Moderna
- Country
- 🇺🇸United States
- Ownership
- Public, Subsidiary
- Established
- 2010-01-01
- Employees
- 5.6K
- Market Cap
- $30.3B
- Website
- http://www.modernatx.com
- Introduction
Moderna, Inc. engages in the development of transformative medicines based on messenger ribonucleic acid (mRNA). Its product pipeline includes the following modalities: prophylactic vaccines, cancer vaccines, intratumoral immuno-oncology, localized regenerative therapeutics, systemic secreted therapeutics, and systemic intracellular therapeutics. The company was founded by Noubar B. Afeyan, Robert S. Langer, Jr., Derrick J. Rose and Kenneth R. Chien in 2010 and is headquartered in Cambridge, MA.
Clinical Trials
149
Trial Phases
5 Phases
Drug Approvals
0
Drug Approvals
No drug approvals found
This company may not have drug approvals in our database
Clinical Trials
Distribution across different clinical trial phases (121 trials with phase data)• Click on a phase to view related trials
A Study of mRNA-1345 Following a Primary Dose of a Licensed Protein Subunit Respiratory Syncytial Virus (RSV) Vaccine in Adult Participants ≥60 Years of Age
- First Posted Date
- 2025-08-12
- Last Posted Date
- 2025-08-12
- Lead Sponsor
- ModernaTX, Inc.
- Target Recruit Count
- 500
- Registration Number
- NCT07117487
- Locations
- 🇺🇸
Velocity Clinical Research, Denver, Denver, Colorado, United States
🇺🇸Indago Research & Health Center, Inc., Hialeah, Florida, United States
🇺🇸Velocity Clinical Research, Savannah, Savannah, Georgia, United States
A Study of mRNA-2808 in Participants With Relapsed or Refractory Multiple Myeloma
- Conditions
- Relapsed or Refractory Multiple Myeloma
- Interventions
- Drug: mRNA-2808
- First Posted Date
- 2025-08-11
- Last Posted Date
- 2025-08-11
- Lead Sponsor
- ModernaTX, Inc.
- Target Recruit Count
- 166
- Registration Number
- NCT07116616
- Locations
- 🇺🇸
University of Alabama at Birmingham Hospital, Birmingham, Alabama, United States
🇺🇸UCSF, San Francisco, California, United States
🇺🇸Emory University Hospital, Atlanta, Georgia, United States
A Study to Evaluate the Immunogenicity and Safety of mRNA-1283 COVID-19 Variant-containing Formulations
- Conditions
- COVID-19
- Interventions
- Biological: mRNA-1283 Variant-containing Formulation
- First Posted Date
- 2025-07-28
- Last Posted Date
- 2025-08-08
- Lead Sponsor
- ModernaTX, Inc.
- Target Recruit Count
- 260
- Registration Number
- NCT07089706
- Locations
- 🇺🇸
DelRicht Research-Atlanta, Atlanta, Georgia, United States
🇺🇸DelRicht Research-Baton Rouge, Baton Rouge, Louisiana, United States
🇺🇸DelRicht Research-New Orleans, New Orleans, Louisiana, United States
A Study of mRNA-4106 Administered Alone and in Combination With Immune Checkpoint Blockade in Participants With Solid Tumors
- Conditions
- Advanced Solid Tumors
- Interventions
- Biological: mRNA-4106
- First Posted Date
- 2025-03-17
- Last Posted Date
- 2025-03-17
- Lead Sponsor
- ModernaTX, Inc.
- Target Recruit Count
- 57
- Registration Number
- NCT06880536
- Locations
- 🇺🇸
START Midwest, Grand Rapids, Michigan, United States
🇺🇸START San Antonio, San Antonio, Texas, United States
🇺🇸START Mountain Region, West Valley City, Utah, United States
A Study of mRNA-4106 Administered Alone and in Combination With Immune Checkpoint Blockade in Participants With Solid Tumors
- Conditions
- Advanced Solid Tumors
- Interventions
- Biological: mRNA-4106
- First Posted Date
- 2025-03-17
- Last Posted Date
- 2025-05-02
- Lead Sponsor
- ModernaTX, Inc.
- Target Recruit Count
- 57
- Registration Number
- NCT06880549
- Locations
- 🇺🇸
START Midwest, Grand Rapids, Michigan, United States
🇺🇸START San Antonio, San Antonio, Texas, United States
🇺🇸START Mountain Region, West Valley City, Utah, United States
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News
IO Biotech's Melanoma Vaccine Narrowly Misses Primary Endpoint in Phase 3 Trial Despite Promising Subgroup Results
IO Biotech's cancer vaccine Cylembio combined with Keytruda showed a 23% relative risk reduction in disease progression or death compared to Keytruda alone, but narrowly missed statistical significance with a p-value of 0.056.
FDA Considers Revoking Pfizer COVID-19 Vaccine Authorization for Children Under 5
The FDA is considering not renewing Pfizer's emergency use authorization for its COVID-19 vaccine in children aged 6 months to 4 years for the upcoming respiratory season.
Genvira and Labskin Secure £1.2 Million UK-Canada Grant for Melanoma Immunotherapy Development
Genvira Biosciences and Labskin Limited have received £1.2 million ($2.0 million) in funding through the Canada-UK Biomanufacturing of Biologics and Advanced Therapies program to develop novel melanoma immunotherapies.
Moderna Announces 10% Workforce Reduction as Part of $1.5 Billion Cost-Cutting Initiative
Moderna plans to cut approximately 10% of its global workforce by year-end, reducing employee count from roughly 5,800 to under 5,000 as part of broader cost reduction efforts.
UNLV Researchers Achieve 99% Pancreas-Specific mRNA Delivery Using Novel ENDO Nanoparticle Platform
UNLV researchers developed ENDO (Endogenous Targeting Lipid Nanoparticles) that achieve 99% selectivity for pancreatic delivery of mRNA therapeutics via intravenous injection.
Aldevron Establishes Innovation Center in Boston Biotech Hub to Accelerate Genomic Medicine Development
Aldevron, a Danaher-owned leader in DNA, RNA, and protein manufacturing, has opened a new Innovation Center in Waltham, Massachusetts, positioning itself at the heart of the Boston biotech corridor.
EU Regulatory Approval Advances Pfizer-BioNTech LP.8.1-Adapted COVID-19 Vaccine for 2025-2026 Season
The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended approval for Pfizer and BioNTech's LP.8.1-adapted COMIRNATY vaccine targeting XFG and NB.1.8.1 variants.
Absci Raises $50 Million to Advance AI-Driven Drug Discovery Platform and Internal Pipeline
Absci Corporation completed a $50 million public offering of 16.67 million shares at $3.00 per share to fund its AI-powered drug discovery programs and internal pipeline development.
Turkish Study Links Pfizer COVID-19 Vaccine to Corneal Structural Changes
A Turkish study of 64 patients found measurable corneal changes 75 days after receiving two doses of the Pfizer-BioNTech COVID-19 vaccine, including 2% increased thickness and 8% reduced endothelial cell density.
Moderna Cancels mRNA Manufacturing Plant in Japan Amid Declining Vaccine Demand and Regulatory Uncertainty
Moderna has canceled plans to build an mRNA vaccine manufacturing plant at Shonan Health Innovation Park in Kanagawa Prefecture due to weak global vaccine demand and challenging business conditions.