•
Jun 30, 2021

Lyra Q2 2021 Earnings Report

Lyra Therapeutics reported financial results and highlighted recent accomplishments.

Key Takeaways

Lyra Therapeutics reported a net loss of $11.0 million for the second quarter of 2021. The company's cash and cash equivalents were $69.0 million as of June 30, 2021, and they expect it to fund operations into 2023. They also announced a licensing agreement with LianBio for LYR-210 and have a clear path forward to advance LYR-210 into Phase 3 clinical development.

Successful EOP2 FDA meeting for LYR-210 in CRS, with Phase 3 program on track to begin around year-end 2021.

Entered into a licensing agreement with LianBio for LYR-210 in Greater China and other Asian markets.

Reported positive topline results from an LYR-210 PK study, supporting a 505(b)(2) NDA pathway.

Cash and cash equivalents were $69.0 million as of June 30, 2021, expected to fund operations into 2023.

EPS
-$0.85
Previous year: -$0.56
+51.8%
Cash and Equivalents
$69M
Previous year: $86.6M
-20.3%
Free Cash Flow
$2.76M
Total Assets
$76.3M

Lyra

Lyra

Lyra Revenue by Segment

Forward Guidance

Lyra Therapeutics expects to advance LYR-210 into Phase 3 clinical development for the treatment of Chronic Rhinosinusitis around year-end. LYR-220 for post-surgical CRS patients, is also advancing and remains on track to enter Phase 2 later this year.

Positive Outlook

  • Clear path forward to advance LYR-210 into Phase 3 clinical development for the treatment of Chronic Rhinosinusitis.
  • LYR-220 for post-surgical CRS patients is advancing and remains on track to enter Phase 2 later this year.
  • LYR-210 and LYR-220 will disrupt the current CRS treatment landscape.
  • Provide a new pharmacologic solution for the full spectrum of the 4 million U.S. CRS patients who fail medical management each year.
  • Cash balance to be sufficient to fund its planned operations into 2023.

Challenges Ahead

  • Incurred significant losses since inception and expects to incur losses for the foreseeable future.
  • Need for additional funding, which may not be available.
  • Limited operating history.
  • No approved products.
  • Product candidates are in various stages of development.