Skip to main content
VSTMVerastem, Inc.Sell5.6·$6.62-0.75%
SellModerate Confidence
Investment thesis

Verastem pairs a perfect 4-quarter earnings beat streak and positive insider signals with real technical risk, an RSI of 92 inside a still-confirmed downtrend and 28% short interest the engine calls justified, leaving the position at zero conviction ahead of an earnings catalyst in 19 days.

Thesis pillars

  • Perfect Earnings Beat Streak CatalystDeteriorating
  • Positive Insider Activity Bull CaseImproving
  • Overbought Bear Rally RiskDeteriorating
  • +2 more pillars — see the Why tab for full reasoning

Full reasoning →

Open full analysis

Verastem, Inc. (VSTM) Stock Analysis

Momentum Cont setup · Inst Constrain edge

SellGrowthShortModerate Confidence

Healthcare · Biotechnology

Sell if holding. Engine safety override at $6.62: Risk below floor (2.5 < 3.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.6/10 and A.R:R 6.3:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 22%; Elevated put/call ratio: 35.71; Below-average business quality.

Verastem is a commercial-stage biopharmaceutical company focused on RAS/MAPK pathway-driven cancers, marketing AVMAPKI FAKZYNJA CO-PACK (avutometinib plus defactinib) as the first FDA-approved treatment for KRAS-mutated recurrent low-grade serous ovarian cancer following... Read more

$6.62+95.0% A.UpsideScore 5.6/10#78 of 240 Biotechnology
QualityF-score4 / 9FCF yield-17.36%
Stop $6.12Target $12.83(analyst − 13%)A.R:R 6.3:1
Analyst target$14.75+122.8%8 analysts
$12.83our TP
$6.62price
$14.75mean
$18

Sell if holding. Engine safety override at $6.62: Risk below floor (2.5 < 3.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.6/10 and A.R:R 6.3:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 22%; Elevated put/call ratio: 35.71; Below-average business quality. Chart setup: Trend continuation, RSI 59, MACD bullish. Score 5.6/10, moderate confidence.

Passes 7/9 gates (favorable risk/reward ratio, clean insider activity, no SEC red flags, news events none recent, earnings proximity 79d clear, semi cycle peak clear, materials cycle peak clear). Fails on weak momentum and death cross (50MA < 200MA). Suitability: speculative.

10-K grounded · weekly refresh

About Verastem, Inc.

About Verastem, Inc.

Verastem's AVMAPKI FAKZYNJA CO-PACK, the first FDA-approved treatment for KRAS-mutated recurrent low-grade serous ovarian cancer, received accelerated approval on May 8, 2025 and generated $30.9 million in net product revenue during its first seven months of commercial launch. The combination therapy is only commercially available in the United States, where an estimated 6,000 to 8,000 women live with LGSOC, and roughly 30% carry a KRAS mutation.

AVMAPKI FAKZYNJA CO-PACK reaches patients through designated specialty pharmacies and distributors, with the product available within five days of approval through two specialty pharmacies onboarded in the second quarter of 2025 and four specialty distributors added in the third quarter; the company estimates the top 100 commercial healthcare organizations in the U.S. represent approximately 50% of the sales opportunity for the drug. Verastem licensed its KRAS G12D inhibitor VS-7375 from GenFleet Therapeutics in January 2025, with GenFleet separately developing the same molecule as GFH375 in China under its own trials. A September 2021 clinical collaboration with Amgen to combine avutometinib with Amgen's LUMAKRAS was discontinued in December 2025 so the company could redirect resources toward VS-7375. Verastem competes against numerous large pharmaceutical and biotechnology companies pursuing RAS/MAPK pathway therapies, including AbbVie and AstraZeneca.

Show full overview

Verastem's business rests on a single approved product still under conditional authorization: the 10-K states the company is highly dependent on the commercial success of AVMAPKI FAKZYNJA CO-PACK for the foreseeable future, and because the drug holds accelerated rather than full approval, continued marketing depends on confirming clinical benefit in the ongoing Phase 3 RAMP 301 trial, with a topline progression-free-survival readout not expected until mid-2027. Enrollment finished a quarter ahead of schedule in October 2025, but a negative or inconclusive result at that 2027 readout could jeopardize the product's continued approval, not just future label expansion.

See also: Healthcare · Biotechnology

From Verastem, Inc.'s most recent 10-K filing, extracted July 19, 2026.

news + 30-day 8-K events · 5-min refresh

Recent developments

updated 2026-08-17
TrendMatrix Research · upcoming catalyst calendar

Upcoming dated catalysts

Tue, Nov 3, 202679d to earnings· next earnings call

Thesis

Rewards
No bull case signals
Risks
Concentration risk — Product: AVMAPKI FAKZYNJA CO-PACK
Risk below floor (2.5 < 3.0)

Key Metrics

P/E (TTM)
P/E (Fwd)-8.8
Mkt Cap$596M
EV/EBITDA-3.4
Profit Mgn-231.6%
ROE-471.2%
Rev Growth1775.4%
Beta0.29
DividendNone
Rating analysts15

Quality Signals

Piotroski F4/9MoatNarrow

Options Flow

P/C35.71bearish
IV234%elevated

Concentration Risks(10-K Item 1A)

  • HIGHProductAVMAPKI FAKZYNJA CO-PACK
    10-K Item 1A: 'We are highly dependent on the commercial success of AVMAPKI FAKZYNJA CO-PACK (avutometinib capsules; defactinib tablets) in the U.S for the foreseeable future.'
  • MEDIUMCustomertop 100 commercial healthcare organizations50%
    10-K Item 1: 'the top 100 commercial healthcare organizations in the U.S. comprise approximately 50% of the sales opportunity'

Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results.

Show full disclosure ▾

About TrendMatrix. TrendMatrix is a publisher of general securities research and market commentary. We publish on a regular schedule. All content is the same for every subscriber in a tier — we do not provide personalized investment advice and we do not take into account any individual subscriber's financial situation, investment objectives, risk tolerance, tax situation, or holdings.

Not investment advice. TrendMatrix is not a registered investment adviser. Our content is for informational and educational purposes only. Consult your own licensed investment adviser, broker, or tax professional before making any investment decision.

Conflicts and positions. The TrendMatrix editorial team frequently holds personal long-term positions in securities discussed. We disclose positions held at the time of publication on each piece. We maintain a trading-window policy: we do not initiate or close positions in the same direction as a TrendMatrix publication within 24 hours before or 72 hours after publication.

No paid promotion. TrendMatrix does not accept payment from any issuer, broker, or third party in exchange for coverage of any security. Our sole compensation is subscription revenue.

No fiduciary duty. No fiduciary, advisory, or agency relationship is created between you and TrendMatrix by reading our content or subscribing to our service.

Performance. Past performance is not indicative of future results. Performance figures reflect the published model only and do not reflect any individual subscriber's actual results.

Methodology · Editorial policy & full disclaimer

Rating Breakdown

2 floor-breakers

Volatile — 6.4% daily ATR makes tight stops impractical. Position-size conservatively.static

Volatility
0.0
Put Call
0.0
Implied Vol
0.0
Short Interest
1.3
Days To Cover
2.5
Debt Equity
3.6
Beta
10.0
High short interest justified: 22%Elevated put/call: 35.71High IV: 234%Concentration risks: 1 HIGH, 1 MED (10-K Item 1A — sized via position_sizing, validated via buy_confidence)

Technicals below the gate floor. Component breakdown shows what dragged the score down.static

52w Position
1.7
Bollinger
2.8
Support Resistance
3.7
GatesMomentum 4.4<4.5Death cross (50MA < 200MA)A.R:R 6.3 ≥ 1.5Insider activity: OKNo SEC red flagsNEWS EVENTS NONE RECENTEARNINGS PROXIMITY 79d clearSEMI CYCLE PEAK CLEARMATERIALS CYCLE PEAK CLEARMomentum ContSuitability: Speculative
RSI
59 · Neutral
20D MA 50D MA 200D MADEATH CROSSSupport $5.54Resistance $7.18

Price Targets

$6
$13
A.Upside+95.0%
A.R:R6.3:1

Position Sizing

ConvictionNone
Suggested %0.5%
Max %1%
RegimeSteady

Risk Alerts

! Risk below floor (2.5 < 3.0)
! momentum at 4.4 (below the engine's 4.5 threshold)
! Death cross — 50-day MA below 200-day MA

Earnings

B
B
B
B
4/4 beats
Next Earnings2026-11-03 (79d)

Verdict History

reverse chrono — latest first
Loading history...
Verdicts are recorded on every nightly pipeline run. Rows capture transitions (verdict flips, score deltas ≥0.3, entry/TP/SL changes). Rows with a ▶ can be expanded to see the change reason. Aggregate cohort performance is tracked in the recommendation ledger.
Frequently Asked Questions
Is VSTM stock a buy right now?

Sell if holding. Engine safety override at $6.62: Risk below floor (2.5 < 3.0) triggers a hard block regardless of the otherwise-positive setup — overall score 5.6/10 and A.R:R 6.3:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 22%; Elevated put/call ratio: 35.71; Below-average business quality. Chart setup: Trend continuation, RSI 59, MACD bullish. Prior stop was $6.12. Score 5.6/10, moderate confidence.

What is the VSTM stock price target?

Take-profit target: $12.83 (+95.0% upside). Prior stop was $6.12. Stop-loss: $6.12.

What are the risks of investing in VSTM?

Concentration risk — Product: AVMAPKI FAKZYNJA CO-PACK; Risk below floor (2.5 < 3.0).

Is VSTM overvalued or undervalued?

Verastem, Inc. trades at a P/E of N/A (forward -8.8). TrendMatrix value score: 7.6/10. Verdict: Sell.

What do analysts say about VSTM?

15 analysts cover VSTM with a consensus score of 4.3/5. Average price target: $15.

What does Verastem, Inc. do?Verastem is a commercial-stage biopharmaceutical company focused on RAS/MAPK pathway-driven cancers, marketing AVMAPKI...

Verastem is a commercial-stage biopharmaceutical company focused on RAS/MAPK pathway-driven cancers, marketing AVMAPKI FAKZYNJA CO-PACK (avutometinib plus defactinib) as the first FDA-approved treatment for KRAS-mutated recurrent low-grade serous ovarian cancer following accelerated approval on May 8, 2025. The product generated $30.9 million in net product revenue during its first seven months of commercial launch in 2025, while the company advances VS-7375, a KRAS G12D inhibitor licensed from GenFleet Therapeutics in January 2025, through Phase 1/2 trials.

Related stocks: HRMY (Harmony Biosciences Holdings, I) · CRMD (CorMedix Inc.) · ZVRA (Zevra Therapeutics, Inc.) · AUPH (Aurinia Pharmaceuticals Inc) · MGTX (MeiraGTx Holdings plc)
Home Stocks VSTM

Latest news

Latest News

Kalkine Media18d ago
Kalkine Media19d ago
BioSpace19d agoProduct
TradingKey19d ago
Stock Titan11d ago
TipRanks18d agoProduct
Dars.gov.et18d agoEarnings
TradingKey18d ago
TradingKey18d ago
TradingKey18d ago
Tradingkey.com18d ago
Finance.yahoo.com10d ago
Yahoo Finance10d ago
Investing.com UK10d ago
GuruFocus11d agoLeadership Change
GuruFocus11d ago
Investing.com11d ago
富途牛牛16d agoEarnings
TradingKey17d ago
TradingKey17d ago
Loading more...