Study to Explore the Pharmacokinetics and Pharmacodynamics of Epinephrine in Healthy Male and Female Subjects With Different Skin to Muscle Depth (STMD)
- Conditions
- Anaphylaxis
- Interventions
- Device: Part 1Device: Part 2 Group 1Drug: Part 2 group 2Device: Part 2 group 3Device: Part 2 Group 4
- Registration Number
- NCT03282929
- Lead Sponsor
- Bausch & Lomb Incorporated
- 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
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 43
- Healthy male and female subjects, between 18 and 54 years of age (inclusive).
- Subjects who are able and willing to give written informed consent.
- 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.
- Compressed STMD of 10 mm and above (Part 1+2).
- Non-smoker for at least 6 months.
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Receipt of medication (prescription or non-prescription) within 14 days prior to the planned drug administration, except for occasional use of paracetamol or ibuprofen.
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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.
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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.
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Presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.
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Hypersensitivity to epinephrine or any of the excipients (e.g. metabisulphite).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Part 1 Group 1 Part 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. Part 2 group 1 Part 2 Group 1 300 μg epinephrine auto-injector (Emerade, Bausch and Lomb, 23 mm needle length) Part 2 Group 2 Part 2 group 2 500 μg epinephrine auto-injector (Emerade, Bausch and Lomb, 23 mm needle length) Part 2 Group 3 Part 2 group 3 300 μg epinephrine auto-injector (Fastjekt, MEDA Pharma, 16 mm needle length) Part 2 Group 4 Part 2 Group 4 300 μg epinephrine auto-injector (Jext, Alk-Abelló, 15 mm needle length)
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Nuvisan GmbH
🇩🇪Neu-Ulm, Wegenerstrasse 13, Germany