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INSM

INSMED Inc

Biopharma developer (SEC filing verified)·Commercial·Bridgewater, NJ, United States·CEO: Mr. William H. Lewis J.D., M.B.A.
OncologyRare DiseaseNeurologyImmunologyCardiovascularInfectious DiseaseMetabolicRespiratoryDermatologyNephrologyGastroenterologyEndocrinology

INSM evidence brief

What we can confirm

BioSniper Score:
5.1 / 10
Market Cap:
$27.27B
Next Catalyst:
Phase1_Start · Oct 29, 2026

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $27.27B · Next Catalyst: Phase1_Start · Oct 29, 2026
BioSniper AIPage evidence connected

Prepared research question

What matters most for INSM—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · INSM

Insmed Inc. is a global biopharmaceutical company focused on developing and commercializing first- and best-in-class therapies for patients with serious diseases in respiratory, immunology & inflammation, and neuro & other rare therapeutic areas.

Key risk: Dependence on commercial success

5.1/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$27.27B

Cash Runway

—

Lead Asset

—

Financial data as of Jun 30, 2026.

Tracking 70 clinical trials · 3 catalysts · 2 FDA decisions for INSMED Inc.

AI OverviewAI overview is shown in English only.

Insmed Inc. is a global biopharmaceutical company focused on developing and commercializing first- and best-in-class therapies for patients with serious diseases in respiratory, immunology & inflammation, and neuro & other rare therapeutic areas.

  • Insmed has two marketed products: ARIKAYCE (amikacin liposome inhalation suspension) for MAC lung disease and BRINSUPRI (brensocatib) for non-cystic fibrosis bronchiectasis, with BRINSUPRI approved in the US, EU, and UK as of early 2026 [sec_mda · as of 2026-08-06].
  • As of June 30, 2026, the company reported cash and cash equivalents of $544.8 million and marketable securities of $615.5 million, with an accumulated deficit of $5.8 billion [sec_mda · as of 2026-08-06].
  • Insmed's pipeline includes Phase 3 studies for TPIP (treprostinil palmitil inhalation powder) in pulmonary hypertension associated with interstitial lung disease and progressive pulmonary fibrosis, and a Phase 2b study for TPIP in pulmonary arterial hypertension reported positive topline results in June 2025 [sec · filed 2026-04-01].
  • The company is advancing early-stage gene therapy programs INS1201 for Duchenne muscular dystrophy and INS1202 for amyotrophic lateral sclerosis, both in Phase 1 studies [sec · filed 2026-04-01].
  • In December 2025, Insmed acquired global rights to INS1148, an investigational monoclonal antibody being developed as a potential first-in-class therapy for respiratory, immunological, and inflammatory diseases [sec · filed 2026-04-01].

What works

  • Insmed has two approved commercial products (ARIKAYCE and BRINSUPRI) generating revenue, with BRINSUPRI recently launched in the US and EU, providing a foundation for top-line growth [sec_mda · as of 2026-08-06].
  • The company maintains a strong cash position of $544.8 million as of June 30, 2026, which management expects to fund operations for at least the next 12 months [sec_mda · as of 2026-08-06].
  • Insmed's pipeline includes multiple late-stage clinical programs (Phase 2/3) in respiratory diseases with high unmet need, such as TPIP for PAH and PH-ILD, and a recently submitted sNDA for ARIKAYCE in all MAC lung patients [sec_mda · as of 2026-08-06].

What to weigh

  • Insmed has an accumulated deficit of $5.8 billion as of June 30, 2026, and continues to incur operating losses, with a net loss of $13.2 million reported for the period ending that date [sec_mda · as of 2026-08-06].
  • The company's ability to reduce operating losses and generate positive cash flow depends on continued commercial success of ARIKAYCE and BRINSUPRI, as well as obtaining full approval of ARIKAYCE in the US, which remains uncertain [sec_mda · as of 2026-08-06].
  • A Phase 2 study of brensocatib in chronic rhinosinusitis without nasal polyps failed to meet primary or secondary efficacy endpoints, leading to program discontinuation in that indication [sec · filed 2026-04-01].

From the filings

Quoted directly from source documents.

  • Insmed's cash position and accumulated deficit as of June 30, 2026

    “As of June 30, 2026, we had cash and cash equivalents of $544.8 million, as compared to $510.4 million as of December 31, 2025. In addition, as of June 30, 2026, we had marketable securities of $615.5 m”

    SEC MD&A · August 6, 2026

  • Insmed's accumulated deficit as of June 30, 2026

    “through June 30, 2026, we had an accumulated deficit of $5.8 billion.”

    SEC MD&A · August 6, 2026

  • BRINSUPRI approval and regulatory status

    “BRINSUPRI, was approved in the US, E U, and UK in August 2025, November 2025, and February 2026, re”

    SEC MD&A · August 6, 2026

  • Discontinuation of brensocatib in CRSsNP

    “The study did not meet its primary or secondary efficacy endpoints, and we discontinued our development program for brensocatib in CRSsNP.”

    SEC filings · April 1, 2026

Catalyst timeline

  • 2026-10-29 · Phase1_Start: A Phase 1, Open-Label, Fixed Sequence, Drug-Drug Interaction Study Assessing the Potential CYP3A Induction Effect of Brensocatib on the Pharmacokinetics of Midazolam in Healthy Participants — This study will evaluate whether brensocatib induces CYP3A, which could affect its drug interaction profile.
  • 2026-12-01 · Phase3_Start: A Phase 3, Randomized, Double-Blind, Placebo-controlled, Multicenter, Parallel Group Study of Efficacy and Safety of Treprostinil Palmitil Inhalation Powder in Participants With Progressive Pulmonary Fibrosis (PPF)-PALM-PPF — This pivotal Phase 3 trial will assess TPIP's efficacy and safety in progressive pulmonary fibrosis, a key pipeline asset.
  • 2040-02-21 · Patent_Expiry: NDA217673 — Patent expiry for brensocatib (BRINSUPRI) is far in the future, indicating long-term exclusivity if approved.
Risks & what to watch (4)›

Key risks

  • Dependence on commercial success — Profitability depends on continued commercial success of ARIKAYCE and BRINSUPRI and full US approval of ARIKAYCE [sec_mda · as of 2026-08-06].
  • Accumulated deficit and operating losses — Accumulated deficit of $5.8B and ongoing net losses; cash runway may require additional capital [sec_mda · as of 2026-08-06].
  • Clinical trial failures — Brensocatib failed in CRSsNP; other pipeline candidates may face similar setbacks [sec · filed 2026-04-01].
  • Regulatory and policy uncertainty — Evolving US policies may impact international launch timing for BRINSUPRI [sec_mda · as of 2026-08-06].

What to watch

  • Regulatory decision for brensocatib (BRINSUPRI) in Japan for NCFB expected in the second half of 2026 [sec_mda · as of 2026-08-06].
  • FDA review of the supplemental new drug application (sNDA) for ARIKAYCE in newly diagnosed MAC lung disease patients, submitted July 2026 [sec_mda · as of 2026-08-06].
  • Phase 3 study start for TPIP in progressive pulmonary fibrosis (PALM-PPF) scheduled for December 2026 [catalyst].
  • Enrollment progress and data readouts from Phase 1 studies of INS1201 (DMD) and INS1202 (ALS) [sec · filed 2026-04-01].

Sources: Catalysts · SEC filings · SEC MD&A · Generated October 13, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Pipeline inputs are unavailable for this score. It uses only the available signals shown below.

Cash RunwayN/A

Cash runway data unavailable

Financial Health7.3

D/E 1.78 · 0% dilution

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum8.0

3 upcoming, next in ~15d

Insider Signal0.0

0 buys · 43 sells (180d)

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

665

Total value held

$33.77B

HolderSharesValue
jpmorgan chase & co24,150,499$3.70B
blackrock, inc.16,678,146$2.73B
darwin global management, ltd.16,805,184$2.58B
fmr llc13,160,167$2.15B
vanguard portfolio management llc10,371,802$1.70B
vanguard capital management llc9,642,131$1.58B
baker bros. advisors lp7,421,111$1.21B
artisan partners limited partnership6,527,301$1.07B
d. e. shaw & co., inc.5,625,825$919.9M
capital international investors5,595,194$914.9M

Showing top 10 of 665 institutional holders of INSMED Inc. Open the full 13F history after sign-in.

Short Interest

as of Apr 30, 2026
% of float
7.2%
Days to cover
5.4
Shares short
13,855,201
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

INSM short interest

Governance

Frequently asked questions

What is the AI investment thesis for INSMED Inc?

Insmed Inc. is a global biopharmaceutical company focused on developing and commercializing first- and best-in-class therapies for patients with serious diseases in respiratory, immunology & inflammation, and neuro & other rare therapeutic areas.

What is INSMED Inc's next catalyst?

INSMED Inc's next tracked catalyst is a Phase1_Start event — "Phase1_Start: A Phase 1, Open-Label, Fixed Sequence, Drug-Drug Interaction Study Assessing the Potential CYP3A Induction Effect of Brensocatib on the Pharmacokinetics of Midazolam in Healthy Participants" — expected October 29, 2026.

Who is the CEO of INSMED Inc?

Mr. William H. Lewis J.D., M.B.A. is the chief executive officer of INSMED Inc (INSM).

Where is INSMED Inc headquartered?

INSMED Inc (INSM) is headquartered in Bridgewater, NJ, United States.

What therapeutic areas does INSMED Inc focus on?

INSMED Inc develops therapies across Oncology, Rare Disease, Neurology, Immunology, Cardiovascular, Infectious Disease, Metabolic, Respiratory, Dermatology, Nephrology, Gastroenterology, Endocrinology.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.