Chemgenex pharmaceuticals steroids

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Pooja Agarwal provides technical and strategic leadership to the Research and Development group at Krystal, and is critically involved in all aspects of product development from concept to to joining Krystal, she was Senior Director, Human Therapeutics, at Intrexon Corporation where she managed the preclinical development of several gene therapy programs in Ophthalmology, Oncology, and Neuropathic Diseases, as well as strategic alliances with internal and external partnerships.
Pooja holds a PhD in Biomedical Sciences from University of California San Francisco, a Masters of Science in Molecular and Medical Genetics from University of Toronto, and a Bachelors of Science (Summa Cum Laude) in Biochemistry from McMaster University.
When not immersed in work, she loves hiking and spending time with her family, or curling with a good book and a glass of wine.

ChemGenex Pharmaceuticals Limited (ASX:CXS) and Hospira, Inc. (NYSE:HSP) announced today that they have entered into an exclusive agreement to license, develop and commercialize ChemGenex’s product candidate omacetaxine mepesuccinate, a novel targeted cytotoxic pharmaceutical product, in Europe, the Middle East and parts of Africa (the Territory). Applications for marketing approval of the product have been accepted for regulatory review in both the United States and Europe for treatment of patients with chronic myeloid leukemia (CML) who have failed to respond to the current standard of care treatment, imatinib mesylate, and who have the Bcr-Abl T315I mutation.

Chemgenex pharmaceuticals steroids

chemgenex pharmaceuticals steroids

ChemGenex Pharmaceuticals Limited (ASX:CXS) and Hospira, Inc. (NYSE:HSP) announced today that they have entered into an exclusive agreement to license, develop and commercialize ChemGenex’s product candidate omacetaxine mepesuccinate, a novel targeted cytotoxic pharmaceutical product, in Europe, the Middle East and parts of Africa (the Territory). Applications for marketing approval of the product have been accepted for regulatory review in both the United States and Europe for treatment of patients with chronic myeloid leukemia (CML) who have failed to respond to the current standard of care treatment, imatinib mesylate, and who have the Bcr-Abl T315I mutation.

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