- Tonix Pharmaceuticals Holding Corp TNXP and privately-held OyaGen Inc have entered into an exclusive worldwide licensing agreement for TNX-3500 (sangivamycin, formerly OYA1) for the treatment of COVID-19 and potentially other viral disorders.
- Under the terms of the agreement, Tonix will conduct further studies to test the safety and efficacy of TNX-3500 in treating COVID-19.
- The financial details of the deal were not disclosed.
- TNX-3500 (sangivamycin) has demonstrated broad-spectrum antiviral activity in laboratory-based assays against the coronaviruses SARS-CoV-2 and MERS-CoV. Sangivamycin also demonstrated that it acts as a dual target-specific antiviral against filoviruses such as the Ebola virus in cell culture infectivity studies.
- Tonix is also developing a COVID-19 vaccine, TNX-1800, which is currently in preclinical studies.
- Last month, the company reported interim data demonstrating that all eight of the TNX-1800 vaccinated animals made anti-CoV-2 neutralizing antibodies against none in the control arm and placebo group after a single dose.
- The human study will start in the second half of this year.
- Also, Tonix announced its plans to develop a diagnostic skin test, TNX-2100, to measure the delayed-type hypersensitivity reaction to SARS-CoV-2.
- Price Action: TNXP shares are up 9.2% at $1.07 in the premarket trading session on the last check Monday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in