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BioWorld - Thursday, April 30, 2026
Home » Authors » Nuala Moran

Articles by Nuala Moran

Phytopharm Gets Rights Back To P57 Due To Merger Talks

Aug. 7, 2002
By Nuala Moran

Vernalis, Roche Stop Phase I Study Due To Pharmacokinetics

Aug. 7, 2002
By Nuala Moran

Celltech Misses Main Endpoint In Phase III Crohn's Disease Trial

Aug. 7, 2002
By Nuala Moran
LONDON - Celltech Group plc failed to reach the primary endpoint in Phase III trials of CDP 571, a humanized antibody for the treatment of Crohn's disease, leaving the future of the compound hanging on discussions with regulators to see if approval can be granted for the management of disease flares.(BioWorld International)
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Phytopharm Gets Rights Back To P57 Due To Merger Talks

Aug. 7, 2002
By Nuala Moran

Celltech Misses Main Endpoint In Phase III Crohn's Disease Trial

Aug. 7, 2002
By Nuala Moran
LONDON - Celltech Group plc failed to reach the primary endpoint in Phase III trials of CDP 571, a humanized antibody for the treatment of Crohn's disease, leaving the future of the compound hanging on discussions with regulators to see if approval can be granted for the management of disease flares.(BioWorld International)
Read More

Vernalis, Roche Stop Phase I Study Due To Pharmacokinetics

Aug. 7, 2002
By Nuala Moran

OGS Gains European Approval, Partner For Gaucher's Product

July 31, 2002
By Nuala Moran

BresaGen, British Biotech See Setbacks Continue As E21R Fails

July 31, 2002
By Mark Lawson and Nuala Moran
SYDNEY, Australia - Unfavorable results from clinical trials have stopped another collaborative project involving an Australian biotech company, despite favorable preclinical trials. BresaGen Ltd. and British Biotech plc abandoned a collaborative agreement to develop E21R as a treatment for acute myeloid leukemia (AML). (BioWorld International)
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OGS Gains European Approval, Partner For Gaucher's Product

July 31, 2002
By Nuala Moran

OGS Gains European Approval, Partner For Gaucher's Product

July 29, 2002
By Nuala Moran
LONDON - Oxford GlycoSciences plc said Friday it received approval in Europe for Vevesca, an oral treatment for Gaucher's disease that was turned down by the FDA on June 24. (BioWorld Today)
Read More
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