Trial for Patients w/ Advanced Hematologic Malignancies Undergoing Allogeneic HCT

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorStanford University

About this trial

The study goal is to characterize the safety of the combination of Orca-T with dual agent GVHD prophylaxis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Acute myeloid, lymphoid or mixed phenotype leukemia in complete remission (CR) or CR with incomplete hematologic recovery (CRi) as defined in Section 6.1.3; with or without the presence of known minimal residual disease, or

Myelodysplasic syndrome (MDS) myelodysplastic syndromes eligible for alloHSCT and/or treatment-related MDS <10% blasts

Age ≥ 18 and ≤ 70 years at the time of enrollment.

Eligible for myeloablative alloHCT including one of two the myeloablative conditioning regimens (fractionated total body irradiation plus cyclophosphamide or busulfan, fludarabine, and thiotepa)

Disqualifiers

Prior allogeneic HCT.

Currently receiving corticosteroids or other immunosuppressive therapy. Topical corticosteroids or oral systemic corticosteroid doses less than or equal to 10 mg/day are allowed.

Planned donor lymphocyte infusion (DLI).

Planned pharmaceutical in vivo or ex vivo T cell depletion, e.g., post-transplant cyclophosphamide (Cy), peri-transplant anti-thymocyte globulin (ATG), or alemtuzumab. For patients that have previously been exposed to a T cell-depleting agent, a 5 half-life washout of the agent must occur prior to planned Day 0 (day of infusion of Orca-T HSPC and Tregs ).

Trial design

Design model

Single group

Treatments tested in this trial

  • ORCA-T

    Drug

    On Day 0, participants will receive an infusion of Orca-T HSPCs and Orca-T Tregs. On Day +2 or +3 (between approximately 48 to 72 hours of Day 0), patients will receive an infusion of the Orca-T Tcons. There is no dose escalation or de-escalation planned for the Orca-T investigational product.

Treatment groups

24 Participants
are divided into 1 treatment group
Group A: ORCA-T + (tacrolimus and ruxolitinib)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Proportion of Patients Without Severe Transplant-Related Adverse Events at Day +100

The proportion of patients who, at Day +100 have not experienced any severe transplant-related adverse events including non-relapse mortality (NRM), primary graft failure, acute GVHD (grade 2-4), acute GVHD grade 3-4, or opportunistic infections (grade 4-5).

Time frame
18 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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Stanford University

Lead sponsor

Incyte Corporation

Collaborator