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CytoDyn Inc says published paper shows leronlimab activity against 4-class drug resistant HIV-1

Nader Pourhassan, CytoDyn’s CEO, noted that leronlimab’s potential role in cancer treatment could help HIV patients with a long history of.

United kingdomBritish columbiaNader pourhassanSanta maria annunziataScotta kellyRaffaele vitaUniversity of rome tor vergataUniversity of perugiaDrug administrationCytodyn incLazzaro spallanzani national institute for infectious diseasesSalute universityUniversity of sienaUniversity of bresciaUniversity of milanBritish columbia based

Leronlimab 14-Week, NASH Clinical Trial Met Primary Endpoint (PDFF) and Secondary Endpoint (cT1) for

Primary endpoint (PDFF) was achieved in both Intention to Treat and Per Protocol PopulationsVANCOUVER, Wash. (BUSINESS WIRE) CytoDyn Inc. (OTCQB: CYDY) ("CytoDyn" or the "Company"), a late-stage biotechnology company developing leronlimab, a CCR5 antagonist with the potential for multiple therapeutic indications,.

United kingdomUnited statesBritish columbiaChristopherp recknorNader pourhassanExchange commissionDrug administrationCytodyn incPer protocolSenior executive vice presidentClinical operationsChief executive officerNonalcoholic steatohepatitisCytodyn fast trackHuman immunodeficiency virusFast track

CytoDyn Receives Positive Response From FDA in Regard to its Phase 3, Registrational Trial in COVID-19 Critically Ill Population

Press release content from Business Wire. The AP news staff was not involved in its creation.

British columbiaUnited statesNader pourhassanDan zacchei joe germaniExchange commissionDrug administrationCytodyn incSloane companyInvasive mechanical ventilationExtracorporeal membrane oxygenationChief executive officerSpecial permitCytodyn fast trackHuman immunodeficiency virusFast trackBiologics license application

CytoDyn Inc receives positive response from US FDA for conducting a Phase III trial in critically ill COVID-19 pneumonia patients

The trial will be performed in combination with the standard of care for critically ill patients with COVID-19 pneumonia with the need for.

Nader pourhassanDrug administrationCytodyn incInvasive mechanical ventilationExtracorporeal membrane oxygenationSpecial permitCytodyn fast trackHuman immunodeficiency virus

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

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