Scimega Launches New Reverse Feasibility Resource Center to Attract the Best Oncology Compounds for Canadian Cancer Patients
Scimega Research is pleased to announce the launch of its new Reverse Feasibility Resource Center
Scimega Research, (www.scimega.com) the experts in clinical oncology, is pleased to announce the launch of its newReverse Feasibility Resource Centre, a unique initiative that complements its highly successful Reverse Feasibility Program that matches the patient recruitment needs of U.S. oncology sponsors with the scientific interests of Canadian investigators and the treatment needs of their patients.
This microsite will enhance sponsor access to the program by providing regular updates that highlight Canada’s expertise in both early and late phase oncology trials. It currently features important information such as the number of oncology sites, key investigators, and catchment area size for each of the ten Canadian provinces.
Sponsors can sign up to receive free quarterly updates on the types of trials Scimega’s Reverse Feasibility Champions are looking to participate in. The Oncology Trial Needs Report for Canada will highlight the number of sites actively looking for trials, based on lines of treatment, tumor types and targets.
“The Reverse Feasibility Program was launched in 2009 to attract state-of-the-art clinical research to Canada,” said Denise Deakin, President & co-founder of Scimega Research. “It was founded on the premise that long-standing relationships between Scimega and top performing oncology sites could be leveraged by sponsors to maximize the performance and quality of their trials, while enhancing the overall clinical trial experience for both investigators and patients,” continued Ms. Deakin.
“Using this approach, we’ve seen as much as a 50% reduction is study start-up times, while meeting targeted patient recruitment objectives. It’s really proven to be win-win situation as sponsors are thrilled with the performance metrics, while clinicians and their patients are happy to take participate in well designed, cutting-edge trials. We’re hoping the new Resource Centre will help facilitate many more of these positive experiences.”
Empowering Sites and Patients: The Impact of Personalized Support in Clinical Trials
November 26th 2024To meet the growing demands of clinical research, sponsors must prioritize comprehensive support models, such as clinical site ambassadors and patient journey coordinators, who can address operational challenges and improve site relationships, patient satisfaction, and overall trial efficiency.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
FDA Finalizes Decentralized Clinical Trial Guidance
November 25th 2024The FDA's guidance is part of a broader effort to modernize clinical trials, improve efficiency, reduce participant burden, and expand access, particularly for underrepresented populations and those in geographically or economically constrained areas.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
