Buparlisib hydrochloride is under clinical development by Adlai Nortye Biopharma and currently in Phase I for Acute Lymphocytic Leukemia (ALL, Acute Lymphoblastic Leukemia). According to GlobalData, Phase I drugs for Acute Lymphocytic Leukemia (ALL, Acute Lymphoblastic Leukemia) have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Buparlisib hydrochloride’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.
Buparlisib hydrochloride overview
Buparlisib hydrochloride (BKM-120) is under development for the treatment of advanced solid tumors, relapsed or refractory thymomas, ovarian cancer, relapsed and refractory chronic lymphocytic leukemia, mantle cell lymphoma, follicular lymphoma, metastatic transitional cell cancer (urothelial cell cancer), cervical cancer, metastatic colorectal cancer, recurrent glioblastoma, relapsed and refractory acute myelogenous leukemia (AML), acute lymphoblastic leukemia (ALL) and pancreatic cancer, recurrent or metastatic head and neck squamous cell carcinoma and solid tumor. BKM-120 targets specific oral pan-class I phosphatidylinositol-3-kinase (PI3K).
It was also under development for thrombocythaemia myelofibrosis, HER2-positive breast cancer, myelofibrosis, post-polycythemia vera myelofibrosis (PPV-MF), newly diagnosed glioblastoma, metastatic hormone refractory prostate cancer, estrogen receptor positive and HER2-negative (ER+/HER2-) stage IV metastatic breast cancer and melanoma, advanced or metastatic squamous non-small cell lung cancer and non-small cell lung cancer, diffuse large B-Cell lymphoma, gastrointestinal stromal tumor (GIST), thyroid cancer (third line therapy), triple negative breast cancer (TNBC) and prostate cancer
Adlai Nortye Biopharma overview
Adlai Nortye Biopharma (Adlai Nortye) is a biopharmaceutical company that discovers and develops drugs for oncology indications. The company is investigating AN2025, a trial-stage pan-PI3K inhibitor for the treatment of recurrent and metastatic head and neck squamous cell carcinoma; and AN0025, an EP4 antagonist designed against triple negative breast cancer, non-small-cell lung carcinoma, bladder, rectum and cervical cancer, and microsatellite stable colorectal cancer. It is also evaluating AN1004 to treat human epidermal growth factor receptor-2-negative metastatic breast cancer; AN4005 against advanced tumors; AN3025 and AN6025 for solid tumors. Adlai Nortye utilizes PAINT-2D and ANEAT-Id platform technologies to identify and develop immunotherapies and antibodies. The company operates research and development, clinical operation centers in China, and the US. Adlai Nortye is headquartered in Hangzhou, Zhejiang, China.
For a complete picture of Buparlisib hydrochloride’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.
