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BioWorld - Friday, January 16, 2026
Home » Authors » Kim Coghill

Articles by Kim Coghill

Guilford Begins Phase III Program For Aquavan Injection In Sedation

May 11, 2004
By Kim Coghill
Guilford Pharmaceuticals Inc. on Monday said it initiated a Phase III development program for Aquavan Injection, a candidate for procedural sedation. (BioWorld Today)
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Guilford Begins Phase III Program For Aquavan Injection In Sedation

May 11, 2004
By Kim Coghill
Guilford Pharmaceuticals Inc. on Monday said it initiated a Phase III development program for Aquavan Injection, a candidate for procedural sedation. (BioWorld Today)
Read More

Adolor, GSK File First Section Of Entereg Rolling NDA In POI

May 10, 2004
By Kim Coghill
Adolor Corp. and partner GlaxoSmithKline plc submitted the first portion of a new drug application for Entereg, a candidate for the management of postoperative ileus. (BioWorld Today)
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Adolor, GSK File First Section Of Entereg Rolling NDA In POI

May 10, 2004
By Kim Coghill
Adolor Corp. and partner GlaxoSmithKline plc submitted the first portion of a new drug application for Entereg, a candidate for the management of postoperative ileus. (BioWorld Today)
Read More

ISTA Receives Approval For Vitrase As Spreading Agent

May 7, 2004
By Kim Coghill
ISTA Pharmaceuticals Inc. won FDA approval of Vitrase for use as a spreading agent to facilitate the dispersion and absorption of other drugs. Meanwhile, the firm is awaiting approval on an earlier new drug application for Vitrase as a single injection to the eye for vitreous hemorrhage. (BioWorld Today)
Read More

ISTA Receives Approval For Vitrase As Spreading Agent

May 7, 2004
By Kim Coghill
ISTA Pharmaceuticals Inc. won FDA approval of Vitrase for use as a spreading agent to facilitate the dispersion and absorption of other drugs. Meanwhile, the firm is awaiting approval on an earlier new drug application for Vitrase as a single injection to the eye for vitreous hemorrhage. (BioWorld Today)
Read More

FDA's Annual Report States Goals For PDUFA III Reached

May 6, 2004
By Kim Coghill

FDA's Annual Report States Goals For PDUFA III Reached

May 6, 2004
By Kim Coghill

ODAC In Favor Of Safety Trials For Amgen, J&J EPO Products

May 5, 2004
By Kim Coghill
GAITHERSBURG, Md. - The Oncologic Drugs Advisory Committee generally agreed that it is reasonable to ask makers of Aranesp and Procrit to conduct placebo-controlled trials to assess possible adverse events. (BioWorld Today)
Read More

ODAC In Favor Of Safety Trials For Amgen, J&J EPO Products

May 5, 2004
By Kim Coghill
GAITHERSBURG, Md. - The Oncologic Drugs Advisory Committee generally agreed that it is reasonable to ask makers of Aranesp and Procrit to conduct placebo-controlled trials to assess possible adverse events. (BioWorld Today)
Read More
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