INSM.O Hits 52-Week High on BRINSUPRI Approval
Shares of INSM.O surged today, reaching a 52-week high following the European Commission's approval of BRINSUPRI (brensocatib) as the first treatment for non-cystic fibrosis bronchiectasis (NCFB). This significant milestone signals a bullish sentiment among investors, as the stock broke through previous resistance levels, reflecting strong market confidence in the drug's potential. BRINSUPRI has shown promising clinical trial results, demonstrating a 19.4% reduction in exacerbation rates, which could greatly enhance the quality of life for approximately 600,000 diagnosed individuals in the EU. Insmed's proactive plans to ensure patient access starting in early 2026 further bolster the stock's outlook, making it a key player in the respiratory treatment market.
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- Leadership Expansion: Definium Therapeutics announces the appointment of Roger Adsett to its Board of Directors, leveraging over 20 years of experience in biopharmaceuticals to drive the company's success in three anticipated Phase 3 trials in 2026.
- Strategic Optimization: Adsett's proven track record at Insmed, particularly in launching ARIKAYCE® and BRINSUPRI®, indicates he will provide valuable commercial execution capabilities to enhance Definium's market impact in mental health treatments.
- Commitment to Scientific Rigor: Adsett expressed admiration for Definium's commitment to scientific rigor in mental health, indicating his dedication to translating clinical research into valuable therapies, thereby strengthening the company's leadership position in the industry.
- Educational Background and Experience: With an MBA from the Wharton School at the University of Pennsylvania and a bachelor's degree in English and economics from Bucknell University, Adsett's extensive educational and professional background will provide robust support for Definium's strategic development.
- Research Presentation: Insmed will showcase four abstracts on TPIP at the 2026 PVRI congress, including the Phase 3 PALM-PAH study design and topline results from the Phase 2b study, highlighting TPIP's potential in treating pulmonary arterial hypertension.
- Clinical Trial Design: The Phase 2b study recruited 102 adult participants across 44 centers to evaluate the efficacy and safety of TPIP, with patients self-administering doses up to 640 µg daily, aimed at improving pulmonary vascular resistance.
- Market Potential Analysis: With approximately 35,000 patients diagnosed with pulmonary arterial hypertension in the U.S. and 40,000 in the EU5, there is significant market demand for TPIP as a potential treatment option, reflecting Insmed's commitment to addressing unmet medical needs.
- Strategic Development Direction: The TPIP research not only lays the groundwork for multiple upcoming Phase 3 clinical trials but also underscores Insmed's ongoing investment and innovation in rare diseases, aiming to enhance patient quality of life.
- Research Presentation: Insmed will present four abstracts on TPIP at the 2026 PVRI congress, including the Phase 3 PALM-PAH study design, highlighting its potential in treating pulmonary arterial hypertension (PAH), which may enhance the company's market position in this field.
- Clinical Data Review: An encore presentation of the Phase 2b trial results for TPIP will provide an in-depth analysis of its efficacy and safety, potentially boosting investor confidence in Insmed's future developments.
- New Technology Application: New data from Functional Respiratory Imaging analysis will be showcased, further supporting TPIP's application in PAH patients, which could open new treatment avenues and market opportunities for the company.
- Future Development Plans: Insmed plans to initiate multiple Phase 3 programs aimed at improving patient outcomes, demonstrating the company's ongoing commitment and strategic positioning in innovative drug development.

- Optimistic Sales Outlook: Roth has initiated coverage on Insmed (INSM) with a Buy rating, anticipating that Brinsupri (brensocatib) and Arikayce (amikacin liposome inhalation suspension) will achieve above-consensus sales, indicating strong market potential for the company's products.
- Price Target Set: The analyst has set a price target of $212, representing approximately 32% upside from the January 22 close, reflecting market confidence in Insmed's future growth trajectory.
- Peak Sales Forecast: Analyst Adam Walsh projects peak sales of $8.1 billion for Brinsupri and $1.3 billion for Arikayce, showcasing Insmed's robust performance in the therapeutic space.
- New Drug Potential: Walsh also highlighted the potential of treprostinil palmitil inhalation powder (TPIP) for pulmonary arterial hypertension, with probability-adjusted peak sales expected to reach $5 billion following positive mid-stage trial results anticipated in June 2025, further enhancing the company's market outlook.
- Clinical Data Potential: Roth analysts believe that upcoming clinical data later this year, combined with above-consensus expectations for Insmed's lead drug Brinsupri, could drive significant stock price appreciation, indicating a robust market outlook.
- Sales Performance Exceeds Expectations: Brinsupri achieved first full-quarter sales of $144.6 million post-FDA approval, significantly surpassing market expectations of $65 million, demonstrating strong market acceptance in treating non-cystic fibrosis bronchiectasis.
- Revenue Forecast Upgrade: Analysts project 2026 revenue to reach $1.2 billion, notably higher than the pre-announcement consensus of $726 million, indicating Insmed's competitive edge and future growth potential in the market.
- Pipeline Diversity: Insmed's broader pipeline offers additional growth potential beyond its lead assets, particularly with positive data from the TPIP drug targeting pulmonary arterial hypertension, which could position it as a best-in-class therapy and enhance the company's long-term outlook.









