Curated News
By: NewsRamp Editorial Staff
November 10, 2025
NanoViricides Wins Congo Approval for MPox Antiviral Trial
TLDR
- NanoViricides' NV-387 Phase II approval positions the company as a leader in antiviral therapy with potential to dominate treatment for up to 95% of human pathogenic viruses.
- NV-387 mimics human cells to trap and destroy viruses through nanoviricide technology, with Phase II trials now approved to assess safety and effectiveness against MPox.
- This broad-spectrum antiviral could transform global health by providing effective treatment for multiple viral diseases, potentially reducing suffering from infections like COVID, influenza and MPox.
- NanoViricides' virus-trapping nanotechnology represents a breakthrough approach that could revolutionize antiviral treatment similar to how antibiotics transformed bacterial disease management.
Impact - Why it Matters
This development matters because it represents a potential paradigm shift in how we combat viral diseases. Current antiviral treatments typically target specific viruses, leaving populations vulnerable to new outbreaks and pandemics. NV-387's broad-spectrum approach could provide a universal defense mechanism against multiple viral threats, much like antibiotics work against various bacterial infections. In a world increasingly facing emerging viral threats like MPox, COVID-19, and future pandemics, a successful broad-spectrum antiviral could transform public health preparedness, reduce treatment development timelines for new viruses, and provide healthcare systems with versatile tools to combat multiple viral diseases simultaneously. For patients, this could mean faster access to effective treatments during outbreaks rather than waiting for virus-specific therapies to be developed.
Summary
NanoViricides, Inc. (NYSE American: NNVC) has achieved a significant regulatory breakthrough as the Democratic Republic of Congo's regulatory agency, ACOREP, has approved the initiation of a Phase II clinical trial for NV-387, the company's innovative antiviral drug candidate targeting MPox caused by hMPXV infection. This milestone represents a crucial step forward in the regulatory development pathway, with the trial set to evaluate both safety and effectiveness once final document submissions are completed. Dr. Anil R. Diwan, President and Executive Chairman, emphasized the importance of this achievement, highlighting NV-387's unique mechanism that mimics human cells to trap and destroy viruses. The company believes this drug could revolutionize antiviral therapy in a manner comparable to how antibiotics transformed bacterial disease treatment, potentially targeting up to 95% of human pathogenic viruses.
NanoViricides operates as a clinical-stage company creating special purpose nanomaterials for antiviral therapy through its novel nanoviricide technology platform. The company's business model involves licensing technology from TheraCour Pharma, Inc. for specific viral applications, with NV-387 serving as the lead drug candidate intended for development against multiple respiratory viral infections including RSV, COVID, Long COVID, Influenza, and MPOX/Smallpox. The company maintains a comprehensive portfolio targeting various viral diseases including Herpes, Shingles, HIV, Hepatitis C, and Ebola, among others. For investors seeking the latest updates, the company's newsroom at https://ibn.fm/NNVC provides ongoing information about NNVC developments within the broader InvestorBrandNetwork portfolio.
Source Statement
This curated news summary relied on content disributed by InvestorBrandNetwork (IBN). Read the original source here, NanoViricides Wins Congo Approval for MPox Antiviral Trial
