Download the free whitepaper: Unravelling the complexities of genomics-driven drug discovery

Genomics-driven drug discovery holds immense promise in developing targeted therapies by leveraging genetic and biomarker information to understand the root causes of diseases. However, the field faces significant hurdles.

In this whitepaper, we examine the obstacles of limited recontactability, scarcity of multi-omics data sets, lack of diversity in data, and the challenge of scaling research for rare diseases. By addressing these challenges and proposing strategies to address them, this whitepaper aims to chart a path by which we can harness the full potential of genomics-driven drug discovery.

 

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Genetic hearing loss case study

Sano designed and executed a patient finding protocol across the US and UK to raise awareness of a gene therapy trial for genetic hearing loss (GHL) caused by OTOF variants, a rare and often overlooked genetic cause. The work called for careful, educational messaging given the sensitivities around newborn genetic testing and the vulnerability of new parents.

We built a custom study page and screening flow, referred eligible participants to genetic testing, and reached families through patient advocacy groups and targeted digital outreach, turning a sensitive topic into a trusted path to research.

Download the case study to see how Sano is helping accelerate research into genetic hearing loss.

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