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Challengers received the Abbreviated New Drug Application (ANDA) pathway, which allows a generic to demonstrate bioequivalence to the reference listed drug without repeating the innovators clinical trials, plus a research safe harbor allowing them to conduct development activities during the patent term without infringement liability, and the 180-day exclusivity reward for challenging brand patents via P.IV certification

This finding provides a novel framework for the development of novel therapeutic interventions for cervical cancer [38]

Patient adherence Ultimately, patient adherence may be influenced by the physical properties of the formulation