ARMONK, NY-February 19, 2009-A new survey released today by IBM and Silico Research reveals that if biopharmaceutical-or life-sciences-companies fail to collaborate, they risk costly delays in the production of new medicines, medical devices, diagnostics and support services.
The survey, An Imperfect Harmony: Alliances within the life sciences industry, spotlights a paradox: while the number of alliances between larger and smaller life-sciences companies has increased over the past decade, their ability to effectively work together and produce new medicines has not been achieved. In fact, the IBM study found 55 percent of Life Sciences Chief Executives surveyed do not plan to partner extensively over the next three years. Moreover, while many large biopharmaceutical companies have the strength to collaborate, they fail to act.
According to the IBM study, many large life-sciences companies have made marginal three to four percent improvements in their abilities to find new partners, negotiate terms, and manage the alliances they have established over the past two years.
For life sciences companies to grow smarter about healthcare, they must attract the best scientists, develop targeted treatments and services for specific disease pathologies, and move into new or emerging markets. To accomplish this goal, especially in the current economic environment, companies must collaborate even more extensively than they currently plan to do.
The IBM study uncovered many factors that drive a company to partner with another. Size is not one of them. Larger companies do not always dictate the terms when it comes to alliances. Today, smaller companies with promising molecules can drive a much harder bargain. Development expertise and overall reputation are among the top factors companies seek. Conversely, scientific expertise ranks only eighth on the list of factors, primarily because most companies believe they have a strong background in pure research.
Creative Partnering
The growing use of co-promotion and equity arrangements is an important sign that biopartnering is maturing. Almost half of biopharmaceutical companies are now using more creative, risk-sharing arrangements to finance the development of new medicines.
Several companies have adopted new business models for developing products using different partners at different stages in the R&D process. For example, Debiopharma in-licenses the molecules it develops and registers them before out-licensing for sales and marketing.
Furthermore, many large firms are expanding their links with academia and adopting a more strategic approach to such alliances. Rather than using academic medical centers to design and conduct clinical trials, pharmaceutical companies are now commissioning university scientists to solve specific research problems in areas of mutual interest.
Four steps to becoming an alluring biopartner
IBM survey analysis suggests that life-sciences companies can take four steps to developing productive partnerships in a world where delivery models are rapidly changing.
The 2008 biopartnering survey-the fifth to be conducted since 1999-aims to assess how well large pharmaceutical and biotech companies interact with their partners. It draws on the responses of 223 people from 209 commercial and academic organizations around the world. Fifty-five percent of the 223 respondents work in biotech companies, while 29 percent work in other areas of the life sciences sector (including pharmaceuticals, medical device manufacturing, contract research and contract services). Academic researchers comprise 16 percent of the total sample.
For more information and to download the study, please visit www.ibm.com.
For more information on Silico Research please visit
www.silico-research.com
.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.