Likelihood of Approval and Phase Transition Success Rate Model – Cabozantinib S-malate in Gastric Cancer

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lgp loa report cover Likelihood of Approval and Phase Transition Success Rate Model – Cabozantinib S-malate in Gastric Cancer

Published: November 17, 2023 Report Code: GDHCDR16306LOA-MP-L5

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How likely is it that a drug will get approved? Will the drug transition to the next phase of its clinical pathway? This report provides you with the data that allows you to track and predict the specific likelihood of approval (LOA) and phase transition success rate (PTSR) of a drug using GlobalData’s proprietary machine learning algorithms developed using over 10 years of historical data.


Cabozantinib S-malate in Gastric Cancer Drug Details:

Cabozantinib s-malate (XL184, BMS907351, Cometriq) is a s-malate salt form of cabozantinib. It is formulated as hard gelatin capsules for oral route of administration. Cometriq is indicated for the treatment of patients with progressive, metastatic medullary thyroid cancer.Cabozantinib is under development for the treatment of metastatic cervical cancer, metastatic castration-resistant prostate cancer (mCRPC), clear cell renal cell carcinoma, advanced or metastatic urothelial cancer, carcinoid tumor, gastroesophageal adenocarcinoma, metastatic melanoma, thyroid cancer, neuroendocrine gastroenteropancreatic tumors, hepatocellular carcinoma, pheochromocytoma, paraganglioma (glomus jugulare tumor), pancreatic neuroendocrine tumor, endometrial cancer, rhabdomyosarcoma, non-rhabdomyosarcoma, Wilms’ tumor (nephroblastoma), Ewing sarcoma, osteosarcoma, soft tissue sarcoma, recurrent head and neck cancer squamous cell carcinoma, squamous cell carcinoma, metastatic colorectal cancer, colorectal cancer, gastric cancer, plexiform neurofibroma, penile cancer, adenocarcinoma of the gastroesophageal junction, advanced melanoma, non-small cell lung cancer, esophageal cancer, small cell lung cancer (SCLC), recurrent or progressive meningioma, papillary thyroid carcinoma (PTC), follicular thyroid carcinoma (FTC) and triple-negative breast cancer (TNBC).The drug candidate was also under development for the treatment of relapsed/refractory acute myeloid leukemia, anaplastic thyroid cancer, astrocytoma, glioblastoma multiforme, renal failure, Merkel cell carcinoma, metastatic renal cell carcinoma, urethral cancer, ureter cancer, peritoneal cancer, pancreatic tumor, metastatic adenocarcinoma of the pancreas, bladder cancer, metastatic uveal melanoma, epithelial ovarian cancer, fallopian tube cancer, hormone-receptor-positive breast cancer with bone metastases, relapsed/refractory multiple myeloma, papillary renal cell carcinoma and gastroesophageal (GE) junction carcinomas.

Report Coverage

The data is segmented by drug name per indication and shows the current likelihood of approval for the drug compared to the indication benchmark and the industry benchmark.

The Likelihood of Approval data is updated regularly based on events that take place which impact the clinical development process and regulatory considerations. GlobalData’s proprietary machine learning models consider these events in real time, to produce quantitative changes to the LOA and PTSR along with qualitative reasoning why the likelihood of approval has changed.

Quick View – Cabozantinib S-malate LOA Data
Report Segments
· Drug type

· Intervention type
Drug Name
· Cabozantinib S-malate
Administration Pathway
· Oral
Therapeutic Areas
· Genito Urinary System And Sex Hormones| Non Malignant Disorders| Oncology
Key Manufacturers
· Exelixis Inc
Drug Development Status
· Exelixis Inc

Reasons to Buy

  • Predict the specific likelihood of approval and phase transition success rates of a drug using a combination of machine learning and proprietary models

  • Get information on LOA and PTSR for competitors’ drugs to plan your clinical development, commercialization and marketing strategies

  • Track event-driven changes in LOA and PTSR benchmarked against indication LOA/PTSR

  • Use PTSR and LOA information and event-driven changes for your investment decisions.

This is an on-demand report that will be delivered upon request. The report will be delivered within 2 business days of the purchase, excluding weekends and holidays. Certain sections of the report may be removed or altered based on data availability and relevance.

Frequently asked questions

    The probability of a drug ultimately receiving market authorization

    The probability of a drug’s advancement to the next stage of clinical development

    GlobalData’s  Drug-Specific Likelihood of Approval (LoA) calculates the  Phase Transition Success Rate (PTSR) and  Likelihood of Approval (LoA) customized to individual drug. The model uses a combination of  Machine Learning (ML) and a  GlobalData proprietary algorithm to process data points from the  Drugs, Clinical Trials, Regulatory Milestones, Company, and  Financial databases.

     

    Inclusion

    Data Scope:

    • Drugs which have been approved in the past 10 years
    • Drugs which have failed during clinical development in the past 18 years
    • Drugs which are currently in development

    Drug Phase Scope:

    • Phase I, Phase II, Phase III, and Pre-Registration development stage

    Drug Geography Scope:

    • Drugs must meet one of the following criteria to be included in the model:
    • The developer has specified the US as an intended market for approval.
    • The developer has not specified any country as an intended market for approval, i.e. the “Drug Geography” is listed as “Global”

    Drug Type Scope:

    • Innovator drugs and biosimilars

    Entity Type Scope:

    Only drugs in development by companies are included in the model.

    Exclusion

    • Diagnostics, Imaging Agents, Biomarkers, stents and other drug delivery devices (covered in GlobalData’s Medical Intelligence Center).
    • Nutraceuticals, dietary supplements, alternative medicines, imaging agents, radio emitter, transplants, transfusions, fillers, cosmetics, probiotics, antiseptics, antacids, mobilizing agents, veterinary drugs and drugs not seeking approval.
    • Generic drugs
    • Innovative drugs in Preclinical or Discovery Stage.
    • Pipeline drugs sponsored by a Government or Institution.
    • Drugs with a specific Drug Geography not the United States.

     

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