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市場調查報告書

歐洲及日本的生物製劑開發動向

Key Issues to Consider When Bringing Biologics to Market in Europe and Japan

出版商 Decision Resources, Inc.
出版日期 2008年07月 商品編碼 71046
內容資訊 英文 34 Pages
價格
US $ 2250 PDF by E-mail (Global License)


歐洲及日本的生物製劑開發動向 是由出版商Decision Resources, Inc.在2008年07月所出版的。 這份英文市場調查報告書包含34 Pages 價格從美金2250起跳。

簡介

本報告書內容包括:歐洲及日本的生物製劑醫療實驗過程實例介紹、主要企業評析、企業合作及M&A動向、未來這兩大地區的生物製劑市場前景預測等。內容綱要摘要如下:

實施概要

  • 策略課題
  • 對利害關係人造成的影響

概要

  • 透過數字分析生物製劑
  • 本報告書的範圍

在歐洲及日本將生物製劑商品化時的考量事項

  • 規範限制流程
  • 藥價制定

歐洲的生物製劑環境前景

  • 新治療方法的評估時間
    • 加速評估
    • 附加條件行銷
  • 孤兒藥品的動向

日本的生物製劑環境前景

  • 醫療實驗的基礎環境尚未完善
  • 規範限制的阻礙

生物製劑製造商如何打進歐洲及日本市場的?

  • 歐洲的環境
  • 日本的環境

生物製劑的藥價及補貼

  • 歐洲
  • 日本
    • 相同的效益比較方法
    • 成本計算方法

生物學名藥對生物製劑市場造成的影響

  • 歐洲
  • 日本

歐洲及日本生物製劑的未來

圖表

目錄

Abstract

Introduction

In the past 25 years, more than 100 recombinant proteins and MAbs have reached the global market. Biologics have scored most of their successes in the United States, but they are a growing force in Europe and Japan, where they are well represented in companies' product pipelines. Issues that will make or break the successful integration of biologics in European and Japanese biopharmaceutical market include clinical trial design, patient recruitment, pricing methodology, reimbursement, treatment for orphan diseases and serious illnesses, and responding to a high unmet need.

Get the Answers You Need to Shape Your Strategy

  • As the biopharma market continues to grow in Europe and Japan, various region-specifi c factors will infl uence the performance of biologics in these markets. What factors will facilitate (or frustrate) market penetration of biologics in Europe? In Japan? What steps, if any, can companies take to enhance or mitigate these market conditions?
  • As seen by GlaxoSmithKline' s decision to set lower prices of its biologics in Europe, companies are adjusting their strategies to respond to a slow growth of biologics. Which strategies are sustainable and reproducible? How will changes at the individual company level affect the whole biologics industry?
  • The performance of biologics depends not only on pricing and reimbursement but also on the impact of biosimilars. Is the outlook for biologics better as a result of biosimilars, or worse? Based on its recent experience with biosimilars, what impact does the European market anticipate from these agents? How will the Japanese experience mirror or differ from this example?

Scope

  • Case studies: two examples of the commercialization and clinical development process of biologics, one in Europe and one in Japan.
  • Companies: a review of leading European and Japanese companies that offer biologics.
  • Deals: collaborations, M&As, and licensing deals in biologics.
  • Strategic decisions: company- and country-level changes are causing waves in the biologics industry. Neil Grubert explores this specifi cally for reimbursement, using the EUnetHTA as an example.
  • Outlook: our forecast for the biologics landscape in Europe and Japan.

Table of Contents

  • Executive Summary
    • Strategic Considerations
    • Stakeholder Implications
  • Overview
    • Biologics by the Numbers
    • Scope of This Report
  • Key Elements to Consider in Commercializing Biologics in Europe and Japan
    • Regulatory Process
    • Price Setting
  • European Perspective on the Biologics Environment
    • Review Times for Novel Therapies
      • Accelerated Assessment
      • Conditional Marketing Authorization
    • Orphan Drug Status
  • Japanese Perspective on the Biologics Environment
    • Inadequate Infrastructure for Clinical Development
    • Regulatory Barriers
  • How Are Biologics Makers Pursuing the European and Japanese Markets?
    • The European Landscape
    • The Japanese Landscape
  • Pricing and Reimbursement of Biologics
    • Europe
    • Japan
      • Similar-Effi cacy Comparison Method
      • Cost-Calculation Method
  • Impact of Biosimilars on the Biologics Market
    • Europe
    • Japan
  • The Future of Biologics in Europe and Japan

Expert Commentary

  • Health Technology Assessment: A Growing Challenge for the Biologics Industry in Europe Neil Grubert, M.A.

Sidebars

  • Clinical Requirements Case Study: Why Amevive Failed and Raptiva Succeeded in Gaining Approval
  • Pricing Methodology Case Study on Avastin: When Market Size Matters

Tables

  • 1. Number of Drug Approvals via the Centralised Procedure, 2005-2008
  • 2. Prices of Leading Biologics in Europe and Japan as a Percentage of U.S. Prices, 2006
  • 3. Best-Selling Biologics in Japan, 2006-2007
  • 4. Select Biologics Collaborations, January 2007-June 2008
  • 5. Select Japanese Pharma Companies' Biologics Sales in Proportion to Total Sales,
  • 6. Japanese Company Pipelines: Late-Stage Biologics
  • 7. Comparative Price and Sales of Key Biologics in Japan (vs. U.S. Prices), 2006
  • A. Price of Chugai' s Avastin (Bevacizumab) in Select Major Markets

Figures

  • 1. Worldwide Sales of the Top 100 Pharmaceutical Drugs, by Type
  • 2. Average Prices of Leading Biologics, Small-Molecule Drugs, and Pharmaceuticals Overall in Europe and Japan as a Percentage of U.S. Prices
  • 3. Biologics as a Proportion of All Drugs Across the Major Markets, by Development Status
  • 4. Number of Conventional-Technology Blockbusters vs. Biotechnology Blockbusters, 1997-2007
  • 5. Market of First Launch of New Molecular Entities, 2005-2007
  • 6. Number of Biologics Approved in Japan, 2005-2007
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