New York, NY -- December 22, 2020 -- InvestorsHub NewsWire -- Traders News Source, a leading independent equity research and corporate access firm focused on small cap growth companies issues new research.

SAMM SOLUTIONS, INC. (DBA BTS Research) has been engaged by Enzolytics, Inc. (OTCPINK: ENZC) to conduct a toxicity study on the Company's Flagship compound ITV-1. The Company has previously tested the compound in successful Clinical Trials in Bulgaria, but FDA regulations require separate Toxicity tests before an Investigational New Drug process may begin in the United States. Harry Zhabilov, CSO stated " This is a big step for our organization, and we hope to be able to use most if not all of the information from our already successful Clinical Trials in Bulgaria to speed our attempt to meet the requirements in the US for approval."

The long phase 3 clinical trial conducted by Northwest Biotherapeutics, Inc. (OTCQB: NWBO) to evaluate its one and only immunotherapy candidate, DCVax-L, as a treatment for glioblastoma, concluded in October. Neither the Company nor any party other than the independent statisticians will have access to any unblinded data from the clinical trial at this stage.
"We are excited to be so close to the finish line now, after such a long road" commented Linda Powers, the Company's CEO. "We are hopeful that DCVax®-L can become an important new treatment option for patients who urgently need more and better treatments for Glioblastoma brain cancer."

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Vyrologix™, being developed by CytoDyn Inc. (OTCQB: CYDY) reached full enrollment in its Phase 3 registrational trial for patients with severe-to-critical COVID-19. The 390-patient data will be analyzed in approximately 28 days, with expected results to be announced shortly thereafter. CytooDyn’s Phase 2b/3 trial to evaluate the efficacy and safety of Vyrologix™, for patients with severe-to-critical COVID-19 indications is a two-arm, randomized, double blind, placebo controlled, adaptive design multicenter study.
CytoDyn completed enrollment of 390 patients in its Phase 2b/3 randomized clinical trial for the severe-to-critically ill COVID-19 population and expects to release results in mid-January 2021.


Innovation Pharmaceuticals Inc. (OTCQB: IPIX) is developing Brilacidin, a Host Defense Protein (HDP) mimetic representing a new class of drug with antiviral, anti-inflammatory, and anti-bacterial properties.
This week, the FDA has approved the Company’s Investigational New Drug (IND) application to proceed with initiation of a Phase 2 clinical trial of Brilacidin in hospitalized patients with COVID-19. With its unique HDP mimetic properties, Brilacidin has potential to exert antiviral activity across SARS-CoV-2 variants. The sudden emergence of highly contagious new variants of the coronavirus illuminates the urgent need for drugs, like Brilacidin, with a different mechanism of action from current antivirals to get this resilient virus under control.

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Innovation Pharmaceuticals (QB) (USOTC:IPIX)
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