Anti-CD30 biAb-AATC in Patients With Relapsed/Refractory CD30 Positive Hematopoietic Malignancies

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorMedical College of Wisconsin

About this trial

This first-in-human trial will assess the safety, feasibility, and efficacy of an immunotherapy with a novel CD30 antibody conjugated to a CD3 antibody that is preloaded onto a patient's own T-cells, generating a CD30 bispecific antibody-armed, anti-CD3-activated, autologous T-cells (CD30 biAb-AATC).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Direct Bilirubin <1.5 x upper limit of normal (ULN) for age. For patients with documented Gilbert's syndrome (unconjugated hyperbilirubinemia) the bilirubin must be ≤3 x ULN for age.

SGPT (ALT) <3 x ULN.

Serum albumin >2 g/dL.

Female patients of childbearing potential must have a negative urine or serum pregnancy test confirmed within 7 days prior to enrollment.

Disqualifiers

None

Trial design

Design model

Sequential

Treatments tested in this trial

  • anti-CD30 Bispecific Antibody-armed anti-CD3-Activated Autologous T-cells (CD30 biAb-AATC)

    Drug

    anti-CD30 Bispecific Antibody-armed anti-CD3-Activated Autologous T-cells

  • GM-CSF

    Drug

    Hematopoietic agent that helps form white blood cells.

Treatment groups

42 Participants
are divided into 5 treatment groups
Group A: CD30biAb-AATC (Dose Level -1 -- 40 x 10^6 cells/kg/infusion + GM-CSF 250 μg/m^2)Experimental treatment 2 interventions
Group B: CD30biAb-AATC (Dose Level 1 -- 80 x 10^6 cells/kg/infusion + GM-CSF 250 μg/m^2)Experimental treatment 2 interventions
Group C: CD30biAb-AATC (Dose Level 2 -- 120 x 10^6 cells/kg/infusion + GM-CSF 250 μg/m^2)Experimental treatment 2 interventions
Group D: CD30biAb-AATC (Dose Level 3 -- 160 x 10^6 cells/kg/infusion + GM-CSF 250 μg/m^2)Experimental treatment 2 interventions
Group E: CD30biAb-AATC Recommended Phase 2 Dose (RP2D)Experimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Maximum Tolerated Dose

To determine the MTD and recommended Phase II dose of CD30 biAb-AATC administered once weekly for a total of 4 doses per cycle

Time frame
2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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