According to filing with the US Securities and Exchange Commission, the city-based pharma company is expected to file the New Drug Application (NDA) with US Food and Drug Administration with regard the migraine drug in 2018 while it is expected to submit license application for the cancer drug, it may approach the drug regulator in 2019.
"As of March 31, 2017, we had 16 active product development programs in our pipeline (for DFN-02- the drug to treat acute treatment of migraines, with or without aura in adults) Phase 3 is completed. Submission of NDA to USFDA is planned for 2018," it said.
It however, said the timelines for expected filing may change due to various factors including outcome of Phase 3 studies, completion of Integrated Summary of Safety/Integrated Summary of effectiveness outcome of stability data and internal reprioritization of portfolio.
The company's principal research and development facilities are located in Telangana-India, Cambridge-United Kingdom and Leiden- the Netherlands while the principal manufacturing facilities are located in Telangana, Andhra Pradesh and Himachal Pradesh in India, Cuernavaca-Cuautla, Mexico, Mirfield, United Kingdom, Louisiana and Tennessee, United States.
"This increase was in accordance with our strategy to expand our research and development efforts in complex formulations, differentiated formulations and bio-similar compounds," the company said in the filing.
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