Likelihood of Approval and Phase Transition Success Rate Model – Vorinostat in Cervical Cancer

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lgp loa report cover Likelihood of Approval and Phase Transition Success Rate Model – Vorinostat in Cervical Cancer

Published: November 17, 2023 Report Code: GDHCDR11290LOA-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.


Vorinostat in Cervical Cancer Drug Details:

Vorinostat is a anticancer agent. it is formulated as hard gelatin capsules for oral route of administration. It is indicated for for the treatment of newly diagnosed glioblastoma and gliosarcoma, refractory/relapsed follicular lymphoma, diffuse large B-cell lymphoma, B-cell non-Hodgkin lymphoma, mantle cell lymphoma, indolent lymphoma, non-small cell lung cancer, soft tissue sarcoma and metastatic uveal melanoma.Vorinostat is under development for the treatment of metastatic squamous cell carcinoma of vulvar cancer, penile cancer, cervix cancer, head and neck squamous cell carcinoma anal cancer, newly diagnosed glioblastoma and gliosarcoma, refractory/relapsed follicular lymphoma, diffuse large B-cell lymphoma (first-line), B-cell non-Hodgkin lymphoma, mantle cell lymphoma, indolent lymphoma, non-small cell lung cancer (third line). It was also under development for Niemann-Pick type-C, cutaneous T-cell lymphoma, metastatic colorectal cancer, pancreatic cancer, epithelial ovarian cancer, fallopian tube cancer, peritoneal cancer, malignant pleural mesothelioma, non-small cell lung cancer (first line), refractory/relapsed multiple myeloma, prostate cancer, small-cell lung cancer (First Line Therapy), metastatic breast cancer, myelodysplastic syndrome, recurrent glioblastoma multiforme, malignant glioma, metastatic clear cell renal cell carcinoma, metastatic, refractory/relapsed acute myeloid leukemia, soft tissue sarcoma and metastatic uveal melanoma.

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 – Vorinostat LOA Data
Report Segments
· Drug type

· Intervention type
Drug Name
· Vorinostat
Administration Pathway
· Oral
Therapeutic Areas
· Metabolic Disorders| Oncology
Key Manufacturers
· Merck & Co Inc
Drug Development Status
· Merck & Co 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.

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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