We recently sat down with one of our partners, Rare Patient Voice, to discuss clinical research, patient centricity, and more.

In honor of Lupus Awareness Month, we chatted with the Lupus Foundation of America about clinical trials, community building, and more.

With data from over 16,000 patients with CVD, Antidote has gathered insights into demographics, racial disparity, prevalence, and more.

From site staff and research coordinators to doctors and nurses, there are many industry professionals that make a difference in patients’ lives.

The patient experience is crucial to a clinical trial’s success, and these actionable tips can help ensure that participants have a positive outlook.

Eosinophilic esophagitis is a rare disease with no known cure. In this blog, we’re sharing some key information about the condition and how it’s treated.

Homocystinuria is a rare disease that often impacts children. Learn more about this condition and what it entails here.

Though asthma can affect anyone, the condition has a disproportionate impact on minority populations.

Finding clinical trials near you can be a challenge, but this blog has all the details about how to make it easier.

This National Kidney Month, we’re raising awareness of IgA nephropathy and what differentiates it from other kidney diseases.

Though many things remain unknown about blood disorders, these facts about hemophilia can be a helpful place to start.

After analyzing over 1,900 individuals searching for depression clinical trials, we've gained valuable insight into patient demographics and motivation.