Entrectinib is under clinical development by F. Hoffmann-La Roche and currently in Phase II for Renal Cell Carcinoma. According to GlobalData, Phase II drugs for Renal Cell Carcinoma have a 29% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Entrectinib’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.
Entrectinib (Rozlytrek) belongs to phenylpiperazines class of compounds, acts as an anti-neoplastic agent. It is formulated as hard gelatin capsules for oral route of administration. Rozlytrek is indicated for the treatment of adult and pediatric patients with neurotrophic tyrosine receptor kinase (NTRK) fusion-positive, advanced recurrent solid tumours including pancreatic cancer, thyroid cancer, salivary gland cancer, breast cancer, colorectal cancer, and non small cell lung cancer, and also indicated for the treatment of TrkA-positive, TrkB-positive, TrkC-positive ROS1-positive or ALK-positive non-small cell lung cancer.
Entrectinib (RXDX-101) is under development for the treatment of solid tumors including non-small cell lung cancer (NSCLC), metastatic colorectal cancer, anaplastic large cell lymphoma, leptomeningeal disease, metastatic pancreatic cancer, salivary gland cancer, brain tumor, astrocytoma, synovial sarcoma, fibrosarcoma, triple negative, HER-2 positive, ER or PR positive breast cancer, head and neck cancer, ovarian cancer, neuroblastoma, central nervous system (CNS) tumor, cholangiocarcinoma, papillary thyroid cancer, renal cell carcinoma, metastatic melanoma, mammary analog secretory carcinoma, acute myeloid leukemia, squamous non-small cell lung cancer and stages I-III non-small cell lung cancer with ALK, ROS1, NTRK, or BRAF v600E molecular alterations. The drug candidate is administered orally. The drug candidate is a selective tyrosine kinase inhibitor of the TrkA, TrkB and TrkC, ROS1 and ALK proteins. It is developed based on Rx/Dx technology platform.
F. Hoffmann-La Roche overview
F. Hoffmann-La Roche (Roche) is a biotechnology company that develops drugs and diagnostics to treat major diseases. It provides medicines for the treatment of cancer, other auto-immune diseases, central nervous system disorders, ophthalmological disorders, infectious diseases, and respiratory diseases. The company also offers in vitro diagnostics, tissue-based cancer diagnostics, and diabetes management solutions. Roche conducts research to identify novel methods to prevent, diagnose, and treat diseases. The company offers its products and services to hospitals, healthcare professionals, commercial laboratories, researchers, and pharmacists. Together with its subsidiaries and partners, the company has operations in various countries. Roche is headquartered in Basel, Switzerland.
For a complete picture of Entrectinib’s drug-specific PTSR and LoA scores, buy the report here.