BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Duodenal Ulcer. According to GlobalData, Phase I drugs for Duodenal Ulcer have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how BR-6002’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
BR-6002 overview
BR-6002 is under development for the treatment of cardiovascular disease, gastric ulcers and duodenal ulcers. It is administered through oral route.
Boryung Pharmaceutical overview
Boryung Pharmaceutical (Boryung)is a pharmaceutical company. It manufactures and distributes pharmaceutical products including cardiovascular, anticancer and gastrointestinal drugs. The company offers products such as kanarb, gelfos, maxpim injection, mayact tablet, among others. The company’s product portfolio focusses on the chronical diseases including hypertension, dyslipidemia, diabetes, CNS disorders, and cancers. It also offers products including Dukarb Plus, Zepzelca, Finjuve Spray, among others. The company also provides marketed API along with anti-cancer injection facilities. Boryung is headquartered in Seoul, South Korea.
For a complete picture of BR-6002’s drug-specific PTSR and LoA scores, buy the report here.
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