Rheumatoid Arthritis Clinical Trials Heat Map and Analysis Forecast To 2022

Rheumatoid Arthritis - Heat Map and Analysis - Rheumatoid Arthritis - Heat Map and Analysis report provides heat map framework for Rheumatoid Arthritis, designed to provide an easily digestible summary of these clinical characteristics, provides detailed readouts of all late-stage clinical trial results for products. All safety and efficacy endpoints reported in these trials are displayed, for both the drug and comparison groups. 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.

Complete report on Rheumatoid Arthritis - Heat Map and Analysis Spread across 15 pages is available at http://www.reportsnreports.com/reports/807454-rheumatoid-arthritis-heat-map-and-analysis.html

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.

Major Points Covered in Table of Contents

• Changes to Conventional Synthetic Disease Modifying Anti-Rheumatic Drugs, 2015-2022.

• Changes to Anti-Tumor Necrosis Factor Alpha Biologic Disease Modifying Anti-Rheumatic Drugs, with or without Concomitant Conventional Synthetic Disease Modifying Anti-Rheumatic Drugs, 2015-2022.

• Changes to Non-Anti-Tumor Necrosis Factor Alpha Biologic Disease Modifying Anti-Rheumatic Drugs, with or without Concomitant Conventional Synthetic Disease Modifying Anti-Rheumatic Drugs, 2015-2022.

•Changes to Targeted Synthetic Disease Modifying Anti-Rheumatic Drugs with or without Concomitant Conventional Synthetic Disease Modifying Anti-Rheumatic Drugs, 2015-2022.

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Scope
The rheumatoid arthritis market landscape is expected to change substantially with the advent of promising novel pipeline products.

·         What are the clinical characteristics of currently approved therapies for rheumatoid arthritis, 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 IL-6 inhibitors affect the market for biologic DMARDs, and are they able to yield comparable clinical efficacy results to TNF-therapies?

·         With four targeted synthetic DMARDs present in the late-stage pipeline, do they have sufficient differentiating characteristics to make a strong impact on the market?

·         How will the influx of biosimilar TNF-a inhibitors affect the competitive landscape?

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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 considers 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.

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