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Pharmion And MethylGene Announce U.S. Orphan Drug Designation Granted For MGCD0103 For The Treatment Of Acute Myelogenous Leukemia
Pharmion Corporation (Nasdaq: PHRM) and MethylGene Inc. (TSX: MYG) announced that the U.S. Food and Drug Administration (FDA) has designated the Companies’ histone deacetylase (HDAC) inhibitor, MGCD0103, as an Orphan Drug for the treatment of acute myelogenous leukemia (AML) in the United States.
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BioNumerik Pharmaceuticals And ASKA Pharmaceutical Co. Announce Results From Phase III Clinical Trial Of Tavocept(TM)
BioNumerik Pharmaceuticals, Inc. (”BioNumerik”) and ASKA Pharmaceutical Co., Ltd. (”ASKA”) announced the results of a Phase III clinical trial of Tavocept(TM) in patients with advanced non-small cell lung cancer. Tavocept is an investigational new drug with potential for oncology and non-oncology indications that was originated and
Hepatitis B Foundation Testifies Before Congressional Appropriation Committee And Urges More Federal Funding For Hepatitis B
Hepatitis B Foundation President Dr. Timothy Block testified about the public health challenge of chronic hepatitis B before the Congressional Appropriations Subcommittee on Labor, Health and Human Services on March 13 in Washington, DC, at the request of Honorable David Obey, chairman, Committee on Appropriations. Dr.
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