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September 9, 2022

Gatehouse Bio and AstraZeneca to develop RNA therapeutics for heart failure

The partnership is expected to expedite the development of a range of new therapeutics using the small non-coding genome area.

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US-based biotech company Gatehouse Bio is extending its collaboration with AstraZeneca for developing RNA therapeutics to treat heart failure with preserved ejection fraction (HFpEF).

Initially, the companies partnered to identify new targets for respiratory and cardiovascular diseases using Gatehouse Bio’s artificial intelligence (AI)-powered platform in December 2019.

The expanded partnership will combine the scientific expertise and investment of AstraZeneca in RNA therapeutics with Gatehouse Bio’s capabilities in developing disease-modifying small RNA compounds.

It is expected to expedite the development of a wide range of new therapeutics using the small non-coding area of the genome that is not explored.

AstraZeneca Oligonucleotide Discovery vice-president Dr Shalini Andersson said: “Gatehouse Bio’s expertise and platform in small RNA together with our own scientific expertise presents a significant opportunity for targeting the drivers of disease in heart failure.

“Together, we are steadily closing the gap between RNA modality, AI, and disease biology with the shared goal of discovering and developing novel treatments in heart failure.”

Gatehouse Bio is engaged in developing small RNA-based therapeutics using AI technology.

Using its platform, the company has discovered mutations that are associated with disease and also designs therapeutics for counteracting their effect.

Gatehouse Bio chief business officer Neal Foster said: “Our ability to identify small RNA mutations opens a novel class of targetable biology and an opportunity for a portfolio of oligonucleotide therapeutics that target specific groups of patients.”

The company discovered mutations in small RNA genes that are connected to microvascular dysfunction in a previous study.

The mutations were expected to regulate biological pathways that are related to a clinical syndrome.

Cell & Gene Therapy coverage on Pharmaceutical Technology is supported by Cytiva.

Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content.

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