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Completed

NCT Number: NCT03282929

Study to Explore the Pharmacokinetics and Pharmacodynamics of Epinephrine in Healthy Male and Female Subjects With Different Skin to Muscle Depth (STMD)

A single dose, open label, randomized cross-over study to explore the pharmacokinetics and pharmacodynamics of epinephrine in healthy male and female subjects

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Key information

Age range

18 year–54 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Nuvisan GmbH

Neu-Ulm, Wegenerstrasse 13, 89231, Germany

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • Receipt of medication (prescription or non-prescription) within 14 days prior to the planned drug administration, except for occasional use of paracetamol or ibuprofen.
  • 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.
  • 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.

  • Presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.
  • Hypersensitivity to epinephrine or any of the excipients (e.g. metabisulphite).

Treatment and study plan

Part 1

Device

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

Other names: Group 1

Part 2 Group 1

Device

300 μg epinephrine auto-injector (Emerade, Bausch and Lomb, 23 mm needle length)

Other names: Group 1

Part 2 group 2

Drug

500 μg epinephrine auto-injector (Emerade, Bausch and Lomb, 23 mm needle length)

Other names: Group 2

Part 2 group 3

Device

300 μg epinephrine auto-injector (Fastjekt, MEDA Pharma, 16 mm needle length)

Other names: Group 3

Part 2 Group 4

Device

300 μg epinephrine auto-injector (Jext, Alk-Abelló, 15 mm needle length)

Other names: Group 4

Primary outcomes

  1. Cmax

    Time frame: 14 days

    Maximum observed drug concentration

  2. tmax

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

Bausch & Lomb Incorporated

Industry

Registry information

Official study title

An 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)

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Sep 14, 2017
Registry last updated
Jun 21, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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