Evidence map›Paper›PMID 42583051›Full record

ArticleTranslational andrology and urology2026

Peyronie's disease patients with pain: a post hoc analysis of the IMPRESS I/II studies.

Jesse N Mills, Gregory A Broderick, James P Tursi, Marian Ayad, Tina Rezakhani, Jeffrey Andrews, Sajel Patel, Landon Trost

2 registry-linked trialsAbstract read
In one paragraph

Article in Translational andrology and urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01221597 phase3completednot on this map

A Phase 3, Double-blind, Randomized, Placebo-controlled Study of the Safety and Effectiveness of AA4500 Administered Twice Per Treatment Cycle for up to Four Treatment Cycles (2 x 4) in Men With Peyronie's Disease

TypeinterventionalSponsorEndo USA Inc., a Keenova Therapeutics CompanyRan2010 to 2012Enrolled418ConditionsPeyronie's DiseaseArmsAA4500, Placebo
NCT01221623 phase3completednot on this map

A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of the Safety and Effectiveness of AA4500 Administered Twice Per Treatment Cycle for Up to Four Treatment Cycles (2 x 4) in Men With Peyronie's Disease

TypeinterventionalSponsorEndo USA Inc., a Keenova Therapeutics CompanyRan2010 to 2012Enrolled418ConditionsPeyronie's DiseaseArmsAA4500, Placebo
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jesse N MillsDivision of Andrology, Department of Urology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Gregory A BroderickMayo Clinic, Jacksonville, FL, USA.
James P TursiEndo USA, Inc. (a Keenova Therapeutics Company), Malvern, PA, USA.
Marian AyadEndo USA, Inc. (a Keenova Therapeutics Company), Malvern, PA, USA.
Tina RezakhaniEndo USA, Inc. (a Keenova Therapeutics Company), Malvern, PA, USA.
Jeffrey AndrewsEndo USA, Inc. (a Keenova Therapeutics Company), Malvern, PA, USA.
Sajel PatelEndo USA, Inc. (a Keenova Therapeutics Company), Malvern, PA, USA.
Landon TrostDepartment of Urology, Mayo Clinic, Rochester, MN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Significant clinical variations exist in the definitions of acute/active vs. chronic/stable Peyronie's disease (PD), limiting treatment options. To determine whether penile pain should inform PD treatment timing, we analyzed the association between baseline penile pain levels and treatment efficacy using data from the IMPRESS (Investigation for Maximal Peyronie's Reduction Efficacy and Safety Studies) I/II studies of collagenase clostridium histolyticum (CCH). Methods: A post hoc analysis of pooled data from 2 phase 3 randomized double-blind trials of CCH in PD (IMPRESS I, NCT01221597; IMPRESS II, NCT01221623) was conducted. CCH-treated participants were stratified by baseline penile pain levels using investigator-assessed and patient-reported measures. A subgroup analysis stratified participants with Any Pain by disease duration. Results: At total of 364 CCH-treated men were included. Mean penile curvature improvements at week 52 were similar across all 4 investigator-assessed and patient-reported penile pain measures (35.0-36.7% improvement for the No Pain group Conclusions: Men with PD who were treated with CCH experienced similar curvature improvements regardless of baseline pain status or disease duration among those who experienced any pain. Findings support the literature that demonstrate similar efficacy when treating men with active

Indexed as

maleMicrobial collagenaseoutcome assessmentpenile induration/drug therapy

Identifiers

PMID42583051
PMCPMC13458737

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.