Teligent has been surprised by a complete response letter issued over an abbreviated new drug application for its first complex drug indicated for an orphan disease population. “In the letter, the US Food and Drug Administration requested further information and raw data to support the ANDA,” revealed the US niche generics specialist, which is working on the orphan generic with an undisclosed development partner.
“This latest response from the FDA is unexpected given the time and opportunity that the FDA had to request the information during the ANDA’s active review,” commented Teligent’s president and...
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