A Study Comparing User Experience of Different Delivery Devices for Glucagon

Inclusion Criteria:

All participants (Trained Users, Persons with Diabetes [PWDs] and Untrained Users):

- Are able to understand the purpose and procedure of the study and to give written
informed consent to show willingness to participate in the study

Trained Users only:

- Are persons who are not diagnosed with Type 1 Diabetes Mellitus (T1DM) or Type 2
Diabetes Mellitus (T2DM)

- Are close friends/relatives of a patient with T1DM or T2DM on insulin

- Have not previously administered any rescue medications (e.g. epinephrine, glucagon,
narcan or seizure medications)

Untrained Users only:

- Have not been diagnosed with T1DM or T2DM, and are not a Trained User of a person with
T1DM or T2DM

- Have not previously administered any rescue medications (e.g. epinephrine, glucagon,
narcan or seizure medications)

Exclusion Criteria:

All participants (Trained Users, PWDs and Untrained Users):

- In the opinion of the investigator or sponsor, are unsuitable for inclusion in the
study

Trained Users and Untrained Users only (i.e. the participants involved in the simulations):

- Are currently enrolled in a clinical study involving any type of medical research
judged not to be scientifically or medically compatible with this study

- Are judged by the investigator as being likely to have difficulty performing the
administration due to physical, cognitive and/or severe psychiatric disorder

- Are judged by the investigator as being trained or experienced in performing rescue
drug administration

- Are judged by the investigator as being trained or experienced in performing
high-fidelity simulations of drug administration

- Have received formal training in a medical field, and/or worked in this field within
the prior 5 years; or otherwise are judged by the investigator as being trained or
experienced as a first responder