is a cell based product, manufactured with mobilized peripheral blood.
No Intervention: Donor; -Donors will undergo apheresis from peripheral blood after daily G-CSF administration (for up to 5 days prior to Day -1)

Outcome Measures

Primary Outcome Measures :

1. Safety and tolerability of ApoGraft as measured by adverse events related to ApoGraft product [ Time Frame: From day 0 to 1 year post-transplantation of ApoGraft product ]
   -The descriptions and grading scales found in the revised NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 will be utilized for all toxicity reporting.

Secondary Outcome Measures :

1. Cumulative incidence of graft failure [ Time Frame: 35 days post haplo-HCT ]
   -Failure to engraft will be defined as failure to achieve absolute neutrophil count > 500 for 3 days by Day 35
2. Treatment related mortality [ Time Frame: Through 1 year post-transplantation of ApoGraft product ]
   -Death that results from a transplant procedure-related complication (e.g. infection, organ failure, hemorrhage, GVHD) rather than from relapse of the underlying disease or an unrelated cause.
3. Time of neutrophil engraftment as determined by number of days for reaching first of 3 consecutive days with ANC ≥ 500/mm3 [ Time Frame: 35 days post haplo-HCT ]
4. Rate of neutrophil engraftment as determined by number of days for reaching first of 3 consecutive days with ANC ≥ 500/mm3 [ Time Frame: 35 days post haplo-HCT ]
5. Time of platelet engraftment determined by number of days for reaching first measurement of 3 consecutive measurements with platelets ≥ 20,000/mm3 in the absence of platelet administration during the prior 7 days [ Time Frame: 35 days post haplo-HCT ]
6. Rate of platelet engraftment determined by number of days for reaching first measurement of 3 consecutive measurements with platelets ≥ 20,000/mm3 in the absence of platelet administration during the prior 7 days [ Time Frame: 35 days post haplo-HCT ]
7. Incidence of Grade 2-4 acute GVHD [ Time Frame: Day 180 ]
   -Acute GVHD will be assessed using MAGIC criteria
8. Time to development of Grade 2-4 acute GVHD [ Time Frame: Day 180 ]
   -Acute GVHD will be assessed using MAGIC criteria
9. Incidence of Grade 3-4 acute GVHD [ Time Frame: Day 180 ]
   -Acute GVHD will be assessed using MAGIC criteria
10. Time to development of Grade 3-4 acute GVHD [ Time Frame: Day 180 ]
    -Acute GVHD will be assessed using MAGIC criteria

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 70 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

Recipient Inclusion Criteria:

• Adult male or female subjects, 18-70 years of age.
• Availability of an HLA-haploidentical-HSCT related donor with a minimum match of 5/10 at the HLA A, B, C, DR and DQ loci.

• Hematologic malignancy in remission or controlled as below:

  • Acute myelogenous leukemia (AML) and Acute lymphoblastic leukemia (ALL) in 1st or subsequent complete remission (CR)
  • Non-Hodgkin's Lymphoma (NHL) in CR by CT or PET/CT
  • Hodgkin's disease (HD) in 1st or subsequent CR by CT or PET/CT
  • Intermediate or high risk Myelodysplastic syndrome (MDS) (IPSS-R criteria)
• ECOG performance status score 0-1 at time of the screening visit
• Cardiac left ventricular ejection fraction ≥ 40% in adults within 90 days of start of lymphodepleting chemotherapy
• Pulmonary function test with DLCO, FEV1 and FVC of ≥ 50% within 90 days of start of lymphodepleting chemotherapy.
• Oxygen saturation ≥ 90% on room air at screening visit.

• Subjects must have adequate organ function as defined below within 2 weeks of Day 0:

  • AST (SGOT)/ALT (SGPT) ≤ 2.5 × upper limit of normal (ULN).
  • Serum bilirubin <3 mg/dL.
  • Estimated creatinine clearance >50
• If female of childbearing potential, agree to use an acceptable method of birth control or be surgically sterile, and have a negative pregnancy test.
• Available HLA-haploidentical donor
• Must be able to receive GvHD prophylaxis with tacrolimus, mycophenolate mofetil, and cyclophosphamide
• Able to understand and willing to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable). Subjects requiring a guardian to sign informed consent will not be included.

Recipient Exclusion Criteria:

• If a matched related donor is available and able to donate
• Participation in an interventional investigational trial within 30 days of Day 0.
• Subject suffering from any active or ongoing malignancy (other than the reason for HSCT) in the last 5 years prior to baseline; excluding basal cell carcinoma, in situ malignancy, low-risk prostate cancer, cervix cancer after curative therapy.
• Uncontrolled infections (bacterial, viral or fungal including sepsis, pneumonia with hypoxemia, persistent bacteremia, or meningitis within two weeks of the screening visit).
• Current known active acute or chronic infection with HBV or HCV.
• Known human immunodeficiency virus (HIV) infection or AIDS.
• Subjects with severe or symptomatic restrictive or obstructive lung disease or respiratory failure requiring ventilator support.
• Subjects with other concurrent severe and/or uncontrolled medical condition, which could compromise participation in the study (i.e. active infection, uncontrolled diabetes, uncontrolled hypertension, congestive cardiac failure, ventricular arrhythmias, and chronic liver or renal disease)
• History of any of the following within 12 months prior to screening: Uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4), unstable angina, myocardial infarction, cerebrovascular accident, coronary/peripheral artery bypass graft surgery, transient ischemic attack, or pulmonary embolism.
• Any form of substance abuse (including drug or alcohol abuse), psychiatric disorder or any chronic condition susceptible, in the opinion of the investigator, of interfering with the conduct of the study.
• Organ allograft transplant recipient.
• If female of childbearing potential, agree to use an acceptable method of birth control or be surgically sterile, and have a negative pregnancy test.
• Pregnancy or lactation
• Must not have undergone a prior allogeneic donor (related, unrelated, or cord) transplant. Prior autologous transplant is not exclusionary.
• Presence of donor-specific anti-HLA antibodies.
• Must not receive antithymocyte globulin as part of pre-transplant conditioning regimen, plan to receive a T-cell depleted product, or have planned donor leukocyte infusions post-transplant.
• Immunosuppressive doses of steroids. Subjects with steroids for adrenal insufficiency will not be excluded.

Donor Inclusion Criteria

• Adult male or female subjects, 18-65 years of age.

• Donor criteria according to standard NMDP criteria for donor selection.

  • Blood-related family member (sibling (full or half), offspring, parent, cousin, niece or nephew, aunt or uncle, or grandparent).
  • HLA-haploidentical donor/recipient match by at least low-resolution typing per institutional standards.
  • In the investigator's opinion, donor is in general good health, and medically able to tolerate leukapheresis required for harvesting HSC.
• Fit to receive G-CSF and donate peripheral blood stem cells.
• Able to sign written informed consent including consent for 2nd donation in the event of graft failure in the recipient.

Donor Exclusion Criteria

• HIV, HBV or HCV positive subjects within 30 days prior to day 0.
• Pregnant or lactating women.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Graft donation with less than 0.3% CD34+ cells

Contacts and Locations

Contacts

Contact: Mark Schroeder, M.D.; 314-454-8306; markschroeder@wustl.edu

Locations

United States, Missouri

Washington University School of Medicine; Recruiting

Saint Louis, Missouri, United States, 63110

Contact: Mark Schroeder, M.D. 314-454-8306 markschroeder@wustl.edu

Principal Investigator: Mark A Schroeder, M.D.

Sub-Investigator: John F DiPersio, M.D., Ph.D.

Sub-Investigator: Peter Westervelt, M.D., Ph.D.

Sub-Investigator: Camille Abboud, M.D.

Sub-Investigator: Amanda Cashen, M.D.

Sub-Investigator: Keith Stockerl-Goldstein, M.D.

Sub-Investigator: Ravi Vij, M.D.

Sub-Investigator: Geoffrey Uy, M.D.

Sub-Investigator: Mathew Walter, M.D.

Sub-Investigator: Todd Fehniger, M.D., Ph.D.

Sub-Investigator: Armin Ghobadi, M.D.

Sub-Investigator: Meagan Jacoby, M.D., Ph.D.

Sub-Investigator: Iskra Pusic, M.D.

Sub-Investigator: Lukas Wartman, M.D.

Sub-Investigator: John Welch, M.D., Ph.D.

Sub-Investigator: Francesa Ferraro, M.D.

Sub-Investigator: Matthew Christopher, M.D., Ph.D.

Sponsors and Collaborators

Washington University School of Medicine

Cellect Biotechnology

Investigators

• Principal Investigator: Mark Schroeder, M.D.; Washington University School of Medicine

More Information

Additional Information:

Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine 

• Responsible Party: Washington University School of Medicine
• ClinicalTrials.gov Identifier: NCT04006652
• Other Study ID Numbers: 201911131
• First Posted: July 5, 2019
• Last Update Posted: July 13, 2022
• Last Verified: July 2022

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Product Manufactured in and Exported from the U.S.: No

Additional relevant MeSH terms:

Graft vs Host Disease; Immune System Diseases