Evaluate the Safety and Feasibility of Injecting PMD-MSC Into the Penis to Treat the Symptoms of PD (PMD-MSC-PD-01)

March 16, 2015 updated by: Melissa Marchand

Evaluate the Safety and Feasibility of Injecting Placental Matrix-Derived Mesenchymal Stem Cells Into the Penis to Treat the Symptoms of Peyronie's Disease

Prospective, open labeled, non-randomized, study to be conducted at a single center. Ten subjects will undergo an injection of Placental Matrix-Derived Mesenchymal Stem Cells (PMD-MSCs) into the penis for the treatment of Peyronie's Disease. Follow up visits will be conducted at 6 weeks, 3 months, 6 months, and 12 months. Subjects will be eligible for re-injection at 3 months and/or 6 months as determined by the clinician based on patient reported treatment satisfaction.

Study Overview

Detailed Description

Symptoms of Peyronie's disease include penile pain and curvature of the penis that prevents penetration and/or causes erectile dysfunction (ED). It is characterized by plaques that form along the top or bottom side of the penis inside the tunica albuginea; the plaque begins as a localized inflammation then develops into a hardened scar. Cases can range from mild to severe. In several cases, the hardened plaque reduces flexibility, causing the penis to curve during erection. The sexual problems as a result can lower a man's self-esteem and interfere with a couple's physical and emotional relationship.

The cause is unknown; however, possibilities include trauma, inherited conditions, Vitamin E deficiency, diabetes, and vascular disease.

Conservative treatments used in the acute phase (initial onset of symptoms) include oral therapies. Vitamin E and antioxidants can decrease the build-up of harmful chemicals that can cause injury to tissue. It is often used as the traditional treatment; it is inexpensive and with proper dosing, there are minimal side effects. Other oral agents include Potaba (aminobenzoates potassium); however, it is expensive ($1000 per year) and has associated gastrointestinal side effects.

Other therapies involve injections directly in the plaques (intralesional) with chemicals such as collagenase or calcium-channel blockers.

Surgical therapies are offered once the disease is stable (symptoms present for one year). Invasive surgical options consist of correction of the penile curvature or the placement of a penile prosthesis to straighten the penis to allow for erections.

Mesenchymal stem cells (MSCs) have been used for a variety of medical treatments to repair and regenerate acute and chronically damaged tissues. These cells have the potential to repair human tissue by forming cells of mesenchymal origin, such as cartilage, bone, fat, muscle, and blood vessels. Most research has focused on bone marrow derived stem cells (BMC) however the process for harvesting the cells is invasive, painful, and yields a low cell count. The human placenta offers an alternative source form MSCs. Placental Matrix-Derived Mesenchymal Stem Cells (PMD-MSCs) are compromised of a novel cellular repair matrix derived from placental mesenchyme. Mesenchyme is the meshwork of embryonic connective tissue in the mesoderm, from which are formed the muscular and connective tissues of the body and also the blood vessels. PMD-MSCs provide the extracellular matrix viable mesenchymal stem cells (MSCs) that coordinate the tissue repair process, regenerative growth factors, and anti-inflammatory cytokines required to regenerate the damaged vasculature of the penile corpora.

The research proposed here will establish the safety and feasibility of utilizing intracavernosal, intralesional injections of PMD-MSCs to treat Peyronie's disease with the intent of avoiding surgery.

Study Type

Interventional

Enrollment (Actual)

5

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Florida
      • Coral Springs, Florida, United States, 33076
        • Z Urology

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  1. acquired penile curvature >15 and <90 degrees associated with palpable penile plaque on physical examination
  2. 1 or 2 penile plaque at screening

Exclusion Criteria:

  1. taking the medication Coumadin
  2. unable to achieve adequate erection with penile injection to access degree of curvature
  3. undergone definitive treatment for prostate cancer, bladder cancer, or other pelvic malignancies including surgery, external beam radiation therapy, brachytherapy, cryotherapy
  4. prior history of prostate cancer, hematologic disorders, chronic liver disease including cirrhosis and hepatitis C, disorders affecting the immune system, including infection with the human immunodeficiency virus, or psychiatric disorder including major depression, schizophrenia, bipolar disease
  5. history of cerebrovascular accident, history of deep venous thrombosis within the past 5 years or history of untreated or severe sleep apnea
  6. clinically significant abnormal lab results that would put the subject at increased risk or compromise the integrity of the study data, in the opinion of the investigator
  7. received any other investigational drug within 30 days

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Injection of PMD-MSCs into the penis
Subjects will receive an initial injection of 1.0cc of Placental Matrix-Derived Mesenchymal Stem Cells (PMD-MSCs). Subjects will be eligible for re-injection at 3 months and/or 6 months as determined by the clinician based on ultrasound guided measurements of penile plaque(s) post treatment and on patient reported treatment satisfaction.
Other Names:
  • Ovation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Peak Systolic Velocity without trimix (cm/s)
Time Frame: Baseline
Baseline
Peak Systolic Velocity without trimix (cm/s)
Time Frame: 6 weeks
6 weeks
Peak Systolic Velocity without trimix (cm/s)
Time Frame: 3 months
3 months
Peak Systolic Velocity without trimix (cm/s)
Time Frame: 6 months
6 months
Peak Systolic Velocity without trimix (cm/s)
Time Frame: 12 months
12 months

Secondary Outcome Measures

Outcome Measure
Time Frame
End Diastolic Velocity without trimix (cm/s)
Time Frame: Baseline
Baseline
End Diastolic Velocity without trimix (cm/s)
Time Frame: 6 weeks
6 weeks
End Diastolic Velocity without trimix (cm/s)
Time Frame: 3 months
3 months
End Diastolic Velocity without trimix (cm/s)
Time Frame: 6 months
6 months
End Diastolic Velocity without trimix (cm/s)
Time Frame: 12 months
12 months

Other Outcome Measures

Outcome Measure
Time Frame
International Index of Erectile Function (IIEF)
Time Frame: 6 weeks
6 weeks
Peak Systolic Velocity with trimix (cm/s)
Time Frame: Baseline
Baseline
Peak Systolic Velocity with trimix (cm/s)
Time Frame: 6 weeks
6 weeks
Peak Systolic Velocity with trimix (cm/s)
Time Frame: 3 months
3 months
Peak Systolic Velocity with trimix (cm/s)
Time Frame: 6 months
6 months
Peak Systolic Velocity with trimix (cm/s)
Time Frame: 12 months
12 months
End Diastolic Velocity with trimix (cm/s)
Time Frame: Baseline
Baseline
End Diastolic Velocity with trimix (cm/s)
Time Frame: 6 weeks
6 weeks
End Diastolic Velocity with trimix (cm/s)
Time Frame: 3 months
3 months
End Diastolic Velocity with trimix (cm/s)
Time Frame: 6 months
6 months
End Diastolic Velocity with trimix (cm/s)
Time Frame: 12 months
12 months
Rigidity test (Pass or Fail)
Time Frame: Baseline
Baseline
Rigidity test (Pass or Fail)
Time Frame: 6 weeks
6 weeks
Rigidity test (Pass or Fail)
Time Frame: 3 months
3 months
Rigidity test (Pass or Fail)
Time Frame: 6 months
6 months
Rigidity test (Pass or Fail)
Time Frame: 12 months
12 months
Stretched Penile Length before trimix (cm/s)
Time Frame: Baseline
Baseline
Stretched Penile Length before trimix (cm/s)
Time Frame: 6 weeks
6 weeks
Stretched Penile Length before trimix (cm/s)
Time Frame: 3 months
3 months
Stretched Penile Length before trimix (cm/s)
Time Frame: 6 months
6 months
Stretched Penile Length before trimix (cm/s)
Time Frame: 12 months
12 months
Post Penile Width with trimix
Time Frame: Baseline
Baseline
Post Penile Width with trimix
Time Frame: 6 weeks
6 weeks
Post Penile Width with trimix
Time Frame: 3 months
3 months
Post Penile Width with trimix
Time Frame: 6 months
6 months
Post Penile Width with trimix
Time Frame: 12 months
12 months
International Index of Erectile Function (IIEF)
Time Frame: Baseline
Baseline
International Index of Erectile Function (IIEF)
Time Frame: 3 months
3 months
International Index of Erectile Function (IIEF)
Time Frame: 6 months
6 months
International Index of Erectile Function (IIEF)
Time Frame: 12 months
12 months
#1 Penile Plaque (Location) Size (mm^3)
Time Frame: Baseline
Baseline
#1 Penile Plaque (Location) Size (mm^3)
Time Frame: 6 weeks
6 weeks
#1 Penile Plaque (Location) Size (mm^3)
Time Frame: 3 months
3 months
#1 Penile Plaque (Location) Size (mm^3)
Time Frame: 6 months
6 months
#1 Penile Plaque (Location) Size (mm^3)
Time Frame: 12 months
12 months
#2 Penile Plaque (Location) Size (mm^3)
Time Frame: Baseline
Baseline
#2 Penile Plaque (Location) Size (mm^3)
Time Frame: 6 weeks
6 weeks
#2 Penile Plaque (Location) Size (mm^3)
Time Frame: 3 months
3 months
#2 Penile Plaque (Location) Size (mm^3)
Time Frame: 6 months
6 months
#2 Penile Plaque (Location) Size (mm^3)
Time Frame: 12 months
12 months
#3 Penile Plaque (Location)Size (mm^3)
Time Frame: Baseline
Baseline
#3 Penile Plaque (Location)Size (mm^3)
Time Frame: 6 weeks
6 weeks
#3 Penile Plaque (Location)Size (mm^3)
Time Frame: 3 months
3 months
#3 Penile Plaque (Location)Size (mm^3)
Time Frame: 6 months
6 months
#3 Penile Plaque (Location)Size (mm^3)
Time Frame: 12 months
12 months
Penile Curvature Angle (degrees)
Time Frame: Baseline
Baseline
Penile Curvature Angle (degrees)
Time Frame: 6 weeks
6 weeks
Penile Curvature Angle (degrees)
Time Frame: 3 months
3 months
Penile Curvature Angle (degrees)
Time Frame: 6 months
6 months
Penile Curvature Angle (degrees)
Time Frame: 12 months
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Michael P. Zahalsky, M.D., Z Urology

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2013

Primary Completion (Actual)

December 1, 2014

Study Completion (Actual)

March 1, 2015

Study Registration Dates

First Submitted

March 9, 2015

First Submitted That Met QC Criteria

March 16, 2015

First Posted (Estimate)

March 20, 2015

Study Record Updates

Last Update Posted (Estimate)

March 20, 2015

Last Update Submitted That Met QC Criteria

March 16, 2015

Last Verified

March 1, 2015

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • PMD-MSC-PD-01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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