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SMMTSummit Therapeutics Inc.Sell5.1·$14.14+3.51%
SellModerate Confidence
Investment thesis

Summit Therapeutics has a single clinical asset, ivonescimab, licensed exclusively from Akeso, with analysts projecting 102% upside and a risk-reward ratio of more than 10 to 1, but the quality score of 1.8, 27% short interest, and 3 consecutive earnings misses before the most recent quarter reflect the binary nature of the investment.

Thesis pillars

  • Analyst Consensus 100pct UpsideDeteriorating
  • Ivonescimab Single Asset BinaryStable
  • High Short Interest Informed BearsStable
  • +1 more pillar — see the Why tab for full reasoning

Full reasoning →

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Summit Therapeutics Inc. (SMMT) Stock Analysis

Falling Knife setup

SellQualityShortModerate Confidence

Healthcare · Biotechnology

Sell if holding. Engine safety override at $14.14: a dimension score below its floor triggers a hard block regardless of the otherwise-positive setup — overall score 5.1/10 and A.R:R 6.2:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 25%; Below-average business quality; Negative price momentum.

Summit Therapeutics is a clinical-stage biopharmaceutical company with a single development candidate, ivonescimab, a PD-1/VEGF-A bispecific antibody licensed from Akeso Inc. in January 2023. Summit has no approved products or revenue; a BLA for ivonescimab in EGFR-mutated NSCLC... Read more

$14.14+73.6% A.UpsideScore 5.1/10#144 of 254 Biotechnology
QualityF-score4 / 9FCF yield-1.28%
Stop $13.11Target $24.47(analyst − 13%)A.R:R 6.2:1
Analyst target$28.13+98.9%13 analysts
$24.47our TP
$14.14price
$28.13mean
$10
$41

Sell if holding. Engine safety override at $14.14: a dimension score below its floor triggers a hard block regardless of the otherwise-positive setup — overall score 5.1/10 and A.R:R 6.2:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 25%; Below-average business quality; Negative price momentum. Chart setup: Death cross, below all MAs, RSI 36, MACD bearish. Score 5.1/10, moderate confidence.

Passes 7/10 gates (favorable risk/reward ratio, clean insider activity, no SEC red flags, news boost analyst 0.50, earnings proximity 84d clear, semi cycle peak clear, materials cycle peak clear). Fails on weak momentum and death cross (50MA < 200MA) and news bankruptcy. Suitability: speculative.

10-K grounded · weekly refresh

About Summit Therapeutics Inc.

About Summit Therapeutics Inc.

Summit Therapeutics' entire pipeline rests on a single asset — ivonescimab, a PD-1/VEGF-A bispecific antibody licensed from Akeso Inc. in January 2023 for $474.9 million upfront in cash and stock. The company has no approved products and no revenue. The HARMONi Phase III trial demonstrated a PFS hazard ratio of 0.52 (p<0.00001) in EGFR-mutated NSCLC; a BLA was submitted in Q4 2025, accepted by FDA in January 2026, with PDUFA date of November 14, 2026.

Summit earns no product revenue and funds operations through capital markets. The license from Akeso covers commercialization rights in the United States, Canada, Europe, Japan, Latin America, Middle East, and Africa, while Akeso retains rights for China — where ivonescimab was approved by the NMPA in May 2024 for EGFR-mutated NSCLC in combination with chemotherapy and again in April 2025 as monotherapy for PD-L1 positive NSCLC. Akeso supplies drug substance and drug product under a supply agreement, and Summit pays a low-double-digit royalty on annual revenues plus milestone payments on regulatory approvals and commercial targets. Summit is running three additional Phase III trials — HARMONi-3 (first-line metastatic NSCLC vs. pembrolizumab), HARMONi-7 (high PD-L1 monotherapy vs. pembrolizumab), and HARMONi-GI3 (colorectal cancer) — with enrollment completions targeted between 2026 and 2027.

Show full overview

The PDUFA date of November 14, 2026 represents a binary regulatory event: the FDA noted that a statistically significant overall survival benefit is necessary to support marketing authorization in the EGFRm NSCLC 2L+ setting, yet the HARMONi primary analysis did not achieve statistical significance for OS (HR=0.79; p=0.057). Approval would initiate commercialization across the Licensed Territory; a Complete Response Letter would leave Summit with no approved product, no alternative revenue source, and ongoing Phase III spend across four concurrent trials.

See also: Healthcare · Biotechnology

From Summit Therapeutics Inc.'s most recent 10-K filing, extracted June 11, 2026.

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

Recent developments

updated 2026-07-27

Recent Developments — Summit Therapeutics Inc.

Generated 2026-07-27T14:48:12Z.

TrendMatrix Research · upcoming catalyst calendar

Upcoming dated catalysts

Mon, Oct 19, 202684d to earnings· next earnings call

Thesis

Rewards
Recent Analyst detected in news
Risks
Concentration risk — Pipeline: ivonescimab
Concentration risk — Counterparty: Akeso license
Quality below floor (2.2 < 4.0)

Key Metrics

P/E (TTM)
P/E (Fwd)-11.5
Mkt Cap$10.9B
EV/EBITDA-11.7
Profit Mgn0.0%
ROE-192.5%
Rev Growth
Beta-1.26
DividendNone
Rating analysts24

Quality Signals

Piotroski F4/9

Options Flow

P/C1.02bearish
IV109%elevated
Max Pain$14-4.5% vs spot

Concentration Risks(10-K Item 1A)

  • HIGHpipelineivonescimab
    10-K Item 1A: 'We depend heavily on the success of ivonescimab. If we are unable to successfully develop and commercialize ivonescimab, or experience significant delays in doing so'
  • HIGHcounterpartyAkeso license
    10-K Item 1A: 'We depend on our relationship with, and the intellectual property licensed from Akeso'
  • HIGHSupplierAkeso
    10-K Item 1A: 'We rely on the use of third parties, including Akeso, to manufacture our product candidate'

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.

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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

3 floor-breakers·1 ceiling hit

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

Gross Margin
0.0
Operating Margin
0.0
Net Margin
0.0
Fcf Quality
0.0
Piotroski F
4.4
Moat
4.8
Current Ratio
6.0
Cash-burning (FCF negative)No competitive moatQuality concerns

Price action weak — below key moving averages, no momentum carry. Needs a base before trend-continuation setups apply.static

Volume
0.0
Ma Position
1.0
Macd
3.3
Rsi
3.5
Obv
5.0
Below 200-MA, MA slope -5.4%/30d — confirmed downtrend

No near-term catalyst priced in. Thesis progression will come from fundamentals grinding, not event reaction.static

Surprise Avg
0.0
Earnings History
1.1
Erm
5.0
Earnings Timing
5.0
News Activity
8.0
Earnings concerns: 1B/2M
GatesMomentum 2.6<4.5Death cross (50MA < 200MA)NEWS BANKRUPTCYA.R:R 6.2 ≥ 1.5Insider activity: OKNo SEC red flagsNEWS BOOST ANALYST 0.50EARNINGS PROXIMITY 84d clearSEMI CYCLE PEAK CLEARMATERIALS CYCLE PEAK CLEARFalling KnifeSuitability: Speculative
RSI
36 · Neutral
20D MA 50D MA 200D MADEATH CROSSSupport $13.20Resistance $16.05

Price Targets

$13
$24
A.Upside+73.6%
A.R:R6.2:1

Position Sizing

ConvictionNone
Suggested %0.5%
Max %1%
RegimeSteady

Risk Alerts

! Quality below floor (2.2 < 4.0)
! momentum at 2.6 (below the engine's 4.5 threshold)
! Death cross — 50-day MA below 200-day MA

Earnings

B
M
M
M
1/4 beats
Next Earnings2026-10-19 (84d)

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 SMMT stock a buy right now?

Sell if holding. Engine safety override at $14.14: a dimension score below its floor triggers a hard block regardless of the otherwise-positive setup — overall score 5.1/10 and A.R:R 6.2:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 25%; Below-average business quality; Negative price momentum. Chart setup: Death cross, below all MAs, RSI 36, MACD bearish. Prior stop was $13.11. Score 5.1/10, moderate confidence.

What is the SMMT stock price target?

Take-profit target: $24.47 (+73.6% upside). Prior stop was $13.11. Stop-loss: $13.11.

What are the risks of investing in SMMT?

Concentration risk — Pipeline: ivonescimab; Concentration risk — Counterparty: Akeso license; Quality below floor (2.2 < 4.0).

Is SMMT overvalued or undervalued?

Summit Therapeutics Inc. trades at a P/E of N/A (forward -11.5). TrendMatrix value score: 9.0/10. Verdict: Sell.

What do analysts say about SMMT?

24 analysts cover SMMT with a consensus score of 3.8/5. Average price target: $28.

What does Summit Therapeutics Inc. do?Summit Therapeutics is a clinical-stage biopharmaceutical company with a single development candidate, ivonescimab, a...

Summit Therapeutics is a clinical-stage biopharmaceutical company with a single development candidate, ivonescimab, a PD-1/VEGF-A bispecific antibody licensed from Akeso Inc. in January 2023. Summit has no approved products or revenue; a BLA for ivonescimab in EGFR-mutated NSCLC was accepted by the FDA in January 2026 with a PDUFA date of November 14, 2026.

Related stocks: AUPH (Aurinia Pharmaceuticals Inc) · INCY (Incyte Corporation) · ARGX (argenx SE) · HRMY (Harmony Biosciences Holdings, I) · HALO (Halozyme Therapeutics, Inc.)
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