UTILISATION OF HOME NURSING TO MITIGATE THE IMPACT OF COVID-19 ON THE CONDUCT OF THE GANTENERUMAB GRADUATE TRIALS

Session Type
SYMPOSIUM
Date
10.03.2021, Wednesday
Session Time
08:00 - 09:45
Room
On Demand Symposia A
Lecture Time
09:15 - 09:30
Presenter
  • Alison Searle, United Kingdom
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On-Demand

Abstract

Aims

COVID-19 has impacted clinical study conduct significantly, particularly in Alzheimer’s disease, which includes an aged population with increased comorbidities. Perceived risk of infection by traveling to a clinic, together with widespread clinical site closures and movement restrictions, reduced study drug compliance. This study evaluated the utilization of home administration of the study drug in the Phase III trials GRADUATE I and II (NCT03444870; NCT03443973), intended to improve study drug compliance and thus preserve study integrity.

Methods

The GRADUATE studies are ongoing and will evaluate gantenerumab versus placebo administered subcutaneously. The protocol allows home administration for consenting participants. After the COVID-19 outbreak, home nursing scope was expanded. Uptake of home nursing administration prior to and during different phases of the pandemic was analyzed.

Results

From March 2019-February 2020, 94 participants from 11 of 31 countries utilized home nursing, contributing to an average of approximately 35 home nursing visits per month. Between March-August 2020, this increased to 234 participants actively utilizing home nursing in 15 countries and an average of approximately 300 monthly visits. The highest peak in uptake was observed between March-April 2020.

Conclusions

The availability of home nursing in GRADUATE, including its expansion in response to the COVID-19 pandemic, resulted in a large and rapid increase in uptake – likely facilitated by gantenerumab’s subcutaneous route of administration. Expanding home administration reduced the risk of study drug non-compliance, thereby helping to preserve study integrity. Such benefits of home administration could extend beyond clinical trials to the real world, once drugs are approved.

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