Insmed Inc

Stock Chart, Company Information, and Scan Results

$193.59(as of Oct 31, 10:06 AM EST)

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Insmed Inc Company Information, Fundamentals, and Technical Indicators

Stock Price$193.59
Ticker SymbolINSM
ExchangeNasdaq
SectorHealthcare
IndustryBiotechnology
Employees1,271
CountyUSA
Market Cap$35,289.0M
EBIDTA-917.5M
10-Day Moving Average166.96
P/E Ratio-35.55
20-Day Moving Average164.40
Forward P/E Ratio0.00
50-Day Moving Average150.79
Earnings per Share-5.67
200-Day Moving Average101.09
Profit Margin-299.48%
RSI82.73
Shares Outstanding211.4M
ATR6.11
52-Week High194.70
Volume6,709,759
52-Week Low60.40
Most Recent Support Level154.79
Book Value1,249.7M
Most Recent Resistance Level168.22
P/B Ratio29.42
Upper Keltner178.14
P/S Ratio92.35
Lower Keltner150.66
Debt-to-Equity Ratio178.14
Next Earnings DateUnknown
Cash Surplus972.6M
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 Oct 31, 2025
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