Status:
NOT_YET_RECRUITING
A Dose Ranging Study to Examine TDS-Testosterone 5%
Lead Sponsor:
Transdermal Delivery Solutions Corp
Collaborating Sponsors:
Advanced Therapies Centre, The London Clinic
Conditions:
Hypogonadotropism
Eligibility:
MALE
18-75 years
Phase:
PHASE2
Brief Summary
This study is a continuation of previous studies done in healthy volunteers to prove the efficacy of delivering Testosterone, the male hormone, rapidly across intact skin in s series of doses from low...
Detailed Description
48 Patients will be enrolled following 2 independent verifying blood tests of their diagnosis of Hypogonadism. there will be 4 cohorts of 12 subjects, each receiving doses of the trail materials, titr...
Eligibility Criteria
Inclusion
- Hypogonadal Male subjects - morning testosterone level ≤300 ng/dL (10.4 ng/L).
- 18 and 75 years of age, inclusive.
- The subject is willing and able to read, understand the Subject Information Sheet and provide written informed consent.
- The subject has a body mass index (BMI) within 18-30 kg/m2.
- The subject is in otherwise good health as determined by medical history and physical examination.
- The subject is a non-smoker.
- The subject must agree to comply with the placement of an indwelling catheter on two separate occasions and the drawing of blood samples for the pharmacokinetic assessments.
- The subject is willing and able to comply with all testing and requirements defined in the protocol.
- The subject is willing and able to return to the study site for all visits.
Exclusion
- The subject has any relevant deviations from normal in physical examination, electrocardiogram (ECG), or clinical laboratory tests, as evaluated by the investigator, particularly an elevated PSA reading \>4.0 ng/ml or ALT and AST greater than 2 times the upper limit of normal, clinically significant anemia (hematocrit \<35%) or renal dysfunction (creatinine \>2mg/dL), active deep vein thrombosis, thromboembolic disorders or history of these conditions.
- The subject has had a clinically significant illness within 30 days preceding entry into this study.
- The subject has a history of significant neurological, hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, or metabolic disease.
- The subject has a known allergy or history of hypersensitivity to Testosterone or similar compounds.
- The subject has used any prescription medication within 14 days or over-the-counter (OTC) medication or alcohol within 48 hours of dosing or intends to use any prescription or OTC medication during the study that may interfere with the evaluation of study medication.
- The subject has donated or lost a significant volume of blood (\>450 mL) within four (4) weeks of the study, and their haemoglobin concentration and haematocrit have not returned to within 5% of normal.
- The subject has a Hematocrit level \> 51%
- The subject has a history of substance abuse or a current positive urine drug screen or urine alcohol test.
- Alcohol consumption greater than community norms (i.e. more than 21 standard drinks per week for males).
- Subjects who have received an investigational drug or have used an investigational device in the 30 days prior to study entry.
- Subjects with an American Urological Association System Index for Prostatism score greater than 7
- Subjects with a history of prostate or breast carcinoma.
- Subjects with prostatic mass on screening physical examination.
- Subjects with a history of significant skin disease.
- Subjects with a history of sleep apnea.
- Subject with a partner with a history of breast cancer.
- Subject with a partner of child bearing potential who is not willing to use adequate contraception for the duration of the trial.
- Subject whose partner is pregnant.
Key Trial Info
Start Date :
June 1 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
February 1 2027
Estimated Enrollment :
48 Patients enrolled
Trial Details
Trial ID
NCT01894308
Start Date
June 1 2026
End Date
February 1 2027
Last Update
September 3 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Advanced Therapies Centre, The London Clinic
London, United Kingdom, NW1 4LJ