Stock Quote        
  Join        Login  
logo

ERYTECH Pharma Announces the Oral Presentation of Positive Phase II Clinical Trial Results in Acute Lymphoblastic Leukemia

Sunday, June 17, 2012 5:00 AM

The oral presentation will be held on June 17th 2012 by Prof. Dr. Hervé Dombret, Hospital Saint Louis, Paris (France) at the 17th Annual Meeting of European Hematology Association (EHA) in Amsterdam (The Netherlands).

Thirty patients over 55-years old, newly diagnosed with Acute Lymphoblastic leukemia (ALL) were included in this Phase II trial. The patients received different doses of erythrocyte encapsulated Asparaginase in combination with the chemotherapy recommended by the European Working group for Adult Lymphoblastic Leukemia (EWALL). Asparaginase is a major and mainstay drug to treat ALL, but current formulations are not recommended in induction therapy for these older patients who are particularly frail for toxicity reasons.

Erythrocyte encapsulated Asparaginase introduced in first line induction therapy showed a good safety profile even in the elderly patients and is efficient for asparagine depletion. At the optimal dose (100IU/Kg), 91% of the patients at the end of induction therapy reached a complete remission and the median overall survival was 15.6 months. The enrollment of the patients was finished 2 months in anticipation to the expectations. The study was performed in close collaboration to the cooperative group GRAALL (Group for Research in Adult Acute Lymphoblastic Leukemia).

“I would like to thank the investigators of the GRAALL for their collaboration in setting up and conducting this important clinical trial. The results demonstrate that our asparaginase formulation offers the possibility to safely administrate this very useful drug in fragile older ALL patients for which today no alternative exist.” says Dr Yann Godfrin, Executive Vice President Preclinical and Clinical Reseach.

About ERYTECH

ERYTECH Pharma SA is a late-stage French biopharmaceutical company developing medicinal products for oncology and rare diseases. The company's patented core technology is based on the use of human red blood cells (RBCs) to improve the pharmacokinetic (PK) and pharmacodynamic (PD) properties of therapeutic enzymes (eg asparaginase). ERYTECH's lead product, GRASPA® for the treatment of Acute Lymphoblastic Leukemia (ALL), holds orphan designation in Europe and the US an is in a pivotal Phase II/III clinical trial in Europe.

www.erytech.com
ERYTECH Pharma, 60 Avenue Rockefeller, Bâtiment Adénine, F-69008 Lyon, France
ERYTECH Pharma (US Office), 3711 Market Street, 19104 Philadelphia PA, USA

(Source: Business Wire )
(Source: Quotemedia)

Follow iStockAnalyst on Twitter Follow iStockAnalyst on Twitter
Subscribe to Email Alerts
Advertisement
Post Comment -- Login is required to post message
Name:  
Alert for new comments:
Your email:
Your Website:
Title:
Comments:
 




Fundamental data is provided by Zacks Investment Research, and Commentary, news and Press Releases provided by YellowBrix and Quotemedia.
All information provided "as is" for informational purposes only, not intended for trading purposes or advice. iStockAnalyst.com is not an investment adviser and does not provide, endorse or review any information or data contained herein.
The blog articles are opinions by respective blogger. By using this site you are agreeing to terms and conditions posted on respective bloggers' website.
The postings/comments on the site may or may not be from reliable sources. Neither iStockAnalyst nor any of its independent providers is liable for any informational errors, incompleteness, or delays, or for any actions taken in reliance on information contained herein. You are solely responsible for the investment decisions made by you and the consequences resulting therefrom. By accessing the iStockAnalyst.com site, you agree not to redistribute the information found therein.
The sector scan is based on 15-30 minutes delayed data. The Pattern scan is based on EOD data.