- A company is conducting clinical trials and seeking drug approval for the U.S. market under the FDA.
Teva's asset received FDA Orphan Drug and Fast Track designations after announcing an acquisition from Tel Aviv.
3 reports, 2 independent
Updated Aug 28
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- Developments
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- Repetition
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New informationRepeats or wire copies
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What happened
Teva's asset received FDA Orphan Drug and Fast Track designations after announcing an acquisition from Tel Aviv.
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
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Teva Pharmaceutical Industries Ltd.
Israeli pharmaceutical company
- FDA
Related events
- Teva's acquired product is currently undergoing review by the FDA.
- Teva Pharmaceutical Industries Ltd. submitted an NDA for ecopipam to the FDA.
- Teva Pharmaceutical Industries discussed company strategy at an event hosted by Morgan Stanley.
- Leerink partners issued an 'outperform' rating on Teva stock, while an insider sold shares of the company.
- The market capitalization of Teva Pharmaceutical Industries was overtaken by another entity on the Tel Aviv Stock Exchange.