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Insmed INSM reported a first-quarter 2025 loss of $1.42 per share, which was wider than the Zacks Consensus Estimate of a loss of $1.36. In the year-ago quarter, the company posted a loss of $1.06 per share.
The company generated total quarterly revenues of $92.8 million, which rose 23% year over year. Quarterly sales were in line with the Zacks Consensus Estimate. (Find the latest EPS estimates and surprises on Zacks Earnings Calendar)
INSM Stock’s Performance
Shares of the company were down 4% yesterday, likely due to the earnings miss.
Year to date, the stock has lost 9% compared with the industry’s 5% decline.
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More on Insmed’s Quarterly Results
In the reported quarter, total revenues were generated entirely by the company’s only marketed drug, Arikayce, which is approved for treating refractory mycobacterium avium complex (“MAC”) lung disease in adults with limited or no alternative treatment options.
The rise in Arikayce sales was driven by continued growth in demand across all marketed regions. Sales of the drug increased 14% to $64.3 million in the United States and 48% to $22.1 million in Japan. Sales in Europe and the rest of the world rallied 52% to $6.5 million.
In the reported quarter, research and development expenses rose 26% year over year to $152.6 million. Selling, general and administrative expenses amounted to $147.5 million, up 58% from the year-ago figure. The uptick in both expenses can be attributed to a rise in employee headcount, resulting in increased compensation and benefit-related expenses as well as stock-based compensation costs.
As of March 31, 2025, Insmed had cash, cash equivalents and marketable securities of around $1.2 billion compared with $1.4 billion as of Dec. 31, 2024.
INSM Maintains 2025 Guidance
Insmed reiterated its sales guidance for the full year. It expects product sales for Arikayce to be between $405 million and $425 million, indicating 14% year-over-year growth at the midpoint of the range.
Updates on INSM’s Pipeline
During fourth-quarter 2024, the company completed enrolling patients in the confirmatory phase III ENCORE study, which is evaluating Arikayce as a potential treatment for newly infected patients with MAC lung disease. While top-line data from this study is expected in the first half of 2026, Insmed intends to submit a regulatory filing with the FDA for the drug before 2026-end.
In February, Insmed announced that the FDA accepted its regulatory filing seeking approval for brensocatib in bronchiectasis indication. The agency has granted a priority review to this filing and a final decsion is expected by Aug.12, 2025. If approved, Insmed plans to commercialize the drug immediately in the United States. While similar regulatory filings are currently under review in the European Union and the United Kingdom, a regulatory submission is planned for Japan later this year.