Study of mRNA-4359 Administered Alone and in Combination With Immune Checkpoint Blockade in Participants With Advanced Solid Tumors
Phase 1/2 Study of mRNA-4359 Administered Alone and in Combination With Immune Checkpoint Blockade in Participants With Advanced Solid Tumors
2 other identifiers
interventional
361
4 countries
27
Brief Summary
The primary goal of this study is to assess the safety and tolerability of mRNA-4359 administered alone and in combination with pembrolizumab or ipilimumab and nivolumab.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1
Started Sep 2022
Longer than P75 for phase_1
27 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 23, 2022
CompletedStudy Start
First participant enrolled
September 1, 2022
CompletedFirst Posted
Study publicly available on registry
September 9, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 18, 2032
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 18, 2032
February 6, 2026
February 1, 2026
9.5 years
August 23, 2022
February 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Arms 1a and 1b: Maximum Tolerated Dose (MTD) or Recommended Dose for Expansion (RDE) of mRNA-4359
Days 1-21 (Cycle 1)
Arms 1, 2a, 2b, and 2c: Number of Participants with Dose Limiting Toxicities (DLTs)
Days 1-21 (Cycle 1)
Arms 1, 2a, 2b, and 2c: Number of Participants with Adverse Events (AEs), AE of Special Interest (AESIs), and Serious AEs (SAEs)
Up to 27 months
Arm 2d: Objective Response Rate (ORR) Based on Blinded Independent Central Review (BICR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1)
Day 1 up to 60 months
Secondary Outcomes (11)
Arms 1, 2a, 2b, and 2c: ORR Based on Investigator Assessment Per RECIST v1.1
Day 1 up to 27 months
Arms 1, 2a, 2b, and 2c: Disease Control Rate (DCR) Based on Investigator Assessment Per RECIST v1.1
Day 1 up to 27 months
Arms 1, 2a, 2b, and 2c: Duration of Response (DOR) Based on Investigator Assessment Per RECIST v1.1
Day 1 up to 27 months
Arms 1, 2a, 2b, and 2c: Progression Free Survival (PFS) Based on Investigator Assessment Per RECIST v1.1
Day 1 up to 27 months
Arms 1, 2a, 2b, and 2c: Percent Change from Baseline in T Cell Profile in the Tumor
Baseline up to 27 months
- +6 more secondary outcomes
Study Arms (9)
Arm 1a (Dose Escalation): mRNA-4359 Alone
EXPERIMENTALAdult participants with locally advanced or metastatic cancer will be administered mRNA-4359 at an applicable dose as monotherapy.
Arm 1b (Dose Confirmation): mRNA-4359 in Combination with Pembrolizumab
EXPERIMENTALParticipants with locally advanced or metastatic, and checkpoint inhibitor (CPI) refractory melanoma or locally advanced or metastatic, and CPI refractory non-small-cell lung carcinoma (NSCLC) will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
Arm 1b (Melanoma Expansion Cohort): mRNA-4359 in Combination With Pembrolizumab
EXPERIMENTALParticipants 18 years or older with CPI refractory, advanced/metastatic melanoma with a programmed cell death ligand-1 (PD-L1) tumor proportion score (TPS) of ≥1% who have had progression on at least 1 prior CPI-based systemic therapy in the advanced/metastatic disease setting will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
Arm 2a (Dose Expansion): mRNA-4359 in Combination with Pembrolizumab
EXPERIMENTALAdult participants with locally advanced or metastatic melanoma who have not yet received any prior systemic therapy for their melanoma in this setting will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
Arm 2b (Dose Expansion): mRNA-4359 in Combination with Pembrolizumab
EXPERIMENTALAdult participants with locally advanced or metastatic NSCLC with a PD-L1 TPS of ≥50%, with no known epidermal growth factor receptor (EGFR)- or anaplastic lymphoma kinase (ALK)-positive tumor mutations who have not yet received any prior systemic therapy for their NSCLC will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
Arm 2c (Dose Expansion): mRNA-4359 in Combination with Ipilimumab and Nivolumab
EXPERIMENTALAdult participants with locally advanced or metastatic melanoma who have not yet received any prior systemic therapy in this setting will be administered mRNA-4359 at an applicable dose in combination with ipilimumab and nivolumab.
Arm 2d (Dose Expansion): mRNA-4359 in Combination with Pembrolizumab
EXPERIMENTALParticipants 12 years or older with CPI refractory, advanced/metastatic melanoma with a PD-L1 TPS of ≥1% who have had progression on at least 1 prior CPI-based systemic therapy in the advanced/metastatic disease setting will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
Pharmacodynamic (PD) Arm (Group 1): mRNA-4359 in Combination with Pembrolizumab
EXPERIMENTALParticipants with locally advanced or metastatic, and CPI refractory melanoma will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
PD Arm (Group 2): mRNA-4359 in Combination with Pembrolizumab
EXPERIMENTALParticipants with locally advanced or metastatic, and CPI refractory NSCLC with a PD-L1 TPS ≥1% will be administered mRNA-4359 at an applicable dose in combination with pembrolizumab.
Interventions
Intramuscular Injection
Intravenous infusion
Intravenous infusion
Intravenous infusion
Eligibility Criteria
You may qualify if:
- Males or females ≥18 years of age who have provided written informed consent prior to completing any study-specific procedure. For Arm 2d, participants ≥12 years are eligible with informed consent/assent.
- Dose Escalation (Arm 1a): Participant has histologically confirmed locally advanced or metastatic cancer (cutaneous melanoma, NSCLC, non-muscle invasive bladder cancer, head and neck squamous cell carcinoma, microsatellite stable colorectal cancer \[MSS CRC\], basal cell carcinoma, or triple negative breast cancer) with measurable disease as determined by RECIST v1.1. Arm 1a participants must have received, and then progressed, relapsed, or been intolerant to, or ineligible for, at least 1 standard treatment regimen in the advanced or metastatic setting. Participants with a known driver mutation must have also received or been offered a mutation-directed therapy, where indicated. Participants must have a tumor lesion amenable to biopsy and must have another lesion that can be followed for response.
- Dose Confirmation (Arm 1b): Participant has histologically confirmed locally advanced or metastatic, and CPI refractory melanoma or locally advanced or metastatic, and CPI refractory NSCLC with measurable disease as determined by RECIST v1.1 who has disease progression after, at least 1 line of standard therapy (no limit to prior lines of therapy), and has been treated with or refused standard of care treatment. Participants in PD arm Group 2 must also have PD-L1 TPS ≥1%. Participants must have primary refractory or acquired secondary resistance to prior immune checkpoint treatments. Primary refractory is defined as prior exposure to anti-programmed death-1 (PD-1)/PD-L1 antibody for at least 6 weeks but no more than 6 months with demonstration of progression on 2 separate scans at least 4 weeks apart but no more than 12 weeks apart and progression occurring within 6 months after first dose of anti-PD-1 antibody. Acquired secondary resistance must have confirmed objective response or prolonged stable disease (SD) (\>6 months), followed by disease progression in the setting of ongoing treatment and confirmed progression on scans at least 4 weeks apart. Participants must have a tumor lesion amenable to biopsy and must have another lesion that can be followed for response.
- For NSCLC participants with known EGFR, ALK, proto-oncogene tyrosine-protein kinase reactive oxygen species (ROS1), or other actionable mutations for which there are approved targeted therapies, participants must have received prior approved targeted therapy or have been offered and declined approved targeted therapy.
- Expansion of the melanoma Arm 1b cohort (up to approximately 16 additional evaluable participants) will require prospective central testing of Screening tumor biopsies to confirm PD-L1 TPS ≥1% for eligibility.
- Dose Expansion Arms (Arm 2): Participant has histologically confirmed:
- Arm 2a: Locally advanced or metastatic melanoma who have not yet received any prior systemic therapy for their melanoma in this setting.
- Arm 2b: Newly diagnosed locally advanced or metastatic NSCLC with a PD-L1 TPS of ≥50% with no known EGFR or ALK positive tumor mutations who have not yet received any prior systemic therapy for their NSCLC (that is, treatment-naive).
- Arm 2c: Locally advanced or metastatic melanoma in participants who have not received prior systemic therapy for melanoma in the advanced/metastatic setting.
- Arm 2d: Advanced/metastatic melanoma that is CPI refractory and having a centrally confirmed PD-L1 TPS of ≥1% on their Screening tumor biopsy.
- All participants must have measurable disease as determined by RECIST v1.1.
- Participants must have a tumor lesion amenable to biopsy and must provide tumor biopsy sample at baseline (archival formalin-fixed, paraffin-embedded \[FFPE\] tissue collected within 90 days of informed consent is accepted as long as no intervening therapy is received, during this time), and optionally at all on-treatment timepoints (including response or progression) if medically feasible. Participants in Arm 2c: Sufficient tumor tissue (slides or FFPE block) for PD-L1 testing is required as per Laboratory Manual. Participants in Arm 2c may be replaced in this cohort if not PD-L1 evaluable. Participants in Arm 1b melanoma expansion cohort and Arm 2d: Central confirmation of PD-L1 TPS score is required prior to enrollment.
- If the participant is undergoing a new biopsy, they must have another lesion outside of the lesion biopsied at baseline that can be followed as a RECIST v1.1 target lesion for response.
- Participant has an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1.
- Participant has adequate hematological and biological function.
You may not qualify if:
- Participant has active central nervous system tumors or metastases.
- Participant has required the use of additional immunosuppression (for example, infliximab) other than corticosteroids for the management of an AE, has experienced recurrence of an AE if rechallenged, and currently requires maintenance doses of \>10 milligrams (mg) prednisone or equivalent per day.
- Participant has any plan to receive a live attenuated vaccine during study treatment or has received a live vaccine within 30 days before the first dose of study treatment. Examples of live vaccines include, but are not limited to measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guérin, and typhoid vaccine. Seasonal influenza vaccines and non-live coronavirus disease 2019 (COVID-19) for injection are generally allowed.
- Participant has reversible toxicities from prior cancer therapy that have not recovered to Grade 1 or baseline. Any unresolved toxicity National Cancer Institute (NCI) Common Terminology Criteria for AEs (CTCAE) Grade ≥2 from previous anticancer therapy with the exception of alopecia, vitiligo, and prespecified laboratory values.
- Participant who is pregnant, breastfeeding, or is of childbearing potential, defined as those who are capable of becoming pregnant who are not willing to employ a highly effective method of contraception during dosing and for 90 days after the last dose of mRNA-4359 or 4 months after the last dose of pembrolizumab or 5 months after the last dose of ipilimumab/nivolumab administrations, whichever is longer.
- Sexually active participants who refuse to use a condom during intercourse or participants who will not refrain from sperm donation while taking study treatment and for 90 days after the last dose of mRNA-4359 or 4 months after the last dose of pembrolizumab or 5 months after the last dose ipilimumab/nivolumab, whichever is longer, or who will not refrain from sperm donation for the same time period.
- Participant has any unstable or clinically significant concurrent medical condition (for example, substance abuse, uncontrolled intercurrent illness including active infection, arterial thrombosis, and symptomatic pulmonary embolism) that would, in the opinion of the Investigator, jeopardize the safety of a participant, impact their expected survival through the end of the study participation, and/or impact their ability to comply with the protocol. Also including but not limited to, ongoing or active infection, interstitial lung disease, serious chronic gastrointestinal conditions associated with diarrhea, active gastrointestinal bleeding or hemoptysis or history of bleeding disorder, or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs, or compromise the ability of the participant to give written informed consent.
- Participant has concurrent enrollment in another clinical study (unless it is an observational noninterventional clinical study).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- ModernaTX, Inc.lead
Study Sites (27)
UCSF Helen Diller Family Comprehensive Cancer Center
San Francisco, California, 94143, United States
University of Colorado Cancer Center
Aurora, Colorado, 80045, United States
George Washington University
Washington D.C., District of Columbia, 20037, United States
Orlando Health UF Health Cancer Center
Orlando, Florida, 32806, United States
The University of Chicago Medicine
Chicago, Illinois, 60637, United States
Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
Dana Farber Cancer Institute
Boston, Massachusetts, 02215, United States
Henry Ford Hospital
Detroit, Michigan, 48202, United States
Washington University
St Louis, Missouri, 63110, United States
John Theurer Cancer Center
Hackensack, New Jersey, 07601, United States
NYU Langone Health-Perlmutter Cancer Center
New York, New York, 10016, United States
Carolina BioOncology Institute
Huntersville, North Carolina, 28078, United States
Oregon Health Sciences University
Portland, Oregon, 97239, United States
Sara Cannon Research Institute Tennessee
Nashville, Tennessee, 37203, United States
Southside Cancer Center
Miranda, New South Wales, 2228, Australia
Melanoma Institute Australia
Wollstonecraft, New South Wales, 2065, Australia
Austin Hospital
Melbourne, Victoria, 3084, Australia
One Clinical Research
Nedlands, Western Australia, 6009, Australia
NEXT Oncology Barcelona
Barcelona, 08023, Spain
NEXT Oncology Madrid
Madrid, 28223, Spain
Beatson West of Scotland Cancer Centre
Glasgow, Scotland, G12 0YN, United Kingdom
Queen Elizabeth Hospital Birmingham
Birmingham, B15 2GW, United Kingdom
University College London Hospitals NHS Foundation Trust
London, NW1 2PG, United Kingdom
Guy's and St. Thomas' NHS Foundation Trust
London, SE1 7EH, United Kingdom
Imperial College London
London, W12 0HS, United Kingdom
Churchill Hospital
Oxford, OX3 7LE, United Kingdom
University Hospital Southampton NHS Foundation Trust
Southampton, SO16 6YD, United Kingdom
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 23, 2022
First Posted
September 9, 2022
Study Start
September 1, 2022
Primary Completion (Estimated)
February 18, 2032
Study Completion (Estimated)
February 18, 2032
Last Updated
February 6, 2026
Record last verified: 2026-02