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CYDY News and Press, CytoDyn Inc From 07/19/21

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Company Name: CytoDyn Inc
Stock Symbol: CYDY
Market: OTC
Website: cytodyn.com

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CYDY - CytoDyn Announces Preliminary Results from 30 mTNBC Patients Treated with Leronlimab. Decreases in CAMLs after 4 Doses of Leronlimab were Identified in Over 70% of Patients and were Associated with a 450% Significant Increase in Overall Survival at 12-Mon

VANCOUVER, Washington, July 19, 2021 (GLOBE NEWSWIRE) -- 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, announced today strong preliminary resul...

CYDY - CytoDyn advances leronlimab into Phase 2 stage in breast cancer trial

MicroStockHub/iStock via Getty Images CytoDyn (CYDY) says that its clinical development of leronlimab in combination with chemotherapy, carboplatin for the treatment of metastatic triple-negative breast cancer (mTNBC) has progressed from Phase 1b stage to a Phase 2 trial. Leronlimab...

CYDY - CytoDyn's Trial for Metastatic Triple-Negative Breast Cancer Demonstrates Safety with 350 mg, 525 mg and 700 mg Dosages; Officially Advances to Phase 2 from Phase 1b

CytoDyn anticipates preliminary efficacy data regarding potential responders in metastatic triple-negative breast cancer in approximately two weeks VANCOUVER, Washington, July 12, 2021 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTCQB: CYDY) ("CytoDyn" or the "Company"), a late-stage biot...

CYDY - CytoDyn Granted a Significant Patent by USPTO for Methods of Treating Coronavirus Infection with Leronlimab

VANCOUVER, Washington, July 06, 2021 (GLOBE NEWSWIRE) -- 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, announced today its drug candidate, le...

CYDY - CytoDyn submits dose justification report to FDA for leronlimab BLA in HIV

CytoDyn (CYDY) has submitted a dose justification report to the FDA, which will be followed by an official submission to CytoDyn’s IND.The dose justification report is a key component for the BLA and includes receptor occupancy analysis, among other factors, to determine the optimal ma...

CYDY - CytoDyn Submits Dose Justification Report to FDA to Begin Overcoming Deficiencies in its BLA for HIV

Management works to advance its BLA filing seeking FDA approval for leronlimab as a combination therapy for HIV patients while continuing its evaluation of other potential indications VANCOUVER, Washington, July 01, 2021 (GLOBE NEWSWIRE) -- CytoDyn Inc. (OTCQB: CYDY) , ("CytoD...

CYDY - Group of Cytodyn Stockholders Nominates Five Highly Qualified Director Candidates to Replace Board Responsible for Mismanagement and Value Destruction

Change Desperately Needed to Reverse Operational Failures, Underperformance, and Realize Significant Value Potential of Company’s Leronlimab Drug Sends Letter to Stockholders Urging Support of Nominees With Deeply Relevant Experience and Critical Independent Persp...

CYDY - Merck Desperate To Get Back In Coronavirus Race, With A Pill

Competitors beating Merck for COVID-19 treatment. Proof of Molunupiravir efficacy is elusive. Merck's track record in this area is poor. For further details see: Merck Desperate To Get Back In Coronavirus Race, With A Pill

CYDY - Lawsuit for Investors in CytoDyn Inc. (OTCQB:CYDY) shares announced by Shareholders Foundation

SAN DIEGO, CA / ACCESSWIRE / June 22, 2021 / The Shareholders Foundation, Inc. announces that a lawsuit is pending for certain investors in CytoDyn Inc. shares. Investors, who purchased shares of CytoDyn Inc. (OTCQB:CYDY) prior to March 2020 and continue to hold any of their (OTCQB:CYDY) sh...

CYDY - CytoDyn posts preliminary results from COVID-19 long-haulers study

CytoDyn ([[CYDY]]) announces preliminary results after unblinding the data from its COVID-19 long-haulers clinical trial.The purpose of the trial was to assess the safety and efficacy of leronlimab administered as weekly subcutaneous injection in subjects experiencing prolonged symptoms (>...

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