02Jul/13

Piper Jaffray Reiterates “Neutral” Rating for Biogen Idec (BIIB) – Watch List News (press release)

Piper Jaffray Reiterates “Neutral” Rating for Biogen Idec (BIIB)
Watch List News (press release)
in particular unpublished estimates) now fully reflect Tecfidera’s strong launch, in our view, and upside in BIIB shares will likely require pipeline success, which is not expected until 2014 data readouts from anti-LINGO Phase II (optic neuritis

02Jul/13

JIM – Un nouvel anticorps monoclonal pour le traitement de la sclérose en plaques – Journal International de Médecine (Inscription)

JIM – Un nouvel anticorps monoclonal pour le traitement de la sclérose en plaques
Journal International de Médecine (Inscription)
Ainsi, le daclizumab est un anticorps monoclonal humanisé spécifique du récepteur CD25 diminuant l’activation immunitaire via l’interleukine 2. Plus de 600 patients ont été inclus dans l’étude SELECT, randomisée, en double aveugle et contre placebo

02Jul/13

BioInvent extends collaboration for the discovery and development of … – PharmiWeb.com (press release)

BioInvent extends collaboration for the discovery and development of
PharmiWeb.com (press release)
BioInvent International AB (OMXS: BINV) today announces that it has signed an extension to its 2009 license agreement with Mitsubishi Tanabe Pharma Corporation for the development of antibodies from BioInvent’s n-CoDeR® library. Under the terms of 

02Jul/13

BioInvent extends collaboration for the discovery and development of … – PipelineReview.com (press release)

BioInvent extends collaboration for the discovery and development of
PipelineReview.com (press release)
LUND, Sweden I July 2, 2013 I BioInvent International AB (OMXS: BINV) today announces that it has signed an extension to its 2009 license agreement with Mitsubishi Tanabe Pharma Corporation for the development of antibodies from BioInvent’s 

and more »

02Jul/13

NICE issues second draft guidance on the use of Pixuvri as monotherapy to … – pharmabiz.com

NICE issues second draft guidance on the use of Pixuvri as monotherapy to
pharmabiz.com
The European Medicines Agency’s (the EMA) Committee for Medicinal Products for Human Use has accepted PIX306, CTI’s ongoing randomized controlled Phase 3 clinical trial, which compares Pixuvri-rituximab to gemcitabine-rituximab in patients who have 

01Jul/13

Stock Analysts' Ratings Reiterations for July, 1st (AMP, BBRY, BIIB, COH, CRM … – Zolmax

Stock Analysts’ Ratings Reiterations for July, 1st (AMP, BBRY, BIIB, COH, CRM
Zolmax
in particular unpublished estimates) now fully reflect Tecfidera’s strong launch, in our view, and upside in BIIB shares will likely require pipeline success, which is not expected until 2014 data readouts from anti-LINGO Phase II (optic neuritis

and more »