CytoDyn Inc. (OTCMKTS:CYDY) Files An 8-K Regulation FD Disclosure
Item 7.01 Regulation FD Disclosure.

CytoDyn Inc. Exhibit
EX-99.1 2 d610798dex991.htm EX-99.1 EX-99.1 Exhibit 99.1   CytoDyn Announces Productive Pre-BLA Meeting with FDA for PRO 140 Combination Therapy – Rolling BLA Submission Starting as Early as the End of 2018 – FDA Provides Guidance on Ongoing Requirements VANCOUVER,…
To view the full exhibit click here

About CytoDyn Inc. (OTCMKTS:CYDY)

CytoDyn Inc. is a clinical-stage biotechnology company. The Company is focused on the clinical development and commercialization of humanized monoclonal antibodies to treat Human Immunodeficiency Virus (HIV) infection. The Company’s lead product candidate, PRO 140, belongs to a class of HIV therapies known as entry inhibitors that block HIV from entering into and infecting certain cells. The Company’s product pipeline also includes Cytolin and CytoFeline. Cytolin is a mouse monoclonal antibody developed to identify a specific type of immune cell called a cytotoxic T cell, or cytotoxic T lymphocyte (CTL). CytoFeline is an anti-lymphocyte function-associated antigen-1 (LFA-1) antibody for the treatment of Feline Immunodeficiency Virus (FIV) infection. PRO 140 blocks HIV from entering a cell by binding to a molecule called C-C chemokine receptor type 5 (CCR5). The Company has finished Phase II clinical trials for PRO 140 with demonstrated antiviral activity in man.