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Platinum-resistant Ovarian Cancer - A Pipeline Analysis Report

  • Published: Jun 2018
  • Pages: 166
  • SKU: IRTNTR22397
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This pipeline analysis report provides detailed insights into the clinical trials landscape of the drug development for platinum-resistant ovarian cancer including molecules at pre-clinical and discovery stage. The report also offers comprehensive information about the therapeutic assessment of the pipeline molecules based on various segmentations such as therapy, route of administration, and target.

Overview of the drug development pipeline for platinum-resistant ovarian cancer

Ovarian cancer is the most lethal gynecologic malignancy. It is formed in or on an ovary. This cancer can spread to the abdominal lining, lungs, and liver. It is difficult to detect ovarian cancer in the early stages, giving the asymptomatic nature of this indication. It reduces patients’ survival span, which is usually less than five years since the genesis of the tumor. Ovarian cancer can be classified in two types on the reaction to chemotherapy drugs. The types are platinum-sensitive and platinum-resistant ovarian cancer. As per the NIH, patients with ovarian cancer have less than 47% chances of surviving for more than five years. The prevalence of this disease in unevenly distributed while being more common in less developed countries compared to the advanced economies. About 58% of ovarian cancer cases are from less developed countries. The disease is also very common in older women. In 2015, 28% of all the new cases of ovarian cancer were in women aging above 75 years. Consequently, Technavio’s market research analysts suggest with the increase in instances of ovarian cancer, the drug development for platinum-resistant ovarian cancer has been promoted.

According to this pipeline analysis report, most of the drug development molecules in the pipeline are being developed for the treatment of platinum-resistant recurrent ovarian cancer. Our market research analysts have also identified that most of these molecules are in the pre-clinical development stage and a considerable number of molecules have been discontinued from development.

Companies covered

This pipeline analysis report provides a detailed analysis of the companies that are involved in the development for the drug development molecules for the treatment of ovarian cancer. In addition to providing information on the various stages of molecules developed by companies for different indications, this pipeline analysis report also provides information about the drug development molecules discontinued by companies.

Some of the companies covered in this pipeline analysis report are –

  • Bayer
  • Novartis
  • Celgene
  • Eli Lilly
  • Pfizer

Therapeutic assessment of the drug development pipeline for platinum-resistant ovarian cancer by route of administration

  • Intravenous
  • Oral
  • Subcutaneos
  • Intradermal
  • Intraperitoneal

The intravenous route of administration (ROA) involves the application of the drug directly into the veins, which will have a more direct effect on the target cells.

Therapeutic assessment of the drug development pipeline for platinum-resistant ovarian cancer by therapy

  • Monotherapy
  • Combination therapy

According to this pipeline analysis report, all the molecules that are currently in the drug development pipeline for platinum-resistant ovarian cancer are being developed as combination therapy drugs and most of these molecules are in the pre-clinical stage of development.

Key questions answered in the report include

  • What are the drug development molecules in the various development stages for platinum-resistant ovarian cancer?
  • What are the companies that are currently involved in the development of drug development molecules for platinum-resistance ovarian cancer?
  • Insight into discontinued/inactive molecules with appropriate reasoning?
  • What are the major regulatory authorities approving drugs in various regions?
  • Detailed profiling of each active molecule

 

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PART 01: EXECUTIVE SUMMARY

PART 02: SCOPE OF THE REPORT

PART 03: RESEARCH METHODOLOGY

PART 04: INTRODUCTION

PART 05: MAJOR REGULATORY AUTHORITIES

  • US
  • Europe
  • China

PART 06: PIPELINE LANDSCAPE

PART 07: COMPARATIVE ANALYSIS

  • Discovery stage molecules
  • Pre-clinical stage molecules
  • Inactive and discontinued molecules

PART 08: INDICATION ANALYSIS

PART 09: THERAPEUTIC ASSESSMENT (THERAPY BASED)

PART 10: THERAPEUTIC ASSESSMENT (ROA BASED)

PART 11: THERAPEUTIC ASSESSMENT BY TARGET

PART 12: KEY COMPANIES

  • Active companies: Category and parameters

PART 13: APPENDIX

  • List of abbreviations

Research Framework

Technavio presents a detailed picture of the market by way of study, synthesis, and summation of data from multiple sources. The analysts have presented the various facets of the market with a particular focus on identifying the key industry influencers. The data thus presented is comprehensive, reliable, and the result of extensive research, both primary and secondary.

TechnavioINFORMATION SOURCES

Primary sources

  • Manufacturers and suppliers
  • Channel partners
  • Industry experts
  • Strategic decision makers

Secondary sources

  • Industry journals and periodicals
  • Government data
  • Financial reports of key industry players
  • Historical data
  • Press releases
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TechnavioDATA ANALYSIS

Data Synthesis

  • Collation of data
  • Estimation of key figures
  • Analysis of derived insights

Data Validation

  • Triangulation with data models
  • Reference against proprietary databases
  • Corroboration with industry experts
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TechnavioREPORT WRITING

Qualitative

  • Market drivers
  • Market challenges
  • Market trends
  • Five forces analysis

Quantitative

  • Market size and forecast
  • Market segmentation
  • Geographical insights
  • Competitive landscape
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