PT-101 is under clinical development by Merck and currently in Phase II for Vitiligo. According to GlobalData, Phase II drugs for Vitiligo 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 PT-101 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.
PT-101 is under development for the treatment of ulcerative colitis, systemic lupus erythematosus, atopic dermatitis, non-segmental vitiligo and other autoimmune diseases. The drug candidate is tissue-specific immune modulators. It is administered through subcutaneous route. It was also under development for autoimmune liver disease, kidney diseases, type 1 diabetes and autoimmune skin conditions.
Merck is a biopharmaceutical company focused on the discovery, development, manufacturing and marketing of prescription medicines, biologic therapies, vaccines, and animal health products. It offers prescription products for therapy areas related to cardiovascular, cancer, immune disorders, infectious, respiratory, and diabetes. The company provides animal health products such as vaccines, poultry products, livestock products and aquaculture products. Merck sells medicines to drug wholesalers, retailers, hospitals, government agencies and managed health care providers; and animal health products to veterinarians, distributors and animal producers. The company and its subsidiaries operate in the Americas, Europe, the Middle East, Africa, Asia Pacific, and Latin America. Merck is known as MSD outside the US and Canada and is headquartered in Kenilworth, New Jersey, the US.
For a complete picture of PT-101’s drug-specific PTSR and LoA scores, buy the report here.