blog-icon

Clinical research blog

Explore our blog for insights into the big questions in precision medicine and clinical research.

Clinical trial site partnerships in 2025: What sponsors need to know

At the Partnerships with Sites summit in September 2025, new data from the Tufts Center for the Study of Drug Development (Tufts CSDD) underscored how the globa...
Continue reading

Behind the scenes at Sano: Navigating the patient journey

Advocating for patients is one of the core pillars of Sano’s mission. Our approach to clinical trials is patient-centered and entails deep and meaningful engage...
Continue reading

Overcoming rare disease trial hurdles: Q&A with Sano's Head of Clinical Engagement 

Rare disease trials are among the most challenging to design and execute. Patient populations are small and hard to reach, and personal and disease-related burd...
Continue reading

Podcast recap: Wanda Smith on turning a family diagnosis into CureGRN

In last week’s episode of The Genetics Podcast, Patrick Short sat down with Wanda Smith, founder of CureGRN and long-time advocate for families affected by prog...
Continue reading

Building trust in clinical trial patient matching: Takeaways from DPHARM 2025

At this year’s DPHARM conference, Sano’s VP of Commercial, Ben Jackson, joined a panel on clinical trial patient matching moderated by a clinical expert from No...
Continue reading

Podcast recap: Terry Pirovolakis on turning his son’s diagnosis into Elpida Therapeutics

On the most recent episode of The Genetics Podcast, we hosted Terry Pirovolakis, founder and CEO of Elpida Therapeutics. Terry’s journey began the day his young...
Continue reading

Q3 product spotlight: New testing options and smarter operations

At Sano, our mission is to accelerate precision medicine research through technology, making it easier for sponsors to run trials efficiently and effectively. E...
Continue reading

The power of natural history studies in rare disease R&D

Natural history studies are central to rare disease research. Rare diseases are defined as conditions that affect less than 1 in 200,000 people in the US or les...
Continue reading

Podcast recap: Samuli Ripatti on turning biobank data into clinical impact

On the most recent episode of The Genetics Podcast, Patrick speaks with Samuli Ripatti, director of the Institute for Molecular Medicine Finland (FIMM) and prof...
Continue reading

Podcast recap: Jonathan Marchini on scaling statistical genetics from HapMap to millions of exomes

On the latest episode of The Genetics Podcast, Patrick sat down with Jonathan Marchini, Head of Statistical Genetics & Machine Learning at the Regeneron Gen...
Continue reading