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.

TQB-2223 overview

Sym-022 is under development for the treatment of advanced/ unresectable or metastatic solid tumor malignancies and lymphomas, bile duct cancer (cholangiocarcinoma), advanced or metastatic esophageal squamous cell carcinoma, metastatic biliary tract carcinoma including adenocarcinoma of the intra- and/or extra-hepatic bile ducts, hepatocellular carcinoma and gallbladder carcinoma. It is administered through the intravenous route. It is a recombinant, fully human antibody. The drug candidate acts by targeting lymphocyte activation gene 3 (LAG-3). It is developed based on sympress platform technology.

It was under development for the treatment of small-cell lung cancer, transitional cell cancer (urothelial cell cancer), bladder cancer, endometrial cancer.

Chia Tai Tianqing Pharmaceutical Group overview

Chia Tai Tianqing Pharmaceutical Group (CTTQ) subsidiary of Sino Biopharmaceutical Ltd, is a pharmaceutical company that offers integrated R&D, manufacturing, marketing, sales and distribution services. The company manufacture prescription medicines in various core therapeutic areas, including liver diseases, oncology, respiratory diseases, antibiotics and diabetes. CTTQ produces dosage forms such as freeze-dried powder, large and small volume injections, hard capsules, sheet pills, granules, powders, soft capsules, pills, ointments, creams, pastes, gels, transdermal patches and herbal extracts, and others. It conducts research activities in the areas of anti-tumor, and liver disease. The company operates through its technology and research and development centers in Jiangsu. Its APIs and FDFs are sold to all major continents including Americas, Europe, Asia, and Africa. CTTQ is headquartered in Lianyungang, Nanjing, China.

For a complete picture of TQB-2223’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 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.