Kestra Medical Technologies, Ltd. (NASDAQ: KMTS), a US-based wearable medical device and digital healthcare company, announced on Tuesday that it has entered a strategic collaboration with Israeli-American medical technology company Biobeat Technologies, Ltd. to expand diagnostic insight for patients prescribed the ASSURE Wearable Cardioverter Defibrillator.
The agreement includes an exclusive licence and co-development arrangement, alongside a USD5m equity investment by Kestra in Biobeat's Series B financing. Biobeat has developed an FDA-cleared, cuffless, patch-worn ambulatory blood pressure monitoring device that uses photoplethysmography to deliver continuous, non-invasive 24-hour blood pressure data.
Kestra plans to integrate Biobeat's technology into its product portfolio, enabling ambulatory blood pressure monitoring data for patients using the ASSURE Wearable Cardioverter Defibrillator.
The collaboration follows Kestra's publication of the prospective real-world study of wearable defibrillators, the ASSURE Wearable Cardioverter Defibrillator Clinical Evaluation Post-Approval Study. Data from the study showed that 72% of patients were hypertensive, underlining the challenges of blood pressure management during cardiac recovery and optimisation of guideline-directed medical therapy.
Summit Therapeutics submits FDA application for ivonescimab in EGFR-mutated lung cancer
Sanofi's Teizeild approved in EU to delay stage 3 type 1 diabetes
Renalytix expands US clinical footprint with three kidneyintelX.dkd integrations
EQT Life Sciences exits Vivasure Medical in EUR185m sale to Haemonetics
FDA accepts NDA resubmission for Camurus' acromegaly drug Oclaiz
Saluda Medical secures CE certification for EVA Sensing Technology in Europe
Arbele's ARB1002 receives US FDA Orphan Drug Designation
Compass Pathways wins FDA IND acceptance for COMP360 PTSD trial
Merck completes acquisition of Cidara Therapeutics for USD9.2bn
GSK wins European Commission approval for Shingrix prefilled syringe