Insmed Inc

Stock Chart, Company Information, and Scan Results

$177.11(as of Dec 19, 12:51 PM EST)

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Insmed Inc Company Information, Fundamentals, and Technical Indicators

Stock Price$177.11
Ticker SymbolINSM
ExchangeNasdaq
SectorHealthcare
IndustryBiotechnology
Employees1,271
CountyUSA
Market Cap$42,326.3M
EBIDTA-978.8M
10-Day Moving Average193.94
P/E Ratio-29.75
20-Day Moving Average199.79
Forward P/E Ratio0.00
50-Day Moving Average186.64
Earnings per Share-6.18
200-Day Moving Average121.17
Profit Margin-259.95%
RSI29.93
Shares Outstanding213.3M
ATR9.10
52-Week High212.75
Volume13,446,145
52-Week Low60.40
Most Recent Support Level192.50
Book Value945.6M
Most Recent Resistance Level205.23
P/B Ratio37.24
Upper Keltner220.26
P/S Ratio78.78
Lower Keltner179.33
Debt-to-Equity Ratio220.26
Next Earnings Date02/19/2026
Cash Surplus-82.5M
Next Ex-Dividend DateUnknown

Insmed Incorporated develops and commercializes therapies for patients with serious and rare diseases in the United States, Europe, Japan, and internationally. The company offers ARIKAYCE for the treatment of refractory nontuberculous mycobacterial lung infections, as well as is in phase 3 clinical trial for the treatment of mycobacterium avium complex lung disease as part of a combination antibacterial drug regimen for adult patients. It also devlops brensocatib, an oral reversible inhibitor of dipeptidyl peptidase 1(DPP1) that is in phase 3 clinical trial for the treatment of bronchiectasis; and in phase 2 clinical trial for the treatment of chronic rhinosinusitis without nasal polyps and hidradenitis suppurativa. In addition, the company is developing treprostinil palmitil inhalation powder, an inhaled formulation of a treprostinil prodrug treprostinil palmitil, which is in phase 3 clinical trial for the treatment of pulmonary hypertension associated with interstitial lung disease; and phase 2 clinical trial for the treatment of pulmonary arterial hypertension. Further, it develops gene therapy, a microdystrophin adeno-associated virus gene replacement therapy which is in phase 1 clinical trial for the treatment of Duchenne muscular dystrophy, as well as is in pre-clinical development for gene therapy, next generation DPP1 inhibitor, deimmunized therapeutic protein, and synthetic rescue. The company was founded in 1988 and is headquartered in Bridgewater, New Jersey.

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As of Dec 19, 2025
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