Sector News

Lilly partners with Haya for lncRNA obesity target deal worth $1bn

September 7, 2024
Life sciences

Pharma giant Eli Lilly is teaming up with Haya Therapeutics in a $1bn deal to find multiple regulatory-genome-derived RNA-based drug targets, as it eyes up new targets in obesity.

Under the deal, the companies will use Haya’s proprietary regulatory genome discovery platform to identify and validate long non-coding RNA (lncRNA) targets for developing potential treatments for obesity and related metabolic disorders.

Until now, Haya has focused its drug discovery platform on fibrotic diseases, cardiovascular and metabolic diseases, and cancer. However, preclinical studies – including one published in the journal Non-coding RNA Research – have demonstrated that lncRNAs also play a role in the development of adipose cells and obesity.

Switzerland-based Haya’s platform focuses on tissue, disease, and cell-specific lncRNA and RNA molecules more than 200 nucleotides long, which regulate gene expression without coding for proteins.

The company’s lead development candidate, HTX-001, is an antisense oligonucleotide targeting the lncRNA Wisper, which is associated with myocardial fibrosis and heart failure.

It comes as no surprise that Lilly is eyeing up new targets in obesity, as it is one of the frontrunners in the space. Its blockbuster drug tirzepatide, which is marketed as Mounjaro for type 2 diabetes and Zepbound for obesity is the main competitor for Novo Nordisk’s semaglutide versions, Ozempic and Wegovy. Lilly reported $5.34bn in sales for both Mounjaro and Zepbound last year, as per the company financials.

This is among a series of deals Lilly has made to identify new obesity drug candidates, including a $1.92bn agreement to acquire Boston-based Versanis and its lead asset bimagrumab in July 2023. Bimagrumab, a monoclonal antibody that attaches to activin type II A and B receptors, is currently being evaluated in the Phase IIb BELIEVE clinical trial both as a monotherapy and along with semaglutide in adults who are obese or overweight.

Lilly also isn’t the first big pharma company to jump into the lncRNA space. This deal comes one week after Bayer teamed up with lncRNA-focused NextRNA in a $547m deal. The companies will collaborate on two oncology programmes, the first involving a lncRNA-targeting small molecule in early preclinical development at NextRNA, and a new target identified by NextRNA’s platform, with Bayer having the option to choose one target for joint development.

In the announcement accompanying the deal, Haya’s CEO Samir Ounzain said: “This partnership with Lilly demonstrates the significant advances we have made with our revolutionary regulatory genome RNA-guided platform and validates the potential of targeting lncRNA for chronic conditions.”

by Jenna Philpott

Source: pharmaceutical-technology.com

comments closed

Related News

September 13, 2024

MedTrace accelerates Phase III trial and announces appointment of Nicholas Borys as Chief Medical Officer

Life sciences

Pharma and medical imaging company MedTrace announced the appointment of Nicholas Borys, M.D., as Chief Medical Officer (CMO). Dr. Borys is a skilled and experienced healthcare executive with over 25 years experience in advancing portfolios of novel therapies across diverse indications in cardiovascular, cancer, and central nervous system disease.

September 13, 2024

Eli Lilly to invest $1.8bn in manufacturing capacity in Ireland

Life sciences

Eli Lilly and Company has announced a significant expansion of its manufacturing presence in Ireland, with a $1bn investment earmarked for its Limerick site. The move is aimed at boosting the company’s production of biologic active ingredients, including those for its approved Alzheimer’s treatment.

September 13, 2024

Lonza completes expansion of microbial manufacturing facility

Life sciences

Lonza recently announced that it has completed a planned expansion of the mid-scale microbial manufacturing facility at its Visp, Switzerland site. This multi-product facility was recently granted a GMP license, allowing cGMP manufacturing and release of biologics produced using microbial fermentation.