Precision health company Helix announced on Monday that it is introducing a new comprehensive clinico-genomic dataset of more than 15,000 patients treated with glucagon-like-peptide-1 (GLP-1) agonists including semaglutide, tirzepatide, liraglutide and dulaglutide.
The research-ready Virtual Registry was built as part of the Helix Research Network (HRN). The cohort consists of whole Exome+ sequencing profiles for 15,000 GLP-1 agonist treated patients combined with longitudinal and regularly refreshed EHR data including demographics, clinical diagnosis (T2D, CVD, kidney diseases, etc), major lab results and procedures, as well as insights from medical and mortality claims data.
James Lu, MD, PhD, Helix CEO, said: "The success of GLP-1 agonists like semaglutide and tirzepatide have created incredible advances in the treatment of cardiometabolic disease and obesity, and the demand for and uptake of these therapies are not slowing down anytime soon. Our registry has more than tripled in less than a year, and will continue to meet and even outpace usage trends, allowing insights from deep real-world data coupled with broad genomic data to play a key role in monitoring safety profiles, determining cost-effectiveness and improving treatment efficacy in select populations."
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA