GLPG-3667 is under clinical development by Galapagos and currently in Phase II for Systemic Lupus Erythematosus. According to GlobalData, Phase II drugs for Systemic Lupus Erythematosus have a 39% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how GLPG-3667’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
GLPG-3667 overview
GLPG-3667 is under development for the treatment of inflammation and moderate to severe plaque psoriasis, dermatomyositis, psoriatic arthritis and ulcerative colitis. The drug candidate is a small molecule. It is administered by oral route. It acts by targeting nonreceptor tyrosine protein kinase (TYK2).
Galapagos overview
Galapagos is a clinical-stage biotechnology company that specializes in the discovery and development of small-molecule medicines. The company conducts clinical trials in several areas, including inflammatory indications, cystic fibrosis, fibrosis and osteoarthritis. Its pipeline products include 5101, 5201, 5301 and 3667 for the indications of non-hodgkin’s lymphoma, chronic lymphocytic leukemia, multiple myeloma, systemic lupus erythematosus, dermatomyositis and other rare diseases. Galapagos collaborates with various partners and alliances to accelerate pipeline development. It operates in Belgium, the Netherlands, the US, Switzerland, France, Germany, Finland, Norway, Austria and Ireland, among others. Galapagos is headquartered in Mechelen, Belgium.
For a complete picture of GLPG-3667’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.
