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RVVTF / Revive Therapeutics to seek data safety board nod for emergency use application to FDA for Bucillamine in COVID-19 in 2Q

Revive Therapeutics to seek data safety board nod for emergency use application to FDA for Bucillamine in COVID-19 in 2Q
Revive Therapeutics Ltd (CSE:RVV, OTCQB:RVVTF) has provided an update on the company's US Food and Drug Administration (FDA) Phase 3 clinical trial (NCT04504734) to evaluate the safety and efficacy of Bucillamine, an oral drug with anti-inflammatory and antiviral properties, in patients with mild-to-moderate coronavirus (COVID-19.) The Toronto-based life sciences company said it now expects to complete full enrollment in second-quarter 2022 and to also submit the study data for 800 subjects to the data safety monitoring board (DSMB) to seek its approval to proceed with an Emergency Use Authorization (EUA) application to the FDA. Read More
Posted: Mar 29 2022, 09:59
Author Name: Proactive Investors
Views: 111532

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Revive Therapeutics Ltd (CSE:RVV, OTCQB:RVVTF). said it has filed a provisional patent application for the use of Bucillamine as a potential treatment more_horizontal

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Revive Therapeutics Ltd (CSE:RVV, OTCQB:RVVTF) has issued an update on the Phase 3 trial of its drug Bucillamine in patients with mild to moderate COV more_horizontal

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Revive Therapeutics Ltd (CSE:RVV, OTCQB:RVVTF) saidĀ its Phase 3 clinical trial evaluating Bucillamine, an oral drug with anti-inflammatory and antivi more_horizontal

Revive Therapeutics says date set for independent Data and Safety Monitoring Board meeting for its Bucillamine Phase 3 clinical trial

By Proactive Investors
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Revive Therapeutics says date set for independent Data and Safety Monitoring Board meeting for its Bucillamine Phase 3 clinical trial

Revive Therapeutics Ltd (CSE:RVV, OTCQB:RVVTF) has revealed that the independent Data and Safety Monitoring Board (DSMB) meeting for its Bucillamine P more_horizontal

Revive Therapeutics to review next steps for Phase 3 Bucillamine study in COVID-19 patients

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