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RVMD — Revolution Medicines Inc.

RVMD (Revolution Medicines Inc.) stock: $192.28, $41.59B market cap, $3.65B cash, $37.94B EV, $48.19B fully diluted market cap. Lead program: RMC-6236 (Pancreatic Cancer), Phase 3. Data from Fully Diluted's biotech stocks database.

What they do

We are a clinical-stage precision oncology company developing novel targeted therapies for RAS-addicted cancers. We possess sophisticated structure-based drug discovery capabilities built upon deep chemical biology and cancer pharmacology know-how and innovative, proprietary technologies that enable the creation of small molecules tailored to unconventional binding sites.

Source: 10-K FY2025 via SEC EDGAR

Share price
$192.28
Market cap
$41,588.7M
Cash
$3,651.4M
Enterprise value
$37,937.3M

Balance sheet

Cash$3,651.4M
Debt$0.0M
Net cash$3,651.4M
Enterprise value$37,937.3M
Basic shares216.3M shares
Fully diluted shares250.6M shares
Fully diluted market cap$48,191.5M
Cash per share$16.88
Quarterly burn$387.3M
Cash runway10.2 quarters

Cash figures as of 2026-09-30. Database snapshot: 2026-11-07.

Share structure

Common
216.3M
Pre-funded warrants
0.0M
Options
17.7M
RSUs
4.8M
Warrants
2.2M
Converts
2.5M
Conv preferred
0.0M
ESPP reserve
7.1M
FDSO
250.6M

Cap table as of 2026-09-30.

Price history

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Next catalyst

RMC-9805 · Feb 11 - Mar 25 in 14 wks · Phase 1 · Non-small Cell Lung Cancer (NSCLC); Colorectal Cancer (CRC); Pancreatic Ductal Adenocarcinoma (PDAC)

Recently reported

Daraxonrasib Phase 3 Positive · 2026-10-15
Primary: Overall survival and progression-free survival in the Phase 3 RASolute 302 trial versus investigator's-choice chemotherapy in metastatic pancreatic adenocarcinoma — In the ITT population, overall survival HR 0.40 (95% CI 0.30-0.53; p<0.0001) with median OS 13.2 months versus 6.7 months, and progression-free survival HR 0.49 (95% CI 0.38-0.64; p<0.0001) with median PFS 7.2 versus 3.6 months
· Trial met all primary and key secondary endpoints in both the RAS G12-mutant and overall intent-to-treat populations
· Later ad hoc OS analysis showed median OS 12.4 versus 6.7 months (HR 0.49)
· CHMP positive opinion recommending EU marketing authorization as monotherapy after at least one prior systemic therapy
· European Commission decision pending
· RASONQUE was FDA-approved on August 26, 2026
Safety: Most common adverse reactions were diarrhea, dermatitis acneiform, stomatitis, nausea, vomiting and fatigue
Source release →
RMC-6236 Mixed · 2026-04-13
Source release →
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