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BioWorld - Monday, June 15, 2026
Home » Authors » Cormac Sheridan

Cormac Sheridan

Articles

ARTICLES

Santhera, Takeda Extend Pact For Idebenone In DMD

Aug. 8, 2007
By Cormac Sheridan
Santhera Pharmaceuticals AG licensed European rights to idebenone in Duchenne muscular dystrophy (DMD) to Takeda Pharmaceutical Co. Ltd., in return for an up-front payment of €2 million, another €18 million (US$24.6 million) in milestones and royalties on eventual product sales. (BioWorld International)
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Rheoscience, Dr. Reddy's Move Balaglitazone Into Phase III Trial

Aug. 8, 2007
By Cormac Sheridan

GPC Biotech Withdraws Satraplatin NDA - For Now

Aug. 1, 2007
By Cormac Sheridan

Fusion Raises $2.4M To Build Antibody Development Pipeline

Aug. 1, 2007
By Cormac Sheridan

GPC Biotech Withdraws Satraplatin NDA - For Now

Aug. 1, 2007
By Cormac Sheridan

Fusion Raises $2.4M To Build Antibody Development Pipeline

Aug. 1, 2007
By Cormac Sheridan

Strong Data Has Trion, Fresenius Optimistic About Removab Filing

July 25, 2007
By Cormac Sheridan
Trion Pharma GmbH and its partner Fresenius Biotech GmbH remain on track to file for approval in Europe this year for their 'trifunctional antibody' removab (catumaxomab), which attained the primary endpoint and several secondary endpoints in a Phase II/III clinical trial in advanced cancer patients with malignant ascites. (BioWorld International)
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Strong Data Has Trion, Fresenius Optimistic About Removab Filing

July 25, 2007
By Cormac Sheridan
Trion Pharma GmbH and its partner Fresenius Biotech GmbH remain on track to file for approval in Europe this year for their 'trifunctional antibody' removab (catumaxomab), which attained the primary endpoint and several secondary endpoints in a Phase II/III clinical trial in advanced cancer patients with malignant ascites. (BioWorld International)
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GlycoVaxyn Gets $9.6M In Series A For Conjugated Vaccines

July 18, 2007
By Cormac Sheridan

Arpida Gains On Iclaprim Data From Second cSSSI Pivotal Trial

July 18, 2007
By Cormac Sheridan
Arpida AG remains on track to file for marketing approval for the intravenous antibiotic iclaprim in the U.S. and Europe before the year-end, following positive topline data from a second pivotal trial of the compound in patients with complicated skin and skin structure infection (cSSSI). (BioWorld International)
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View All Articles by Cormac Sheridan

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