NanoDOX is under clinical development by Ology Bioservices and currently in Phase II for Wounds. According to GlobalData, Phase II drugs for Wounds does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the NanoDOX LoA Report. 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.
NanoDOX overview
NanoDOX is under development for the treatment of atopic dermatitis and wound healing. The drug candidate contains 1 percentage doxycycline monohydrate hydrogel. It is applied topically as a gel. It acts by targeting matrix metalloproteinase (MMP).
It was under development for the treatment of dermal ulcers such as diabetic ulcers of the foot and lower limbs, trauma.
Ology Bioservices overview
Ology Bioservices is an US based integrated biopharmaceutical company. The company provides contract development and manufacturing services. The company manufactures biopharmaceutical products which include vaccines, antibodies, protein therapies and medical devices.
For a complete picture of NanoDOX’s drug-specific PTSR and LoA scores, buy the report here.
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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 clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
