Re: Farmas USA
RTTR dedícale un rato que es interesante la historia del tal Andrew Ritter
http://beta.latimes.com/business/la-fi-himi-andrew-ritter-20161130-story.html
RTTR dedícale un rato que es interesante la historia del tal Andrew Ritter
http://beta.latimes.com/business/la-fi-himi-andrew-ritter-20161130-story.html
Conocía la historia de los Ritter.
Para guión de Hollywood.
Si lo consigue heroe y si no villano.
Tiene merito
Creo que este artículo de SA no se había colgado...
Acadia Remains Significantly Undervalued
https://seekingalpha.com/article/4135660-acadia-remains-significantly-undervalued
ACAD
CELG
Posible BO.
Barclays:
$CELG WSJ Reports Celgene likely to acquire Impact Biomedicines for $7bn
Only late-stage asset is fedratinib in phase 3 trials for myelofibrosis. This afternoon, the WSJ (link) reported that Celgene could buy Impact Biomedicines (private) for nearly $7bn in a three-stage deal, with $1bn upfront and the rest dependent on FDA approval and successful commercialization. Fedratinib is an oral JAK2 inhibitor, currently in phase 3 development for myelofibrosis (off of a clinical hold in October 2017). As Celgene has not formally announced a transaction, we have little other details regarding the likely deal structure. From the WSJ report, we are encouraged with the potential structuring, with payments tied to milestones - essentially de-risking both FDA approval and commercialization.
We note that the myelofibrosis space is not without competition, as Incyte (along with partner Novartis) has successfully commercialized Jakafi with >$1bn in US sales expected in 2017. Even if approved in 2019 (best case given currently available data), fedratinib would have to compete against a drug with a similar mechanism and already successfully commercialized. We note that this drug could be used in patients resistant or intolerant to Jakafi. Given today’s news, Celgene could update its 2020 guidance during tomorrow’s presentation in San Francisco to include potential revenues from fedratinib. We would have preferred to see business development with a commercial-ready asset in a space with a higher-unmet need or novel MOA. Reiterate EW and $105 PT.
Development of fedratinib has not been smooth with a clinical hold in 2013. Only recently (October 2017) has the development of the drug resumed following the 2013 clinical hold (and development discontinuation by Sanofi) due to reports of Wernicke’s encephalopathy (WE). We have few details of the result of the FDA Type-A meeting by Impact. Given the history, it is possible that Impact and Celgene could have additional clinical work beyond the ongoing phase 3. We would expect more details following a formal announcement by Celgene, if the WSJ report is accurate.
CELG
http://www.businesswire.com/news/home/20180107005114/en/
Feliz año a todos!
Nadie en ARDM por aqui? AdCom en breve.
En seguimiento las CRISPRs hoy por si bajan en referencia al nuevo articulo ciencifico
Viernes añadí SGYP
DVAX
Y después de varios años y varias CRL por fin llegó el día...
Dynavax Announces HEPLISAV-B™ is Now Available in the United States for the Prevention of Hepatitis B in Adults
http://investors.dynavax.com/releasedetail.cfm?ReleaseID=1053522
TGTX
TG Therapeutics and Jiangsu Hengrui Medicine Announce Global License Agreement for Development and Commercialization of Novel BTK Inhibitor Program for the Treatment of Hematologic Malignancies
US IND Filing Expected in the First Half of 2018
Hengrui is Eligible to Receive Collaboration and Licensing Payments of Approximately $350MM, in Addition to Royalties on Future Sales