“And then hopefully, you can make something meaningful out of it.”īut a growing number of large biopharma companies are moving to the concept of a technology platform that gives them an end-to-end view of their supply chain. “If you want to take a look holistically at what’s happening in your supply chain, you have to go to many systems and consolidate everything yourself in something like an Excel environment,” Kappelle said. But often, sponsor companies working with multiple contract manufacturers face the challenge of dealing with various ERP or MRP systems. Occasionally, a company will use an integrated enterprise resource planning (ERP) or material requirements planning (MRP) system to keep track of such disparate elements. “The manufacturing activities, including the packaging and labeling, the drug product, manufacturing, drug substance manufacturing - all of those things are generally managed in different systems,” Kappelle said.
Supply chain digitization promises to help tame the chaos. “But if you look into managing the clinical supply chain, a lot of the activities are done in a fragmented way,” Kappelle said. Still, a growing number of clinical trials use wearables to collect data from patients.
“The whole IoT component is not well matured in clinical trials.” Fast-forward to today, IoT adoption in the pharmaceutical sector remains at an early phase. The digitization of clinical supply chains continuesĪ few years ago, the hype was high regarding the promise of the Internet of Things (IoT), which promised to optimize nearly every conceivable industry. “Patients are getting much more vocal,” Kappelle said. But as the internet continues to grow, patients have become better informed about active clinical trials. Conversely, patients in the past tended to have a more passive role. “The voice of the patient becomes much more important,” Kappelle said.
#Drug free clinical trials trial#
“In a DCT trial setting, you have a much greater access to patients, which on the sponsor side is very much appreciated because this can accelerate your enrollment of patients in the study.”ĭCT trials also are empowering for clinical trial volunteers. First, it makes it easier to optimize clinical trial diversity and accelerate enrollment. “There’s an interest from industry and people who acknowledge that the DCT structure makes a lot of sense for the future,” he said. As a result, some drug developers have returned to traditional strategies for managing clinical trials.īut growth in DCT trial designs remains strong, Kappelle said. Biogen Trial Link: Learn more about clinical trials, why they are important, what they involve, and view our currently enrolling U.S.Jan Pieter Kappelle, VP of strategy of 4G Clinical But the DCT model is easier to pull off in some geographies and medical specialties than others.See detailed information on currently enrolling clinical trials for Biogen investigational and marketed therapies on.View our current pipeline to learn more about clinical trials for specific conditions.By volunteering for a clinical trial, you are helping the medical community determine whether new treatments are safe and effective.īiogen is conducting numerous clinical trials in neurologic and immunologic diseases to evaluate the efficacy and safety of potential therapies. The benefits and risks of taking the treatment are not completely known. In most cases, the therapies investigated in clinical trials are not yet approved by regulatory agencies like the Food and Drug Administration (FDA) in the United States.
Each individual’s participation contributes enormously to our understanding of disease and has the potential to benefit patients around the world.ĭeciding to participate in a clinical trial requires careful consideration. We are grateful to the patients, healthy volunteers, families, hospitals and clinics that participate in the clinical trials for testing our potential therapies. Biogen’s mission is to discover, develop and deliver innovative therapies that improve the lives of patients.
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