A Phase 1 Open-Label Multicenter Study to Assess the Safety Tolerability and Immunogenicity of mRNA-4157 Alone or in Combination in Participants with Solid Tumors
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Resected Solid Tumors And Unresectable Solid Tumors
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Age: Between 18 Year(s) - 100 Year(s)
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Gender: Male or Female
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Other Inclusion Criteria:
Patients with any of the following solid malignancies: a. Non-small cell lung cancer lacking EGFR sensitizing mutant on or ALK translocation per local test results b. Small cell lung cancer c. Melanoma d. Bladder urothelial carcinoma e. Human papillomavirus-negative HNSCC f. Any solid malignancy known to be MSI high MMR efficient (including but not limited to; CRC, stomach adenocarcinoma, esophageal adenocarcinoma and endometrial cancer) 2. Patients must have resolution of toxic effect(s) from prior therapy 3. Patients must have one of the histologically-confirmed solid malignancies OR Patients must have one of the histologically- or cytological -confirmed unresectable (locally advanced or metastatic) solid malignancies
You may not be eligible for this study if the following are true:
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1. Active central nervous system metastases and/or carcinomatous meningitis. 2. Active autoimmune disease that has required systemic treatment in past 2 years 3. Has a history of (noninfectious) pneumonitis that required steroids or current pneumonitis.
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.
