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About This Webinar
Sponsors must be able to balance the need for efficiency and inclusivity on the path to seeking drug approval for rare cancer. Focusing on this topic, our oncology experts will share valuable insights and strategies for developing and operationalizing clinical trials in this space in this free educational webinar.
Agenda
- Defining what rare cancer means
- Considerations for protocol design- including patient-reported outcomes (PRO)
- Evolving approaches to feasibility
- Strategies for operational delivery
- Q&A with our experts
Language:
English
Who can attend? Anyone with the event link can attend
Featured Presenters
Senior Vice President, Oncology Strategy & Innovation, Ergomed
Debra Kientop is an experienced, strategic leader in oncology clinical development across Pharma, Biotech, and CRO industries. She has focus on patient-centricity and incorporating innovative solutions into clinical delivery. Her role is strategic and executive oversight of clinical trials, sponsor and KOL engagement.
Senior Vice President, Global Medical Affairs, Ergomed
Dr. Marie-Edith A. Bonneterre, is based in Lille, France, and is board-certified in Medical Oncology. Her experience in both the hospital setting and the pharma industry, biotechnology and CRO arenas is focused on clinical development and innovative strategies. Her role is strategic and medical oversight of clinical trials, innovative development strategies.
Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed Clinical Research is a complete, global Phase I-IV clinical development and trial management service with a strong heritage in the development of drugs in rare diseases and oncology.
Founder & Managing Director
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