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FDA Grants 37 Breakthrough Designations in 2013

2014年01月16日 PM11:25
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LONDON & BOSTON & TOKYO

Since the FDA’s breakthrough therapy designation (BTD) was put into effect in July of 2012, pharma and biotech companies have certainly taken note, according to the new report, “Breakthrough Therapy Designation: A Breakthrough Year for Unmet Diseases,” from EP Vantage, the editorial arm of Evaluate. The FDA data indicate that no fewer than 141 BTDs have been applied for, of which 37 have been granted. Thus far, three breakthrough-designated products have received US approval: Roche’s Gazyva, J&J/Pharmacyclics’ Imbruvica and Gilead’s Sovaldi.

The jury is still out, however, on what it actually means in practice for a project to be designated a breakthrough therapy, and attempts to highlight evidence of shortened approval times for BTD products look premature. The new EP Vantage report takes a deeper look at this new designation and how small and large pharma are looking to reap the benefits the designation is touted to provide.

“Although many companies have been quick to play up the potential advantages of a breakthrough designation, the fact is that no one actually knows what these are in practice,” said Jacob Plieth, report author and EP Vantage senior editorial analyst. “Little can be gleaned from the three products to have already received US approval, and many uncertainties still abound.”

A list of the 30 disclosed breakthrough projects reveals that the vast majority have favoured big pharma and big biotech – despite the fact that the FDA’s promise to provide assistance on clinical trial design and guidance on development was aimed at small, cash-strapped biotechs, notes Plieth. According to the report, the hope is that this trend will shift as the programme matures.

The report, based on market intelligence and analysis from EvaluatePharma, can be downloaded at http://www.evaluategroup.com/EPVantage-Breakthrough-Therapies.

About EP Vantage

Written by a team of award-winning journalists, EP Vantage provides daily financial analysis of key industry catalysts including: regulatory and patent decisions, marketing approvals, licensing deals, and M&A – giving fresh angles and insight to both current and future industry triggers. Launched in 2007 by EvaluatePharma®, EP Vantage’s unique access to EvaluatePharma and EvaluateMedTech data allows unrivalled, forward-looking coverage of the pharmaceutical, biotech and medtech industries. Visit www.epvantage.com to sign up for a free trial. On Twitter: @EPVantage.

About Evaluate Ltd.

Evaluate is the trusted source for life science market intelligence and analysis with exclusive consensus forecasts to 2018. We support life science and healthcare companies, financial institutions, consultancies and service providers in their strategic decision-making. Our services include EvaluatePharmaEvaluateClinicalTrials and EvaluateMedTech. Our global team of dedicated healthcare analysts employs rigorous methodologies to deliver strategic commercial analysis. We make our services valuable by combining superior quality content, user-friendly reporting tools and outstanding customer service to solve client problems. For more information visit: www.evaluategroup.com. On Twitter: @evaluatepharma, @evaluatemedtech, @epclinicaltrial.

CONTACT

Media Contacts: (for general questions)
Evaluate and EP
Vantage
Christine Lindgren
+1 617-866-3906
christine.lindgren@evaluategroup.com
or
Chempetitive
Group (for U.S. media)
Rachel Lear
+1 781-775-3640
+1
858-997-9462
rlear@chempetitive.com
or
College
Hill (for non-U.S. media)
Melanie Toyne Sewell
Stefanie Bacher
Gemma
Howe
+44 (0) 20 7457 2020
evaluate@collegehill.com

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