Progress Towards YUTREPIA Approval
Liquidia Corporation is on track to receive final approval for YUTREPIA for PAH and PH-ILD patients following the expiration of TYVASO DPI's clinical exclusivity on May 23, 2025.
Successful Legal Outcomes
The Supreme Court's decision has exhausted the legal process regarding three patents initially asserted against Liquidia, removing impediments to YUTREPIA's commercialization.
Positive Clinical Developments
The ASCENT study has shown encouraging preliminary data on YUTREPIA's safety and efficacy in PH-ILD patients, with 1/3 of patients enrolled and high tolerability noted.
Expanded Partnerships and Resources
Liquidia expanded its relationship with Pharmosa, including a license agreement for L606 in the EU and other territories, and secured rights to a next-generation nebulizer.
Strengthened Financial Position
The company closed several financings, bringing in approximately $100 million, and ended Q3 2024 with $204.4 million in cash, supporting its corporate objectives.
Revenue Growth
Q3 2024 revenue increased to $4.4 million from $3.7 million in Q3 2023, largely due to higher sales quantities from the promotion agreement with Sandoz.