Étude de cas : Celerion propose une surveillance continue de la pression artérielle pour un client pharmaceutique


Les sociétés de recherche contractuelle (CRO) comme Celerion mènent des études de recherche sur les médicaments pour le compte de sociétés pharmaceutiques, en utilisant des cohortes de sujets en bonne santé, qui sont payés pour leur participation. Une étude peut durer d’un jour à deux mois, parfois plus, et pendant l’essai, les signes vitaux des sujets sont surveillés.

Cela peut faire appel à des collectes de sang, d’urine ou de selles et dans certains essais, les sujets sont alités pendant toute leur durée. Ces types d’études sont difficiles à mener et souvent éprouvantes pour les sujets. Au plus l’expérience du sujet est confortable, au plus le taux d’abandon sera faible, de sorte que les CRO sont toujours à la recherche de moyens de rendre leurs essais plus confortables pour leurs sujets.

In 2019 and 2020, Celerion was contracted to conduct two studies to investigate a novel bi-dose nasal delivery drug/device combination that would be used to treat severe allergies, such as anaphylaxis at its center in Lincoln, Nebraska.  The drug would be dosed nasally, using a novel bi-dose nasal spray device, with subjects in bed, with multiple vital sign checks, including blood pressure, heart rate, at very frequent intervals taken using a traditional Welch Allyn pole-mounted device. Celerion was looking for a better way to monitor vital signs more quickly and conveniently to identify changes continuously in real-time, and approached Caretake Medical to ask how readily we could produce the data they needed for this study.

Our wireless Caretaker 4 wearable vital signs monitor provided the solution. With beat-by-beat BP data sent via Bluetooth from all the subjects to the monitoring console, it provided the continuous blood pressure monitoring; real-time data that were required.

Moreover, the comfort and convenience of this lightweight, wearable device meant was more comfortable and less intrusive to the subjects with reduced effort required to collect these data by the research staff.  We supplied 18 Caretaker 4 devices for the trial, which spanned several months and multiple subject cohorts.


Celerion is continuing its study of the drug, using the Caretaker 4 not just for BP monitoring but for all the vital signs.  So far 3 studies have been completed for 133 subjects, with 2 more studies planned in 2021 and 120 additional subjects to be enrolled.  Celerion’s client, Bryn Pharma LLC has reported their data generated in their first studies in 2020 and the data from the third study will be presented at the  American Academy of Asthma, Allergy, and Immunology (AAAAI) Feb 26 – Mar 1.

As a result of this trial, Celerion recommended Caretaker for other clients as the preferred technology for other trials, including an advanced hemodynamics use case with Caretaker’s cardiac output and stroke volume as an exploratory endpoint for an investigational new drug trial.  “We found that using Caretaker for continuous blood pressure monitoring and vital signs made it faster and more efficient for our staff, and more comfortable for the patients, and generally the dosing days went more smoothly compared to using traditional monitoring methods” said Kelly Pachunka, Sr. Manager, Clinical Operations at Celerion.


CROs and their Pharma clients always look to safely and efficiently bring therapeutics to market while maximizing patient comfort.  Caretaker allows both.  At Hospital Phase 2 trial sites where staffing and research funding is limited, Caretaker can provide a further advantage.

In certain competitive enrollment trials where total subject numbers are limited, CROs and research hospitals compete for research dollars and are rewarded for the number of subjects they enroll. Caretaker 4 gives them a competitive advantage because it can monitor faster and continuously, is comfortable and so does not cause subjects to drop out, and can also be used to monitor subjects from home.

This remote functionality has enabled research centers to restart trials that had been halted by Covid-19. For example, Yale has been able to recommence a study of Alzheimer’s patients, no longer requiring them to come in for trials but monitoring them from home using the Caretaker 4.

About Celerion

Celerion, a global leader in early clinical research services, “Translates Science into Medicine” with its powerful combination of scientific excellence, medical expertise, and clinical operations experience to give clients the confidence to make fast, accurate decisions about their drug development path during the crucial early development period. For 50 years, Celerion has provided industry leadership and execution of safety/tolerability, pharmacokinetic, and pharmacodynamics studies in highly controlled clinical environments such as firstin-human dose escalation, drug-drug interaction, cardiac safety, bioequivalence and bioavailability, metabolism and excretion program, as well as pharmacokinetic evaluations in patients with impaired renal or hepatic function.  Celerion completes the offering with data management, biostatistics, clinical monitoring, and bioanalytical services. Our founding mission is to help our clients get their drugs to market quickly so that they touch the lives of our families, friends, and people in need around the world. For more information, please visit

About Bryn Pharm LLC.

Bryn Pharma, founded in 2016, is a privately held pharmaceutical company founded by patients for patients. Bryn is focused on positively disrupting the existing market for epinephrine auto-injectors by delivering an accessible, easy-to-use alternative that better meets the needs of patients. Bryn Pharma seeks to provide this growing population at risk for anaphylaxis with A Better Way to be prepared for a life-threatening allergic reaction. For more information visit

For a safer tomorrow, contact Caretaker Medical today!

Caretaker Medical is a Wireless Digital Health company that has developed a continuous Blood Pressure monitoring and vital signs that eliminates blind spots between traditional intermittent spot-check monitors and untethers patients from mobility-restricting wires and hoses. The FDA-Cleared Caretaker4 wireless monitor utilizes a simple finger cuff and patented Pulse Decomposition Analysis technology to measure uninterrupted blood pressure, hemodynamics, and other parameters for wire-free, “touchless” remote patient monitoring that maximizes patient comfort and clinical decision-making. For more information, please visit

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