Status:
COMPLETED
Pharmacokinetic Study of Subcutaneous Testosterone Enanthate
Lead Sponsor:
Antares Pharma Inc.
Conditions:
Hypogonadism
Eligibility:
MALE
18-55 years
Phase:
PHASE1
Brief Summary
Evaluation of pharmacokinetics of subcutaneous testosterone enanthate
Detailed Description
Evaluation of pharmacokinetics and safety profile of testosterone enanthate injected subcutaneously via auto-injector in healthy male volunteers
Eligibility Criteria
Inclusion
- Healthy adult male subjects, 18-55 years of age, inclusive, at the time of signing the informed consent;
- Body weight ≥50 kg and body mass index within the range 19-30 kg/m2, inclusive, at screening;
- Medically healthy subjects with clinically insignificant screening and check-in results (medical history, 12-lead electrocardiogram \[ECG\], physical examination, and laboratory tests); and
- Subjects who are able to understand and are willing and able to give their signed informed consent before any trial-related procedures are performed.
Exclusion
- Currently diagnosed or a history of asthma, urticarial, angioedema, anaphylaxis, atopic dermatitis, clinically significant abnormality of skin of the abdomen, cancer, diabetes, or any other clinically significant cardiovascular, respiratory, metabolic, renal, hepatic, gastrointestinal, hematological, dermatological, venereal, neurological, psychiatric, or other major disorders;
- History of benign prostate hypertrophy (BPH), prostate cancer, or abnormal prostate specific antigen (PSA) values;
- PSA level \> 3 ng/ml at screening;
- Presence or history of gastrointestinal, hepatic or renal disease, or any other condition (including surgery) known to interfere with the absorption, distribution, metabolism, or excretion of medicines;
- Systolic blood pressure outside the range of 90 to 140 mmHg, diastolic blood pressure outside the range of 40 to 90 mmHg, and/or pulse rate outside the range of 40 to 100 beats per minute after one repeat at screening or check-in;
- Abnormal ECG at screening as judged by the Investigator;
- History of clinically significant drug and/or food allergies as determined by the Investigator;
- Allergy to sesame, sesame oil, or a history of hypersensitivity or idiosyncratic reaction to compounds related to the study drug
- Subjects undergoing current treatment with other androgens (i.e. dehydroepiandrosterone \[DHEA\]), anabolic steroids, other sex hormones, or drugs that interfere with the metabolism of testosterone (i.e. opioids, anastrozole, clomiphene, dutasteride, finasteride, flutamide, ketoconazole, spironolactone, and testolactone);
- Subjects treated within the past 12 months with estrogens, gonadotropin releasing hormone (GnRH) agonists, or growth hormone;
- Prescription, over the counter medications, vitamins, herbal and dietary supplements taken within 7 days or 5 half-lives (whichever is longer) prior to the dose of study medication and duration of the study;
- Positive screen for human immunodeficiency virus (HIV), hepatitis B, and/or hepatitis C at screening;
- Positive urine screen for drugs of abuse (amphetamine, barbiturates, benzodiazepines, cocaine, marijuana, methadone, methamphetamines, oxycodone, and opiates) or positive breath alcohol test at screening and check-in
Key Trial Info
Start Date :
September 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2014
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT02233751
Start Date
September 1 2014
End Date
October 1 2014
Last Update
April 19 2019
Active Locations (1)
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1
Medpace Clinical Pharmacology Unit
Cincinnati, Ohio, United States, 45227