ESMO 2026:
Key Findings for Cancer Care and Drug Development

Date
Monday, November 09, 2026Mon, Nov 9, 2026
Time
11am EST (NA) / 4pm GMT (UK) / 5pm CET (EU-Central)11am EST
Duration
60 min— Live + Q&A
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About this webinar

As oncology research continues to advance, understanding the clinical significance of emerging evidence is essential for informing treatment strategies and guiding future research. The European Society for Medical Oncology (ESMO) Congress 2026 brought together healthcare professionals, researchers and industry experts to examine the latest advances in cancer research, treatment and clinical practice.

This webinar will explore key clinical trial results and advances in cancer therapies presented at ESMO 2026, with a focus on their implications for cancer treatment and oncology drug development. By examining these findings alongside existing treatment approaches, the discussion will highlight opportunities to improve patient care and advance therapeutic development.

The featured speakers will place these findings in the context of current evidence, examining their relevance to treatment decisions, remaining uncertainties and priorities for further research. Participants will gain a concise overview of the key messages presented at the congress and their significance for cancer care and oncology development programs.

Register for this webinar to learn how key findings from ESMO 2026 may inform clinical decision-making, cancer treatment strategies and future oncology research.

Who should attend

This webinar will appeal to professionals across the following roles and functions seeking a concise, clinically relevant update on ESMO 2026:
  • Medical/Clinical Oncologists
  • Oncology Fellows and Trainees
  • Clinical Researchers
  • Medical Affairs professionals
  • Medical Directors
  • Translational Medicine Scientists
  • Pharmaceutical and biotechnology R&D professionals

What you will learn

Attendees will gain insight into:
  • Key clinical trial findings and emerging oncology research presented at ESMO 2026
  • Advances in cancer therapies and their potential implications for clinical practice
  • How emerging evidence may inform treatment decisions and future drug development strategies
  • Remaining clinical uncertainties, research gaps and priorities shaping the future of cancer care

Featured Speakers

Cesar Eduardo Carrasco, MD, PhD, Senior Medical Director, Kapadi

Cesar Eduardo Carrasco, MD, PhD

Senior Medical Director · Kapadi

Dr. Cesar Alberto Eduardo Carrasco is a Senior Medical Director at Kapadi, Inc. He is a clinical oncologist and molecular geneticist with more than 20 years in the pharmaceutical and CRO industry, including 15 years running and medically monitoring Phase I–III clinical trials. At Kapadi he works as Global and Regional Medical Advisor on assigned projects. His work covers medical oversight of trials, protocol and eligibility support for investigative sites, Medical Management Plans, medical data review, and review of adverse events (AEs) and serious adverse events (SAEs) in collaboration with Pharmacovigilance.

Before Kapadi, he held Senior Medical Director roles at Parexel International, and Medpace in USA. He was Medical Director at Parexel in Buenos Aires and Associate Global Medical Director at Quintiles. Earlier, he held oncology medical affairs and medical science liaison roles across Latin America at Roche, GlaxoSmithKline, Ferrer-Leti, and Eli Lilly. His medical affairs work included advisory boards, investigator-initiated trials, training programs covering about 20 countries, and engagement with key opinion leaders.

He has supported more than 140 oncology and hematology projects. These include solid tumors (breast, lung, gastric, colorectal, liver, prostate, ovarian, and GIST), hematologic malignancies (B-cell non-Hodgkin lymphoma/CLL, multiple myeloma, mastocytosis, and mycosis fungoides), and cell and gene-based therapies such as CAR-T, CAR-NK, and RNA/antisense. He also brings experience in study start-up, regulatory submissions, preparing informed consent forms (ICFs), and negotiating site contracts.

Dr. Carrasco earned his MD and his clinical oncology specialization at Universidad Central de Venezuela. He also holds a PhD in Molecular Genetics, with a focus on Molecular Oncology, from the Instituto Venezolano de Investigaciones Científicas.

Scott E. Smith, MD, PhD, FACP, Chief Medical Officer, Kapadi

Scott E. Smith, MD, PhD, FACP

Chief Medical Officer · Kapadi

Scott E. Smith, MD, PhD, FACP, is Chief Medical Officer at Kapadi and a Physician-Scientist with more than 20 years of leadership in hematology, oncology and clinical research. As Senior Vice President and Global Head of Hematology at Parexel, he oversaw global clinical trial operations across more than 20 countries. As Founder and CEO of Chemosabe Consulting, he has advised more than 15 pharmaceutical and biotechnology companies on clinical development and immunotherapy strategy, contributing to the launch of four hematology and oncology therapies.

Previously, Dr. Smith served as Associate Cancer Center Director and Section Chief of Hematology at Loyola University Medical Center, where he expanded clinical programs and led teams of more than 50 professionals. His work includes bone marrow transplantation, CAR T-cell therapy, precision medicine initiatives and review for the FDA Orphan Products Development Program. He has authored more than 150 peer-reviewed publications and abstracts and has spoken at international meetings including ASH and ASCO. Dr. Smith earned his MD and PhD at Wayne State University and is board certified in Internal Medicine, Hematology and Medical Oncology.

Partner for this event

Humaneva Group

Humaneva Group: Revolutionizing Oncology Research by a Fully Integrated Approach

Humaneva Group is an integrated clinical research company that brings together specialized research sites, global CRO capabilities, and advanced clinical technology to improve how clinical trials are planned, conducted, and delivered.

Through its interconnected companies (Pratia, Kapadi, and Hyggio), Humaneva connects patients, investigators, research sites, sponsors, and clinical data within a coordinated operating model designed to increase efficiency, data quality, and certainty of execution.

With a particular focus on oncology, Humaneva Oncology combines an embedded oncology site network, purpose-built CRO expertise, patient identification and screening intelligence, and real-time data capabilities. This integrated approach reduces fragmentation, strengthens accountability, and helps sponsors navigate increasingly complex clinical development programs—from early planning and patient access through trial delivery and reliable data generation.

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Live: Mon Nov 9