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Peyronie's DiseasePhase 4NCT05108558

Efficacy of a Novel CCH Protocol for PD Among Prior Non-responders

A Phase 4 study testing CCH administration and RestoreX in people with Peyronie's Disease, run by Charitable Union for the Research and Education of Peyronie's Disease at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Compare key clinical outcomes between controls and men treated with a novel CCH administration protocol among men previously unresponsive to CCH administration. Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Peyronie's Disease
What is being tested?
CCH administration and RestoreX
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteUnited States
Study dates
20 Sep 2021to 13 Jun 2026
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men with Peyronie's Disease
  • >18 years old
  • Curvature ≥30 degrees
  • Previously completed 6-8 CCH injections
  • Prior minimal (<20% and/or <10 degrees) responsiveness to CCH administration
  • Prior CCH injections must have been performed without use of a Restorex traction device and used the IMPRESS protocol
  • Ability to achieve an erection satisfactory for intercourse with or without PDE5 inhibitors
  • The patient exhibits a palpable plaque consistent with Peyronie's Disease

Who cannot join

  • Prior surgical treatment on the penis (other than circumcision)
  • Any contraindications to CCH - as determined by the PI
  • Inability to complete 8 additional CCH injections
  • Severe plaque calcification (i.e. >1 cm shadowing)

Trial locations and contacts

1 site in 1 country.

United States1 site
  • The Male Fertility and Peyronie's Clinic

    Orem, Utah, 84057

Other trials in United States

About this study

Official title: Efficacy of a Novel Collagenase Clostridium Histolyticum Protocol for Peyronie's Disease Among Prior Non-responders: A Randomized, Controlled, Single-Blinded Study

Compare key clinical outcomes between controls and men treated with a novel CCH administration protocol among men previously unresponsive to CCH administration.

Read the detailed description

Beginning approximately 3 years ago, the investigators' team sought to achieve further improvements with CCH through the addition of more aggressive modeling therapies. Results from a comparison of CCH alone vs CCH and traction with RestoreX demonstrated a mean 33.8 degree (49%) curvature improvement with combined therapy compared to 19-20 degrees (30-31%) with CCH alone or CCH and other traction devices). These results currently represent the greatest improvements with CCH in published literature and further build upon phase IIb results which demonstrated that mechanical traction (via manual modeling in the phase IIb trial) represents a critical factor in achieving improvements with CCH.

The investigators' team additionally published a survey of men who had experienced suspected penile fractures with CCH and demonstrated greater curvature improvements without any loss / worsening of erectile function. This critical study highlighted that conservative management of suspected fractures should not only be considered a standard of care in managing suspected fractures, but also that these men achieved better final outcomes (again highlighting the importance of the combination of mechanical curvature correction in addition to CCH management).

Based on the above findings, the investigators' team began performing a more aggressive manual modeling protocol. This novel protocol included several notable innovations: dilution of the 0.9 mg of CCH in 0.7 ml of diluent, injection to the erect penis to assure accurate injection, repeat curvature assessments with each series (due to changing of the point of maximal curvature), incorporation of RestoreX traction therapy post injection, and 'aggressive' manual modeling (equivalent of 10-15 lbs of force) to achieve curvature correction. Preliminary (unpublished - abstract submitted to SMSNA 2021) results from these men demonstrated a median ~60% curvature improvement. Importantly, several of the patients had previously undergone 8 CCH injections with outside providers and were able to similarly achieve a median 60% improvement with the investigators' injection / modeling protocol.

These preliminary findings have several important ramifications for the treatment of PD:

  1. Men who have previously not achieved adequate curvature correction with 4 series of CCH injections may benefit from additional injections using a more aggressive traction protocol.
  2. A more aggressive traction protocol would benefit patients to achieve greater outcomes than with previously reported protocols.

1.2 Investigational Treatments

The current study would randomize men 1:3 into one of two treatment cohorts: 1. Observation followed by CCH or 2. CCH followed by observation. This study design offers the benefits of a randomized, controlled trial (highest level of evidence). RCTs are particularly important in PD, where the disease changes over time in a percentage of men as a function of its natural history. This would also allow blinding of measurements using photographs (single-blinded assessments), which provides further study rigor.

  1. No treatment (control) followed by CCH. Men in this cohort would undergo baseline assessments followed by no treatment for 6 months and then repeat assessments. Men would then cross-over to CCH treatment and undergo up to 8 injections (or until curvature is <15 degrees). Interval assessments would be performed with the 1st injection of each series, and final assessments would then be performed 6 weeks following the final injection.
  2. CCH followed by no treatment. Men in this cohort would undergo baseline assessments followed by up to 8 injections of CCH (or until curvature is <15 degrees). Interval assessments would be performed with the 1st injection of each series and 6 weeks following completion of treatment. Men then would not undergo any additional treatments for 6 months, after which final assessments would then performed.
Being tested
CCH administration, Control - Crossover to CCH, RestoreX
Medical subject headings
Penile Induration

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CCH administrationDrug

    Also called Collagenase Clostridium Histolyticum

    Patients will be randomized 3:1 into the CCH administration arm. After undergoing baseline assessments, this arm will receive up to 8 CCH injections, followed by final assessments 6 weeks later.

  • Control - Crossover to CCHDrug

    Also called Collagenase Clostridium Histolyticum

    Patients will be randomized 1:3 into the control arm. After undergoing baseline assessments, control men will not undergo treatments for 6 months. They will then have repeat assessments and receive up to 8 CCH injections. They will then have final assessments performed 6 weeks after treatment.

  • RestoreXDevice

    Both treatment arms will incorporate the use of RestoreX for 30-60 minutes daily during CCH administration and continued until 6 weeks after final injection administration.

Study groups in NCT05108558
Study groupRoleWhat they receive
Control - Crossover to CCHActive comparatorMen in this cohort would undergo baseline assessments followed by no treatment for 6 months and then repeat assessments. Men would then cross-over to CCH treatment and undergo up to 8 injections (or until curvature is <15 degrees). Final assessments would then be performed 6 weeks following the final injection.
Receives: Drug: Control - Crossover to CCH; Device: RestoreX
Collagenase Clostridium HistolyticumExperimentalMen in this cohort would undergo baseline assessments followed by up to 8 injections of CCH (or until curvature is <15 degrees). Men would then undergo assessments 6 weeks later, followed by a 6-month no treatment phase and then final assessments.
Receives: Drug: CCH administration; Device: RestoreX

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Penile Curvature

    Compare the change in degree of penile curvature from baseline (using a goniometer) between control and treatment groups at 6 months

    Measured: 6 months

  2. Peyronie's Disease Questionnaire Outcomes

    Compare Peyronie's Disease Questionnaire outcomes between control and treatment groups at 6 months using the Peyronie's Disease Questionnaire (15 items; subdomains - psychological and physical (Q1-6, 0-24), penile pain (Q7-9; 0-30), symptom bother (Q10-15; 0-16); 12 and 14 (Y/N q's); lower is better.

    Measured: 6 months

Secondary outcomes (9)
  1. International Index of Erectile Function Outcomes

    Compare International Index of Erectile Function Outcomes between control and treatment groups at 6 months

    Measured: 6 months

  2. Penile Curvature Compared to Baseline

    Compare penile curvature changes (degrees) in control men at baseline and 12 months (i.e. prior to and following cross-over to CCH) - using goniometer

    Measured: 12 months

  3. Penile Length Compared to Baseline

    Compare penile length changes in control men at baseline and 12 months (i.e. prior to and following cross-over to CCH)

    Measured: 12 months

  4. Compare Peyronie's Disease Questionnaire to Baseline

    Compare PDQ changes in control men at baseline and 12 months (i.e. prior to and following cross-over to CCH) using the Peyronie's Disease Questionnaire (15 items; subdomains - psychological and physical (Q1-6, 0-24), penile pain (Q7-9; 0-30), symptom bother (Q10-15; 0-16); 12 and 14 (Y/N q's); lower is better.

    Measured: 12 months

  5. Compare International Index of Erectile Function to baseline

    Compare International Index of Erectile Function changes in control men at baseline and 12 months (i.e. prior to and following cross-over to CCH)

    Measured: 12 months

  6. Penile Length Between Groups

    Compare penile length changes between control and treatment groups at 6 months

    Measured: 6 months

  7. Adverse events - 6 months - pain, sensation, swelling

    Report adverse events at the 6-month time point

    Measured: 6 months

  8. Adverse events - 12 months - pain, sensation, swelling

    Report adverse events at the 12-month time point

    Measured: 12 months

  9. Change in penile curvature durability

    Report changes in penile curvature degree between the 6 and 12-month assessments for CCH men by goniometer.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Nov 2021
  2. Study start20 Sep 2021
  3. Primary completion13 Jun 2026
  4. Study completion13 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Patients meeting criteria who have consented will be randomized to either control or CCH x 6 months, followed by a cross-over phase where controls will receive CCH. See Figure 1 for full study schema. 1. Control. Men in this cohort would undergo baseline assessments followed by no treatment for 6 months and then repeat assessments. Men would then cross-over to the CCH treatment phase and undergo up to 8 injections (or until curvature is \<15 degrees, whichever comes first). Final assessments would then be performed 6 weeks following the final injection. 2. CCH followed by observation. Men in this cohort would undergo baseline assessments followed by up to 8 injections of CCH (or until curvature is \<15 degrees). Assessments would then be performed 6 weeks after completion of treatment. Men then would not undergo any additional treatments for 6 months, after which they would have final assessments performed.
Masking
Double blind
Who is masked
Care provider, Outcomes assessor
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05108558
Sponsor's protocol ID
CUREPD 103
Status last verified
Aug 2026
First submitted
11 Oct 2021
Last updated
26 Aug 2026
Results posted
No
FDA-regulated drug
Yes
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing CCH administration and RestoreX in people with Peyronie's Disease, run by Charitable Union for the Research and Education of Peyronie's Disease at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Penile Curvature (time frame: 6 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Aug 2026.

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