Anaphylaxis
Conditions
Brief summary
A single dose, open label, randomized cross-over study to explore the pharmacokinetics and pharmacodynamics of epinephrine in healthy male and female subjects
Detailed description
A single dose, open label, randomized cross-over study to explore the pharmacokinetics and pharmacodynamics of epinephrine in healthy male and female subjects with different skin-to-muscle depth (STMD) of the thigh after injections with four different marketed auto-injectors
Interventions
DEVICEPart 1
A single dose of 500 μg epinephrine (0.5 mL Suprarenin®) will be administered i.m. and s.c. by using a needle and a syringe in randomized order
DEVICEPart 2 Group 1
300 μg epinephrine auto-injector (Emerade, Bausch and Lomb, 23 mm needle length)
DRUGPart 2 group 2
500 μg epinephrine auto-injector (Emerade, Bausch and Lomb, 23 mm needle length)
DEVICEPart 2 group 3
300 μg epinephrine auto-injector (Fastjekt, MEDA Pharma, 16 mm needle length)
DEVICEPart 2 Group 4
300 μg epinephrine auto-injector (Jext, Alk-Abelló, 15 mm needle length)
Sponsors
Bausch & Lomb Incorporated
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Pharmacokinetics and pharmacodynamics of epinephrine in healthy male and female subjects with different skin-to-muscle depth (STMD) of the thigh after injections with four different marketed auto-injectors
Eligibility
Sex/Gender
ALL
Age
18 Years to 54 Years
Healthy volunteers
Yes
Inclusion criteria
1. Healthy male and female subjects, between 18 and 54 years of age (inclusive). 2. Subjects who are able and willing to give written informed consent. 3. Body mass index (BMI) between 28.0 and 40.0 kg/m² (inclusive). Weight on Day -1 may not have changed by more than 3 kg compared to screening. 4. Compressed STMD of 10 mm and above (Part 1+2). 5. Non-smoker for at least 6 months.
Exclusion criteria
1. Receipt of medication (prescription or non-prescription) within 14 days prior to the planned drug administration, except for occasional use of paracetamol or ibuprofen. 2. Receipt of any of the following medications within the previous 6 months; beta adrenergic blockers, tricyclic antidepressants, monoamine oxidase inhibitors and catechol-O-methyl transferase inhibitors, methylphenidate, amphetamines, any drugs that may sensitize the heart to arrhythmias, including digitalis and quinidine. 3. History or current evidence of a clinically significant disease including, but not limited to: cardiovascular, hepatic, renal, hematological, neuropsychological, endocrine, gastrointestinal or pulmonary diseases especially asthma bronchiale. Significant is defined as any disease that, in the opinion of the investigator, would put the safety of the subject at risk through participation, or which could affect the endpoint analysis if the disease/condition exacerbated during the study. History or presence of silent infections, including positive tests for HIV1, HIV2, Hepatitis B or C. 4. Presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs. 5. Hypersensitivity to epinephrine or any of the excipients (e.g. metabisulphite).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cmax | 14 days | Maximum observed drug concentration |
| tmax | 14 days | Time of the maximum drug concentration (obtained without interpolation). If the maximum value occurs at more than one time point, tmax is defined as the first time point with this value. |
Countries
Germany
Outcome results
None listed