Shire Renews Rare Genetic Disease Collab With Santaris

NewsGuard 100/100 Score

In what was surely music to Santaris' ear, Shire extended an existing agreement, saying, "We are delighted with our partnership with Santaris, whose expertise and capabilities in LNA antisense therapy complement Shire's drug discovery and development strengths."

The long-term partners have been working together in the rare genetic disease space since 2009. Under the terms of the extended agreement, Shire will have the right to nominate additional collaboration targets for drug discovery and development. Santaris will receive an upfront payment and, consistent with the initial agreement, is eligible for research support and preclinical, clinical, and sales milestones and royalties on each product emerging from the collaboration.

The original deal provided Santaris with early-stage payments of $6.5 million covering technology access, exclusivity for three predefined targets and initial discovery funding, and an additional early-stage payment of $13.5 million upon successful completion of certain initial studies.

In addition to the initial payments under the 2009 contract, Santaris received funding for all additional discovery activities to be performed and payments on Shire's nomination of up to two additional targets, and was eligible to receive development, regulatory, and sales-related milestone payments of up to $72 million for each of the potential five drug candidates and customary royalties on the worldwide sales of commercialized products arising from the alliance.

With its LNA Drug Platform and Drug Discovery Engine, Santaris combines LNA chemistry with specialized and targeted drug development capabilities to deliver LNA-based drug candidates against RNA targets, both mRNA and microRNA, for a range of diseases including cardiometabolic disorders, infectious and inflammatory diseases, cancer, and rare genetic disorders.


Genetic Engineering & Biotechnology News (GEN) Genetic Engineering & Biotechnology News (GEN)This article was reprinted from Genetic Engineering & Biotechnology News (GEN) with permission from Mary Ann Liebert, Inc., publishers. Genetic Engineering & Biotechnology News (GEN) has retained its position as the number one biotech publisher around the globe since its launch in 1981. GEN publishes a print edition 21 times a year and has additional exclusive editorial content online, like news and analysis as well as blogs, podcasts, webinars, polls, videos, and application notes. GEN's unique news and technology focus includes the entire bioproduct life cycle from early-stage R&D, to applied research including omics, biomarkers, as well as diagnostics, to bioprocessing and commercialization.

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Exploring how gene variants affect brain cells in children with severe epilepsy