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Clinical research blog

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

Navigating FDA guidance on natural history studies

Developing treatments for rare diseases involves unique obstacles due to the rarity and complexity of these conditions. To address these challenges, the FDA off...
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Understanding disease progression: The power of natural history studies

A natural history study is a preplanned observational study designed to track the course of a disease over time. Its purpose is to identify demographic, genetic...
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Patient-centric innovation: Sano's highlights from the CMO Summit 360°

Last week, Sano had the privilege of travelling to Boston for the Chief Medical Officer Summit 360°, where our Co-founder and COO, Charlotte Guzzo, shared her e...
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Clinical trial design in precision medicine: 7 CROs and protocol partners

Clinical trial design and protocol development sit at the foundation of every successful study. The choices made at this stage, from study type and endpoint sel...
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Navigating smooth clinical trials: Tips for pharma and biotech sponsors to avoid study rescue

Clinical trials play a crucial role in the development of pharmaceutical and biotech products. However, unforeseen challenges can arise during the trial process...
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Webinar recap: Why patient centricity is no longer optional in ALS clinical trials

Patient centricity has become increasingly important in clinical trials for ALS. In this webinar, host Paul Wicks and Cathy Collet discuss the challenges of pat...
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How to pick the right CRO for a clinical trial

Choosing a CRO partner affects every phase of a clinical trial. A mismatch in therapeutic expertise, regulatory experience, or service scope can introduce delay...
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Virtual clinical trials: When to shift and reduce risk

Virtual and decentralized trial models have moved from emergency workaround to strategic default for many precision medicine programs. This article examines whe...
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