Lyra Therapeutics Suspends LYR-210 Development and Reduces Workforce
Lyra Therapeutics, announced that its Board of Directors has decided to suspend further development of LYR-210, the Company's lead product candidate for the treatment of chronic rhinosinusitis. The Company also announced a workforce reduction impacting its remaining 28 employees and other cost-saving actions to preserve capital. Maria Palasis, Ph.D., Chief Executive Officer, President and Chair of the Board, and Jason Cavalier, Chief Financial Officer and Treasurer, are each being retained as consultants to support the Company's pursuit of strategic alternatives. The Company has engaged SSG Capital Advisors to assist with this effort. "In connection with the Company's review of strategic options, which was announced in May 2024, the Board has concluded that it is in the best interests of shareholders to cease Lyra's product development operations," said Dr. Palasis. "We are grateful for the contributions of our employees most of whom will leave Lyra as a result of this decision to discontinue development of LYR-210. Our priority moving forward is to evaluate and explore strategic alternatives to advance LYR-210 for the potential benefit of patients."
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Earnings Performance: Assertio (ASRT) reported quarterly earnings of $0.11 per share, exceeding expectations of a loss of $0.08 per share, marking a significant earnings surprise of +237.50%.
Revenue Growth: The company generated revenues of $49.46 million for the quarter, surpassing the Zacks Consensus Estimate by 83.86% and showing a year-over-year increase from $29.2 million.
Stock Outlook: Assertio shares have declined by 12.7% year-to-date, underperforming the S&P 500, and currently hold a Zacks Rank #3 (Hold), indicating expected performance in line with the market.
Industry Context: The Medical - Drugs industry, to which Assertio belongs, ranks in the top 37% of Zacks industries, suggesting that industry performance could significantly influence Assertio's stock movement in the future.

New Treatment Advances: Upstream Bio's Phase 2 VIBRANT trial for verekitug in chronic rhinosinusitis with nasal polyps showed significant reductions in nasal polyp and congestion scores, with a favorable safety profile and reduced need for surgery or corticosteroids.
Regulatory Developments: The FDA is reviewing GSK's marketing application for depemokimab for chronic rhinosinusitis, while Lyra Therapeutics reported positive results from its Phase 3 trial of LYR-210, indicating effective symptom improvement in patients without nasal polyps.
Financial Performance: Lyra Therapeutics reported a GAAP EPS loss of $5.51 for Q2 2025, which was less negative than expected, but its revenue of $0.18 million fell short of estimates and decreased significantly from the previous year. The company achieved cost reductions leading to a lower net loss compared to Q2 2024.
Clinical and Regulatory Developments: Positive results from the ENLIGHTEN 2 clinical trial for LYR-210 position the company favorably for future regulatory meetings, although no specific timeline for submission has been provided. The company is preparing for a Type C meeting with the FDA to discuss New Drug Application requirements while continuing to manage costs effectively.









