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Articles published by CytoDyn Inc.
CytoDyn Announces FDA Has Lifted Clinical Hold
February 29, 2024
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces Submission of Clinical Protocol to FDA and Initiation of Pre-Clinical Study in Glioblastoma
February 01, 2024
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Appoints Jacob Lalezari M.D. as CEO, Mitchell Cohen as Interim CFO
January 29, 2024
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces Webcast to Provide Company Update
December 07, 2023
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Appoints Jacob Lalezari M.D. as Interim CEO
November 21, 2023
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
November 2023 Letter to Shareholders
November 03, 2023
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces Company Updates and Investment Community Update Webcast
July 11, 2023
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces President Takes Medical Leave of Absence
May 24, 2023
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn to Hold Webcast to Provide a Company Update
April 05, 2023
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn to Hold Webcast to Discuss the Performance of Leronlimab in Clinical Trials and Recent Charges Against Former CEO
December 23, 2022
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn to Host R&D Update on Wednesday, December 7, 2022
November 22, 2022
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces Voluntary Withdrawal of BLA for HIV-MDR Due to CRO Data Management Issues
October 28, 2022
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces Appointment of Additional Directors with Industry Experience
October 20, 2022
From
CytoDyn Inc.
Via
GlobeNewswire
Tickers
CYDY
CytoDyn Announces Leadership Transition Plan to Support Regulatory Approval and Commercialization of Leronlimab
January 25, 2022
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Cancels Webcast and Live Q/A Scheduled for Today
January 13, 2022
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
Published Paper Indicates Leronlimab Shows Activity Against 4-Class Drug Resistant HIV-1 From Heavily Treatment Experienced (“HTE") Subjects
January 10, 2022
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
Leronlimab 14-Week, NASH Clinical Trial Met Primary Endpoint (PDFF) and Secondary Endpoint (cT1) for Per Protocol Population in 350 mg Weekly Dose
January 05, 2022
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Announces Favorable Ruling Granting Injunction Against Former CRO
December 22, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Receives Positive Response From FDA in Regard to its Phase 3, Registrational Trial in COVID-19 Critically Ill Population
December 21, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
NASH Phase 2 Trial Open-Label Portion Demonstrates Average 80 msec cT1 Reduction in 50% of Patients and Reduction of Nearly 50 msec in 80% of Patients
December 13, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Submits Protocol with the FDA for Phase 3 Registrational Trial of Leronlimab for Critically Ill COVID-19 Population
December 09, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Files for Expanded Access Use of Leronlimab for Multi-Drug Resistance HIV Patients
December 09, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn’s CRO in Brazil Met with ANVISA to Modify CD16 Trial for Critically Ill COVID-19 Patients to Expedite Interim Analysis After 51 Patients, Potentially in 1Q2022
December 08, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Submits CMC (Manufacturing) Section of HIV BLA to FDA Under Previously Authorized Rolling Review; Last (Clinical) Section Will Complete Full BLA Submission
December 01, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn’s Chairman, CMO, and Head of Business Development Dr. Scott A. Kelly to Present at World Antiviral Congress 2021 Beginning Tomorrow
November 29, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
Leronlimab (350 mg) Weekly Use for 14 Weeks in Open Label Arm of NASH Trial Produces Fibrosis Reduction as High as 93 msec Amongst First 15 Patients with Average Reduction of 24 msec
November 24, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Research Paper on Leronlimab Published in Frontiers in Immunology Journal
November 19, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
Health Canada Authorizes Emergency Use of Leronlimab for Treatment of First Triple-Negative Breast Cancer Patient in Canada
November 16, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Inc. Announces Adjournment of Annual Meeting of Shareholders to November 24, 2021 Due to Lack of Quorum
October 28, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
CytoDyn Announces Delaware Court Has Denied Activist Group’s Motion to Prevent Annual Meeting from Taking Place
October 20, 2021
From
CytoDyn Inc.
Via
Business Wire
Tickers
CYDY
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