Illumina and Ovation.io launching first-of-kind GLP-1 dataset to accelerate new therapy development

On May 1, 2025 Illumina, Inc. (NASDAQ: ILMN), and Ovation.io, Inc., an organization dedicated to building best-in-class multiomics datasets, reported the development of the largest commercially available clinical multiomic dataset from 25,000 patients treated with glucagon-like peptide-1 (GLP-1) receptor agonist therapies (Press release, Illumina, MAY 1, 2025, View Source [SID1234652464]). The dataset will be made available to the pharma community to advance drug discovery and development. This collaboration is the latest in a series of efforts to partner across the ecosystem, and deploy multimodal data to advance a deeper understanding of biology.

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One in eight adults in the United States have used a GLP-1 receptor agonist, according to a 2024 health tracking poll conducted by the Kaiser Family Foundation. However, roughly 40% of users with Type 2 diabetes do not respond effectively to GLP-1 receptor agonists, according to a study published in Diabetes & Metabolic Syndrome in 2024. The collaboration aims to accelerate GLP-1 therapy development, indication expansion research, and discovery of novel biomarkers and drug targets in nonresponsive populations.

"The power of whole-genome and multiomic insights to impact all diseases is coming into focus, and metabolic disease is a prime example," said Todd Christian, senior vice president of Services, Arrays, and Genomic Access at Illumina. "This collaboration and its novel clinical dataset will be crucial to advancing the next wave of these potential life-changing therapies, and ensuring more patients can benefit from them."

Through a multiyear agreement, Illumina and Ovation are launching an integrated dataset of phenotypic, genomic, and proteomic data from patients treated with GLP-1 therapies, including therapy-responsive and nonresponsive populations. This critical dataset is designed to enable deeper understanding of molecular pathways involved in GLP-1 response, which can unlock new indications where GLP-1 therapies may be effective, as well as new biomarkers and drug targets for patients who do not respond to GLP-1 therapies today.

"We’re proud to collaborate with Illumina to develop one of the world’s largest WGS omics datasets, supporting the millions of patients with diabetes and obesity," said Marty Miller, chief revenue officer of Ovation. "Through this effort—and for the first time at scale with the inclusion of proteomics—we aim to equip the pharmaceutical industry with the insights needed to better understand the varying effectiveness and side effects of GLP-1 receptor agonists across individual patients."

The initiative leverages end-to-end Illumina NGS technologies to sequence 25,000 whole genomes and to profile the protein expression of 5000 samples, using the Illumina Protein Prep (IPP) assay, which detects 9500 human proteins per sample. The initiative aims to include a longitudinal subset of proteomes from paired samples collected before and after patient exposure to GLP-1 therapy.

IPP enables the discovery of new protein quantitative trait loci (pQTL), which are emerging as a vital tool for drug discovery, linking genetic variation with protein expression data and disease or other phenotypes. The pQTL dataset is processed using Illumina’s industry-leading DRAGEN secondary analysis and the newly released Illumina Connected Multiomics for tertiary analysis and visualizations. The data is stored for future large-scale studies in Illumina Connected Analytics.

Ovation is providing samples from its biobank of over 1.7 million de-identified, consented, and tokenized samples, linked to rich, longitudinal phenotypic data.

Ovation announced an original agreement with Illumina in 2024, aimed at addressing challenges in drug development through genomic data solutions. The initial phase of the collaboration focused on creating pilot datasets from patients with liver disease, chronic kidney disease, and patients treated with GLP-1 receptor agonists. The companies plan to explore opportunities to scale the GLP-1 dataset and generate others in the future.

First patient enrolled in Phase 1 clinical trial of Akiram’s cancer drug candidate AKIR001

On April 30, 2025 Akiram Therapeutics, a Swedish biotech company specializing in targeted radiotherapy, reported that the first patient has been enrolled in the Phase 1 clinical trial of its drug candidate 177Lu-AKIR001 (Press release, Akiram Therapeutics, APR 30, 2025, View Source [SID1234652375]). The trial is being conducted at Karolinska University Hospital, which also acts as the study sponsor, and marks an important milestone in Akiram’s efforts to develop a new targeted treatment for difficult-to-treat cancers.

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This is the first-in-human trial with AKIR001 and aims to evaluate the drug’s safety, tolerability, and pharmacokinetic profile. The trial follows a dose-escalation design and targets patients with advanced, difficult-to-treat tumors.

Akiram’s drug candidate 177Lu-AKIR001 is a targeted radiopharmaceutical that combines an antibody directed against CD44v6—a cancer marker associated with several aggressive tumor types—with the therapeutic radioisotope lutetium-177. Through this mechanism, radiation can be delivered directly to tumor cells while minimizing damage to surrounding healthy tissue.

The trial is enrolling patients with anaplastic and iodine-refractory thyroid cancer, head and neck squamous cell carcinoma, gynecological squamous cell carcinoma, and non-small cell lung cancer. It is expected to run for 18–24 months with patients recruited on a rolling basis. As the sponsor, Karolinska University Hospital is responsible for conducting the trial in accordance with applicable regulations and with patient safety as a top priority.

"The launch of the clinical trial with AKIR001 marks the beginning of a new chapter for Akiram. Our vision has always been to develop a treatment that can offer new opportunities for patients with difficult-to-treat cancers, where treatment options are often limited. Seeing our drug candidate now being evaluated in collaboration with Karolinska University Hospital—one of Europe’s leading cancer centers—is a major milestone and a strong motivator for our continued work," says Marika Nestor, CEO of Akiram Therapeutics.

"The enrollment of the first patient means that we have now initiated dose escalation and systematic evaluation of AKIR001’s safety and potential. This is an important first step in understanding how the drug behaves clinically and the potential role a CD44v6-targeted therapy could play in tumor types where treatment options today remain limited," says Dr. Luigi De Petris, Principal Investigator at Karolinska University Hospital.

The trial is registered at ClinicalTrials.gov: NCT06639191.

Jazz Pharmaceuticals to Participate in the BofA Securities 2025 Healthcare Conference

On April 30, 2025 Jazz Pharmaceuticals plc (Nasdaq: JAZZ) reported that the Company will participate in the BofA Securities 2025 Healthcare Conference. Company management will participate in a fireside chat on Wednesday, May 14, 2025, at 10:00 a.m. PT / 1:00 p.m. ET / 6:00 p.m. IST (Press release, Jazz Pharmaceuticals, APR 30, 2025, View Source [SID1234652395]).

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An audio webcast of the fireside chat will be available via the Investors section of the Jazz Pharmaceuticals website at View Source A replay of the webcast will be archived on the website for 30 days.

Quarterly Activities/Appendix 4C Cash Flow Report

On April 30, 2025 Imugene reported results for quarter ended March 2025 (Presentation, Imugene, APR 30, 2025, View Source [SID1234654357]).

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Nain Biopharmaceuticals Presents World-First R&D Results at AACR 2025

On April 30, 2025 Nain Biotech reported the company presents World-First R&D Results at AACR (Free AACR Whitepaper) 2025 Chicago (Press release, Nain Biotech, APR 30, 2025, View Source [SID1234654627]). This international conference, steeped in a century of academic heritage, once again captured global attention with its groundbreaking themes and unprecedented attendance. According to official data, the conference brought together over 20,000 leading oncology scholars, clinicians, and industry representatives from over 60 countries. They engaged in in-depth discussions on cutting-edge fields such as precision medicine, immunotherapy, and gene editing, exploring more feasible technological approaches to advance humanity’s fight against cancer.

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