A Study of Imvotamab Monotherapy and in Combination in Subjects With Relapsed/Refractory Non-Hodgkin Lymphoma

I

IGM Biosciences

Status and phase

Active, not recruiting
Phase 2
Phase 1

Conditions

Marginal Zone Lymphoma
Mantle Cell Lymphoma
Follicular Lymphoma
DLBCL
Non-Hodgkin Lymphoma

Treatments

Drug: imvotamab

Study type

Interventional

Funder types

Industry

Identifiers

NCT04082936
IGM-2323-001

Details and patient eligibility

About

This is a Phase 1/2 study of imvotamab in adult subjects with relapsed or refractory B-cell Non-Hodgkin Lymphoma. This study will consist of a dose-escalation stage, a combination stage, and a randomized dose-expansion stage where subjects will be enrolled into indication-specific expansion cohorts. imvotamab will be administered intravenously (IV). Additional CD20-positive NHL histologies (e.g. MZL and MCL), may be allowed with Medical Monitor approval during the Dose-Escalation Phase of the study.

Full description

Imvotamab is an engineered bispecific IgM antibody for the treatment of patients with CD20-positive cancers. It contains ten high affinity binding domains for CD20, and one binding domain for CD3. Imvotamab is able to eliminate CD20-positive lymphoma cells by engaging T-cells and lymphoma cells, leading to T-cell dependent cellular cytotoxicity. Additionally, imvotamab is also able to eliminate lymphoma cells by recruiting complement to the surface of lymphoma cells, leading to complement dependent cytotoxicity. In our preclinical studies, we observed activity against rituximab resistant cells carrying low levels of CD20. We have also observed much lower cytokine release with imvotamab relative to comparable IgG format bispecific T-cell engaging antibodies, which is expected to result in reduced risk of the serious adverse effects from cytokine release syndrome (CRS). For the combination stage, imvotamab will be combined with loncastuximab tesirine, a CD19-targeting antibody drug conjugate.

Enrollment

97 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria:

  • > 18 years of age: ECOG PS 0 or 1
  • Relapsed or Refractory Follicular Lymphoma (FL), and Diffuse Large B-cell Lymphoma (DLBCL), Mantle cell Lymphoma (MCL), Marginal Zone Lymphoma (MZL) in dose escalation
  • Relapsed or refractory to at least two prior systemic treatment regimens (must include anti-CD20 chemo-immunotherapy regimen). FL/MZL may be enrolled with a least 2 prior systemic regimens which must include an anti-CD20, without the need for a prior chemotherapy regimen)
  • At least one bi-dimensionally measurable lesion (>1.5cm in it's longest dimension by computerized tomography (CT scan)
  • Good organ function
  • Not eligible for autologous stem cell transplant (DLBCL subjects), due to chemoresistant disease, medically unfit (organ function), or unwilling.

Key Exclusion Criteria:

  • Prior allogeneic transplant
  • ASCT within 100 days prior to the first imvotamab administration.
  • Lack of response to prior treatment with CAR-T therapy, subjects with less than 3 months from prior CAR-T therapy to first dose of imvotamab, and prior CAR-T therapy only allowed with Medical Monitor approval.
  • Concurrent serious co-morbidities that could limit patients full participation and compliance.
  • Prior CD-targeting bispecific antibodies.
  • Prior loncastuximab tesirine.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

97 participants in 6 patient groups

Phase 1a (Dose Escalation)
Experimental group
Description:
Subjects will receive imvotamab via intravenous (IV) infusion weekly. No longer enrolling.
Treatment:
Drug: imvotamab
Phase 1a (Q3W)
Experimental group
Description:
Subjects will receive imvotamab via intravenous (IV) infusion every 3 weeks. No longer enrolling.
Treatment:
Drug: imvotamab
Phase 1a (Prior bi-specific)
Experimental group
Description:
Subjects treated with prior bi-specifics will receive imvotamab via IV infusion weekly. No longer enrolling.
Treatment:
Drug: imvotamab
Phase 2 (DLBCL)
Experimental group
Description:
DLBCL subjects will receive imvotamab via IV infusion at a dose and schedule to be determined after reviewing all available response and safety data. No longer enrolling.
Treatment:
Drug: imvotamab
Phase 2 (FL)
Experimental group
Description:
FL subjects will receive imvotamab via IV infusion at a dose and schedule to be determined after reviewing all available response and safety data. No longer enrolling.
Treatment:
Drug: imvotamab
Phase 1b (Combination)
Experimental group
Description:
Subjects will receive imvotamab via IV infusion weekly and loncastuximab tesirine via IV infusion every 3 weeks.
Treatment:
Drug: imvotamab

Trial contacts and locations

27

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Central trial contact

Ibrahim Qazi

Data sourced from clinicaltrials.gov

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