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Outlook Therapeutics (OTLK) was back in the spotlight on Thursday as Wall Street looked ahead to a crucial U.S. Food and Drug Administration (FDA) decision on its therapy to treat wet age-related macular degeneration (Wet AMD), with the regulator reviewing the company’s biologics license application for a third time after two previous setbacks.
At the time of writing, OTLK stock was down 0.4%, having closed in the red in five of the previous six sessions.
Last month, the FDA accepted Outlook Therapeutics’ biologics license application for Lytenava for a third review after previously rejecting it in August 2023 over manufacturing issues and again in late 2025, citing insufficient confirmatory efficacy evidence and requesting additional data.
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The FDA has set July 29, 2026, as its target date to decide on the application, while the company has already begun pre-launch preparations.
If approved, Lytenava would become the first FDA-approved ophthalmic formulation of Bevacizumab for wet AMD. The therapy is already approved in the European Union and the United Kingdom and is designed to treat a progressive eye disease that can lead to severe vision loss if left untreated.
Meanwhile, unit sales of Lytenava in Europe in the second quarter fell around 10% compared to the previous quarter. The company stated that it has taken steps to reduce costs in Europe in an effort to improve margins in future quarters.
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Retail sentiment surrounding OTLK on Stocktwits trended in the ‘bullish’ territory over the past 24 hours, amid an 80% jump in message volumes.
One user expects a “big boom” in the stock’s price after the FDA decision, implying approval.
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Another user said they were hoping the stock could climb to $9 to $12.
Meanwhile, analysts on average have set a 12-month price target of $5.5, an over 300% upside potential from current levels, according to Koyfin.
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OTLK shares have seen significant buying interest so far this year, surging more than 100%.
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