Patient Engagement

ÐǺ£ÆåÅÆ receives and shares insights and knowledge to help patients and care partners make the most of their lives – both during and after treatment.
By working with patients, advocates, and professional organizations, we gain a deeper understanding of the patient and care partner perspective. This collaboration directs us to incorporate real world learnings from every stage and aspect of developing a medicine.
Three ÐǺ£ÆåÅÆ employees smile in conversation while walking their bikes outside the office.Three ÐǺ£ÆåÅÆ employees smile in conversation while walking their bikes outside the office.
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Creating a positive impact for patients

By 2030, ÐǺ£ÆåÅÆâ€™s antibody medicines will be fundamentally transforming the lives of people with cancer and other serious diseases.

This is ÐǺ£ÆåÅÆâ€™s vision for the future and to make the vision come to life, we include the patient voice into every possible aspect of our work. 

We work with a patient-first mindset while engaging with patients and organizations to learn and share experiences and knowledge. Together we can provide education that empowers patients and care partners for self-advocacy, and help progress towards equitable access and optimal care while advancing the science. 

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Headshot of Mark Peters, ÐǺ£ÆåÅÆ Senior Director of Patient Advocacy, smiling.
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The insights from patients, care partners, patient advocacy groups, and professional organizations are integral to our work at ÐǺ£ÆåÅÆ. From early-stage research and development to clinical trials and commercialization, we are committed to incorporating their perspectives into all aspects of our work.

Mark Peters

Senior Director, Patient Advocacy


Our commitment to improving the lives of patients

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Our Patient Advisory Council
As part of our commitment to listen to patients and put them at the center of our work, our patient advocacy team facilitates opportunities with patients and patient advocacy organizations to share insights. The ÐǺ£ÆåÅÆ Patient Advisory Council meets regularly to dive deep into topics such as clinical trial recruitment and diversity in clinical trials, providing patient perspectives on the cancer experience and how ÐǺ£ÆåÅÆ can better serve patient and care partners. Members of the Council represent people with a variety of tumor types, ages, geographies and socioeconomic backgrounds. The perspectives of patient advisors are integrated into all aspects of our work. 

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Resources for patients and care partners
Navigating a cancer diagnosis is challenging. Finding all the information about living with cancer can be hard for patients and their care partners. Follow the link below for resources offered by patient advocacy and professional organizations.