Revolution Medicines

- Country
- 🇺🇸United States
- Ownership
- Public
- Established
- 2015-01-01
- Employees
- 378
- Market Cap
- $7.2B
- Website
- http://www.revmed.com
- Introduction
Revolution Medicines, Inc. is a clinical-stage precision oncology company, which engages in developing novel targeted therapies. It engages in the discovery and development of cancer treatment by pioneering novel combination and monotherapy treatment regimens to maximize the depth and durability of clinical benefit and circumvent adaptive resistance mechanisms for patients which are dependent on the RAS and mTOR pathway. The company was founded by Mark A. Goldsmith, Kevan Shokat, Martin D. Burke, David L. Pompliano and Michael Fischbach in October 2014 and is headquartered in Redwood City, CA.
Clinical Trials
16
Trial Phases
3 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 (16 trials with phase data)• Click on a phase to view related trials
Study of Daraxonrasib (RMC-6236) in Previously Treated Patients With RAS Mutated NSCLC (RASolve 301)
- Conditions
- NSCLC (Non-small Cell Lung Cancer)Non-Small Cell Lung CancerNSCLCNSCLC (Non-small Cell Lung Carcinoma)NSCLC (Advanced Non-small Cell Lung Cancer)
- Interventions
- First Posted Date
- 2025-03-18
- Last Posted Date
- 2025-09-29
- Lead Sponsor
- Revolution Medicines, Inc.
- Target Recruit Count
- 420
- Registration Number
- NCT06881784
- Locations
- 🇺🇸
Alabama Oncology, Birmingham, Alabama, United States
🇺🇸Florida Cancer Specialists & Research Institute - South, Fort Myers, Florida, United States
🇺🇸BRCR Global, Plantation, Florida, United States
Phase 3 Study of Daraxonrasib (RMC-6236) in Patients With Previously Treated Metastatic Pancreatic Ductal Adenocarcinoma (PDAC)
- Conditions
- Pancreatic CancerPDACPDAC - Pancreatic Ductal Adenocarcinoma
- Interventions
- First Posted Date
- 2024-10-03
- Last Posted Date
- 2025-09-16
- Lead Sponsor
- Revolution Medicines, Inc.
- Target Recruit Count
- 460
- Registration Number
- NCT06625320
- Locations
- 🇺🇸
Cedars-Sinai Medical Center, Los Angeles, California, United States
🇺🇸UCLA, Los Angeles, California, United States
🇺🇸UC San Diego Health Moores Cancer Center, San Diego, California, United States
Study of RAS(ON) Inhibitors in Patients With Gastrointestinal Solid Tumors
- Conditions
- PDACCRCPancreatic Ductal AdenocarcinomaMetastatic Pancreatic Ductal AdenocarcinomaColorectal CancerGastrointestinal Cancer
- Interventions
- Drug: mFOLFOX6 regimenDrug: mFOLFIRINOX regimen
- First Posted Date
- 2024-06-06
- Last Posted Date
- 2025-10-01
- Lead Sponsor
- Revolution Medicines, Inc.
- Target Recruit Count
- 1130
- Registration Number
- NCT06445062
- Locations
- 🇺🇸
Ironwood Cancer and Research Centers, Chandler, Arizona, United States
🇺🇸Mayo Clinic Hospital, Phoenix, Arizona, United States
🇺🇸HonorHealth Research Institute, Scottsdale, Arizona, United States
Study of RAS(ON) Inhibitors in Patients With Advanced RAS-mutated NSCLC
- Conditions
- Non-Small Cell Lung Cancer, NSCLCKRAS, NRAS, HRAS-mutated NSCLCKRAS G12C-mutated Solid Tumors, Lung CancerLung Cancer Stage IV, Advanced Solid Tumor, CancerRAS G12D-mutated NSCLC
- Interventions
- First Posted Date
- 2023-12-08
- Last Posted Date
- 2025-10-03
- Lead Sponsor
- Revolution Medicines, Inc.
- Target Recruit Count
- 616
- Registration Number
- NCT06162221
- Locations
- 🇺🇸
City of Hope - Duarte, Duarte, California, United States
🇺🇸City of Hope - Lennar, Irvine, California, United States
🇺🇸UC Davis, Davis Comprehensive Cancer Center, Sacramento, California, United States
Study of RMC-6291 in Combination With RMC-6236 in Participants With Advanced KRAS G12C Mutant Solid Tumors
- Conditions
- Colorectal CancerPancreatic Ductal AdenocarcinomaNon-Small Cell Lung Cancer (NSCLC)
- Interventions
- Drug: Assigned interventions
- First Posted Date
- 2023-11-13
- Last Posted Date
- 2025-03-27
- Lead Sponsor
- Revolution Medicines, Inc.
- Target Recruit Count
- 210
- Registration Number
- NCT06128551
- Locations
- 🇮🇹
Niguarda Cancer Center, Milano, Italy
🇺🇸City of Hope, Duarte, California, United States
🇺🇸UC IRVINE Health, Orange, California, United States
- Prev
- 1
- 2
- 3
- Next
News
Revolution Medicines Appoints Alan Sandler as Chief Development Officer to Advance RAS-Targeted Cancer Pipeline
Revolution Medicines has appointed Alan Sandler, M.D. as chief development officer to lead development of RAS(ON) inhibitors for RAS-addicted cancers.
Orbital Therapeutics Appoints Adam Raff as Senior VP to Advance RNA Medicine Platform Toward Clinical Trials
Orbital Therapeutics has appointed Adam Raff, M.D., Ph.D., as Senior Vice President of Clinical Development to oversee clinical and regulatory strategy for the company's RNA medicine portfolio.
Ivonescimab Demonstrates Superior Efficacy in Phase III Lung Cancer Trials, Positioning for Global Regulatory Approvals
Ivonescimab, a PD-1/VEGF bispecific antibody, achieved a 48% reduction in progression-free survival risk compared to chemotherapy in EGFR-mutated NSCLC patients.
Revolution Medicines Partners with Iambic Therapeutics in $25M AI-Driven Drug Discovery Collaboration for RAS-Addicted Cancers
Revolution Medicines and Iambic Therapeutics announced a multi-year collaboration in July 2025 to develop novel drug candidates using AI-driven discovery platforms targeting RAS-addicted cancers.
Revolution Medicines and Summit Therapeutics Launch Clinical Collaboration to Test RAS Inhibitor Combinations with Bispecific Antibody
Revolution Medicines and Summit Therapeutics announced a clinical collaboration to evaluate three RAS(ON) inhibitors in combination with ivonescimab, a PD-1/VEGF bispecific antibody, across multiple solid tumor types.
Revolution Medicines Secures $2 Billion Funding Deal with Royalty Pharma for RAS Cancer Drug Development
Revolution Medicines partnered with Royalty Pharma on a $2 billion flexible funding agreement to support global development and commercialization of its RAS(ON) inhibitor portfolio for cancer treatment.
Revolution Medicines Advances First-in-Class KRAS(G12D) Molecular Glue Inhibitor RMC-9805 with Novel Cyclophilin A Mechanism
Revolution Medicines has developed RMC-9805, a first-in-class covalent KRAS(G12D)(ON) molecular glue inhibitor that targets the previously "undruggable" KRAS(G12D) mutant using a cyclophilin A-recruiting tricomplex mechanism.
Revolution Medicines Reports Promising Results for Zoldonrasib in KRAS G12D Mutant Lung Cancer
• Revolution Medicines announced new clinical data for zoldonrasib (RMC-9805) showing a 61% objective response rate in patients with KRAS G12D mutant non-small cell lung cancer at the AACR Annual Meeting. • The RAS(ON) G12D-selective inhibitor demonstrated an acceptable safety profile with primarily Grade 1 or 2 adverse events and a favorable mean dose intensity of 98% in the Phase 1 study. • These results build on earlier promising data in pancreatic ductal adenocarcinoma, supporting further evaluation of zoldonrasib as both monotherapy and in combination treatments for these difficult-to-treat cancers.
AACR Annual Meeting 2025 to Bridge Gap Between Cancer Science and Clinical Practice
The American Association for Cancer Research (AACR) Annual Meeting 2025 in Chicago will focus on "Unifying Cancer Science and Medicine" with presentations spanning from basic research to practice-changing clinical trials.
Revolution Medicines' Novel Drug Shows Promise in Advanced Pancreatic Cancer Treatment
• A groundbreaking experimental drug, daraxonrasib by Revolution Medicines, demonstrates encouraging results in treating late-stage pancreatic cancer patients, offering new hope in a traditionally difficult-to-treat disease. • One stage-four pancreatic cancer patient has achieved a remarkable 17-month survival while participating in the clinical trial, significantly exceeding typical survival expectations for advanced cases. • The development represents a potential breakthrough in pancreatic cancer treatment, where current five-year survival rates for late-stage patients stand at only 3%, with median survival under one year.