Peyronie's Disease Treatment Protocol

Peyronie's Disease Clinical Trial

Official title:

A Sequential, Randomized, Double-blind, Placebo-controlled, Prospective Study to Evaluate the Safety and Efficacy of the H-100 Treatment in Adult Male Volunteers With Peyronie's Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02072018
• Other study ID #: PDTP1
• Status: Completed
• Phase: Phase 1
• First received: July 9, 2013
• Last updated: February 24, 2014
• Start date: June 2013
• Est. completion date: December 2013

Study information

• Verified date: February 2014
• Source: Hybrid Medical
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Treatment of Peyronie's disease remains difficult. The purpose of this study is to test the safety and efficacy of a new compound to treat this disease.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: December 2013
• Est. primary completion date: December 2013
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Have symptom(s) of Peyronie's disease (pain, curvature or plaque)

2. Be judged to be in good health, based upon the results of a medical history, physical examination, and laboratory profile

3. Voluntarily sign and date an informed consent agreement approved by the Institutional Review Board/Independent Ethics Committee (IRB/IEC). The subject must also sign an authorization form to allow disclosure of his protected health information (PHI). The PHI authorization form and informed consent form may be an integrated form or may be separate forms depending on the institution

4. Be able to read, complete and understand the informed consent and various rating instruments in English

Exclusion Criteria:

1. Inability to understand study goals and risks

2. Inability to understand the informed consent

3. Inability to achieve erection with or without PDE5 inhibitor use adequate for penetration if penile curvature is not a limiting factor

4. Peyronie's disease symptoms greater than one year duration

5. Chordee in the presence or absence of hypospadias Thrombosis of the dorsal penile artery or vein Infiltration by a benign or malignant mass resulting in penile curvature Infiltration by an infectious agent, such as lymphogranuloma venereum Ventral curvature from any cause Presence of an active sexually transmitted disease Known active hepatitis B or C Known immune deficiency disease or be positive for human immunodeficiency virus (HIV)

6. Has previously undergone surgery for Peyronie's disease

7. Fails to have an erection which in the opinion of the investigator is sufficient to accurately measure the subject's penile deformity

8. Has an isolated hourglass deformity of the penis (curvature caused by a plaque that is noncontiguous with the hourglass deformity may be treated)

9. Has the plaque causing curvature of the penis located proximal to the base of the penis

10. Has previously received alternative medical therapies for Peyronie's disease administered by the intralesional route (including, but not limited to, steroids, verapamil, and the naturally occurring low molecular weight protein, interferon-a2b) within 3 months before the first dose of study drug or plans to use any of these medical therapies at any time during the study

11. Has received alternative medical therapies for Peyronie's disease administered by the oral (including, but not limited to, vitamin E [>500 U], potassium aminobenzoate [Potaba], tamoxifen, colchicine, pentoxifylline, over-the-counter erectile dysfunction medications, or steroidal anti-inflammatory drugs) or topical routes (including, but not limited to, verapamil applied as a cream) within 3 months before the first dose of study drug or plans to use any of these medical therapies at any time during the study

12. Has had extracorporeal shock wave therapy (ESWT) for the correction of Peyronie's disease within the 6- month period before screening or plans to have ESWT at any time during the study

13. Has used any mechanical type device for correction of Peyronie's disease within the 2-week period before screening or plans to use any these devices at any time during the study

14. Has used a mechanical device to induce a passive erection within the 2-week period before screening or plans to use any of these devices at any time during the study

15. Has significant erectile dysfunction that has failed to respond to oral treatment with phosphodiesterase type 5 (PDE5) inhibitors

16. Has uncontrolled hypertension, as determined by the investigator

17. Has a known recent history of stroke, bleeding, or other significant medical condition, which in the investigator's opinion would make the subject unsuitable for enrollment in the study

18. Is unwilling or unable to cooperate with the requirements of the study including completion of all scheduled study visits

19. Has received an investigational drug or treatment within 30 days before the first dose of study drug

20. Has a known systemic allergy to any H-100 component

21. Has received any collagenase treatments within 30 days of the first dose of study drug

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Penile Induration
• Peyronie's Disease

Intervention

Drug:
• H-100
H-100 is a new compound to be applied to Peyronie's disease tissue with the intention of reducing disease symptoms.
• Placebo
Placebo is an established, standard compound to be applied to Peyronie's disease tissue that will have no effect on disease symptoms.

Locations

Country	Name	City	State
United States	North Memorial Medical Center	Robbinsdale	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Hybrid Medical

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety measure	Number of participants with adverse events. Continuous monitoring for adverse events. An adverse event is the development of an undesirable medical condition - e.g. symptoms or abnormal results of an investigation - or the deterioration of a pre-existing medical condition (not relevant in this study). Per the subject description, adverse events will be reported as: mild, moderate or severe.	Up to six months	Yes
Secondary	Efficacy measure	Measure for change in pain, curvature, length, plaque hardness and plaque size. At the end of three months the Placebo group will change from Placebo to H-100 for the remaining three months. The H-100 group will receive H-100 for six months.; Monitor for adverse events.	Up to three and six months (the Placebo group will change from Placebo to H-100 at the end of three months)	Yes