CytoDyn announces FDA has lifted clinical hold on leronlimab

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VANCOUVER, Washington, Feb. 29, 2024 — CytoDyn Inc. (OTCQB: CYDY) (“CytoDyn” or the “Company”), a biotechnology company developing leronlimab, a CCR5 antagonist with the potential for multiple therapeutic indications, announced today that the FDA has lifted the clinical hold on leronlimab. The Company is now free to proceed with its proposed HIV clinical trial exploring leronlimab and its effects on chronic inflammation.

CytoDyn’s CEO, Dr. Jacob Lalezari, stated, “We are excited that the clinical hold on leronlimab has been lifted by the FDA. CytoDyn is grateful for the FDA’s guidance on our protocol and we are excited to open a new chapter in the development of leronlimab as a therapy that provides clinical benefit by modulating chronic inflammation.”

Read the full press release here.

 

Source : CytoDyn Inc.

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