ACTengine® IMA203 Combined With mRNA-4203
a study on Skin Cancer/Melanoma Sarcoma Synovial Sarcoma
Summary
- Eligibility
- for people ages 18 years and up (full criteria)
- Location
- at UCSF
- Dates
- study startedstudy 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 Francisconot yet accepting patients 
 San Francisco 5391959 California 5332921 94143 United States
- MD Anderson Cancer Centeraccepting new patients 
 Houston 4699066 Texas 4736286 77030 United States
- Memorial Sloan Kettering Cancer Centeraccepting new patients 
 New York 5128581 New York 5128638 10065 United States
- Dana Farber Cancer Institutenot 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
