Bevacizumab-vikg is under clinical development by Outlook Therapeutics and currently in Phase III for Diabetic Macular Edema. According to GlobalData, Phase III drugs for Diabetic Macular Edema have a 67% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Bevacizumab-vikg’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Bevacizumab-vikg overview

Bevacizumab-vikg is under development for the treatment of wet age related macular degeneration, diabetic macular edema, branch retinal vein occlusion and other retinal diseases. The drug candidate is a monoclonal antibody developed based on Biosymphony platform. It is administered through intravitreal route in the form of solution. It acts by targeting vascular endothelial growth factor A (VEGFA).

Outlook Therapeutics overview

Outlook Therapeutics is a biopharmaceutical company. It develops, manufactures, and commercializes biosimilar products in the areas of ophthalmology. The company pipeline product includes ONS-5010 Lytenava, Repackaged Bevacizumab, Ophthalmic anti vegf among others. The company is investigating its lead product candidate, ONS-5010 an ophthalmic formulation of bevacizumab-VIKG intended to treat wet age-related macular degeneration (AMD), diabetic macular edema (DME), branch retinal vein occlusion (BRVO) and other retinal diseases. It works in collaboration with biotechnology and pharmaceutical companies to develop its products. Outlook Therapeutics is headquartered in Cranbury, New Jersey, the US.

For a complete picture of Bevacizumab-vikg’s drug-specific PTSR and LoA scores, buy the report here.


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.