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Revive Therapeutics Provides Update on Phase 3 Clinical Trial for Bucillamine in COVID-19

by rvvadmin | Mar 29, 2022 | 2022

Expected to seek DSMB approval to proceed with EUA application to the FDA in Q2-2022 Ongoing regulatory package activities for submission to international regulatory authorities for drug approvals TORONTO, March 29, 2022 – Revive Therapeutics Ltd. (“Revive” or...

HAVN Life Secures Purchase Order for Controlled Substance Sale to Revive Therapeutics Ltd. for Use in Clinical Research

by rvvadmin | Feb 24, 2022 | 2022

The naturally derived GMP psilocybin will be exported through distribution partner Mycrodose Therapeutics Inc. to the University of Wisconsin-Madison, Contract Research Organization for Revive Therapeutics VANCOUVER, BC, Feb. 24, 2022  – HAVN Life Sciences...

Revive Therapeutics Receives FDA Orphan Drug Designation for Bucillamine in the Prevention of Ischemia-Reperfusion Injury During Liver Transplantation

by rvvadmin | Feb 15, 2022 | 2022

TORONTO, Feb. 15, 2022 – Revive Therapeutics Ltd. (“Revive” or the “Company”) (OTCQB: RVVTF) (CSE: RVV) (FRANKFURT:31R), a specialty life sciences company focused on the research and development of therapeutics for medical needs and rare disorders, is pleased to...

Revive Therapeutics Provides Update on Phase 3 Clinical Trial for Bucillamine in COVID-19

by rvvadmin | Feb 14, 2022 | 2022

Ethics Committee approval to proceed with Phase 3 clinical trial in Turkey 13 clinical sites selected to date in Turkey TORONTO, Feb. 14, 2022 – Revive Therapeutics Ltd. (“Revive” or the “Company”) (OTCQB: RVVTF) (CSE: RVV) (FRANKFURT:31R), a specialty life...

Revive Therapeutics Provides Update on Phase 3 Clinical Trial for Bucillamine in COVID-19

by rvvadmin | Jan 18, 2022 | 2022

701 subjects dosed to date Initiating enrollment activities in Turkey as part of its clinical diversification plans to support global regulatory approvals On-track to complete enrollment in Q1-2022 and FDA submission thereafter Commencing regulatory package activities...
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