Altasciences完成Gimsilumab用于新冠肺炎（COVID-19）患者ARDS的一期研究
28 mars 2020 06h57 HE
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Altasciences Company Inc.
魁北克拉瓦尔, March 28, 2020 (GLOBE NEWSWIRE) --...
Altasciences Completes Phase I Study on Gimsilumab for ARDS in COVID-19
27 mars 2020 13h48 HE
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Altasciences Company Inc.
LAVAL, Quebec, March 27, 2020 (GLOBE NEWSWIRE) -- Altasciences has completed a Phase I study for the development of gimsilumab, a fully human monoclonal antibody that targets granulocyte-macrophage...
WPD Pharmaceuticals Provides 2019 Corporate Year End Review
08 janv. 2020 03h05 HE
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WPD Pharmaceuticals
VANCOUVER, British Columbia, Jan. 08, 2020 (GLOBE NEWSWIRE) -- Westcot Ventures Corp. (CSE: WBIO) (the “Company”), and its wholly-owned subsidiary WPD Pharmaceuticals sp. z.o.o (“WPD”), a clinical...
ObsEva SA Announces Completion of Patient Recruitment in IMPLANT 4 Phase 3 Clinical Trial of Nolasiban for Improving IVF Outcomes
04 juin 2019 01h00 HE
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ObsEva SA
Geneva, Switzerland and Boston, MA – June 4, 2019 – ObsEva SA (NASDAQ: OBSV / SIX: OBSN), a clinical-stage biopharmaceutical company focused on the development and commercialization of novel...
ObsEva SA Announces Initiation of Phase 3 EDELWEISS 2 and 3 Trials of Linzagolix for Endometriosis Associated Pain in U.S., Canada and Europe
09 mai 2019 01h00 HE
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ObsEva SA
Geneva, Switzerland and Boston, MA – May 9, 2019 – ObsEva SA (NASDAQ: OBSV / SIX: OBSN), a clinical-stage biopharmaceutical company focused on the development and commercialization of novel...
ObsEva SA reports additional positive Phase 3 results of IMPLANT 2 trial showing significant increase of Live Birth Rate (LBR) following IVF with Single Embryo Transfer (SET)
03 oct. 2018 01h00 HE
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ObsEva SA
Phase 3 IMPLANT 2 trial results showed Live Birth Rate increased by up to 35% with Nolasiban treatment Nolasiban safety profile not different from placebo in IMPLANT 2 European MAA submission...
Celixir announces US FDA approval of the IND application for cell therapy Heartcel
08 juin 2018 02h00 HE
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CELIXIR Plc
Celixir announces US FDA approval of the IND application for cell therapy HeartcelTM FDA IND and UK MHRA CTA approval both achieved in H1 2018 Potentially pivotal heart failure trial of up to 250...
3D Signatures Inc. Announces Closing of Second Tranche of Brokered Private Placement
22 déc. 2016 16h38 HE
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3D Signatures Inc
WINNIPEG, MB--(Marketwired - December 22, 2016) - NOT FOR DISTRIBUTION TO U.S. NEWSWIRE SERVICES OR FOR DISSEMINATION IN THE UNITED STATES 3D Signatures Inc. (TSX VENTURE: DXD) (the "Company" or...
3D Signatures Appoints Two Industry Specialists to Board Positions
09 déc. 2016 07h00 HE
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3D Signatures Inc.
WINNIPEG, MB--(Marketwired - December 09, 2016) - 3D Signatures Inc. (TSX VENTURE: DXD) (the "Company" or "3DS") is pleased to announce two additional strategic appointments to its Board of Directors...
Are You Ready to Be An Expert Witness?
14 avr. 2010 11h17 HE
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Author Judd Robbins
ASHLAND, OR--(Marketwire - April 14, 2010) - Judd Robbins did not get into computers to become an expert witness.
He has advanced degrees from UC Berkeley and the University of Michigan,...