Multiple Sclerosis Drug Discoveries: What the future holds

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Description: This 102 page reports analyzes brand positioning and the development of oral formulations as well as the recent R&D and products in development to treatment multiple sclerosis.



Research Report Overview

Published Date: 19/10/2010
Category: Therapies & Markets

Research Report Decription

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The recent approval in the US of Novartis orally administered Gilenya (fingolimod) heralds a new phase in the treatment of Multiple Sclerosis (MS).Over the last few years, the MS market has been driven by five disease-modifying agents: Teva’s Copaxone (glatiramer acetate), Biogen Idec’s Avonex (interferon beta-1a) and Tysabri (natalizumab), Merck KGaA’s Rebif (interferon beta-1a) and Bayer’s Betaferon (interferon beta-1b). From 2009, interferon beta-1b has also been available from Novartis as Extavia; this is the same formulation as Betaferon.In addition to these, Amgen’s Novantrone (mitoxantrone) has been available to treat MS. Generic mitoxantrone is also available. Avonex, Betaferon/Extavia, Rebif and Copaxone are all used in first-line therapy for RRMS. They are generally well accepted and have accumulated comprehensive safety and clinical trial data supporting their use in modifying the course of the disease. Tysabri and mitoxantrone are generally used in second-line therapy in RRMS. Mitoxantrone is also approved to treat SPMS and PRMS. Both of these agents are associated with serious side-effects.The arrival of oral treatments brings big clinical advantagesThe development of oral therapies for MS has attracted significant investment from pharmaceutical companies and the first of these have begun to receive marketing approvals, signalling another major change in the way MS is treated. In September 2010, Novartis won the race to gain the first oral approval in the US with its sphingosine-1-phosphate (S1P) receptor agonist, Gilenya. The product was also approved in Russia in the same month. Merck’s oral product, Movectro (cladribine) was approved in Russia in July 2010 and in Australia in September 2010 for the treatment of RRMS for a maximum duration of two years. However, the European Medicine Agency’s CHMP issued a negative opinion for Movectro for the treatment of RRMS. 

Key Questions Answered:

  • What are the four main types of MS?
  • Research into MS vaccines has stalled. What is the current situation and are there still opportunities in this area?
  • How might the asthma treatment salbutamol (albuterol) help control MS?
  • Which countries have the highest prevalence of patients per 100,000 population?
  • MS is a geographically specific condition – what are the theories as to why this is so?
  • Despite having patent protection until 2014, generic companies are already making a play for Teva’s Copaxone. Who’s involved and what is the current status?
  • What are the expected sales in 2016 of Novartis’ novel oral MS treatment Gilenya?
  • What are the patient safety concerns with Acorda’s Ampyra (dalfampridine), the first in class treatment for treating MS symptoms?
  • How many Phase III products are in the pipeline and when are they expected to launch?
  • What positive clinical trial results did sanofi-aventis report for its oral MS drug teriflunomide?

Companies Mentioned:

Acorda, Amgen, Bayer Schering, Biogen Idec, Elan, Merck Serono, Novartis, Teva Pharmaceutical Industries

Paper Highlights:

Multiple Sclerosis is a chronic autoimmune neurological disease affecting up to 2.5 million people worldwide, the majority of whom live in North America and Europe. It is a complex disorder that affects people in different ways. Around 85% of patients are initially diagnosed with relapsing remitting MS (RRMS). Up to half of these will go on to develop secondary-progressive MS (SPMS).The other main types identified are primary progressive MS (PPMS), which affects around 10% of patients at onset, and progressive-relapsing MS (PRMS) which affects up to 5% of patients. There is currently no cure for MS and treatment is aimed at its symptoms and slowing disease progression. The launch of interferons during the 1990s transformed the treatment of MS but there is still a large unmet clinical need in reducing disease progression.Shape of the industry in 2010...At the forefront of the MS market is Biogen Idec, with a market share of 27% due to sales of Avonex and Tysabri. Following closely are Teva and sanofi-aventis who currently market Copaxone, giving them a combined share of the market by sales value of around 30%. With the third biggest seller, Rebif, Merck Serono has been attributed with a market share of 19%; Bayer Schering takes 15% of the market with Betaferon sales; while Elan’s share of Tysabri sales provide the company with around 4%....and in 2016By 2016, a number of new agents will be available to treat MS, and their contribution to revenues will enhance Biogen Idec’s leading position. In addition, Teva’s Copaxone will lose patent protection in the US in May 2014. If approved, generic versions of Copaxone would undoubtedly put pricing pressures on both the branded version and related therapies. The combined effect of an influx of new therapies and generic competition for the market leader is likely to cause a ripple through the entire MS therapy market. Consequently, the current market leaders will all have their share of the US$15.3 billion market reduced as competition increases. Over US$4 billion of the MS market will be generated by recently approved or developmental products that will be launched in the near term.