At a glance
- Company
- Adherium Limited
- Ticker
- ASX: ADR
- Announcement
- Partnership
- Location
- Atlanta, Georgia, United States
Key figures
- SENTA locations
- 48
- SENTA states
- six
- SENTA specialists, physician assistants and nurse practitioners
- 88
Products and programs
November 21, 2023 -- Adherium Limited (ASX: ADR), a leading digital health company specialising in remote patient monitoring and data solutions for respiratory patients, confirms the first patients have been enrolled and remote patient monitoring underway as part of the SENTA’s commercial roll out of the Hailie® platform.
In September Adherium entered a partnership with SENTA (Southern Ear, Nose, Throat and Allergy), one of the largest, premier specialty allergy and asthma medical groups in the United States. The first patients are now being monitored and managed at SENTA clinics in Atlanta, Georgia.
Enrollment will expand and scale to more patients and providers into 2024 within SENTA’s 48 locations in six states with 88 specialist allergy, asthma and ENT physicians, physician assistants and nurse practitioners.
Hailie’s FDA 510(k) cleared advanced, drug agnostic sensors are the first to measure inhaler use and inspiratory flow rate. Adherium's state-of-the-art Hailie sensor technology and software platform empower patients and their doctors with information to improve adherence, reduce exacerbations and improve quality of life.
Hailie enables doctors to bill for long-term, remote patient management under established US reimbursement codes. Adherium is paid for sensor sales and receives monthly, per patient fees for generating and transmitting respiratory data.
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Questions around this news
What does the SENTA rollout of Hailie involve?
The release says the first patients were being monitored at SENTA clinics in Atlanta, Georgia, after a partnership announced in September. It describes plans to extend enrollment to more patients and providers across SENTA’s locations into 2024. The monitoring uses sensors and software to collect respiratory data for patients and their doctors.
What does FDA 510(k) clearance mean?
510(k) clearance is a U.S. regulatory decision that allows a medical device to be marketed when it is found substantially equivalent to a legally marketed device, called a predicate. It is distinct from approval through a process that requires a different level of evidence. The specific requirements depend on the device and its intended use.
What is inspiratory flow rate?
Inspiratory flow rate is the speed at which a person draws air into their lungs during inhalation. In respiratory care, measuring it can help assess how someone breathes and whether their inhalation technique is suitable for a particular inhaler. The measurement is different from simply recording whether or when an inhaler was used.
