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AGIOAgios Pharmaceuticals, Inc.Sell4.9·$31.20
SellModerate Confidence
Investment thesis

Agios is a cash-burning biotech whose value rests on PYRUKYND and AQVESME, with 30.6% analyst-target upside offset by negative FDA-related news, weak quality scores and earnings due in 4 days.

Thesis pillars

  • Negative Fda News Event↑Improving
  • Cash Burning Biotech Profile→Stable
  • Single Product Concentration↑Improving
  • +2 more pillars — see the Why tab for full reasoning

Pillars as of Nov 1, 2026, based on the 10-K filed Feb 12, 2026

Full reasoning →

Open full analysis

Agios Pharmaceuticals, Inc. (AGIO) Stock Analysis

SellGrowthModerate Confidence

Healthcare · Biotechnology

Earnings today — results expected after close (2026-11-05). Expect elevated volatility around the report — consider waiting for post-earnings price action before new entries.

Sell if holding. Engine safety override at $31.20: Quality below floor (2.2 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 4.9/10 and A.R:R 2.0:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 12%; Below-average business quality; Negative price momentum.

Agios Pharmaceuticals is a commercial-stage rare hematology company with two approved medicines: PYRUKYND® (mitapivat) for PK deficiency in the U.S. and EU, and AQVESME™ (mitapivat) FDA-approved in December 2025 for thalassemia. PYRUKYND® generated $54.0 million in net product... Read more

$31.20+27.9% A.UpsideScore 4.9/10#178 of 241 Biotechnology
QualityF-score4 / 9FCF yield-14.74%
Stop $29.02Analyst target $39.91(−13% haircut)A.R:R 2.0:1
Analyst consensus$45.88+47.0%8 analysts with price targets
$39.91Analyst target
$31.20price
$45.88mean
$72

Sell if holding. Engine safety override at $31.20: Quality below floor (2.2 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 4.9/10 and A.R:R 2.0:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 12%; Below-average business quality; Negative price momentum. Chart setup: No clear chart pattern; technical signals are mixed. Score 4.9/10, moderate confidence.

Passes 6/9 gates (favorable risk/reward ratio, clean insider activity, no SEC red flags, news boost analyst 0.50, semi cycle peak clear, materials cycle peak clear). Fails on weak momentum and news soft fda negative and earnings proximity 0d<=7d. Suitability: speculative.

10-K grounded · weekly refresh

About Agios Pharmaceuticals, Inc.

About Agios Pharmaceuticals, Inc.

Agios Pharmaceuticals' two approved medicines—PYRUKYND for PK deficiency (approved in the U.S., EU, and Great Britain) and AQVESME for thalassemia (FDA-approved December 2025)—both contain mitapivat, an oral pyruvate kinase activator. PYRUKYND generated $54.0 million in net product revenues in the year ended December 31, 2025, compared with $36.5 million in 2024 and $26.8 million in 2023. AQVESME launched commercially in late January 2026 following FDA approval and implementation of a Risk Evaluation and Mitigation Strategy to monitor hepatocellular injury risk.

Agios earns product revenue from direct U.S. sales of PYRUKYND and AQVESME, and rest-of-world royalties under two distribution agreements: the Avanzanite Agreement (European Economic Area, Switzerland, and the United Kingdom, signed June 2025) and the NewBridge Agreement (Gulf Council Countries, signed July 2024). The company retains full ownership of both approved medicines and funds their development and commercialization costs. The commercial patient population is narrow—PK deficiency affects an estimated 3,000–8,000 individuals in the U.S. and EU5, while thalassemia prevalence in those same markets is roughly 18,000–23,000. Beyond product revenue, Agios retains a 3% earn-out on vorasidenib U.S. net sales above $1.0 billion per year following the August 2024 sale of the Vorasidenib Royalty Rights to Royalty Pharma for $905.0 million. The remaining pipeline includes tebapivat for lower-risk MDS and SCD, AG-181 for phenylketonuria, and AG-236 licensed from Alnylam Pharmaceuticals targeting TMPRSS6 for polycythemia vera.

Show full overview

The next significant binary event is FDA review of the sickle cell disease application for mitapivat: the Phase 3 RISE UP trial achieved the hemoglobin response primary endpoint (40.6% response vs. 2.9% placebo, p<0.0001) but missed the co-primary annualized pain crises endpoint (p=0.1213). Agios plans a pre-supplemental NDA meeting with the FDA in the first quarter of 2026 before submitting the U.S. marketing application; regulatory acceptance of a mixed-endpoint package could expand the mitapivat franchise into a U.S. and EU5 patient population of approximately 120,000–135,000—substantially larger than either current approved indication.

See also: Healthcare · Biotechnology

From Agios Pharmaceuticals, Inc.'s most recent 10-K filing, extracted June 9, 2026.

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

Recent developments

updated Oct 30, 2026

Recent Developments — Agios Pharmaceuticals, Inc.

Latest item Oct 30, 2026 · Generated 2026-11-04T12:04:35Z.

TrendMatrix Research · upcoming catalyst calendar

Upcoming dated catalysts

Thu, Nov 5, 2026Earnings today — results expected after close· next earnings call

Thesis

Rewards
Recent Analyst detected in news
Risks
Concentration risk — Product: PYRUKYND® / AQVESME™
Quality below floor (2.2 < 4.0)

Key Metrics

P/E (TTM)—
P/E (Fwd)-7.7
Mkt Cap$1.9B
EV/EBITDA-2.8
Profit Mgn0.0%
ROE-34.3%
Rev Growth259.3%
Beta0.62
DividendNone
Analysts with ratings16

Quality Signals

Piotroski F4/9MoatNarrow

Options Flow

P/C0.77neutral
IV54%elevated

Concentration Risks(10-K Item 1A)

  • HIGHProductPYRUKYND® / AQVESME™
    10-K Item 1A: 'Our ability to generate meaningful revenue from PYRUKYND® and AQVESME™ will depend heavily on our successful development and commercialization of the product'

Model-generated analysis — not investment advice. Not a registered investment advisor. Past performance does not guarantee future results. How we score · Editorial policy

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. People who build TrendMatrix, or entities they control, may hold positions, long or short, in securities it covers, and may trade them at any time. Positions are not disclosed individually. Verdicts are generated by an automated model applied by the same rules to every covered stock, and are not adjusted for any position held by the people who build TrendMatrix. We do not accept payment from issuers for coverage.

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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

2 floor-breakers

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

Macd
0.0
Volume
0.1
Obv
1.0
Ma Position
2.2
Rsi
4.5
Volume distribution (falling OBV)Below 200-MA but MA still rising (+3.0%/30d) — pullback in uptrend, not confirmed weakness

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

Roe
0.0
Roa
0.0
Net Margin
0.0
Fcf Quality
0.0
Piotroski F
4.4
Current Ratio
5.0
Moat
5.8
Cash-burning: FCF -279% of revenueQuality concerns
GatesMomentum 1.6<4.5NEWS SOFT FDA NEGATIVEEARNINGS PROXIMITY 0d<=7dA.R:R 2.0 ≥ 1.5Insider activity: OKNo SEC red flagsNEWS BOOST ANALYST 0.50SEMI CYCLE PEAK CLEARMATERIALS CYCLE PEAK CLEARSuitability: Speculative
RSI
51 · Neutral
↓ 20D MA↓ 50D MA↓ 200D MAGOLDEN CROSSSupport $29.67Resistance $38.69

Price Targets

$29
$40
A.Upside+27.9%
A.R:R2.0:1

Position Sizing

ConvictionNone
Suggested %0%
Max %0%
RegimeSteady

Risk Alerts

! Quality below floor (2.2 < 4.0)
! momentum at 1.6 (below the engine's 4.5 threshold)
! NEWS_SOFT:FDA_NEGATIVE

Earnings

B
B
B
M
3/4 beats
Next Earnings2026-11-05 (Earnings today — results expected after close)

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 AGIO stock a buy right now?

Sell if holding. Engine safety override at $31.20: Quality below floor (2.2 < 4.0) triggers a hard block regardless of the otherwise-positive setup — overall score 4.9/10 and A.R:R 2.0:1 is above the 1.5:1 BUY gate. Specifically: High short interest: 12%; Below-average business quality; Negative price momentum. Chart setup: No clear chart pattern; technical signals are mixed. Prior stop was $29.02. Score 4.9/10, moderate confidence.

What is the AGIO stock price target?

Analyst target: $39.91 (+27.9% upside). Prior stop was $29.02. Stop-loss: $29.02.

What are the risks of investing in AGIO?

Concentration risk — Product: PYRUKYND® / AQVESME™; Quality below floor (2.2 < 4.0).

Is AGIO overvalued or undervalued?

Agios Pharmaceuticals, Inc. trades at a P/E of N/A (forward -7.7). TrendMatrix value score: 5.4/10. Verdict: Sell.

What do analysts say about AGIO?

16 analysts rate AGIO, with a consensus score of 4.1/5. 8 analysts publish price targets averaging $46.

What does Agios Pharmaceuticals, Inc. do?Agios Pharmaceuticals is a commercial-stage rare hematology company with two approved medicines: PYRUKYND® (mitapivat)...

Agios Pharmaceuticals is a commercial-stage rare hematology company with two approved medicines: PYRUKYND® (mitapivat) for PK deficiency in the U.S. and EU, and AQVESME™ (mitapivat) FDA-approved in December 2025 for thalassemia. PYRUKYND® generated $54.0 million in net product revenues in 2025 and AQVESME™ launched commercially in the United States in late January 2026.

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