医療従事者の為の最新医療ニュースや様々な情報・ツールを提供する医療総合サイト

EP Vantage Releases Its Annual Analysis of Pharma & Biotech and Medtech Sector Performance: 2015 in Review Reports

2016年03月16日 PM10:00
このエントリーをはてなブックマークに追加


 

LONDON & BOSTON & SAN FRANCISCO & TOKYO

Funding for early stage biopharma and medtech research dwindled in 2015, as investors shifted their support to more mature companies. These findings and more were released today as part of the Pharma & Biotech 2015 in Review and Medtech 2015 in Review reports by EP Vantage, the editorial arm of life science market intelligence firm Evaluate Ltd.

This venture investment trend, which began five years ago, could constrain future pharmaceutical and medtech innovation, as promising new scientific discoveries fail to progress due to lack of funding.

“Early stage investment is the lifeblood of the industry,” said Lisa Urquhart, Editor of EP Vantage. “Our 2015 reports show it’s being given to an increasingly small pool of companies, which could cause some very serious problems in the future. Both medtech and pharma need a large cohort of startup companies to hedge against failure and foster innovation. Depriving them of funding now could eventually choke the industry.”

Other key findings include:

  • Drug pricing and sustainability issues took the air out of the biotech bubble, leading to the early 2016 market collapse, which negated almost all gains since mid-2014.
  • A shift toward mega investment rounds became evident in the pharma & biotech world. Top-10, triple-digit venture capital raises consumed nearly one quarter of all available funds for development-stage biotechs.
  • Pharma & Biotech FDA approvals jumped from an unprecedented 50 in 2014, to 57 in 2015
  • The total value of mergers and acquisitions in the medtech sector in 2015 reached an unprecedented high; a figure that held true even if the record-breaking acquisition of Covidien by Medtronic was excluded.
  • Questions remain about how the medtech sector can stimulate investing and deals for emerging to mid-size companies, to support sector innovation and growth.
  • A total of 51 novel medical devices were approved by the FDA in 2015, the most in a decade.

The two reports published today offer analysis and expert commentary on M&A deals venture financing, initial public offerings and FDA approvals in the pharma and medtech sectors during 2015. The reports are based on EvaluatePharma® and EvaluateMedTech® data.

To download the complimentary Pharma & Biotech 2015 in Review report, please visit www.evaluategroup.com/PharmaBiotech2015Review. For the Medtech 2015 in Review report, please visit www.evaluategroup.com/Medtech2015Review.

About Evaluate Ltd

Evaluate is the trusted source for life science market intelligence and analysis with exclusive consensus forecasts to 2020. Our subscription services include EvaluatePharmaEvaluateClinical Trials and EvaluateMedTech. Evaluate Custom Services provides project-based analytical and data services. Our award-winning editorial team, EP Vantage, leverages our strategic analysis to cut through the noise, giving you daily opinion and insights. The Evaluate services enable the life science community to make sound business decisions about value and opportunity. For more information please visit www.evaluate.com. On Twitter: @evaluatepharma, @evaluatemedtech, @evaluateJP @epclinicaltrial, @epvantage.

View source version on businesswire.com: http://www.businesswire.com/news/home/20160316005143/en/

CONTACT

Evaluate and EP Vantage (for general questions)
Christine Lindgren,
+1 617-866-3906
christine.lindgren@evaluategroup.com
or
Chempetitive
Group (for U.S. media)
Trisha Rule, +1-858-230-4949
trule@chempetitive.com
or
Instinctif
Partners (for non-U.S. media)
Gemma Howe, +44 (0) 20 7457 2020
evaluate@instinctif.com

同じカテゴリーの記事 

  • La Jolla Institute for Immunology and RevolKa started a Research Collaboration
  • U.S. FDA Approves Subcutaneous Administration of Takeda’s ENTYVIO® (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Crohn’s Disease
  • ESCMID Global 2024: Shionogi presents real-world data demonstrating efficacy of Fetcroja® / Fetroja® (cefiderocol) in critically ill patients with certain difficult-to-treat bacterial infections
  • Renesas’ New FemtoClock™ 3 Timing Solution Delivers Industry’s Lowest Power and Leading Jitter Performance of 25fs-rms
  • 成人向け予防接種プログラムは初期投資の19倍もの社会経済的価値をもたらすとの新レポートを発表