...companies could not show a benefit over existing treatments. The drugs were Onrigin laromustine from Vion Pharmaceuticals Inc.... ...Chicago Medical Center , Chicago, Ill. U.S. Food and Drug Administration (FDA), Silver Spring, Md. Vion...
...leukemia (AML) prior to conducting another Phase III trial. In January, FDA refused to grant Vion... ...additional trial (see BioCentury, Dec. 21). Vion filed for Chapter 11 bankruptcy late last year. Vion Pharmaceuticals Inc....
...FDA refused to grant Vion an SPA for a planned Phase III trial (HOVON AML 92... ...complete response letter from FDA for Onrigin to treat AML (see BioCentury, Dec. 21, 2009). Vion Pharmaceuticals Inc....
...profile for Hexvix to detect papillary bladder cancer using fluorescence cystoscopy (see B14) . Vion Pharmaceuticals Inc. (OTCBB:VION... ...FDA issued a complete response letter to an NDA for Onrigin laromustine. The agency asked Vion... ...ages 60 and up with de novo, poor-risk acute myelogenous leukemia (AML). For the week, Vion...
...that the company conduct an additional randomized trial and addressed clinical pharmacology and manufacturing issues. Vion... ...would be needed for the sulfonyl hydrazine DNA alkylating agent (see BioCentury, Sept. 7). Vion Pharmaceuticals Inc. (OTCBB:VION...
...had previously said that it does not have sufficient funds for a new randomized trial. Vion... ...II testing for myeloproliferative disorders and Phase I testing for solid tumors. At Sept. 30, Vion... ...in cash and a nine-month operating loss of $14.1 million (see BioCentury, Oct. 19). Vion Pharmaceuticals Inc. (OTCBB:VION...
...companies could not show a benefit over existing treatments. The drugs were Onrigin laromustine from Vion Pharmaceuticals Inc.... ...Chicago Medical Center , Chicago, Ill. U.S. Food and Drug Administration (FDA), Silver Spring, Md. Vion...
...leukemia (AML) prior to conducting another Phase III trial. In January, FDA refused to grant Vion... ...additional trial (see BioCentury, Dec. 21). Vion filed for Chapter 11 bankruptcy late last year. Vion Pharmaceuticals Inc....
...FDA refused to grant Vion an SPA for a planned Phase III trial (HOVON AML 92... ...complete response letter from FDA for Onrigin to treat AML (see BioCentury, Dec. 21, 2009). Vion Pharmaceuticals Inc....
...profile for Hexvix to detect papillary bladder cancer using fluorescence cystoscopy (see B14) . Vion Pharmaceuticals Inc. (OTCBB:VION... ...FDA issued a complete response letter to an NDA for Onrigin laromustine. The agency asked Vion... ...ages 60 and up with de novo, poor-risk acute myelogenous leukemia (AML). For the week, Vion...
...that the company conduct an additional randomized trial and addressed clinical pharmacology and manufacturing issues. Vion... ...would be needed for the sulfonyl hydrazine DNA alkylating agent (see BioCentury, Sept. 7). Vion Pharmaceuticals Inc. (OTCBB:VION...
...had previously said that it does not have sufficient funds for a new randomized trial. Vion... ...II testing for myeloproliferative disorders and Phase I testing for solid tumors. At Sept. 30, Vion... ...in cash and a nine-month operating loss of $14.1 million (see BioCentury, Oct. 19). Vion Pharmaceuticals Inc. (OTCBB:VION...