Revolution Medicines, Inc. (RVMD) SEC Filings & Earnings Calls
EquiReason read 16 Revolution Medicines, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-10-13 — Revolution Medicines entered into a Tranche A loan agreement with Royalty Pharma, creating a direct financial obligation. The filing incorporates details from Item 8.01, indicating.
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
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Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
13 Oct 20268-K · 2.03, 8.01Revolution Medicines entered into a Tranche A loan agreement with Royalty Pharma, creating a direct financial obligation. The filing incorporates details from Item 8.01, indicating a material debt financing event.open
Risks flagged
Increased leverage and debt service obligations may strain future cash flows.
“Material direct financial obligation created; no specific terms disclosed in excerpt.”
1 Sep 20268-K · 1.01, 2.03Revolution Medicines entered into four lease agreements for ~672,000 sq ft headquarters in Redwood City, CA. Aggregate monthly base rent ~$2.7M starting, escalating 3% annually. Tenant improvement allowances up to ~$156.2M. Leases commenceopen
Figures in the filing · each found in the filing text
| Rentable Square Feet | 672,000 | |
| Aggregate Monthly Base Rent | $3M | |
| Tenant Improvement Allowances | $116M | |
| Rent Abatement | $23M |
Risks flagged
Related-party transaction risk: Landlord affiliated with Farallon Capital Management, a 6.4% shareholder.
“Farallon reported beneficial ownership of ~6.4% of outstanding common stock; funds managed by Farallon indirectly own majority interest in Landlords.”
Lease commencement subject to Phase II Closing; potential termination if not completed by April 29, 2027.
“Effectiveness subject to acquisition by Landlords; automatic termination if Phase II Closing not occurred by April 29, 2027.”
26 Aug 20268-K · 8.01FDA approved RASONQUE (daraxonrasib) for metastatic pancreatic adenocarcinoma based on Phase 3 RASolute 302 trial. WAC price set at $39,800 for 30-day supply.open
Figures in the filing · each found in the filing text
| Wholesale acquisition cost (WAC) of RASONQUE · RASONQUE · Q3-2026 | $39800.00 |
Risks flagged
Commercial execution risk; pricing and reimbursement uncertainty; competition from other RAS inhibitors.
“First-in-class RAS inhibitor; pricing set at $39,800 per 30-day supply; no revenue history.”
5 Aug 202610-QRevolution Medicines reported Q2 2026 results, highlighting positive Phase 3 data for daraxonrasib in 2L PDAC, NDA acceptance, and strong cash position.earningsopen
Figures in the filing · each found in the filing text
| Net loss · H1-2026 | $-1.10B | |
| Research and development expenses · H1-2026 | $739M | |
| General and administrative expenses · H1-2026 | $211M | |
| Operating cash flow · H1-2026 | $-741M |
Risks flagged
Clinical and regulatory risk
“We have not obtained regulatory approval for any product candidate, and it is possible that none of our current or future product candidates will ever obtain regulatory approval.” · word for word
Financing risk
“We will require substantial additional financing to achieve our goals, which may not be available on acceptable terms, or at all.” · word for word
Competition risk
“We face significant competition, and if our competitors develop and market products that are more effective, safer or less expensive than our product candidates, our commercial opportunities will be negatively impacted.” · word for word
Pricing and reimbursement risk
“Even if we are able to commercialize any product candidates, such products may become subject to unfavorable pricing regulations or third-party coverage and reimbursement policies.” · word for word
5 Aug 20268-K · 2.02FDA accepted NDA for daraxonrasib in pancreatic cancer after positive Phase 3 RASolute 302 results; Breakthrough Therapy Designation in NSCLC; EAP distributed to >2000 patients; commercial launch readiness achieved.open
Risks flagged
Regulatory and commercial execution risk remains until final approval and launch.
“NDA accepted but not yet approved; commercial launch contingent on FDA decision.”
6 May 20268-K · 2.02Released earnings results and quarterly financials; filed financial statements and exhibits with this reportearningsopen
Risks flagged
Regulatory and commercial execution risk for daraxonrasib.
“Submission to global authorities pending; commercialization capabilities still being built.”
Clinical trial risk for other pipeline candidates.
“Multiple Phase 3 trials ongoing; results not yet available.”
6 May 202610-QNet loss $-454Mopen
Figures in the filing · each found in the filing text
| Net loss · Q1-2026 | $-454M |
Risks flagged
Clinical Trial Failure Risk
“Even if we obtain positive results from preclinical studies or initial clinical trials, we may not achieve the same success in future trials.” · word for word
Financing Risk
“If we need to raise additional capital to fund our operations, funding may not be available to us on acceptable terms, or at all.” · word for word
Competition Risk
“Our clinical trials will compete with approved therapies, including sotorasib and adagrasib, as well as other clinical trials for product candidates that are in the same therapeutic areas” · word for word
27 Apr 2026DEF 14AAnnual proxy statement filed, disclosing executive compensation, governance, and stockholder voting matters.open
Figures in the filing · each found in the filing text
| Net Income (Loss) · FY2025 | $-1.13B |
Risks flagged
Pre-commercial stage risk
“The company is a late-stage clinical oncology company with no approved products, as indicated by the compensation discussion focusing on pre-commercial milestones.”
Net loss and negative cash flow
“Net loss of $1,131 million in 2025, as shown in Pay Versus Performance table.”
17 Apr 20268-K · 1.01, 2.03, 8.01Revolution Medicines issued $500M 0.50% Convertible Senior Notes due 2033 via underwriting agreement dated April 14, 2026, creating a direct financial obligation.open
Risks flagged
Increased debt and potential dilution from conversion feature.
“Notes are convertible into common stock; initial conversion price ~$198.80.”
16 Apr 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen
Risks flagged
Dilution to existing shareholders from issuance of 12.15M shares (including overallotment).
“Issued 10,563,381 shares plus 1,584,506 overallotment shares.”
13 Apr 20268-K · 8.01Revolution Medicines reported Phase 3 RASolute 302 trial of daraxonrasib in PDAC met endpoints: median OS 13.2 vs 6.7 months (HR 0.40, p<0.0001), PFS improved.open
Figures in the filing · each found in the filing text
| median overall survival (daraxonrasib) · Q2-2026 | $13.20 | |
| median overall survival (chemotherapy) · Q2-2026 | $6.70 | |
| hazard ratio · Q2-2026 | $0.40 |
Risks flagged
Regulatory and commercial risks remain; filing and approval not guaranteed.
“Forward-looking statements highlight risks in drug development, regulatory approval, and manufacturing.”
25 Feb 20268-K · 2.02Released earnings results and quarterly financials; filed financial statements and exhibits with this reportearningsopen
Risks flagged
No revenue, net loss, cash burn typical for clinical-stage biotech
“No revenue or net income figures provided; company is pre-revenue”
Clinical trial risk: pipeline failure could impair value
“Dependence on Phase 3 readouts; no approved products”
25 Feb 202610-KRisks named: Drug Pricing Pressure, Regulatory Compliance Cost, Clinical Development Failureopen
Risks flagged
Drug Pricing Pressure
“third-party payors are increasingly reducing reimbursements for pharmaceutical products and services” · word for word
Regulatory Compliance Cost
“We may be subject to numerous federal, state and foreign laws, regulations that govern the collection, use, disclosure and protection of health-related and other personal information” · word for word
Clinical Development Failure
“Our business is dependent on the successful development of our current and future product candidates” · word for word
5 Nov 202510-QQuarterly filing with financial results; net loss increased significantly due to higher R&D spending.earningsopen
Figures in the filing · each found in the filing text
| Net loss · Q3-2025 | $-305206.00 | +95% y/y |
| Research and development expense · Q3-2025 | $262506.00 | +73% y/y |
| General and administrative expense · Q3-2025 | $52763.00 | +120% y/y |
| Operating cash flow · 9M-2025 | $-623503.00 | +49% y/y |
Risks flagged
High cash burn rate
“Net cash used in operating activities $ (623,503) for nine months ended September 30, 2025.”
Dependence on clinical trial success
“The Company is a clinical-stage precision oncology company developing novel targeted therapies for RAS-addicted cancers.” · word for word
Liability from royalty sale
“Liability related to the sale of future royalties $256,509 as of September 30, 2025.” · word for word
5 Nov 20258-K · 2.02Released earnings results and quarterly financials; filed financial statements and exhibits with this reportearningsopen
Risks flagged
Clinical trial failure risk.
“Phase 3 trials for daraxonrasib in pancreatic and lung cancer; data readout in 2026.”
No approved products or revenue.
“Company is a late-stage clinical oncology company with no approved products.”
Revolution Medicines, Inc. — questions
- What did Revolution Medicines, Inc. file recently?
- 16 SEC filings in the last 12 months. Latest: 8-K on 2026-10-13 — Revolution Medicines entered into a Tranche A loan agreement with Royalty Pharma, creating a direct financial obligation. The filing incorporates details from Item 8.01, indicating a material debt financing event.
Every figure on this page comes from Revolution Medicines, Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.