Let's talk medical research

Two of the most critical components of any clinical trial recruitment campaign are patient-centricity and trust. Antidote has a robust Contact Center with personable and knowledgeable agents that walk patients through the prescreening process and answer any questions along the way. We spoke with our Contact Center Operations Manager, Andy Schulz, about why he joined the team, what his team’s ...

Clinical trials can’t move forward without volunteers. But, the barrier to entry for clinical trials can be inordinately high, starting with public information like a study page or a listing in a database. We share three tips for people who want to participate in a clinical trial, such as having your medical history handy, using a clinical trial search tool, and creating a list of questions to ...

People of color are largely unrepresented in clinical research studies. However, many factors, including biological sex, disabilities, chronic comorbidities, geographical location, gender identity, race, and ethnic background, can influence how an individual may react to certain drugs, medical devices, and treatment plans. We share three key ways to drive diversity in clinical trials, so that ...

Clinical trial project managers are at the heart of research. They keep studies running on schedule, help manage budgets, choose and liaise between vendors, report on results, enforce compliance, and fulfill other key duties.

When a clinical trial is in danger of not meeting its endpoints, sponsors may consider rescuing the research initiative by bringing a new set of vendors into the mix. With appropriate planning, sponsors can transition to a new team seamlessly, minimize any momentum lost, and ensure that the new vendors are set up for success.

Like clinical trials for medications, devices must go through various testing processes before they can be approved for patients. Medical device trials, however, are typically smaller in scale and require fewer phases.

With 80% of clinical trials failing to meet enrollment timelines and up to 50% of sites enrolling one or no patients at all, there are many opportunities to “rescue” studies. When timelines are at risk, data quality is suspect, and management practices are questionable, a new vendor can be brought in to rescue a study and get it back on track.

Antidote’s new podcast, Talk of the Towne, focuses on the ultimate sweet spot: that special place where science and patients converge. Our host, Rich Towne, was trained in pharmacy and currently works in Clinical Informatics at Antidote. In each episode, Rich welcomes a new guest from an organization with which Antidote is working, and takes an in-depth look at particular therapeutic areas, ...

In our work, we're honored to speak with advocates about their lived experiences, why they participate in research, and how they engage with their communities. Our partners at the Lupus Research Alliance graciously connected us with Carly H., a lupus nephritis advocate from Brooklyn, New York. We were able to chat with Carly over Zoom about her diagnosis story, why it’s so important to have a ...

Patient-centricity is at the heart of the clinical research community. It’s a guiding principle for study design and recruitment efforts that puts the focus on the people at the core of research: volunteers and their loved ones. At Antidote, we think of patient-centricity as letting the patient voice drive how we think about the recruitment component of the clinical trial process. We look at ...