Bridging the Gap: Direct-to-Patient Strategies to Support Diversity in Clinical Trials

I'm Ready to Bridge the Gap in Clinical Trial Diversity

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This webinar will explore the latest trends in the clinical trial industry, emphasizing direct-to-patient trial strategies and their impact on diversity, equity and inclusion (DEI). Reaching marginalized communities is a critical component for fulfilling study enrollment, yet these communities often face unique challenges.

One significant hurdle is the financial burden placed on patients due to the leveraging of patient insurance, which can hinder study enrollment and impact efforts to improve clinical trial diversity in the United States. Current industry trends are centered on patient-centric approaches such as DEI, accelerated start-up timelines and decentralized clinical trials.

Prioritizing patient-centricity can significantly enhance patient experience and enrollment, leading to more successful clinical trials. In addition, as clinical trial sites manage numerous studies simultaneously, it is essential to develop supply strategies that simplify the management of investigational medicinal products (IMPs) and non-IMPs (NIMPs).

The webinar will dive into how patient-centric supply strategies can address these complexities, improve trial efficiency and support clinical trial diversity. Through case studies, the featured speakers will examine various sourcing options for sponsors, highlighting their benefits and drawbacks for sponsors, patients and sites. Additionally, the discussion will cover how comparator drug supply vendors handle complex trial designs and access to specialty drugs, ensuring that patient needs are met efficiently.

Register to learn about innovative, on-demand local sourcing solutions, methods to minimize cost and waste in clinical trials and how clinical trial diversity can benefit both sites and patients.

Samit Bhatt, Vice President, Clinical Trial Patient Solutions

Samit Bhatt is the Vice President for the Clinical Trial Patient Solutions team at Myonex. He is responsible for the team’s growing global operations in North America, Europe, Australia and New Zealand. Samit has over 13 years’ experience in the pharmacy and pharmaceutical industry; managing successful formulary status and relationship management with payers, significant understanding of healthcare contracts and knowledge of medical and pharmacy benefits, including specialized knowledge across different therapeutic areas. Samit holds both a Doctor of Pharmacy degree and an MBA from Drake University.

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Todd Luckritz, Associate Director, Clinical Trial Patient Solutions

Todd Luckritz is the Associate Director for the Clinical Trials Patient Solutions team at Myonex. He is responsible for the team’s operations in North America. He has over 22 years’ experience as a Critical Care Pharmacist and as a Lead Pharmacist for the Investigational Drug Services Pharmacy   Team at the Mayo Clinic in Phoenix, Arizona, where he managed  a diverse portfolio of clinical trials from all therapeutic areas.    Todd has extensive knowledge and experience of clinical trial operations of Phase I-IV studies at clinical trial sites and pharmacies. Todd holds a Doctor of Pharmacy degree.

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This webinar will appeal to professionals in the following fields:
  • Vendor Managers/Clinical Vendors Manager
  • Clinical Trial Operations/Supplies Management/Supply Consultant
  • Clinical Trial Comparator Managers/Clinical Trial Sourcing Managers
  • Clinical Supply Planning
  • Strategy Lead Comparator Managers
  • Clinical Trial Managers
  • Clinical research organisations
Attendees will gain insights into:
  • How direct-to-patient strategies and patient-centric supply chain solutions can enhance clinical trial diversity
  • How patient centricity can significantly enhance patient experience and enrollment
  • The challenges of leveraging patient insurance and how innovative approaches can alleviate financial burdens