Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
study ends around

Description

Summary

This purpose of this clinical trial is to evaluate the safety, tolerability and anti-tumor activity of IMA203 in combination with different doses of mRNA-4203. The trial includes participants with previously treated unresectable or metastatic cutaneous melanoma (CM) or synovial sarcoma (SS).

Official Title

A First-in-human, Open-label Trial to Evaluate the Combination of ACTengine® IMA203 With mRNA-4203 in Previously Treated, Unresectable or Metastatic Cutaneous Melanoma or Synovial Sarcoma Patients (ACTengine® IMA203-102)

Details

This clinical trial is a multi-center, open-label, non-comparative Phase 1 a/b trial to assess the safety, tolerability, and anti-tumor activity of the combination of IMA203 and mRNA-4203 in HLA-A*02:01 positive patients with previously treated, unresectable or metastatic cutaneous melanoma (CM) and synovial sarcoma (SS).

Keywords

Cutaneous Melanoma, Synovial Sarcoma, immunotherapy, T-cell therapy, RNA vaccine, Immatics, Moderna, Melanoma, IMA203, mRNA-4203

Eligibility

You can join if…

Open to people ages 18 years and up

  • Pathologically confirmed and documented cutaneous melanoma (CM) or synovial sarcoma (SS) with unresectable or metastatic disease
  • HLA-A*02:01 positive
  • Adequate selected organ function per protocol
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  • Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
  • Life expectancy more than 5 months
  • CM participants who must have disease progression (resistance, toxicity) on or after at least one PD-1 inhibitor
  • SS participants must have received (or declined) at least one line of treatment (including SoC) and are still in need of further systemic therapy.
  • Female participants of childbearing potential must use adequate contraception prior to trial entry until 12 months after the infusion of IMA203 and 15 days after the last mRNA 4203 dose administration

Other protocol defined inclusion criteria could apply

You CAN'T join if...

  • History of other malignancies (except for adequately treated basal or squamous cell carcinoma or carcinoma in situ) within the last 3 years
  • Pregnant or breastfeeding
  • Serious autoimmune disease
  • History of cardiac conditions as per protocol
  • Prior allogenic stem cell transplantation or solid organ transplantation
  • Concurrent severe and/or uncontrolled medical disease that could compromise participation in the study
  • History of hypersensitivity to cyclophosphamide, fludarabine, or IL-2
  • History of hypersensitivity to mRNA-based medicines
  • Positive for HIV infection or with active hepatitis B virus (HBV) or active hepatitis C virus (HCV) infection
  • Any condition contraindicating leukapheresis
  • Participants with lactate dehydrogenase (LDH) greater than threshold allowed per protocol
  • Participants with active brain metastases prior to lymphodepletion
  • Concurrent treatment in another clinical trial or a device trial that could interfere with the IMA203 treatment
  • Participants with renal impairment AND reduced bone marrow reserve per protocol

Other protocol defined exclusion criteria could apply

Locations

  • University of California San Francisco not yet accepting patients
    San Francisco 5391959 California 5332921 94143 United States
  • MD Anderson Cancer Center accepting new patients
    Houston 4699066 Texas 4736286 77030 United States
  • Memorial Sloan Kettering Cancer Center accepting new patients
    New York 5128581 New York 5128638 10065 United States
  • Dana Farber Cancer Institute not yet accepting patients
    Boston 4930956 Massachusetts 6254926 02215 United States

Details

Status
accepting new patients at some sites,
but this study is not currently recruiting here
Start Date
Completion Date
(estimated)
Sponsor
Immatics US, Inc.
ID
NCT06946225
Phase
Phase 1 research study
Study Type
Interventional
Participants
Expecting 15 study participants
Last Updated