Stories Library

We proudly offer support and resources to researchers, healthcare providers, patients and their advocates as well as our local communities.

Scientists working in a lab

October 18, 2023

Advancing African Ancestry Representation in Genomic Research and STEM Education

Driven to make a difference through the Together for CHANGE™ Initiative

Genetics

Debbie Allen (award-winning actress, dancer, and director) posing and smiling.

September 20, 2023

Prioritizing Eye Health With the Gr8 Eye Movement

Driving awareness for serious retinal diseases among impacted groups with a patient-focused disease awareness campaign.

Clinical Research & Medicines

Bari Kowal, REGENERON Senior Vice President, Head of Development Operations & Portfolio Management

June 26, 2023

Biomarkers Go Digital

Biomarkers Go Digital

Clinical Research & Medicines

A Woman holding a mug

May 23, 2023

Changing the Paradigm in COPD: Rethinking the Science & Removing Barriers

Committed to a patient-centered and science-forward approach

Clinical Research & Medicines

A close-up view of a microscope

May 23, 2023

An Unequivocal Victory for Innovation

A recent Supreme Court decision helps patients by protecting the scientific innovation emerging from America’s thriving biopharma community

Responsibility & Culture

REGENERON employees working with plants

May 03, 2023

Responsible Innovation: Taking a Holistic Approach to Our Mission to Improve Lives

Unlocking the power of our business to “Do Well by Doing Good”

Responsibility & Culture

Diagram showing a therapeutic agent, VEGF molecule and two VEGF receptors.

April 17, 2023

Our Impact on Diseases of the Retina: Always Striving for Innovation

Regeneron’s unique impact on ophthalmology

Clinical Research & Medicines

Scientist holding test tube

January 25, 2023

Más genómica, menos miedo

El genoma es el cómo y el por qué que nos define

Genetics, Research & Preclinical Development

Technical themed image of a test tube

January 25, 2023

More Genomics, Less Fear

The genome is the how and why that define us

Genetics, Research & Preclinical Development

Graphic reading '1 in 700 PEOPLE have the rare loss-of-function CIDEB genetic mutation.'

October 03, 2022

Going “all in” with liver disease genetics

The "Team Science" approach leading to the discovery of CIDEB mutations that protect from liver disease

Genetics