Outlook Therapeutics (NASDAQ:OTLK) announced on Monday that it has submitted a formal dispute resolution request (FDRR) to the U.S. Food and Drug Administration (FDA) regarding its ONS-5010/LYTENAVA.
The update comes after receiving a Complete Response Letter (CRL) in December 2025 for its Biologics License Application (BLA) for the treatment of neovascular age-related macular degeneration.
The FDA has accepted the FDRR and has granted a meeting with the deciding official to be conducted in April 2026.
ONS-5010/LYTENAVA demonstrated clinically meaningful and statistically significant improvements in visual acuity in the NORSE TWO randomized, double-masked, active-controlled Phase 3 trial, which met its primary and key secondary endpoints.
Additional evidence from NORSE EIGHT and other data submitted in the BLA further supports the efficacy and safety profile of ONS-5010, consistent with its anti-VEGF mechanism of action.
The FDA has raised no safety concerns.
In August 2025, the FDA issued a CRL to ONS-5010 resubmission. The CRL included only one deficiency for a lack of substantial evidence of effectiveness.
In August 2023, Outlook Therapeutics received a complete response letter from the FDA regarding ONS-5010.
The FDA noted that the additional mechanistic and natural history data provided in the BLA resubmission do not alter the previous review conclusion.
In the U.S., ONS-5010/LYTENAVA remains investigational, but its potential approval would mark it as the first FDA-approved ophthalmic bevacizumab formulation.
The product has already gained approval in Europe. Outlook Therapeutics emphasizes the robust pharmacovigilance and domestic U.S. manufacturing supply chain supporting ONS-5010/LYTENAVA.
This positions the company to meet regulatory standards and expand its market presence.
OTLK Price Action: Outlook Therapeutics shares were up 4.64% at $0.20 at the time of publication on Tuesday. The stock is trading near its 52-week low of $0.16, according to Benzinga Pro data.
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