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Market Research Report

Pipeline Insight: Disease Modification in Rheumatoid Arthritis - Competition for the anti-TNF failure patient population increases

Published by Datamonitor Contact us : +1-860-674-8796
Published 2007/04 Content info  
Product code DC51296
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Description TOC

Abstract

Overview

Introduction

The treatment of Rheumatoid Arthritis (RA) has been rapidly evolving over the last decade. The success of the next wave of novel RA therapies depends on their ability to address the key issue of cost effectiveness, as the patient population for anti-TNF' s is reaching a maximum and competition moves to anti-TNF failure patients.

Scope

  • Detailed pipeline analysis for key products in a specific RA indication, plus drug sales forecasts to 2016.
  • Overview of patient potential, segmentation by indication and unmet needs in RA across the seven major markets
  • Benchmarking of key clinical and company attractiveness of the late-Phase pipeline products
  • Detailed up to data clinical trial information

Report Highlights

The anti-TNF failure segment will be an area of increased competition over the next five years, as new products avoid direct confrontation with the established anti-TNF' s. This population will increase as more patients use biologics and cycle through the anti-TNF' s, but there are a finite number of eligible patients, especially if prices remain high.

The race is on between the Roche/Genentech/Biogen Idec and the Genmab/GSK partnerships to launch a CD20-inhibiting monoclonal antibody to follow, and build upon, the success shown by Rituxan/MabThera (rituximab) in the RA indication. At present Roche with ocrelizumab have a slight, but uncertain, advantage.

The majority (58%) of projects in human clinical trials are in Phase II development showing the positive growth potential in the RA disease area. However, a large proportion are small molecule, orally available products, which have in the past shown a high attrition rate in Phase II.

Reasons to Purchase

  • Understand why pricing restraint is necessary for the continued exponential uptake and commercial growth of the biologic DMARDs
  • Quantify the size and potential of the market for novel treatments in the RA indication.
  • Use analysis of the common molecular targets under investigation to find gaps in the market for your product
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