Palatin Technologies Unveils Significant Progress in Dry Eye Disease Treatment with PL9643 at ARVO 2025

Palatin Technologies Showcases PL9643's Promising Results at ARVO 2025



Palatin Technologies, Inc., a biopharmaceutical company focused on groundbreaking therapies targeting the melanocortin receptor system, revealed compelling data from its Phase 3 MELODY-1 study on the treatment of dry eye disease (DED) during the 2025 Association for Research in Vision and Ophthalmology (ARVO) Annual Meeting. This meeting, known for showcasing collaboration and advancements in eye research, proved to be a perfect platform for unveiling these results.

Key Findings from PL9643 Clinical Trial


The updated analysis underscores PL9643 as a potential first-in-class medication that not only provides rapid symptom relief but also demonstrates full symptom resolution across multiple clinical endpoints. Key highlights indicate that six out of thirteen symptom endpoints showed statistically significant improvement (p<0.05) when compared to placebo, positioning PL9643 distinctly in the realm of DED therapies.

Importantly, patients under treatment began experiencing symptom relief as early as two weeks into the study, a timeline that continued through to week twelve without plateauing. Symptoms assessed through various measures illustrated that PL9643 effectively enhanced the ocular surface's health, paving the way for a potential new standard in treating this chronic condition.

According to the safety data reported, PL9643 exhibited tolerability rates comparable to or better than the placebo vehicle—typically akin to artificial tears—reinforcing the formulation's safety profile alongside its efficacy.

Clinical Implications and Future Perspectives


Dr. Carl Spana, President and CEO of Palatin, articulated that the results presented are

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