Global Survey on the Impact of Decentralized Clinical Trials (DCTs) on Sponsor-CRO Collaborations
The Tufts Center for the Study of Drug Development at the Tufts University School of Medicine is conducting an ambitious global study to characterize and benchmark the impact of decentralized clinical trials (DCTs) on sponsor-CRO collaborations. This is one of the most comprehensive surveys of its kind among clinical research professionals and it will gather critical baselines to compare against future results. We are focused on gaining insights and perceptions on this topic across a wide range of organizations and appreciate your time on this research.
Please click on the link below to complete the survey: Take the Survey
The survey should take approximately 30 minutes of your time. Your responses will be strictly confidential and will only be reported in the aggregate; none of the study findings can be traced back to any individual or organization. A summary report of de-identified, aggregate results will be shared with 10 pharmaceutical companies and contract research organizations (CROs) that funded the study. In appreciation for completing the survey, we’ll send you a summary of the results. Thank you in advance for your participation in this important research effort!
Please complete the survey by March 25, 2022.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
FDA Grants Ziftomenib with Breakthrough Therapy Designation for NPM1-Mutant Acute Myeloid Leukemia
April 23rd 2024Data from the Phase Ib portion of the KOMET-001 trial showed that the once-daily oral treatment may provide a substantial improvement over available therapies for relapsed/refractory NPM1-mutant acute myeloid leukemia.
