Depleted Donor Stem Cell Transplant in Children and Adults With Fanconi Anemia After Being Conditioned With a Regimen Containing Briquilimab

Fanconi Anemia Clinical Trial

Official title:

TCRαβ+ T-cell/CD19+ B-cell Depleted Hematopoietic Grafts and a Reduced Intensity Preparative Conditioning Regimen Containing JSP191 (Briquilimab) to Achieve Engraftment and Blood Reconstitution in Patients With Fanconi Anemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04784052
• Other study ID #: IRB-60108
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: December 7, 2021
• Est. completion date: April 2028

Study information

• Verified date: February 2023
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this clinical trial is to develop a cell therapy for Fanconi Anemia which enables enhanced donor hematopoietic and immune reconstitution with decreased toxicity by transplanting depleted stem cells from a donor after using an experimental antibody treatment called JSP-191 as a part of conditioning. This experimental treatment will hopefully cause fewer side effects than chemotherapy (the current standard of care method).

Participants will be administered the conditioning regimen, are assessed until they receive the depleted stem cell infusion, and will be followed for up to 2 years after the cell infusion.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 12
• Est. completion date: April 2028
• Est. primary completion date: April 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years and older

Eligibility

Inclusion Criteria:

All patients must have:

1. Fanconi Anemia diagnosis as demonstrated by abnormal chromosome breakage studies with increased sensitivity to mitomycin-C (MMC) or diepoxybutane (DEB) and at least one mutation in a known Fanconi-associated gene

2. Bone marrow failure (defined by reduction in at least one cell line on two separate occasions at least one month apart (e.g., platelet count of <100,000 per cubic millimeter, hemoglobin <9 gm/dl and/or absolute neutrophil count (ANC) of <1000/mm)

3. Age of =2 years

4. Consenting =5/10 HLA-matched related or unrelated donor available for apheresis

5. Organ function defined as:

1. Serum Creatinine <2.0 mg/dL and corrected creatinine clearance/cystatin cL >60 mL/min/1.73m^2 without dialysis

2. Forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC), and diffusing capacity of the lung for carbon monoxide (DLCO) corrected for hemoglobin and volume, >50% predicted by pulmonary function tests (PFTs)

3. For patients unable to cooperate for PFTs, criteria are no evidence of dyspnea at rest, no exercise intolerance, and no requirement for supplemental oxygen with spO2 >93%

4. Shortening fraction of =29% or ejection fraction of =45% by echocardiogram

5. Serum total bilirubin of <4 x ULN

6. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 5 x ULN

7. Prothrombin time international normalized ratio (PT INR) and partial thromboplastin time (PTT) <1.5 x ULN

6. Life expectancy of at least 2 years

7. Patients of childbearing potential must be willing to use an effective contraceptive method for the duration of the peri-transplant conditioning through hematopoietic recovery

8. Patients and/or parents or legal guardians must be able to provide written informed consent and authorize use and disclosure of personal health information in accordance with Health Insurance Portability and Accountability Act

Exclusion Criteria:

1. Patients with available and consenting 10/10 HLA-identical sibling donor for apheresis

2. Patients with any acute or uncontrolled infections at the time of enrollment, including bacterial, fungal or viral

3. Patients who are seropositive for HIV-I/II or HTLV-I/II.

4. Patients receiving any other investigational agents or other biological, chemotherapy, or radiation therapy within 14 days of enrollment

5. Patients with any active malignancies, myelodysplastic syndrome or other concerns for high-risk bone marrow disease

6. Patients who received androgens in last 3 months

7. Pregnant or lactating women

8. Women who are nursing and do not wish to discontinue breastfeeding

9. Lansky/Karnofsky performance score <50%.

10. Any other medical condition or history that, in the opinion of the Principal Investigator, could pose a significant safety risk to the participant or jeopardize the integrity of the study

11. Patients who, in the opinion of the Principal Investigator, may not be able to comply with the safety monitoring requirements of the study

Related Conditions & MeSH terms

• Anemia
• Fanconi Anemia
• Fanconi Syndrome

Intervention

Drug:
• JSP191
Participants will receive a single IV dose at start of conditioning

Device:
• CliniMACS Prodigy System
The device used to remove the aß+T cells from donor stem cell transplant before being given to the recipient

Biological:
• Depleted Stem Cell Transplant
TCRaß+ T-cell/CD19+ B-cell depleted hematopoietic cells will be administered by IV after completion of conditioning regimen.
• Rabbit Anti-Thymoglobulin (rATG)
3 consecutive daily doses of rATG will be given by IV during conditioning

Drug:
• Cyclophosphamide
4 consecutive daily doses of cyclophosphamid will be given by IV during conditioning
• Fludarabine
4 consecutive daily doses of fludarabine will be given by IV during conditioning
• Rituximab
1 dose of rituximab will be given at the end of conditioning

Locations

Country	Name	City	State
United States	Stanford University	Stanford	California

Sponsors (1)

Lead Sponsor	Collaborator
Porteus, Matthew, MD

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants without grade 3 and 4 treatment-emergent adverse events (TEAEs) (infusion related reactions) following administration of JSP191	Recorded and graded according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0	From start of conditioning regimen administration until cell infusion (up to 30 days)
Primary	Number of participants without grade 3 and 4 treatment-emergent adverse events (TEAEs) (infusion related reactions) following infusion of TCRaß+ T-cell/CD19+ B-cell depleted hematopoietic graft transplantation		Up to 2 years post-cell infusion
Primary	Number of participants able to achieve donor engraftment	Participants have achieved engraftment when absolute Neutrophil Count (ANC) is above 500/mm^3 for three consecutive laboratory values obtained on different days post cell transplantation with >1% CD15 donor chimerism	Assessed at Day +42 post-cell infusion
Primary	Number of participants who are able to have donor engraftment persist at the same rate or better compared to alternative hematopoietic cell transplant regimens for this patient population		Assessed at Day +100 post-cell infusion
Secondary	Serum concentration of JSP191	Assessed as serum concentrations in the peripheral blood from administration until time of cell infusion	Prior to start of conditioning regimen, and 5 minutes, 4 hours, +2, +3, +4, +6, +8, +10 days after start of conditioning regimen, and day of cell infusion
Secondary	Serum concentration of rATG	Assessed as serum concentrations in the peripheral blood from administration until time of cell infusion	Prior to start of rATG infusion; 15 minutes after first, second, and third rATG infusion; day of cell infusion; and week +1, week +2 and week +12 post cell infusion
Secondary	Serum concentration of fludarabine	Assessed as serum concentrations in the peripheral blood from administration until time of cell infusion	Prior to start of fludarabine infusion, and 15 minutes, 1 hour, 3 hours, and 6 hours after the fludarabine infusion
Secondary	Participants who do not develop mucositis	Mucositis incidence will be scored using the CTC criteria	Start of conditioning regimen until +12 weeks post-cell infusion (up to 15 weeks)
Secondary	Participants who do not develop veno-occlusive disease (VOD)	VOD incidence will be scored using the Modified Seattle criteria	Start of conditioning regimen until +12 weeks post-cell infusion (up to 15 weeks)
Secondary	Number of participants who achieve hematopoietic recovery	Hematopoietic recovery defined by hemoglobin >8g/dL and platelets >20k/dL without transfusion support achieved on 7 days post-graft transplantation documented on hematologic monitoring	Up to 107 weeks (after start of conditioning regimen through Week +104 post-cell infusion)
Secondary	Number of participants who achieve donor engraftment	Engraftment measured as peripheral blood (total, CD15+, CD3+, CD19+, CD56+, and CD34+) and bone marrow (total and CD34+) chimerism by STR analysis	Weeks +1 through +104 post-cell infusion
Secondary	Number of participants who achieve immunologic recovery	Immunologic recovery defined as >200/uL CD3+ T-cells and as assessed by percent and absolute numbers of T (CD3), B (CD19) and NK (CD56) cells by CBC differential studies and flow cytometry for lymphocyte lineages	Weeks +1 through +104 post-cell infusion
Secondary	Number of participants who develop Grade I-IV acute graft-vs-host disease (GvHD)		Day +100 post-cell infusion
Secondary	Number of participants who develop chronic graft-vs-host disease (GvHD)		Day +100 through Week +104 post-cell infusion
Secondary	Number of participants who achieve disease-free survival	Disease-free defined by improved DEB-induced chromosomal breakage analysis in peripheral blood lymphocyte cultures	Up to 104 weeks (from time of cell infusion through Week +104)