Long-term Safety Study of Intramuscular Injections of 750 mg and 1000 mg Testosterone Undecanoate in Hypogonadal Men

Completed · Phase 3

Conditions studied: Hypogonadism, Primary Hypogonadism, Secondary Hypogonadism

In brief

To evaluate the pharmacokinetics of TU 750 mg and TU 1000 mg via multiple measurements of serum total testosterone.

Key facts

Study ID

NCT00467870

Run by

Endo USA Inc., a Keenova Therapeutics Company

People needed

531

Starts

2006-03-01

Expected to finish

2009-07-01

Last updated by the study team

2017-10-05

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Male with primary or secondary hypogonadism at least 18 years of age and for study part C2 weighs ≥143.3 lb (≥65 kg)
• Morning screening serum testosterone concentration <300 ng/dL

You may not qualify if…

• American Urological Association (AUA) Symptom Score ≥15 or significant prostatic symptoms
• History of carcinoma, tumors or induration of the prostate or the male mammary gland including suspicion thereof
• Screening serum prostate-specific antigen (PSA) level >4 ng/mL or hyperplasia of the prostate (size >75 cm3 as measured by transrectal ultrasonography)
• Past or present liver tumors or acute or chronic hepatic disease with impairment of liver function; liver function tests (alanine aminotransferase [ALT], aspartate aminotransferase [AST]) exceeding 1.5 times upper limit of normal
• History of deep vein thrombosis in the past 5 years or any history of cerebrovascular accident
• Severe acne
• Hypertension (systolic blood pressure >160 mm Hg and diastolic blood pressure >95 mm Hg) or coronary heart disease not stabilized by therapy as assessed by the investigator
• Insulin-dependent diabetes mellitus or uncontrolled non-insulin-dependent diabetes mellitus; patients with diabetes are excluded if screening glycated hemoglobin (HbA1C) level is >9%
• Use of any sex hormones within 28 days (for injectable testosterone preparations) or 7 days (for oral, gel, patch, etc, testosterone preparations) prior to screening visit and throughout the study (exclusive of administered study drug)
• Use of steroidal anabolic drugs or supplements (eg, dehydroepiandrosterone [DHEA]) by any application method within the 28 days prior to first administration of study drug and throughout the study (exclusive of administrated study drug)
• Medication with substances which might interfere with testosterone metabolism within 28 days before the first administration of study drug
• History of sleep apnea Insulin-dependent diabetes mellitus
• Use of steroidal anabolic drugs or supplements by any application method within the 28-days prior to the first administration of the study drug and throughout the study (exclusive of the administered study drug)

Where it is running

• Indevus Pharmaceuticals, Inc. — Lexington, Massachusetts, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.