First-In-Human Study of Apramycin
A Phase I, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of Apramycin Administered Intravenously in Healthy Adults.
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
-
Mannheim, Germany
- CRS Clinical Research Services Mannheim GmbH
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy male and female subjects of non-childbearing potential, 18-45 years of age (both inclusive), body mass index 18.0 - 29.9 kg/m2 (inclusive) and body weight from 50 to 100 kg (inclusive).
- Glomerular filtration rate (GFR) ≥ 90 mL/min /1.73 m2.
- Subjects with systemic hearing, with air conduction thresholds no worse than 20 decibels (dB) hearing loss for the frequencies 0.5-1-2-4-6-8 kilohertz (kHz) bilaterally and, no threshold asymmetry ≥ 20 dB at any frequency, normal (reproducibility 70% or better) transient evoked otoacoustic emissions (TEOAE).
- From the signing of the informed consent until the last follow-up visit, subjects must be willing to avoid exposure to loud noise and Subjects must be willing to avoid excessive physical exercise within 48 h prior to dosing.
- Normal blood pressure and pulse rate, ECG recording without clinically significant abnormalities.
- Thyroid-stimulating hormone, free triiodothyronine and free thyroxine within the reference ranges.
- Having had no febrile or infectious illness for at least 7 days prior to the first administration of the Investigational medicinal product (IMP) of the study.
- Normal microscopic findings in the ears, normal tympanic membrane mobility and stapedial reflex present.
Exclusion Criteria:
- Vegetarian or vegan.
- Demonstrating excess in xanthine consumption.
- More than low-risk alcohol consumption (men: ≥24 g of pure alcohol regularly per day; women: ≥12 g of pure alcohol regularly per day).
- Any history of alcohol or drug abuse or a positive urine drug screen test. Positive alcohol breath test.
- Consumption of xanthine-containing food or beverages within 48 h before dosing.
- Smokers smoking more than 10 cigarettes or equivalent per day.
- Exposure to loud noise within 3 days prior to drug administration.
- Taking any medication on a regular basis, with the exception of solitary doses of up to 1000 mg paracetamol.
- Use of any investigational drug product within 30 days or 5 half-lives before screening.
- Use of aminoglycosides or other antibiotics within 3 months prior to screening.
- Use of neuromuscular blocking agents within 1 week or 5 half-lives prior to screening.
- Use of potentially nephrotoxic medication 2 weeks prior to the drug administration.
- Any history of drug hypersensitivity, asthma, urticaria or other severe allergic diathesis as well as hay fever with ongoing symptoms.
- Any history of hypersensitivity to aminoglycosides.
- Any history or signs of acute, chronic or recurrent metabolic, renal, hepatic, pulmonary, gastrointestinal, neurological, neuromuscular disorders, endocrinological, immunological, psychiatric or cardiovascular disease, myopathies, and bleeding tendency.
- Problems with hearing and/or balance.
- Previous injury or surgery to the middle or inner ears, family history of hearing loss before the age of 60.
- Genetic predisposition to aminoglycoside-driven ototoxicity.
- Laboratory values outside the reference range that are of clinical relevance.
- Positive test for HIV antibodies, hepatitis B-virus surface antigen, or anti-hepatitis C-virus antibodies.
- Blood or plasma donation of 500 mL within 3 months or more than 100 mL within 30 days before signing an informed consent to this trial.
- Judged by the investigator to have occupational noise exposure of high risk during the trial.
- Positive test for SARS-CoV-2.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Apramycin injection in escalating doses
Apramycin, solution for infusion.
|
30-min infusion
|
|
Placebo Comparator: Placebo
Physiological saline, solution for infusion.
|
30-min infusion
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Type and incidence of treatment-emergent adverse events (TEAEs) until 2 weeks after dosing.
Time Frame: until 2 weeks after dosing
|
until 2 weeks after dosing
|
|
|
Type and incidence of TEAEs related to auditory and vestibular function tests.
Time Frame: until 3 months after dosing
|
until 3 months after dosing
|
|
|
Number of subjects with clinically significant vital sign measurement blood pressure.
Time Frame: until 2 weeks after dosing
|
Frequency is defined as number of subjects with clinically significant observations.
|
until 2 weeks after dosing
|
|
Number of subjects with clinically significant vital sign measurement pulse rate.
Time Frame: until 2 weeks after dosing
|
Frequency is defined as number of subjects with clinically significant observations.
|
until 2 weeks after dosing
|
|
Number of subjects with clinically significant observation in physical examination.
Time Frame: until 2 weeks after dosing
|
Frequency is defined as number of subjects with clinically significant observations.
|
until 2 weeks after dosing
|
|
Number of subjects with clinically significant changes in clinical laboratory parameters.
Time Frame: until 2 weeks after dosing
|
Frequency is defined as number of subjects with clinically significant observations.
|
until 2 weeks after dosing
|
|
Number of subjects with clinically significant changes in ECG parameters.
Time Frame: until 2 weeks after dosing
|
ECG parameters include heart rate and PQ, QT, RS.
Frequency is defined as number of subjects with clinically significant observations.
|
until 2 weeks after dosing
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Armin Schultz, Dr.med., CRS Clinical Research Services Mannheim GmbH
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- JUV18-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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