- A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.
Apnimed, a company based in Massachusetts, is seeking FDA approval for its drug candidates targeting the OSA market and is also planning an IPO to fund operations.
1 report, 1 independent
Updated Jul 28
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What happened
Apnimed, a company based in Massachusetts, is seeking FDA approval for its drug candidates targeting the OSA market and is also planning an IPO to fund operations.
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
- Cronus Pharma LLC, headquartered in East Brunswick, is launching products in the U.S. market and seeking FDA approval.
- A study author is based in Johns Hopkins School of Medicine, and the research is connected to Baltimore, now involving the FDA for drug approval.
- Capricor Therapeutics is seeking regulatory approval from the FDA for clinical trials and has listed on the Nasdaq stock exchange, with a law firm based in New York City involved.
- BioPorto is seeking regulatory pathways and activating its first clinical site in collaboration with Massachusetts General Hospital.
- The FDA is overseeing a company that is based in the state of Missouri.
Coverage
Newest first; wire copies grouped- yahoo.comApnimed scouts $160m IPO to back late-stage sleep apnoea pill development