HZB-0071 is under clinical development by Heilongjiang ZBD Pharmaceutical and currently in Phase I for Gastric Cancer. According to GlobalData, Phase I drugs for Gastric Cancer have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how HZB-0071’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.
HZB-0071 overview
HZB-0071 is under development for the treatment of adenocarcinoma, gastric cancer and unspecified cancer. It acts by targeting protein kinase B ( AKT).
Heilongjiang ZBD Pharmaceutical overview
Heilongjiang ZBD Pharmaceutical (ZBD Pharmaceutical) develops pharmaceutical products. The company offers various products which include acanthopanax senticosus injection, astragalus injection, shuxuening Injection for cardiovascular treatment; yanhuning injection, norfloxacin and clindamycin hydrochloride capsules for typhoid, respiratory tract infections and anaerobic bacteria; compound paracetamol capsules, Quinlan oral liquid for fever, cough and sore throat; bone peptide injection and hongbao tablets for fracture healing, bone pain and osteoarthritis; pediatric hot quick clear syrup for purging fire and swallowing; lingua plus oral solution and motherwort granules for treatment of irregular menstruation and calcium deficiency. ZBD Pharmaceutical is headquartered in Harbin, Heilongjiang, China.
For a complete picture of HZB-0071’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.
