Latest
industry research report on: Global Cystic Fibrosis Market : Industry
Size, Share, Research, Reviews, Analysis, Strategies, Demand, Growth,
Segmentation, Parameters, Forecasts
Cystic fibrosis (CF) is
a progressive genetic condition and is the result of a patient
inheriting a faulty cystic fibroses transmembrane conductance regulator
(CFTR) gene from both parents. The defective CFTR genes produce faulty
CFTR proteins on the body?s epithelial cells, and result in the buildup
of a thick and sticky mucus in the lungs and pancreas. Historically
therapeutic options have focused heavily on treating the symptoms, but
despite being clinically and commercially successful have failed to
address the faulty CFTR proteins that cause the disease. This unmet need
has led to the development of CFTR modulators.
The
treatment algorithm patients receive is likely to consist of an
antimicrobial, a mucolytic agent, pancreatic enzymes and possibly a CFTR
modulator. This tabular heatmap framework, designed to provide an
easily digestible summary of these clinical characteristics, provides
detailed information on all late-stage clinical trial results for
products in the CF market and Phase III or Preregistration stages of the
pipeline. These are split along drug class lines, and are therefore
reflective of the treatment algorithm.
All
safety and efficacy endpoints reported in these trials are displayed.
In addition, key study characteristics such as the size, composition and
patient segment of the study population are provided. These results are
presented in a visually accessible, color-coded manner in order to
maximize ease of use.
The
accompanying text provides a detailed analysis of the clinical
benchmarks set by the current market landscape, and the anticipated
changes to these benchmarks, and to the treatment algorithm, as a result
of the late-stage pipeline.
Download Sample copy of this Report at : http://www.marketresearchreports.biz/sample/sample/915807
Scope
- To what extent is the CF market landscape expected to change with the introduction of new CFTR modulators?
- What are the clinical characteristics of currently approved therapies for CF, in terms of specific safety and efficacy parameters?
- What are the key unmet needs in this indication, and which clinical safety and efficacy parameters are the most closely linked to them?
- How will current late-stage CFTR modulators affect the market for symptomatic therapies, and are they able to yield comparable clinical efficacy results to Kalydeco?
- How will the influx of tobramycin generics affect the competitive landscape?
Reasons to buy
- Understand the current clinical landscape by considering the treatment options available for each patient segment.
- Visually compare the currently approved treatments available at each line of therapy, based on the most important efficacy and safety parameters tested in clinical trials.
- Assess the current late-stage pipeline, in terms of the likely positioning of each product and the implications for the clinical landscape at each line of therapy.
- Understand the relative strengths and weaknesses of the studies used to gather these data.
- Build up a nuanced understanding of the clinical benchmarks set by these products, and consider how the current late-stage pipeline will affect these benchmarks.
- Assess your own pipeline programs in light of these benchmarks in order to optimally position them and maximize uptake by clinicians.
Table of Contents
1 Table of Contents
1 Table of Contents 2
2 Introduction 3
2.1 Report Guidance 3
3 Marketed Products 4
3.1 Antimicrobeals 4
3.2 Mucolytic Agents 5
3.3 Pancreatic Enzymes 6
3.4 CFTR modulators 6
4 Pipeline Products 8
4.1 Changes to Antimicrobeals, 2016-2022 8
4.2 Changes to Mucolytic Agents, 2016-2022 8
4.3 Changes to Pancretic Enzymes, 2016-2022 8
4.4 Changes to CFTR Modulators, 2016-2022 9
5 Appendix 10
5.1 Abbreviations 10
5.2 References 10
5.3 Research Methodology 13
5.4 Contact Us 13
5.5 Disclaimer 13
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