Independent Data Monitoring Committee Recommends Marshall Edwards, Inc.'s OVATURE Trial Continue
12 nov. 2008 08h10 HE | Marshall Edwards, Inc.
NEW CANAAN, CT--(Marketwire - November 12, 2008) - The Independent Data Monitoring Committee (IDMC) constituted to oversee the conduct of the Phase III OVArian TUmor REsponse (OVATURE) Trial,...
Mi-Co's Mi-Forms Validated for FDA Regulation 21 CFR Part 11 Compliance
24 janv. 2008 10h13 HE | Mi-Co
RESEARCH TRIANGLE PARK, NC--(Marketwire - January 24, 2008) - Mi-Co, the mobile data capture software company, announced that its Mi-Forms e-forms system has been validated for compliance with FDA...
Pharmexa Files the First Phase III Application
01 févr. 2006 03h20 HE | Pharmexa A/S
HOERSHOLM, Denmark, Feb. 1, 2006 (PRIMEZONE) -- Pharmexa has filed an application to obtain approval to initiate the phase III trial with GV1001 in Ireland. Further applications will be filed in a...
ProtoKinetix CEO and Scientific Advisory Board to Meet in Paris to Discuss Preliminary Results of Third Party RECAF Validation Studies
15 avr. 2004 12h10 HE | ProtoKinetix, Incorporated
VANCOUVER, British Columbia, April 15, 2004 (PRIMEZONE) -- ProtoKinetix Inc. (OTCBB:PKTX), announces today that it has received a preliminary report from their new Director of Medical Research in...