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Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid Tumors
NCT03313778 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to assess the safety, tolerability, and immunogenicity of mRNA-4157 alone and in combination in participants with solid tumors.
Conditions Studied
Interventions
- BIOLOGICAL Pembrolizumab
- BIOLOGICAL mRNA-4157
- BIOLOGICAL SoC Treatment
Study Locations (20)
Florida
- Orlando Health Cancer Institute — Orlando
- Florida Cancer Specialists — Sarasota
- H Lee Moffitt Cancer Center and Research Institute — Tampa
New South Wales
- St Vincents Hospital Sydney — Darlinghurst
- Westmead Hospital-Cnr Hawkesbury and Darcy Road — Westmead
Other
- The Cancer Institute Hospital of Japanese Foundation For Cancer Research — Tokyo
- Imperial College Healthcare NHS Trust Hammersmith Hospital — London
California
- Angeles Clinic and Research Institute — Los Angeles
District of Columbia
- The George Washington Cancer Center — Washington D.C.
Massachusetts
- Massachusetts General Hospital — Boston
New York
- NYU Langone Medical Center — New York
Ohio
- The Cleveland Clinic Foundation — Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 161 participants |
| Start Date | 2017-08-14 |
| Est. Completion | 2027-11-21 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03313778
The ClinicalTrials.gov registry entry for NCT03313778 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 161 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ModernaTX, which has 67 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Solid Tumors appearing as the primary indexed condition, and to 3 interventions — of which Pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03313778 reports 20 study locations spanning 16 distinct geographic areas — top geographies include Florida, New South Wales, Other. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03313778 about?
NCT03313778 is a clinical study titled "Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid Tumors". The purpose of this study is to assess the safety, tolerability, and immunogenicity of mRNA-4157 alone and in combination in participants with solid tumors.
What is the current status of trial NCT03313778?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 161 participants. The study started on 2017-08-14. Estimated completion is 2027-11-21.
What conditions does trial NCT03313778 study?
This clinical trial studies the following conditions: Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03313778?
The interventions under investigation include: Pembrolizumab (BIOLOGICAL), mRNA-4157 (BIOLOGICAL), SoC Treatment (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03313778?
This trial is sponsored by ModernaTX, which has 67 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03313778 being conducted?
This trial has 20 study locations across California, District of Columbia, Florida, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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