RVMD Revolution Medicines, Inc.

BULLISH Impact: 8/10 PRESS-RELEASE
Horizon weeks Filed May 6, 2026 Processed 1mo ago Wire GlobeNewswire
Press release: fda
Latest settled — T+20d
RVMD ▲ +9.46% at T+20d
LONG call ✓ call won +9.46% · α vs SPY +6.32% · entry $142.51 → $155.99
Next anchor: T+60d in 7w
Last close $153.87 (close Jun 12) · +7.97% from $142.51 entry
Entry anchored
May 6, 03:59 PM ET
via Databento tick
T+1d
0.00%
call 0.00% · α -0.83%
$142.51
settled 6w ago
T+5d
+5.21%
call +5.21% · α +3.71%
$149.94
settled 5w ago
T+20d
+9.46%
call +9.46% · α +6.32%
$155.99
settled 11d ago
T+60d
call — · α —
in 7w

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Executive Summary

Revolution Medicines announced that Phase 1/2 data for daraxonrasib in RAS-mutant pancreatic cancer were published in NEJM, complementing recently reported positive Phase 3 topline results showing an unprecedented overall survival benefit. The drug holds FDA Breakthrough Therapy and Orphan Drug Designations, reinforcing its potential as a new standard of care for a deadly cancer with limited treatment options.

Actionable Insight

Traders should expect upward price pressure as the market digests the positive clinical validation. Monitor for regulatory submission milestones and potential partnership or M&A interest given the high unmet need.

Key Facts

  • NEJM published Phase 1/2 data for daraxonrasib in metastatic RAS-mutant PDAC.
  • Company previously announced positive Phase 3 RASolute 302 topline results with unprecedented overall survival benefit vs. standard chemotherapy.
  • Daraxonrasib has FDA Breakthrough Therapy and Orphan Drug Designations for PDAC with G12 mutations.
  • Daraxonrasib is a RAS(ON) multi-selective inhibitor targeting diverse RAS mutations.
  • Three additional global Phase 3 registrational trials are ongoing, including earlier-line PDAC and NSCLC.

Financial Impact

Positive clinical data significantly increases probability of regulatory approval and peak sales potential, estimated by analysts in the multi-billion dollar range for PDAC indication alone.

probability of approvalpeak revenue estimatesvaluation multiples

Risk Factors

  • Regulatory approval not guaranteed; pivotal trial results may not replicate in larger populations.
  • Competition from other RAS inhibitors (e.g., from Mirati, Amgen) could limit market share.
  • Risk of toxicity or safety issues in ongoing broader clinical development.

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
96% bullish (27 analysts)

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3289496
12 reports for RVMD
Performance horizon
75% Hit rate 6 of 8 directional calls best @ T+5▲ +9.96%Apr 17, 2026
Filters
Rows
Reports for RVMD — sortable, filterable
Type Now
Jun 11, 2026
3d ago
144
NEUTRAL ★ 3/10
$149.21 awaiting T+5awaiting T+5$153.87 (+3.12%)
May 31, 2026
14d ago
Press Release
BULLISH ★ 8/10
$163.68 $149.23▼ −8.83%▼ −6.08%$153.87 (−5.99%)
May 6, 2026
5w ago
Press Release
BULLISH ★ 8/10
$142.51 $149.94▲ +5.21%▲ +3.71%$153.87 (+7.97%)
Apr 21, 2026
7w ago
Press Release
BULLISH ★ 8/10
$141.50 $140.80▼ −0.49%▼ −0.55%$153.87 (+8.74%)
Apr 21, 2026
7w ago
Press Release
BULLISH ★ 7/10
$141.50 $140.80▼ −0.49%▼ −0.55%$153.87 (+8.74%)
Apr 21, 2026
7w ago
Press Release
BULLISH ★ 8/10
$148.90 $144.83▼ −2.73%▼ −3.82%$153.87 (+3.34%)
Apr 19, 2026
8w ago
Press Release
BULLISH ★ 8/10
$146.23 $131.67▼ −9.96%▼ −10.87%$153.87 (+5.22%)
Apr 17, 2026
8w ago
Press Release
BEARISH ★ 7/10
$146.23 $131.67▲ +9.96%▲ +10.87%$153.87 (−5.22%)
Apr 15, 2026
8w ago
Press Release
BEARISH ★ 7/10
$152.54 $141.50▲ +7.24%▲ +8.88%$153.87 (−0.87%)
Apr 13, 2026
8w ago
Press Release
BEARISH ★ 7/10
$147.01 $148.90▼ −1.29%▲ +0.11%$153.87 (−4.67%)
Showing 10 of 12

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