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BIOCRYST PHARMACEUTICALS INC (BCRX)
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Create: Alert |
All | News | Filings
Date Filed | Type | Description |
08/03/2023 |
8-K
| Quarterly results |
08/04/2022 |
8-K
| Quarterly results |
05/05/2022 |
8-K
| Quarterly results |
02/23/2022 |
8-K
| Quarterly results |
11/03/2021 |
8-K
| Quarterly results |
08/05/2021 |
8-K
| Quarterly results |
05/06/2021 |
8-K
| Quarterly results |
02/25/2021 |
8-K
| Quarterly results |
11/05/2020 |
8-K
| Quarterly results |
08/06/2020 |
8-K
| Quarterly results |
05/06/2020 |
8-K
| Quarterly results |
03/05/2020 |
8-K
| Quarterly results |
11/06/2019 |
8-K
| Quarterly results |
08/06/2019 |
8-K
| Quarterly results |
05/08/2019 |
8-K
| Quarterly results |
03/04/2019 |
8-K
| Quarterly results |
11/06/2018 |
8-K
| Quarterly results |
08/07/2018 |
8-K
| Quarterly results |
05/08/2018 |
8-K
| Quarterly results |
11/07/2017 |
8-K
| Quarterly results |
08/07/2017 |
8-K
| Quarterly results |
05/04/2017 |
8-K
| Form 8-K - Current report |
11/07/2016 |
8-K
| Quarterly results |
08/04/2016 |
8-K
| Form 8-K - Current report |
05/05/2016 |
8-K
| Form 8-K - Current report |
02/23/2016 |
8-K
| Quarterly results |
11/05/2015 |
8-K
| Quarterly results |
08/07/2015 |
8-K
| Quarterly results |
05/08/2015 |
8-K
| Quarterly results |
02/18/2015 |
8-K
| Quarterly results |
11/06/2014 |
8-K
| Quarterly results |
08/05/2014 |
8-K
| Quarterly results |
05/08/2014 |
8-K
| Quarterly results |
02/26/2014 |
8-K
| Quarterly results
Docs:
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"Amendment #17 to the Agreement between BioCryst Pharmaceuticals, Inc. and the U.S. Department of Health and Human Services",
"BIOCRYST REPORTS FOURTH QUARTER AND FULL YEAR 2013 FINANCIAL RESULTS",
"BIOCRYST ANNOUNCES PERAMIVIR NDA ACCEPTANCE BY THE FDA Research Triangle Park, North Carolina - February 25, 2014 - BioCryst Pharmaceuticals, Inc. , a pharmaceutical company focused on the development and commercialization of treatments for rare and infectious diseases, today announced that the U.S. Food and Drug Administration has accepted for review the New Drug Application for intravenous peramivir that was submitted to the FDA in December 2013. The FDA assigned the NDA a standard review time, resulting in a PDUFA action date of December 23, 2014. The FDA has informed BioCryst that at this time, it does not plan to hold an Advisory Committee review of the NDA. “We are pleased that BioCryst's first NDA filing has been accepted by the FDA. We believe the approval of peramivir and its mode..." |
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