A Phase 2 interventional study of Verteporfin Injection and Saline injection in Surgical Scar, sponsored by Odense University Hospital. Recruiting at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-27.
Sponsored by Odense University Hospital · Phase 2, Interventional, and Prevention
The purpose of this clinical trial is to investigate whether the drug verteporfin can reduce the formation of scars in adult patients undergoing a tummy tuck procedure (abdominoplasty).
The main questions the study aims to answer are:
The researchers will compare three different doses of verteporfin (0.5 mg/mL, 1.0 mg/mL, and 2.0 mg/mL) with placebo. Each participant will receive all three doses as well as placebo, but in different areas of the surgical wound and in different small wounds, allowing comparisons to be made within the same person.
Participants will:
Introduction and Background:
Scar formation after skin injury represents a significant medical challenge with both physical and psychosocial consequences. Scars can cause pain, pruritus, restricted movement, and substantial psychological distress.
While adult wound healing typically results in scar formation, fetal wounds heal with minimal or no scarring, suggesting that regenerative, scarless healing is biologically possible under specific conditions. Recent research has identified the Yes-Associated Protein (YAP)/ Transcriptional Co-Activator with PDZ-binding motif (TAZ) signaling pathway as central to fibrosis development. Inhibition of this pathway has shown promising results in experimental fibrosis models.
YAP is a mechano-sensitive transcription coactivator regulated by the Hippo pathway. Its activity has emerged as a key determinant of whether injured tissues undergo regenerative healing (restoring normal structure) or fibrotic repair (scar formation). Recent studies across multiple organs indicate that the timing and duration of YAP activity is critical: Transient or timely YAP modulation can promote regeneration, whereas sustained YAP activation or complete loss of YAP often skews healing toward fibrosis.
Verteporfin is a Food and Drug Administration (FDA)-approved benzoporphyrin derivative used for treating macular degeneration that also inhibits the YAP/TAZ pathway. Animal studies have demonstrated that verteporfin reduces extracellular matrix deposition in liver, kidney, and retinal fibrosis. Most notably, Mascharak et al. recently showed that a single dose of verteporfin induced scarless wound healing in the Duroc pig, a model with skin healing characteristics closely resembling those of humans. The results were further validated using a human foreskin graft model in nude mice. Despite these promising preclinical results, human evidence for verteporfin's potential as a scar-preventing treatment is lacking. This study represents the first attempt to translate these findings into clinical practice.
Aim:
The aim of this study is to evaluate the safety and tolerability and to identify the most appropriate dose of intradermal verteporfin for the prevention of scar formation in surgical wounds. The results will pave the way for subsequent studies to further investigate the efficacy of verteporfin's anti-fibrotic properties.
Hypothesis:
It is hypothesized that a single intradermal administration of verteporfin at the time of surgery will result in a significant reduction in scar formation compared to placebo. Furthermore, a dose-response relationship is expected, with higher concentrations leading to greater improvement in scar quality without compromising wound healing. Finally, it is hypothesized that the treatment to be safe and well tolerated in humans with no serious adverse effects.
Study Design:
This trial is a phase 2, prospective, randomized, single blinded, placebo-controlled, intra-patient, single center clinical trial where each participant serves as their own control with different dose levels administered to different parts of the wound and different open wounds within the same patient. The total participation period for the individual subjects is 3 months.
The single-blinded study design (blinding of participants and outcome assessors, with the operating surgeon unblinded) was selected due to the visible dark green color of verteporfin, which makes full blinding difficult during administration. An intra-patient design was chosen to minimize inter-patient variability in wound healing.
Randomization and blinding:
Treatment allocation will be randomized using a computer-generated sequence to assign verteporfin dose levels and placebo to wound areas and punch biopsies within each participant.
Sample Size:
A total of 12 participants has been chosen as an appropriate sample size for this study. Due to the intra-patient design, where each participant contributes eight scar outcomes (four closed and four open wounds), a total of 96 observations will be available for safety assessment, exploratory dose-response analysis and estimation of effect. The underlying statistical considerations are presented below:
Fixed effect: treatment dose; random effect: participant. Pairwise comparisons between each verteporfin dose and placebo will be performed using a mixed-effects model with Dunnett's adjustment for multiple testing.
Based on previous scar studies, a 6-point difference in POSAS is considered clinically meaningful. Assuming a standard deviation of 5-7 points and intra-subject correlation of 0.3: With 12 participants, each contributing 4 scars per model (closed and open). The design yields sufficient power (≥80%, α = 0.025 per endpoint after Bonferroni correction). Total of 48 observations per model, supporting separate detection of meaningful differences in both scar types.
Methods:
Verteporfin will be administered by intradermal injection into wound margins at three dose levels:
The drug will be administered after suture in the closed model, and after punch creation in the open model. Punch biopsies will be obtained from the lower abdomen within the pubic hair-bearing region to evaluate whether hair regrowth occurs as part of the regenerative process and to minimize the visibility of any scars resulting from the biopsies. No light activation will be used in this study. Each participant will receive all three dose levels plus one placebo (saline injection) in separate wound segments and separate punch biopsies. A single administration will take place on Day 0 (day of surgery) with no repeat dosing. This timing exploits the critical early YAP/TAZ modulation window.
Participants will be monitored at preplanned follow-up visits on Day 7, Month 1 and Month 3 where scar quality will be assessed via the primary endpoint for both the closed and open model:
Study Limitations:
This study has several limitations. Firstly, the small sample size of 12 participants and the single-centre design limit the generalizability of the findings and the ability to detect rare adverse events or establish clinical efficacy. Secondly, the study population consists of healthy adults undergoing elective abdominoplasty which provides a homogeneous wound model but does not reflect high-risk groups such as patients with diabetes, smokers or individuals prone to hypertrophic scarring, therefore external validity is limited.
The follow-up period of 3 months fails to capture the long-term phases of scar maturation. Additionally, inter-patient dose comparison - while reducing inter-individual variability - introduces the possibility of local interference between the scar segments. Moreover, several outcome measures rely on subjective scar assessment tools (e.g. POSAS, MSS, SCAR-Q) which - despite being validated - carry a risk of observer bias even under blinded evaluation. These limitations will be addressed in future trials with larger study populations, longer follow-up and multicenter variation as well as inclusion of high-risk groups.
Feasibility:
The intra-patient design significantly enhances feasibility by reducing the required sample size as each participant contributes four treatment sites per wound model (open and closed). Recruitment is therefore considered realistic, as eligible patients are routinely available among those undergoing elective abdominoplasty at Odense University Hospital. All study procedures are integrated into the routine surgical workflow and three follow-up visits consisting only of non-invasive assessments are planned, minimizing participant burden and risk of withdrawal.
The research team has full access to surgical facilities, ultrasound equipment and clinical photography tools. Furthermore, the investigational medicinal product, verteporfin, has an established safety profile in humans in other indications, and only a single, local administration is required per participant. Together, these factors ensure that the study is practically, logistically and ethically feasible.
Risks, Adverse Events, and Potential Disadvantages:
Verteporfin has an established safety profile in ocular use but is administered differently in this study. Therefore, additional or previously unobserved adverse effects may occur.
Possible adverse events include:
Common, non-serious adverse events
Rare or potentially serious adverse events
Potential longer-term effects
As with any clinical study, there may be risks that are currently unknown. Participants will therefore be asked to inform the study team if they experience any health-related problems during the course of the study. If new or previously unrecognized adverse effects are identified during the study, participants will be informed promptly and will have the opportunity to decide whether they wish to continue their participation.
Novelty:
This study is the first clinical trial to investigate intradermal verteporfin to reduce scarring in humans. Most available scar treatments focus on symptomatic treatment of cosmetic symptoms addressing established scars rather than preventing their formation. This project offers a unique possibility to introduce a new concept of pharmacological therapy targeting the biological mechanisms of fibrosis (YAP/TAZ signaling pathway) at the time of injury. This study therefore generates safety and preliminary efficacy data for a completely new therapeutic indication of verteporfin with significant translational potential and large global clinical relevance.
Clinical Impact:
Excessive scarring remains a major unmet clinical challenge with functional, aesthetic, and psychological consequences affecting millions of patients worldwide every year. Current treatment options are limited in efficacy and primarily reactive as they largely focus on the management of established scars rather than prevention.
If successful, this study could introduce a paradigm shift in postoperative wound care by demonstrating that scarring can be modulated at the time of injury through targeted biological intervention. Intradermal verteporfin has the potential to become the first pharmacological therapy to actively reduce scar formation by inhibiting fibrotic signaling pathways.
The clinical impact is substantial: Improved patient satisfaction after surgeries with better functional and aesthetic outcomes and significant cost savings for healthcare systems. The findings from this study could benefit a wide range of surgical fields, including plastic and reconstructive surgery, orthopedics, general surgery and dermatology. Ultimately, by bridging strong preclinical evidence with clinical data, this study has the potential to lay the foundation for a new standard of care in scar prevention and personalized wound management.
611 studies on the registry are indexed under Cicatrix; 114 are open to participants now.
This study's planned enrollment of 12 is below the median of 40 across 512 interventional studies indexed under Cicatrix.
Browse Cicatrix studies →Odense University Hospital is the lead sponsor of 479 studies on the registry; 110 are open to participants now.
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Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Moderate hepatic dysfunction, defined as:
Biliary obstruction, defined as:
or fibrotic skin conditions including (but not limited to):
1. Keloids or hypertrophic scars, scleroderma, lupus, GVD, morphea, lichen sclerosus, Ehlers-Danlos syndrome, cutis laxa, Marfan syndrome
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.
Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.
Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.
The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.
“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.
A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.
Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.
A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.
Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.
ASA physical status
The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Excipients
The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ALT and AST (liver enzymes)
Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.
Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ULN (upper limit of normal)
The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.
“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Bilirubin
A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.
Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Autoimmune disease
A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.
Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Saline is used as placebo and administered to one segment of the closed wound and one open wound.
Drug: Saline injection
Will be administered to one segment of the closed wound and one open wound. This dose level is included to explore the minimal effective dose.
Drug: Verteporfin Injection
Will be administered to one segment of the closed wound and one open wound. This dose level reflects the optimal concentration in murine models.
Drug: Verteporfin Injection
Will be administered to one segment of the closed wound and one open wound. This dose level reflects the optimal concentration in porcine models.
Drug: Verteporfin Injection
* Approved Generic Name: Verteporfin * Trade Name: Visudyne® * Chemical Class: Benzoporphyrin derivative * EU Substance No.: SUB00044MIG
Also known as: Visudyne
Sterile saline solution administered intradermally as placebo.
Also known as: Sodium chloride 0.9%
POSAS (Patient and Observer Scar Assessment Scale)
Closed wound endpoint: Difference in scar quality between three verteporfin doses (0.5, 1.0, 2.0 mg/mL) and placebo, assessed in sutured incision segments using the Observer component of the POSAS 3.0. Open wound endpoint: Difference in scar quality between three verteporfin doses (0.5, 1.0, 2.0 mg/mL) and placebo, assessed in punch biopsy wounds using the Observer component of the POSAS 3.0. POSAS Observer scores range from 10 (normal skin) to 50 (worst imaginable scar) and includes ten items assessing clinically relevant scar characteristics and overall scar quality. Each wound type (closed and open) will be evaluated independently.
Time frame: Month 3
Safety and Tolerability
Incidence, severity and type of local and systemic adverse events, including but not limited to injection site reactions, delayed wound healing, infections and systemic symptoms.
Time frame: Day 7, month 1 and month 3
MSS (Manchester Scar Scale)
A clinician-rated scar assessment scale designed for the evaluation of linear surgical scars, primarily based on visual inspection. Total score ranges from 5 to 18 (higher scores indicate worse scar quality). Evaluation will be performed based on standardized clinical photographs. Scale modification The "texture" component (item 5) is omitted, as assessments are performed exclusively based on standardized photographs and do not include physical examination. Therefore, the total score with the modified scale ranges from 4 to 14 (higher scores indicate worse scar quality).
Time frame: Month 3
Ultrasound Assessment of Scar Thickness
Quantitative measurement of dermal thickness using high-frequency ultrasound to assess fibrosis objectively.
Time frame: Month 1 and 3
Photographic Documentation
Standardized clinical photography.
Time frame: Day 7, month 1 and 3
Patient-Reported Scar Outcomes using SCAR-Q Appearance Scale and SCAR-Q Symptom Scale
The SCAR-Q is a validated patient-reported outcome measure designed to assess scar appearance and scar-related symptoms from the patient's perspective. The Appearance and Symptom scales are scored separately. Each scale consists of 12 items rated on a 4-point Likert scale (each likert scale ranges from 12 to 48 with higher scores indicating better outcomes). Likert scores are converted to Rasch-transformed scores ranging from 0 to 100 where higher scores indicate better outcomes (i.e., more favourable appearance or fewer symptoms).
Time frame: Month 1 and 3
Plan to share: No — IPD will not be shared due to data protection regulations and patient confidentiality considerations.
Start is estimated for Oct 2026; primary completion for Aug 2028, 22 months later.
Of 24 phase 2 interventional studies under Cicatrix, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 61. This study's planned 22 months is close to that.
Since we started tracking on Sep 25, 2026, the dates moved once, on Oct 5, 2026: start Jun 2026 → Oct 2026, primary completion Feb 2028 → Aug 2028 and completion Feb 2028 → Nov 2028.
Earlier changes are on the record history on ClinicalTrials.gov ↗
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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Studies of the drug tested here: Verteporfin