DURECT Corporation Receives FDA Breakthrough Therapy Designation For Larsucosterol In Alcohol-Associated Hepatitis
Portfolio Pulse from Benzinga Newsdesk
DURECT Corporation has received FDA Breakthrough Therapy Designation for its drug Larsucosterol, aimed at treating alcohol-associated hepatitis.
May 21, 2024 | 12:03 pm
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DURECT Corporation has received FDA Breakthrough Therapy Designation for its drug Larsucosterol, aimed at treating alcohol-associated hepatitis. This designation could expedite the development and review process, potentially leading to faster market entry and increased investor interest.
The FDA Breakthrough Therapy Designation is a significant milestone that can accelerate the development and review of Larsucosterol. This could lead to faster market entry, which is likely to boost investor confidence and positively impact the stock price in the short term.
CONFIDENCE 95
IMPORTANCE 90
RELEVANCE 100