🏛️ Verified NIH Record • Updated 2026-03-02
Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid Tumors (NCT03313778)
A Phase 1, Open-Label, Multicenter Study to Assess the Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid Tumors
🔵 Active, Not Recruiting Phase1 💊 Investigational Drug / Biologic Sponsor: ModernaTX, Inc.
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Angeles Clinic and Research Institute — Los Angeles, California
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (20 Sites)
- Angeles Clinic and Research Institute — Los Angeles, California
- The George Washington Cancer Center — Washington D.C., District of Columbia
- Orlando Health Cancer Institute — Orlando, Florida
- Florida Cancer Specialists — Sarasota, Florida
- H Lee Moffitt Cancer Center and Research Institute — Tampa, Florida
- Massachusetts General Hospital — Boston, Massachusetts
- NYU Langone Medical Center — New York, New York
- The Cleveland Clinic Foundation — Cleveland, Ohio
- UPMC Hillman Cancer Center — Pittsburgh, Pennsylvania
- UT Southwest Medical Center — Dallas, Texas
- St Vincents Hospital Sydney — Darlinghurst, New South Wales
- Westmead Hospital-Cnr Hawkesbury and Darcy Road — Westmead, New South Wales
- One Clinical Research Perth — Nedlands, Western Australia
- National Cancer Center East — Kashiwa-Shi, Chiba
- National Cancer Center Hospital — Chuo-Ku, Tokyo
- The Cancer Institute Hospital of Japanese Foundation For Cancer Research — Tokyo,
- Kindai University Hospital — Osakasayama-Shi, Ôsaka
- Ninewells Hospital - PPDS — Dundee, Scotland
- Royal Mardsen Sutton — Sutton, Surrey
- Imperial College Healthcare NHS Trust Hammersmith Hospital — London,
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Solid Tumors
- Study of Pembrolizumab Following Surgery in Patients With Microsatellite Instability High (MSI-H) Solid Tumors — Basking Ridge, New Jersey
- Study of the Effect of Rifampicin on the Pharmacokinetics (PK) of Multiple Doses of Cediranib in Patients With Solid Tumours — Edmonton, Alberta
- Study of Anti-CEACAM5 ADC M9140 in Participants With Advanced Solid Tumors (PROCEADE PanTumor) — Santa Monica, California
- A Safety and Efficacy Extension Study of Pertuzumab in Patients With Solid Tumors Previously Enrolled in a Hoffmann-La Roche-Sponsored Pertuzumab Clinical Trial — Porto Alegre, Rio Grande do Sul
- Flavored, Oral Irinotecan VAL-413 (Orotecan®) Given With Temozolomide for Treatment of Recurrent Pediatric Solid Tumors — Phoenix, Arizona
Explore by condition: All Solid Tumors clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.