20Jun/13

Two Studies Evaluating the Combination of REVLIMID(R) and rituximab in Non … – MarketWatch (press release)

Two Studies Evaluating the Combination of REVLIMID(R) and rituximab in Non
MarketWatch (press release)
Celgene International Sarl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ:CELG) , today announced that results from two studies evaluating the combination of REVLIMID(R) (lenalidomide) and rituximab in various non-Hodgkin’s lymphomas 
Two Studies Evaluating the Combination of REVLIMID ® and rituximab in Non EON: Enhanced Online News (press release)

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19Jun/13

GILEAD SCIENCES, INC. : Gilead Announces Interim Phase 2 Data for Idelalisib … – 4-traders (press release)

GILEAD SCIENCES, INC. : Gilead Announces Interim Phase 2 Data for Idelalisib
4-traders (press release)
idelalisib (formerly GS-1101), an investigational, targeted, oral inhibitor of PI3K delta, for the treatment of patients with indolent non-Hodgkin’s lymphoma (iNHL) that is refractory (non-responsive) to rituximab and to alkylating-agent-containing
Gilead Presents Idelalisib DataZacks.com

all 2 news articles »

17Jun/13

New EXTEND Analyses Evaluate Efficacy Of Single Agent PIXUVRI® In 3rd And … – Daily Markets

New EXTEND Analyses Evaluate Efficacy Of Single Agent PIXUVRI® In 3rd And
Daily Markets
Compared to physicians’ choice of other agents given as monotherapy, single agent PIXUVRI resulted in 30 percent of patients who had previously received rituximab achieving a complete or unconfirmed durable complete response lasting on average 9.5 

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17Jun/13

New EXTEND Analyses Evaluate Efficacy of Single Agent PIXUVRI(R) in 3rd … – Wall Street Journal (press release)

New EXTEND Analyses Evaluate Efficacy of Single Agent PIXUVRI(R) in 3rd
Wall Street Journal (press release)
Compared to physicians’ choice of other agents given as monotherapy, single agent PIXUVRI resulted in 30 percent of patients who had previously received rituximab achieving a complete or unconfirmed durable complete response lasting on average 9.5 

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17Jun/13

New EXTEND Analyses Evaluate Efficacy of Single Agent PIXUVRI in 3rd and … – MarketWatch (press release)

New EXTEND Analyses Evaluate Efficacy of Single Agent PIXUVRI in 3rd and
MarketWatch (press release)
Compared to physicians’ choice of other agents given as monotherapy, single agent PIXUVRI resulted in 30 percent of patients who had previously received rituximab achieving a complete or unconfirmed durable complete response lasting on average 9.5 

and more »

17Jun/13

New EXTEND Analyses Evaluate Efficacy of Single Agent PIXUVRI® in 3rd and … – PR Newswire (press release)

New EXTEND Analyses Evaluate Efficacy of Single Agent PIXUVRI® in 3rd and
PR Newswire (press release)
Compared to physicians’ choice of other agents given as monotherapy, single agent PIXUVRI resulted in 30 percent of patients who had previously received rituximab achieving a complete or unconfirmed durable complete response lasting on average 9.5 

and more »

14Jun/13

Zusetzen von Obinutuzumab (GA101) oder Rituximab zu Chlorambucil … – FinanzNachrichten.de (Pressemitteilung)

Zusetzen von Obinutuzumab (GA101) oder Rituximab zu Chlorambucil
FinanzNachrichten.de (Pressemitteilung)
Zugehörigkeit: Deutsche CLL-Studiengruppe, Köln, Deutschland Thema: Zusetzen von Obinutuzumab (GA101) oder Rituximab zu Chlorambucil verbessert Aussichten für ältere Patienten mit chronischer lymphatischer Leukämie (CLL) und Komorbiditäten 

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