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ARWRArrowhead Pharmaceuticals, Inc.Sell5.5·$82.79+0.04%
SellModerate Confidence
Investment thesis

Free cash flow is negative, the Rule of 40 fails at negative 94, a Piotroski F-Score of 3 out of 9 reflects broad financial weakness, and a single approved product carries all commercial risk; with only 1.9% headroom to the near-term resistance target and an unfavorable risk/reward, two recent earnings beats introduce modest optimism but do not yet support an attractive setup at current prices.

Thesis pillars

  • Single Product Concentration RiskImproving
  • Minimal Upside Unfavorable SetupImproving
  • Negative Fcf Weak FundamentalsStable
  • +1 more pillar — see the Why tab for full reasoning

Full reasoning →

Open full analysis

Arrowhead Pharmaceuticals, Inc. (ARWR) Stock Analysis

SellVALUE-TRAP 3/5GrowthModerate Confidence

Healthcare · Biotechnology

Sell if holding. Momentum 3.3/10 is below the 5.0 floor at $82.79 — engine's falling-knife protection flags exit rather than catching a breakdown. Specifics: Concentration risk — Product: single approved product; V7 low-quality RISK_OFF penalty: -0.5 (Q=4.1).

Arrowhead Pharmaceuticals develops RNAi therapeutics using its proprietary TRiM platform, with REDEMPLO (plozasiran) receiving FDA approval in November 2025 for Familial Chylomicronemia Syndrome as its first commercial product, plus 18 drug candidates in clinical trials. Revenue... Read more

$82.79+15.5% A.UpsideScore 5.5/10#73 of 259 Biotechnology
QualityF-score4 / 9FCF yield-0.42%
Stop $77.92Target $95.70(analyst − 13%)A.R:R 2.0:1
Analyst target$110.00+32.9%12 analysts
$95.70our TP
$82.79price
$110.00mean
$126

Sell if holding. Momentum 3.3/10 is below the 5.0 floor at $82.79 — engine's falling-knife protection flags exit rather than catching a breakdown. Specifics: Concentration risk — Product: single approved product; V7 low-quality RISK_OFF penalty: -0.5 (Q=4.1). Chart setup: No clear chart pattern; technical signals are mixed. Score 5.5/10, moderate confidence.

Passes 7/8 gates (favorable risk/reward ratio, clean insider activity, no SEC red flags, news events none recent, earnings proximity 72d clear, semi cycle peak clear, materials cycle peak clear). Fails on weak momentum. Suitability: speculative.

10-K grounded · weekly refresh

About Arrowhead Pharmaceuticals, Inc.

About Arrowhead Pharmaceuticals, Inc.

Arrowhead Pharmaceuticals' first commercial product, REDEMPLO (plozasiran), received FDA approval in November 2025 as the first and only siRNA treatment for Familial Chylomicronemia Syndrome. The company held 18 drug candidates in clinical trials at the time of filing—including Phase 3 studies for severe hypertriglyceridemia—and maintained collaboration agreements with Takeda, GSK, Amgen, Sarepta, and Novartis, which provide non-dilutive capital to support the wholly-owned pipeline through commercialization.

Arrowhead generates revenue through REDEMPLO product sales and licensing and collaboration payments from partners. The Takeda agreement for fazirsiran (ARO-AAT) provides co-development funding and a 50/50 U.S. profit share if approved; outside the United States, Takeda holds an exclusive license and Arrowhead is eligible for 20-25% tiered royalties on net sales. Amgen owns olpasiran (ARO-LPA), a lipoprotein(a)-targeting siRNA in Phase 3 for cardiovascular disease; Arrowhead sold its royalty rights to Royalty Pharma but remains eligible for up to $485 million in remaining milestone payments from Amgen and Royalty Pharma combined. The Sarepta agreement executed in November 2024 covers multiple clinical and preclinical muscle, CNS, and lung programs. The Novartis agreement executed in August 2025 and closed October 2025 covers ARO-SNCA for synucleinopathies including Parkinson's disease. Manufacturing for clinical supplies and commercial products depends on third-party contract manufacturers, as Arrowhead holds limited internal manufacturing capacity.

Show full overview

The plozasiran program carries a distinct Phase 3 readout event beyond the FCS label: SHASTA-3, SHASTA-4, and SHASTA-5 studies for severe hypertriglyceridemia were fully enrolled at the time of filing, with a supplemental NDA planned for 2026 pending successful completion. The 10-K explicitly notes that REDEMPLO's Phase 3 PALISADE success in FCS does not guarantee approval in sHTG because endpoints and clinical data requirements differ between a rare-disease indication and a broader patient population.

See also: Healthcare · Biotechnology

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

TrendMatrix Research · upcoming catalyst calendar

Upcoming dated catalysts

Tue, Nov 24, 202672d to earnings· next earnings call

Thesis

Rewards
Sector modifier (Healthcare): +0.5
Positive news sentiment (+0.67)
Strong growth profile
Risks
Concentration risk — Product: single approved product
V7 low-quality RISK_OFF penalty: -0.5 (Q=4.1)
Leverage penalty (D/E 3.0): -1.5

Key Metrics

P/E (TTM)
P/E (Fwd)-17.2
Mkt Cap$11.7B
EV/EBITDA-57.2
Profit Mgn-47.8%
ROE-55.2%
Rev Growth171.0%
Beta1.28
DividendNone
Rating analysts20

Quality Signals

Piotroski F4/9MoatNarrow

Options Flow

P/C0.71neutral
IV67%elevated

Concentration Risks(10-K Item 1A)

  • HIGHProductsingle approved product
    10-K Item 1A: 'we have only one product based on RNAi and our delivery technologies approved in November 2025'
  • MEDIUMSupplierthird-party manufacturers
    10-K Item 1A: 'must rely on third-party manufacturers to manufacture certain of our clinical supplies and our commercial products'

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

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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

2 floor-breakers·1 ceiling hit

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

Macd
0.0
Obv
1.0
Volume
3.7
Ma Position
4.0
Rsi
7.7
Uptrend pullback (RSI 38) - buy opportunityVolume distribution (falling OBV)Above 200-day MA

Ranks in the bottom of its industry peers on the composite signal. Better names in the same sector exist.static

Quality Rank
2.3
Value Rank
3.1
Growth Rank
9.0
Industry growth leader
GatesMomentum 3.3<4.5A.R:R 2.0 ≥ 1.5Insider activity: OKNo SEC red flagsNEWS EVENTS NONE RECENTEARNINGS PROXIMITY 72d clearSEMI CYCLE PEAK CLEARMATERIALS CYCLE PEAK CLEARSuitability: Speculative
RSI
38 · Neutral
20D MA 50D MA 200D MAGOLDEN CROSSSupport $80.33Resistance $90.21

Price Targets

$78
$96
A.Upside+15.5%
A.R:R2.0:1

Position Sizing

ConvictionNone
Suggested %0.5%
Max %1%
RegimeRisk-Off

Risk Alerts

! momentum at 3.3 (below the engine's 4.5 threshold)

Earnings

B
B
M
M
2/4 beats
Next Earnings2026-11-24 (72d)

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 ARWR stock a buy right now?

Sell if holding. Momentum 3.3/10 is below the 5.0 floor at $82.79 — engine's falling-knife protection flags exit rather than catching a breakdown. Specifics: Concentration risk — Product: single approved product; V7 low-quality RISK_OFF penalty: -0.5 (Q=4.1). Chart setup: No clear chart pattern; technical signals are mixed. Prior stop was $77.92. Score 5.5/10, moderate confidence.

What is the ARWR stock price target?

Take-profit target: $95.70 (+15.5% upside). Prior stop was $77.92. Stop-loss: $77.92.

What are the risks of investing in ARWR?

Concentration risk — Product: single approved product; V7 low-quality RISK_OFF penalty: -0.5 (Q=4.1); Leverage penalty (D/E 3.0): -1.5.

Is ARWR overvalued or undervalued?

Arrowhead Pharmaceuticals, Inc. trades at a P/E of N/A (forward -17.2). TrendMatrix value score: 4.5/10. Verdict: Sell.

What do analysts say about ARWR?

20 analysts cover ARWR with a consensus score of 4.3/5. Average price target: $110.

What does Arrowhead Pharmaceuticals, Inc. do?Arrowhead Pharmaceuticals develops RNAi therapeutics using its proprietary TRiM platform, with REDEMPLO (plozasiran)...

Arrowhead Pharmaceuticals develops RNAi therapeutics using its proprietary TRiM platform, with REDEMPLO (plozasiran) receiving FDA approval in November 2025 for Familial Chylomicronemia Syndrome as its first commercial product, plus 18 drug candidates in clinical trials. Revenue flows from REDEMPLO product sales and licensing and collaboration agreements with Takeda, GSK, Amgen, Sarepta, and Novartis.

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