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INSMInsmed IncorporatedBuy Wait5.6·$96.98
Buy WaitModerate Confidence
Investment thesis

Analyst consensus implying roughly 83% price upside with a risk/reward ratio of nearly 11.8-to-1 reflects strong institutional conviction in this growth-stage biotech, but the business remains a substantial cash burner (free cash flow negative at 74% of revenue), concentrated in two products and a single supplier, and has missed earnings estimates in three of the last four quarters before a single recent beat.

Thesis pillars

  • Exceptional Upside Risk Reward→Stable
  • Elite Growth Metric Vs Cash Burn→Stable
  • Momentum Recovery Not Yet Confirmed↑Improving
  • +1 more pillar — see the Why tab for full reasoning

Pillars as of Jul 3, 2026, based on the 10-K filed Feb 19, 2026

Full reasoning →

Open full analysis

Insmed Incorporated (INSM) Stock Analysis

Recovery setup

Buy WaitVALUE-TRAP 1/5GrowthModerate Confidence

Healthcare · Biotechnology

Earnings today — results expected after close (2026-10-29). Expect elevated volatility around the report — consider waiting for post-earnings price action before new entries.

Wait for pullback to $94.50. BUY gates pass at $96.98, but concentration risk — Product: ARIKAYCE and BRINSUPRI and concentration risk — Supplier: Lamira device argue for a more patient entry. Engine's entry $94.50 (Atr Pullback Sticky) is the shallowest technical level that clears the 2:1 A.R:R minimum.

Insmed Incorporated commercializes two respiratory products—ARIKAYCE (approved US 2018, EU 2020, Japan 2021) for refractory MAC lung disease and BRINSUPRI (approved US August 2025, EU November 2025) for non-cystic fibrosis bronchiectasis. Revenue derives from prescription sales... Read more

$96.98+82.0% A.UpsideScore 5.6/10#91 of 241 Biotechnology
QualityF-score5 / 9FCF yield-2.70%
Entry $94.50(Atr Pullback Sticky)Stop $89.84Target $176.52(analyst − 10%)A.R:R 14.1:1
Analyst consensus$196.14+102.2%22 analysts
$176.52our TP
$96.98price
$196.14mean
$243

Wait for pullback to $94.50. BUY gates pass at $96.98, but concentration risk — Product: ARIKAYCE and BRINSUPRI and concentration risk — Supplier: Lamira device argue for a more patient entry. Engine's entry $94.50 (Atr Pullback Sticky) is the shallowest technical level that clears the 2:1 A.R:R minimum. Chart setup: Death cross but MACD improving, RSI 41. Earnings today. Wait until post-earnings. Score 5.6/10, moderate confidence.

Passes 7/9 gates (positive momentum, favorable risk/reward ratio, clean insider activity, no SEC red flags, news boost earnings 0.80, semi cycle peak clear, materials cycle peak clear). Fails on earnings proximity 0d<=7d. Suitability: speculative.

10-K grounded · weekly refresh

About Insmed Incorporated

About Insmed Incorporated

BRINSUPRI (brensocatib) received FDA approval in August 2025 for non-cystic fibrosis bronchiectasis in patients 12 and older, followed by European Commission approval in November 2025; Insmed Incorporated's first commercial product, ARIKAYCE, received FDA accelerated approval in September 2018 for refractory MAC lung disease and is commercially approved in the US, EU, and Japan. Regulatory submissions for brensocatib in the UK and Japan have been accepted, with decisions anticipated in 2026. No other approved therapies for bronchiectasis exist in the US, Europe, or Japan as of the 10-K filing.

Insmed generates revenue from prescription sales of ARIKAYCE and BRINSUPRI in the US, EU, and Japan through its own sales force. ARIKAYCE is a drug/device combination requiring the Lamira nebulizer manufactured exclusively by PARI; the company cannot sell ARIKAYCE without Lamira, creating a single-source device dependency. Brensocatib was licensed from AstraZeneca in October 2016. The MAC lung disease addressable market spans the US, EU5, and Japan, while BRINSUPRI targets an estimated 500,000 bronchiectasis patients in the US, 600,000 in EU5, and 150,000 in Japan. The clinical pipeline includes TPIP (Phase 3 PALM-ILD study initiated Q4 2025 in PH-ILD; Phase 3 in PAH planned for H1 2026) and brensocatib for hidradenitis suppurativa (Phase 2b CEDAR study completed enrollment Q4 2025, topline data expected Q2 2026).

Show full overview

The confirmatory ENCORE trial—required by the FDA as a condition of ARIKAYCE's accelerated approval—enrolled 425 patients in Q4 2024 with topline data anticipated by April 2026. If ENCORE data are positive, Insmed plans to submit a supplementary NDA for ARIKAYCE in all MAC lung disease patients in H2 2026; if the trial fails, the FDA could withdraw accelerated approval under the Consolidated Appropriations Act, 2023. This binary readout, concurrent with BRINSUPRI's early commercial trajectory in bronchiectasis, makes 2026 a period of substantial clinical and regulatory uncertainty for the company.

See also: Healthcare · Biotechnology

From Insmed Incorporated's most recent 10-K filing, extracted June 10, 2026.

TrendMatrix Research · upcoming catalyst calendar

Upcoming dated catalysts

Thu, Oct 29, 2026Earnings today — results expected after close· next earnings call

Thesis

Rewards
Sector modifier (Healthcare): +0.5
Strong growth profile
Analyst upside: 82%
Risks
Concentration risk — Product: ARIKAYCE and BRINSUPRI
Concentration risk — Supplier: Lamira device
V7 low-quality RISK_OFF penalty: -0.5 (Q=4.0)

Key Metrics

P/E (TTM)—
P/E (Fwd)122.0
Mkt Cap$21.2B
EV/EBITDA-26.1
Profit Mgn-76.9%
ROE-87.2%
Rev Growth296.1%
Beta0.82
DividendNone
Rating analysts31

Quality Signals

Piotroski F5/9MoatNarrow

Options Flow

P/C14.40bearish
IV88%elevated
Max Pain$50-48.4% vs spot

Concentration Risks(10-K Item 1A)

  • HIGHProductARIKAYCE and BRINSUPRI
    10-K Item 1A: 'Our prospects are highly dependent on the success of our approved products, ARIKAYCE and BRINSUPRI'
  • HIGHSupplierLamira device
    10-K Item 1A: 'we cannot sell ARIKAYCE without Lamira'

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

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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. 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·2 ceiling hits

Priced at a premium — multiples above sector norms. Needs delivery on growth + margins to justify.static

Ps
0.0
Forward Pe
1.0
Peg Ratio
6.9
Analyst Target
9.0
Forward P/E: 122.0xPEG: 1.02

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

Quality Rank
0.8
Value Rank
3.3
Growth Rank
9.6
Industry growth leader
GatesEARNINGS PROXIMITY 0d<=7dDeath cross (50MA < 200MA)Momentum 6.3>=5.5A.R:R 14.1 ≥ 1.5Insider activity: OKNo SEC red flagsNEWS BOOST EARNINGS 0.80SEMI CYCLE PEAK CLEARMATERIALS CYCLE PEAK CLEARRecoverySuitability: Speculative
RSI
41 · Neutral
↓ 20D MA↓ 50D MA↓ 200D MADEATH CROSSSupport $92.62Resistance $116.19

Price Targets

$90
$95
$177
A.Upside+82.0%
A.R:R14.1:1

Position Sizing

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

Risk Alerts

! Earnings today - binary event risk
! EARNINGS_PROXIMITY:0d<=7d

Earnings

B
B
M
M
2/4 beats
Next Earnings2026-10-29 (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 INSM stock a buy right now?

Wait for pullback to $94.50. BUY gates pass at $96.98, but concentration risk — Product: ARIKAYCE and BRINSUPRI and concentration risk — Supplier: Lamira device argue for a more patient entry. Engine's entry $94.50 (Atr Pullback Sticky) is the shallowest technical level that clears the 2:1 A.R:R minimum. Chart setup: Death cross but MACD improving, RSI 41. Earnings today. Wait until post-earnings. Target $176.52 (+82.0%), stop $89.84 (−7.9%), A.R:R 14.1:1. Score 5.6/10, moderate confidence.

What is the INSM stock price target?

Take-profit target: $176.52 (+82.0% upside). Target $176.52 (+82.0%), stop $89.84 (−7.9%), A.R:R 14.1:1. Stop-loss: $89.84.

What are the risks of investing in INSM?

Concentration risk — Product: ARIKAYCE and BRINSUPRI; Concentration risk — Supplier: Lamira device; V7 low-quality RISK_OFF penalty: -0.5 (Q=4.0).

Is INSM overvalued or undervalued?

Insmed Incorporated trades at a P/E of N/A (forward 122.0). TrendMatrix value score: 3.4/10. Verdict: Buy (Wait for Entry).

What do analysts say about INSM?

31 analysts cover INSM with a consensus score of 4.3/5. Average price target: $196.

What does Insmed Incorporated do?Insmed Incorporated commercializes two respiratory products—ARIKAYCE (approved US 2018, EU 2020, Japan 2021) for...

Insmed Incorporated commercializes two respiratory products—ARIKAYCE (approved US 2018, EU 2020, Japan 2021) for refractory MAC lung disease and BRINSUPRI (approved US August 2025, EU November 2025) for non-cystic fibrosis bronchiectasis. Revenue derives from prescription sales in the US, EU, and Japan using the company's own sales force. The clinical pipeline includes TPIP in Phase 3 trials for PH-ILD and PAH, plus gene therapy programs.

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