A Study of DA-8159 in Subjects With Erectile Dysfunction

A Randomized, Placebo-Controlled, Double-Blind, Parallel Design Phase 2 Dose Ranging Trial To Assess The Safety and Efficacy of DA-8159 Tablets in Male Subjects With Erectile Dysfunction.

The purpose of this study will be to evaluate the clinical efficacy and safety of DA-8159, an orally administered, potent and selective inhibitor of PDE5, versus placebo for the treatment of subjects with erectile dysfunction (ED).

Study Overview

• Status: Completed
• Conditions: Erectile Dysfunction
• Intervention / Treatment: Drug: DA-8159

Detailed Description

This will be a multi-center, randomized, double-blind, placebo-controlled, parallel-group study in 300 erectile dysfunction patients. Patients will complete a screening visit (V1) to determine eligibility for the study based on the International Index of Erectile Function (IIEF) erectile function (EF) domain scores, patient history and safety measures. Patients that meet the entrance criteria for this study will enter a 4 week, drug-free run-in period to establish a baseline for the erectile function domain score and to meet the criteria for participation in the study.

Patients successfully completing screen will be randomly assigned to one of four treatment groups at Visit 2 (V2): placebo or one of 3 active drug doses of DA-8159 tablets. Patients will be given medication for at-home use and will also be given diaries for recording information regarding sexual encounters, quality of erections and adverse events. At 4-week intervals for 3 months (V3, V4, V5), patients will return to the clinic to review and collect SEP diaries, safety data, 12-lead ECG and medication reconciliation. In addition, at each 4-week interval patients will complete an IIEF, and at Visit 5 will have blood drawn for safety evaluation.

The primary efficacy end points are: a) the change in score (baseline to Visit 5) for the Erectile Function domain score of the IIEF, b) change in response, relative to baseline, for sexual encounter profile (SEP) question 2, and c) change in response, relative to baseline, for SEP question 3. For DA-8159 tablets to be judged efficacious, the DA-8159 tablet groups must be shown superior to the placebo group on all three measures.

• Study Type: Interventional
• Enrollment: 300
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • Alabama
    • Huntsville, Alabama, United States, 35801
      • Medical Affiliated Research Center
  • California
    • Beverly Hills, California, United States, 90212
      • The Male Clinic
    • Laguna Woods, California, United States, 92653
      • South Orange County
    • Newport Beach, California, United States, 92660
      • California Profession Research
    • Tarzana, California, United States, 91356
      • West Coast Clinical Research
  • Colorado
    • Aurora, Colorado, United States, 80012
      • Urology Research Options
  • Connecticut
    • Waterbury, Connecticut, United States, 06708
      • Connecticut Clinical Research Center
  • Florida
    • Aventura, Florida, United States, 33180
      • South Florida Medical Research
    • Ocala, Florida, United States, 34474
      • Florida Foundation for Healthcare Research
  • Indiana
    • Fort Wayne, Indiana, United States, 46825
      • Northeast Indiana Research, LLC
  • Maryland
    • Greenbelt, Maryland, United States, 20770
      • Drs. Werner, Murdock & Francis, P.A. , Urology Associates
  • New York
    • Garden City, New York, United States, 11530
      • AccuMed Research Associates
    • Williamsville, New York, United States, 14221
      • Center for Urologic Research of Western New York
  • Rhode Island
    • Providence, Rhode Island, United States, 02904
      • University Urological Researcgh Institute
  • Texas
    • San Antonio, Texas, United States, 78229
      • Urology San Antonio Research

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 19 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

1. Is male and at least 19 years of age.
2. Has a stable monogamous relationship for at least 6 months with a consenting female partner (vaginal intercourse is a required study activity).
3. Provides written informed consent.
4. The subject's female partner provides written informed consent.
5. Has a history of ED (clinically defined as the inability to attain and maintain an erection of the penis sufficient to permit satisfactory sexual intercourse) of at least 3 months duration. The investigator will record the etiology of the ED (organic, psychogenic or mixed).
6. Has scored between 6-25 for the Erectile Function domain score (Questions Number 1-5, 15) at both Visits 1 & 2.
7. Completes least four diary entries by Visit 2, showing at least 4 attempts at sexual intercourse with a 50% or greater failure rate in achieving or in maintaining an erection sufficient to complete intercourse (defined as answering "no" to SEP questions #2 or #3).
8. The subject's partner is not pregnant or lactating and both subject and partner agree to the use of a medically acceptable form of birth control. Exceptions would be subjects with a vasectomy or partners that are post menopausal, and partners that have had a tubal ligation or hysterectomy.

Exclusion Criteria:

1. Has a history of stroke, myocardial infarction, or coronary artery disease within the past 6 months.
2. Has a history of cardiac failure, angina, or life-threatening arrhythmia within the past 6 months.
3. Is taking nitrate medication in any form(Appendix 7)
4. Is taking alpha blockers.
5. Has a clinically significant abnormal laboratory value as determined by the principal investigator.
6. Has a history of uncontrolled diabetes (HbA1c>9%).
7. Has a history of proliferative diabetic retinopathy.
8. Has a history of spinal cord injury or a radical prostatectomy or radical pelvic surgery.
9. Has a supine blood pressure lower than 90/50mmHg or uncontrolled hypertension higher than 170/100mmHg.
10. Has a anatomical deformity of the penis such as severe penile fibrosis or Peyronie's disease.
11. Has a thyroid stimulating hormone (TSH) level lower than 30% of LLN.
12. Has erectile dysfunction caused by neurological or endocrine factors such as hyperprolactinemia or low serum testosterone levels (<300 ng/dl).
13. Has hepatic impairment (GOT, GPT levels > 3 x ULN).
14. Has renal impairment (serum creatinine ≥ 2.5mg/dl).
15. Has a history of hematological disorder such as bleeding disorder or a risk of GI bleeding such as peptic ulceration.
16. Has a history of retinitis pigmentosa.
17. Has a history of sickle cell disease, multiple myeloma, leukemia or any other disorders that may cause priapism.
18. Has a history of significant psychiatric disorder.
19. Has a history of central nervous system disorders such as stroke, transient ischemic attacks, or spinal cord injury.
20. Has a history of drug abuse (alcohol, marijuana, cocaine, or opiates).
21. Has a known sensitivity to drugs especially to phosphodiesterase type 5 inhibitors such as Viagra, Cialis or Levitra.
22. Has used other erectile dysfunction therapies including nutraceutical and herbal products within 14 days prior to entering into this study.

23. Is using concomitant medications that are known or suspected to interact with PDE 5 inhibitors such as the following:

    1. Antibacterial: erythromycin
    2. Antifungals: itraconazole, ketoconazole
    3. Antivirals: ritonavir, saquinavir, amprenavir, indinavir, nelfinavir
    4. H2 receptor antagonist: cimetidine
    5. Anticoagulants, androgens, trazodone
24. Have other sexual disorders such as hypoactive sexual desire.
25. Have previously failed to respond to PDE-5 inhibitors such as Viagra, Cialis or Levitra.
26. Have a major illness that in the opinion of the investigator would interfere with the conduct of the study.
27. Has not participated in a clinical drug study within the last 30 days prior to entering this study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

What is the study measuring?

Primary Outcome Measures

Outcome Measure
The primary efficacy end points are:
the change in score (baseline to Visit 5) for the Erectile Function domain score of the IIEF;
change in response, relative to baseline, for sexual encounter profile (SEP) question 2, and
change in response, relative to baseline, for SEP question 3.
Safety will be assessed by monitoring adverse events and changes in vital signs, clinical laboratory test results, 12-lead ECG, and physical examinations.

Secondary Outcome Measures

Outcome Measure
The study has several secondary efficacy measurements including:
changes in the satisfaction of intercourse, orgasmic function, sexual desire and overall satisfaction domains of the IIEF,
changes from baseline in SEP questions 1, 4 and 5;
the global assessment questionnaire (GAQ), and
changes from baseline in patient self assessment questionnaire (PSAE) scores.

Collaborators and Investigators

• Sponsor: Dong-A PharmTech Co., Ltd.
• Investigators: Study Director: James L Yeager, RPh., Ph.D.; Principal Investigator: Harin Padma-Nathan, MD, The Male Clinic

Study record dates

Study Major Dates

• Study Start: May 1, 2005
• Study Completion: June 1, 2006

Study Registration Dates

• First Submitted: January 25, 2006
• First Submitted That Met QC Criteria: January 25, 2006
• First Posted (Estimate): January 27, 2006

Study Record Updates

• Last Update Posted (Estimate): February 28, 2007
• Last Update Submitted That Met QC Criteria: February 27, 2007
• Last Verified: February 1, 2007

More Information

Terms related to this study

• Keywords: Erectile Dysfunction
• Additional Relevant MeSH Terms: Mental Disorders; Sexual Dysfunctions, Psychological; Sexual Dysfunction, Physiological; Erectile Dysfunction; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Phosphodiesterase Inhibitors; Phosphodiesterase 5 Inhibitors; Udenafil
• Other Study ID Numbers: DA 2005-001