BI-905711 is under clinical development by Boehringer Ingelheim International and currently in Phase I for Gallbladder Cancer. According to GlobalData, Phase I drugs for Gallbladder Cancer does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the BI-905711 LoA Report. 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.
BI-905711 overview
BI-905711 is under development for the treatment of metastatic colorectal adenocarcinoma, gastric adenocarcinoma, esophageal adenocarcinoma, pancreatic ductal adenocarcinomas. metastatic adenocarcinoma of pancreas, cholangiocarcinoma and gallbladder cancer. It is administered by parenteral route as powder for solution. The therapeutic candidate is a tetravalent bi-specific monoclonal antibody which acts by targeting TNF related apoptosis inducing ligand receptor 2 (TRAILR2) and cadherin 17 (CDH17).
Boehringer Ingelheim International overview
Boehringer Ingelheim International (Boehringer), a subsidiary of CH Boehringer Sohn AG & Co KG, is a pharmaceutical company that develops, manufactures and markets pharmaceuticals, parasiticides, vaccines and therapeutics for unmet medical needs. It offers a wide range of products including human diseases, animal health care products and biopharmaceuticals. The company’s products are used for the treatment central nervous system disorders, cardiometabolic diseases, respiratory diseases, cancer, immunology, and retinal diseases among others. It also offers animal healthcare products for swine, ruminant, poultry, horses and pets among others. Boehringer is headquartered in Ingelheim, Rheinland-Pfalz, Germany.
For a complete picture of BI-905711’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.
