- A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.
ARS Pharmaceuticals, based in San Diego, submitted a generic product application requiring FDA approval.
1 report, 1 independent
Updated Sep 5
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What happened
ARS Pharmaceuticals, based in San Diego, submitted a generic product application requiring FDA approval.
Who's involved
What this event is mainly aboutKeep exploring
Part of
A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.Also in this story
- A partnership with BARDA has accelerated the development of SCY-247 for the company.
- A company plans to submit regulatory applications to the FDA, EMA, and Australian TGA.
- Approval leads to procurement process initiation.
- UroGen Pharma Ltd., headquartered in Princeton, is seeking FDA approval for its products for the U.S. market.
The entities involved
Related events
- FDA approval is the goal for product candidates from Daré Bioscience, Inc.
- Merck announced on September 3, 2025, that it is seeking potential approval for new drugs from the FDA.
- FDA oversees drug trials in the US and Israel for Clearmind Medicine Inc., which is listed on Nasdaq.
- Steriwave requires FDA approval for US market.
- FDA approved a medical device from Abbott and supported a PARADIGM study based on data from the Cleveland Clinic.
Coverage
Newest first; wire copies grouped- Insider MonkeyARS Pharmaceuticals (SPRY) Faces Patent Test as Lupin Files ANDA ARS Pharmaceuticals, Inc. (NASDAQ:SPRY) is among the fastest growing small cap stocks to buy. Lupin Inc., a leading player in the heal