April 15, 2014
Drug Developers Are Using New Models and Methods to Boost Clinical Success Rates
BOSTON – April 15, 2014 – Drug companies and their development partners who are seeking to increase clinical success rates of new drug candidates are developing tools to help them predict the likelihood of marketing approval and incorporating business planning earlier in clinical development, according to R&D leaders who recently participated in a roundtable discussion convened by the Tufts Center for the Study of Drug Development.
“The research-based drug industry is racing to boost its research pipelines, as existing patents expire and development times continue to lengthen,” said Tufts CSDD Director Kenneth I Kaitin. “Drug companies are exploring new approaches to product development that focus on increasing the probability of clinical success and speeding time to market.”
One tactic, Kaitin cited, focuses on statistical models that help predict clinical success. For example, his team, working with a pharmaceutical company, created a simple algorithmic model called the Approved New Drug Index (ANDI) – modeled on the five-factor APGAR score widely used in delivery rooms to evaluate the health of newborns – that reliably predicts which oncology products emerging from Phase II testing are likely to receive marketing approval.
The team concluded that, compared to the prevailing industry metric, the data support assigning a much higher probability of success to oncology drugs with top ANDI scores of 7 and 8, and much lower probabilities of success to those with scores of 0 to 4.
Among other points discussed in the roundtable, summarized in the April Tufts CSDD R&D Management Report, released today:
- A shift in approach to decision making that favors data-driven models over intuition and what is already known can improve drug development success.
- More rigorous use of risk-adjusted net present value calculations earlier in clinical development can improve decision making on how to structure clinical trials.
- Advances in development of personal genomic information, increased voluntary sharing of patient data, and an explosion in data on cell metabolism have significant potential to transform clinical trials, but effectively mining the data these advances create presents a major challenge for research centers.
SCHEDULED TUFTS CSDD EXECUTIVE FORUM ROUNDTABLES
Upcoming Tufts CSDD Executive Forum Roundtable meetings:
- May 15, 2014: Risk-Sharing Partnerships and Alliances: Strategic and Operational Challenges
- Sept. 18, 2014: New Directions in Outsourcing
ABOUT THE TUFTS CENTER FOR THE STUDY OF DRUG DEVELOPMENT
The Tufts Center for the Study of Drug Development (http://csdd.tufts.edu) at Tufts University provides strategic information to help drug developers, regulators, and policy makers improve the quality and efficiency of pharmaceutical development, review, and utilization. Tufts CSDD, based in Boston, conducts a wide range of in-depth analyses on pharmaceutical issues and hosts symposia, workshops, and public forums, and publishes Tufts CSDD Impact Reports, a bi-monthly newsletter providing analysis and insight into critical drug development issues.
Tufts Center for the Study of Drug Development
Sandra Peters – 617-636-2170
Business Communication Strategies
Peter Lowy – 617-734-9980