A Dose Ranging Study to Examine TDS-Testosterone 5% (PARC-T-D)

T

Transdermal Delivery Solutions

Status and phase

Begins enrollment this month
Phase 2

Conditions

Hypogonadotropism

Treatments

Drug: Testosterone
Device: Pump Sprayer

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01894308
2013-001766-42 (EudraCT Number)
IRAS project ID: 146877 (Other Identifier)
PARC-Testosterone-D1/09/13

Details and patient eligibility

About

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 to high in men with low-to-no natural testosterone production to measure their response to the varying doses. The results of this study will inform further studies which will be longer in length, as to the starting doses. The study will be conducted in London, U.K. at the Advanced Therapies Centre, The London Clinic.

Full 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, titrated by means of number of sprays applied. Doses will range from 10 to 70 mgs Testosterone.

Enrollment

48 estimated patients

Sex

Male

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

48 participants in 2 patient groups

Forearm dose
Active Comparator group
Description:
Half of Ss will receive their dose of Testosterone on the inner aspects of their forearms.
Treatment:
Device: Pump Sprayer
Drug: Testosterone
Chest Dose
Active Comparator group
Description:
Half of Ss will receive their dose of Testosterone on the chest.
Treatment:
Device: Pump Sprayer
Drug: Testosterone

Trial contacts and locations

1

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Central trial contact

Shern L. Chew, M.D., Ph.D.; Chandan AS Alam, MD

Data sourced from clinicaltrials.gov

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