Create Account
Log In
Dark
chart
exchange
Premium
Terminal
Screener
Stocks
Crypto
Forex
Trends
Depth
Close
Check out our Level2View


Acer Therapeutics Inc. (ACER) and its collaboration partner, RELIEF THERAPEUTICS Holding SA announced the FDA has accepted for filing the New Drug Application (NDA) for ACER-001 for the treatment of patients with Urea Cycle Disorders. The FDA has assigned a PDUFA target action date of June 5, 2022.


RTTNews | Oct 6, 2021 08:56AM EDT

08:56 Wednesday, October 6, 2021 (RTTNews.com) - Acer Therapeutics Inc. (ACER) and its collaboration partner, RELIEF THERAPEUTICS Holding SA announced the FDA has accepted for filing the New Drug Application (NDA) for ACER-001 for the treatment of patients with Urea Cycle Disorders. The FDA has assigned a PDUFA target action date of June 5, 2022.

"In parallel with Acer's activities, we continue to execute on our global commercial strategy for ACER-001 which includes our intended submission of a Marketing Authorization Application for the treatment of patients with UCDs in Europe in Q2/Q3 2022," said Jack Weinstein, CFO of Relief.

Read the original article on RTTNews ( https://www.rttnews.com/3230867/acer-therapeutics-fda-to-review-nda-for-acer-001-quick-facts.aspx)

For comments and feedback: contact editorial@rttnews.com

Copyright(c) 2021 RTTNews.com All Rights Reserved






Share
About
Pricing
Policies
Markets
API
Info
tz UTC-5
Connect with us
ChartExchange Email
ChartExchange on Discord
ChartExchange on X
ChartExchange on Reddit
ChartExchange on GitHub
ChartExchange on YouTube
© 2020 - 2025 ChartExchange LLC