NanoViricides, Inc. (NASDAQ:NNVC) |
- NanoViricides, Inc. filed its Annual Report on Form 10-K with the SEC, detailing the progress of its antiviral drug NV-387.
- The company is conducting Phase II trials for NV-387 to treat Mpox and Ebola, noting that there is currently no approved drug for Mpox Clade I or Clade II.
- Approval of the drug would provide a critical medical countermeasure for viral infections that cause outbreaks, epidemics, and pandemics.
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NanoViricides, Inc. Has Filed its Annual Report: Broad-spectrum Antiviral NV-387 Is In Phase II Clinical Trials - BioSpace
β’ NanoViricides, Inc. filed its annual report detailing the Phase II clinical trials for NV-387, a broad-spectrum antiviral drug. β’ The company is targeting unmet medical needs for MPox and Ebola, noting that no approved drugs currently exist for the treatment of MPox Clade I or Clade II.
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Read original Β· statnews.com
StatnewsTop U.S. Health Officials to Address Rare Disease Leaders at 2026 NORD Breakthrough Summit in Washington, D.C.
β’ Three top U.S. federal health officials will join over 900 rare disease leaders at the 2026 NORD Rare Diseases and Orphan Products Breakthrough Summit from October 25β27 in Washington, D.C. β’ Attendees will include Kyle Diamantas, the Acting Commissioner of Food and Drugs at the U.S. Food and Drug Administration.
Read original Β· prnewswire.comGastein health conference gets underway β POLITICO
β’ The European Commission adopted a proposal on Monday for a Council recommendation to combat cardiovascular diseases. β’ These heart-related conditions are the leading cause of death in Europe, claiming 1.7 million lives annually.
Read original Β· politico.euMedical News Publisher
β’ A phase 3 clinical trial found that delivering focused radiation therapy over three to five sessions after brain metastasis surgery reduced cancer recurrence compared to a single session. β’ This study represents the first randomized trial to directly compare these two specific radiation delivery schedules.
Read original Β· newswise.comPAHO marks 50 years of strengthening health emergency preparedness and response in the Americas - PAHO/WHO
β’ The Pan American Health Organization (PAHO) marked the 50th anniversary of its Health Emergencies Program on September 28, 2026. β’ Regional coordination mechanisms were activated within hours to support national and international responses after two powerful earthquakes struck Venezuela in June 2026.
Read original Β· paho.orgAI can accelerate medical research, experts say - Oman Observer
β’ Experts at the University Medical City's Second Annual Scientific Research Day discussed how artificial intelligence can accelerate medical research and improve healthcare decision-making. β’ The participants highlighted that AI technology can support more precise treatment for patients.
Read original Β· omanobserver.omCDC Reinstates COVID-19 Vaccine Recommendations Amid Pending Lawsuit
β’ The Centers for Disease Control and Prevention updated its online immunization guidance in late September 2026 to recommend COVID-19 vaccinations for specific groups. β’ The agency now recommends the vaccine for all adults 18 and older and for children aged 6 months to 17 years who are moderately to severely immunocompromised.
Read original Β· newstarget.com
NewstargetThe Americas are making progress in health but must accelerate action on emerging challenges, says PAHO Director - PAHO/WHO
β’ Dr. Jarbas Barbosa, Director of the Pan American Health Organization (PAHO), called for accelerated action on emerging health challenges during the opening of the 63rd Directing Council. β’ The Director identified primary health care, vaccination, digital health, and emergency preparedness as the region's top priorities.
Read original Β· paho.orgManaged Care Considerations and Economic Implications of Vaccination Practices
β’ The FDA approved the once-daily pill Baricitinib for adolescents aged 12 and older suffering from severe alopecia areata, a condition causing patchy hair loss. β’ A large trial found a new type of eye drug performed as well as standard anti-VEGF therapy for treating diabetic macular edema, which affects 1.6 million Americans.
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β’ Nearly 600 postmarket studies for FDA-approved drugs and biologics are currently behind their scheduled completion dates. β’ These delayed studies are required safety and efficacy evaluations that the FDA mandates after a medicine is already available for sale.
Read original Β· inkl.com
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