Decitabine is under clinical development by Dong Wha Pharma and currently in Phase I for Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer). According to GlobalData, Phase I drugs for Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer) have a 90% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Decitabine’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.
Decitabine overview
Decitabine (DW-1018) is under development for the treatment of HER2 negative breast adenocarcinoma and metastatic, locally advanced breast cancer. The drug candidate is administered by intravenous route. Decitabine acts by targeting DNA methyltransferase 1 (DNMT1).
Dong Wha Pharma overview
Dong Wha Pharma (Dongwha Pharm) is a pharmaceutical company that offers generic products. The company offers ethical drugs, over-the-counter products, quasi-drugs, health foods and medical devices. Its products comprise clzapine tablets, valaboom, aripico tablets, intrinsic bubble cleanser, shampoos, tonic, danke cream and lotion. Dongwha Pharm provides muscle relaxants, antibiotics, dermatological, vitamins, anti-smoking agents, hepatic protectors, moega3 capsules, nutrients, tonics, cold remedies, mouth and teeth products and others. The company offers and drugs for the alimentary system, cardiovascular and metabolic system, respiratory system, nervous system and urinary system. It operates in Incheon, Uiwang-si, Wonju-si, Dong-gu, Cheongju-si, and others. Dongwha Pharm is headquartered in Seoul, South Korea.
For a complete picture of Decitabine’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.
