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Progressive Supranuclear Palsy - A Pipeline Analysis Report

  • Published: May 2018
  • Pages: 72
  • SKU: IRTNTR22822
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This pipeline analysis report provides detailed insights into the drug development landscape for the development of drug for progressive supranuclear palsy including molecules at pre-clinical and other developmental stages. The report also offers comprehensive information about the therapeutic assessment of the pipeline molecules based on various segmentations such as indications coverage, therapies employed, preferred route of administration, therapeutic modality, and targets for drugs under development.

Overview of the drug development pipeline for progressive supranuclear palsy

Progressive supranuclear palsy (PSP) is a rare and progressive neurodegenerative disease, which is commonly known as Steele-Richardson-Olszewski syndrome. This condition is caused by the gradual damage of brain cells and the patients suffering from this condition undergo changes in personality, stiffness of muscles, dizziness, arthralgia, challenges with vision, speech, and facial movements, depression, and lack of interest. The prevalence of PSP is high among people above the age of 60. As a result, the growth of the global geriatric population will drive the demand for PSP treatments. Technavio’s market research analysts have predicted that with the introduction of medication, physiotherapy, speech therapy, and feeding tubes as some of the most promising investigational approaches to treat progressive supranuclear palsy, the global progressive supranuclear palsy market will witness growth in the forthcoming years.

According to progressive supranuclear palsy market overview, most of the drug development molecules in the pipeline are under the phase I and phase II development stages. For instance, sponsors such as Asceneuron developed ASN120290 and AbbVie developed ABBV-8E12, which are under phase I and phase II development stages respectively. Our market research analysts have also identified that a small amount of drug molecules that are being developed comes under the phase II/III development stage. The pipeline landscape in the pipeline analysis report mentions the percentage of drug development molecules that are under the pre-clinical stage.

Companies covered

This pipeline analysis report provides a detailed analysis of the companies that are involved in the development of drug molecules for the treatment of progressive supranuclear palsy. 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 –

  • Biogen
  • AlzProtect
  • AbbVie

Therapeutic assessment of the drug development pipeline for progressive supranuclear palsy by preferred route of administration

  • Oral
  • Intravenous

The oral route of administration (ROA) involves the administration of drug substances through mouth cavity. It has been observed that the majority of total therapeutics are being developed for oral administration.

Therapeutic assessment of the drug development pipeline for progressive supranuclear palsy by therapeutic modality

  • Small molecule
  • Vaccine
  • Monoclonal antibody

Based on the progressive supranuclear palsy market forecasts, the majority of molecules that are currently in the drug development pipeline for progressive supranuclear palsy are being developed as small molecules. Small molecules are chemically manufactured active substances that are able to enter the cells easily because of their low molecular weight.

Key questions answered in the report include

  • What are the drug development molecules in the various development stages for progressive supranuclear palsy?
  • What are the companies that are currently involved in the development of drug molecules for progressive supranuclear palsy?
  • 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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