clinicalRSVP Expands Phase 1 Network, Joins Two California Sites
clinicalRSVP
, the nationwide network that prevents research volunteers from enrolling in multiple concurrent research studies, announced the addition of Anaheim Clinical Trials and Profil Institute for Clinical Research, Inc. to the clinicalRSVP network.
The new California sites will join participating sites in Florida and Ontario who access
clinicalRSVP.com
to check subject eligibility requirements before dosing commences. The addition of the two West Coast sites expands the reach of the clinicalRSVP site network, as well as strengthens the relevance of the network for participating sites. The goal of clinicalRSVP.com is to provide a single continental registry for all Phase 1 investigators to check and report subject eligibility criteria, thereby improving data integrity for sponsors and trial safety for participants.
ClinicalRSVP.com began operating in 2009 with five sites located in South Florida, and has since grown the network to eighteen (18) Phase 1 units across the United States and Canada.
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.
