Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 770.00K | 1.53M | 1.56M | 1.36M | 285.00K | 0.00 |
Gross Profit | 570.00K | 1.53M | 1.56M | 296.00K | -716.00K | -95.00K |
EBITDA | -34.86M | -60.26M | -65.25M | -53.92M | -42.61M | -22.11M |
Net Income | -38.84M | -93.44M | -62.68M | -55.28M | -43.51M | -22.05M |
Balance Sheet | ||||||
Total Assets | 52.57M | 66.35M | 142.60M | 109.97M | 54.87M | 80.83M |
Cash, Cash Equivalents and Short-Term Investments | 29.78M | 40.58M | 102.75M | 97.89M | 45.75M | 74.59M |
Total Debt | 32.48M | 34.38M | 26.88M | 4.18M | 1.45M | 2.44M |
Total Liabilities | 50.95M | 54.75M | 53.18M | 29.21M | 20.55M | 6.34M |
Stockholders Equity | 1.62M | 11.59M | 89.42M | 80.75M | 34.32M | 74.49M |
Cash Flow | ||||||
Free Cash Flow | -43.02M | -72.35M | -64.35M | -43.55M | -29.20M | -22.92M |
Operating Cash Flow | -43.01M | -70.01M | -63.30M | -43.38M | -25.82M | -21.14M |
Investing Cash Flow | 36.27M | 80.31M | -12.58M | -65.01M | -3.38M | -1.77M |
Financing Cash Flow | 4.62M | 8.53M | 65.69M | 96.26M | 359.00K | 87.70M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
51 Neutral | $7.83B | -0.18 | -40.10% | 2.29% | 21.46% | -2.03% | |
47 Neutral | $11.82M | ― | -238.26% | ― | -57.69% | 63.76% | |
40 Underperform | $7.26M | ― | 234.90% | ― | ― | 47.54% | |
34 Underperform | $4.06M | ― | -181.99% | ― | ― | 46.96% | |
― | $5.67M | ― | -602.64% | ― | ― | ― | |
35 Underperform | $4.28M | ― | -133.62% | ― | -86.43% | -8.91% | |
― | $4.75M | ― | ― | ― | ― |
On August 20, 2025, Lyra Therapeutics received a Deficiency Letter from Nasdaq indicating that the company’s stockholders’ equity, reported at $1.6 million as of June 30, 2025, did not meet the minimum requirement of $2.5 million for continued listing on the Nasdaq Capital Market. Although this has no immediate effect on the trading of its stock, Lyra has until October 4, 2025, to submit a plan to regain compliance. The company is exploring various strategies to meet Nasdaq’s requirements, but there is no guarantee of acceptance or successful compliance, which could lead to potential delisting.
On August 1, 2025, Lyra Therapeutics announced the immediate termination of Dr. Harlan W. Waksal’s employment as Executive Chairman, following a mutual agreement. Dr. Waksal also resigned from the Board of Directors, and Maria Palasis, the company’s President and CEO, was appointed as the new Chair of the Board, while Jim Tobin continues as Lead Independent Director.
On June 26, 2025, Lyra Therapeutics entered into a securities purchase agreement with accredited and institutional investors, resulting in a registered direct offering and concurrent private placement of shares and warrants, expected to yield approximately $4.3 million in net proceeds. The funds are intended for working capital and potential clinical development of LYR-210, reflecting the company’s strategic efforts to advance its product pipeline despite past challenges, including the failure to meet the primary endpoint in a Phase 3 clinical trial and significant workforce reductions.
On June 13, 2025, Lyra Therapeutics, Inc. received a notification from Nasdaq confirming that its common stock maintained a minimum bid price of $1.00 or more for 12 consecutive business days, from May 28, 2025, to June 12, 2025. This achievement means the company has regained compliance with Nasdaq’s Listing Rule 5550(a)(2), closing the matter.
On June 9, 2025, Lyra Therapeutics announced the posting of a corporate presentation detailing their progress and strategic plans for LYR-210, following the successful ENLIGHTEN 2 Phase 3 trial. The company aims to advance LYR-210 for CRS with polyp indication, with a Phase 3 trial planned for early 2026, highlighting its commitment to addressing the needs of CRS patients and expanding its pipeline opportunities.
On June 2, 2025, Lyra Therapeutics announced positive results from the ENLIGHTEN 2 Phase 3 clinical trial of LYR-210, which met its primary and key secondary endpoints for treating chronic rhinosinusitis (CRS) at 24 weeks. The trial demonstrated statistically significant improvements in symptoms for patients both with and without nasal polyps, positioning Lyra to advance regulatory strategies and potentially become a leader in CRS treatment.