Dr. Reddy’s Laboratories and Promius Pharma announce the filing of an NDA for its migraine candidate

Dr. Reddy’s Laboratories Ltd and its subsidiary, Promius Pharma, LLC announced the filing of New Drug Application (NDA) for its migraine candidate DFN-02 with the U.S. Food and Drug Administration (USFDA).

According to Dr. Anil Namboodiripad, Senior Vice President, Proprietary Products and President, Promius Pharma, the NDA for DFN-02 is an important step forward in the company’s mission to bring solutions that address unmet needs.

“The filing of DFN-02 NDA represents our continuing commitment to bring innovative solutions in migraine treatment,” explains Dr. Namboodiripad. “Acute migraine attacks are typically associated with pain and symptoms, such as nausea, photophobia, and phonophobia. It is important that an effective migraine treatment helps address associated symptoms. Equally important is having a well-tolerated treatment that provides patients a satisfactory resolution of their migraine attack.”

In a multicenter, double-blind, randomized, placebo controlled study with 107 subjects (Clinicaltrials.gov # NCT02856802), DFN-02 has demonstrated that it can effectively treat pain and associated symptoms during a migraine attack and reduce attack-related functional disability. Data from this study show that there was a significantly higher proportion of subjects who experienced 2-hour pain freedom with DFN-02 compared with placebo: 43.8% (n=48) versus 22.5% (n=40), p<.05). DFN-02 was also significantly better than placebo at alleviating the patients’ most bothersome symptom (MBS), including nausea, photophobia, and phonophobia (70.7% versus 39.5% MBS free at 2 hours postdose; p<.01. DFN-02 was well tolerated, with the following Treatment-Emergent Adverse Events: dysgeusia (n = 4), application site pain (n = 2), chest discomfort, burning sensation, rhinorrhea and malaise (n = 1 each), all mild to moderate.

Upon approval, the product will be commercialized by Promius Pharma.