VXAG-1.1NN is under clinical development by Vaxart and currently in the Phase II in clinical pathway. The characteristics of the clinical trial as well as other attributes related to the drug, regulations, and company play a fundamental role in ensuring the likelihood of transition that the drug moves from its current development stage to next.

According to GlobalData, the latest event to affect VXAG-1.1NN’s likelihood of approval (LoA) and phase transition for Norovirus Infections took place on 13 Jan 2022, which increased the likelihood that the drug progresses to the next phase in its clinical pathway.

GlobalData uses proprietary data and analytics to provide a complete picture of this assessment in their VXAG-1.1NN Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.

VXAG-1.1NN overview

VXAG-1.1NN is under development for the prevention of norovirus infections. It is administered through oral route as a tablet. The drug candidate is a recombinant vector vaccine and it is developed based on tablet vaccine technology. The delivery platform consists of an adenovirus type 5 vector (Ad5)-adjuvant combination which is used with a recombinant antigen to create vaccines for oral administration.

Vaxart overview

Vaxart, formerly Aviragen Therapeutics, is a clinical-stage pharmaceutical company that develops oral recombinant vaccines based on its proprietary oral vaccine platform, using state-of-the-art recombinant technology. The platform enables the company to develop oral versions of currently available vaccines, and design recombinant vaccines for new indications. The company is developing prophylactic vaccine candidates for a range of infectious diseases, including norovirus infection, seasonal influenza, respiratory syncytial virus (RSV) infection, and coronavirus (COVID-19) disease. It is also developing a therapeutic immune-oncology vaccine, which targets cervical cancer, and dysplasia caused by human papilloma virus (HPV). Vaxart is headquartered in San Francisco, California, the US.

Quick View VXAG-1.1NN LOA Data

Report Segments
  • Innovator
Drug Name
  • VXAG-1.1NN
Administration Pathway
  • Oral
Therapeutic Areas
  • Infectious Disease
Key Developers
Highest Development Stage
  • Phase II

GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.