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CytoDyn Inc completes submission of all major sections of CMC to FDA for HIV Biologics License Application

This CMC is a critical part of the biotech s Biologics License Application (BLA) for HIV - the request for permission to commercialize a product

Nitya rayNader pourhassanChris recknorCytodyn incFood drug administrationDrug administrationBiologics license application

CytoDyn Inc reveals very strong updated results for cancer patients receiving its flagship drug leronlimab

A 12-month analysis of 28 metastatic triple-negative breast cancer patients receiving leronlimab suggests an increase of 3,600% in 12-month.

United statesBritish columbiaNitya rayNader pourhassanChris recknorCreatv microtech incCato researchDrug administrationCytodyn incMetastatic triple negative breast cancerCompassionate use studyProgression free survivalCreatv microtechChief operating officerBreakthrough therapyUnited states food

CytoDyn Reports Preliminary Results from First Five Patients in Phase 2 NASH Open Label

Press release content from Globe Newswire. The AP news staff was not involved in its creation.

United statesBritish columbiaNader pourhassanDan zacchei joe germaniMelissa carlsonChris recknorCompany board of directorsDrug administrationCytodyn incExchange commissionAlliance advisorsCato researchSloane companySenior executive vice presidentClinical operationsChief executive officer

Senhwa Presents Positive Initial Data from Phase 2 Clinical Trial of Silmitasertib (CX-4945) in Moderate COVID-19 Patients At the ISIRV-WHO Conference

Statistically significant 133% faster time to COVID-19 clinical symptoms recovery versus standard of care (SOC)/best supportive care. Statistically significant.

United statesSan diegoSenhwa biosciencesSenhwa bioscienceChris recknorSenhwa biosciences incUs national institute of healthHuman servicesBiomedical advanced researchUs department of healthDevelopment authorityAdvanced researchCasein kinaseBest supportive careEmergency useFurther study

CytoDyn Receives Clearance from Brazil s ANVISA to Commence Phase 3 Trial for Severe COVID-19 Patients | Business

CytoDyn Receives Clearance from Brazil s ANVISA to Commence Phase 3 Trial for Severe COVID-19 Patients | Business
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United statesBritish columbiaNader pourhassanChris recknorExchange commissionHead of clinical developmentAcademic research organizationDrug administrationCytodyn incNacional de vigilAlbert einstein israelite hospitalChief operating officerClinical developmentLatin americaChief executive officerCytodyn fast track

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