Diabetes management company ALR Technologies SG Ltd (OTC: ALRTF) announced on Monday that it has completed internal manufacturing testing of its GluCurve Pet CGM, confirming accuracy comparable to leading veterinary Blood Glucose Meters (BGM). The company plans to relaunch the device in the Canadian market in January 2026.
GluCurve is the first continuous glucose monitoring system specifically designed for cats and dogs. The sensor attaches painlessly to pets and provides blood sugar readings every three minutes for up to 14 days. Data is accessible to pet owners via the GluCurve app and to veterinarians through the ALRT Veterinary Web Portal, enabling remote or in-clinic insulin management.
An independent non-inferiority study is scheduled for mid-December to further validate GluCurve's efficacy against standard veterinary BGMs.
A US relaunch is expected in early Q2 2026 via a strategic veterinary distributor, followed by global expansion to Europe, Australia, Asia and South America.
ALR Technologies also offers the ALRT Diabetes Solution for human patients, combining FDA-cleared glucose monitoring, predictive A1C tracking, and an insulin dosing adjustment program to optimise diabetes therapy. The GluCurve Pet CGM extends this data-driven approach to companion animals, supporting veterinarians in optimising insulin treatment and improving diabetic care outcomes for pets.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval