260 Participants NeededMy employer runs this trial

Levulan Kerastick + PDT for Actinic Keratosis

Recruiting at 19 trial locations
HR
Overseen ByHead, Regulatory Affairs
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: Sun Pharmaceutical Industries, Inc.
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment for actinic keratosis (AK), which are rough, scaly patches on the skin caused by sun exposure. The study examines the effectiveness of a reformulated version of Levulan Kerastick (a topical solution) combined with blue light therapy in clearing these skin lesions on the arms. Participants will receive either the active treatment or a placebo. The main goal is to determine if the AK spots disappear completely after 12 weeks. The trial is suitable for individuals in good health with 4-8 mild to moderate AK lesions on one arm, who can maintain a consistent skincare routine and avoid tanning. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants a chance to contribute to the potential availability of a new treatment.

Do I have to stop taking my current medications for the trial?

The trial requires you to stop using certain topical therapies on the treatment area within 2 days to 8 weeks before starting, and some systemic therapies within 6 weeks to 6 months before starting. If you're using phototoxic or photoallergic medications, you need to stop them 8 weeks before starting. It's best to discuss your specific medications with the trial team.

Is there any evidence suggesting that this treatment is likely to be safe for humans?

Previous studies have shown that Levulan Kerastick, used with photodynamic therapy (PDT), offers promising safety results for treating actinic keratosis (AK). Research indicates that patients generally tolerate this treatment well. Most side effects are mild and temporary, with skin pain during the light treatment being the most common issue, though it usually resolves quickly. Other reactions, such as redness or swelling, also tend to be short-lived.

Levulan Kerastick has a strong safety record when used on the face and scalp for AKs. Its FDA approval for these areas supports its safety. The combination of Levulan Kerastick with blue light treatment has proven effective, yielding excellent cosmetic results and side effects that diminish over time. Overall, while the treatment may cause some discomfort, it has consistently been found safe for patients.12345

Why do researchers think this study treatment might be promising for actinic keratosis?

Unlike other treatments for actinic keratosis, which often rely on topical creams or cryotherapy, the reformulated Levulan Kerastick with photodynamic therapy (PDT) offers a unique approach by combining a medication with a specialized light treatment. This therapy involves applying Levulan, allowing it to incubate, and then activating it with blue light, which targets and destroys precancerous cells. Researchers are particularly excited because this method could potentially provide more precise and effective treatment with fewer side effects, offering new hope for patients with this common skin condition.

What evidence suggests that this treatment might be an effective treatment for actinic keratosis?

Research has shown that Levulan Kerastick, combined with blue light therapy, effectively treats actinic keratosis (AK), which are rough, scaly patches on the skin. In this trial, participants will receive either the Levulan application or a vehicle application, both followed by blue light therapy. Studies have demonstrated that the Levulan treatment can clear up to 100% of AK spots, completely removing these patches. Patients treated with Levulan and blue light report good cosmetic results, with no scarring or changes in skin color. The FDA has approved this combination, confirming its effectiveness and safety for mild to moderate AK. Overall, the evidence strongly supports its use in effectively clearing AK spots.12367

Are You a Good Fit for This Trial?

This trial is for adults aged 18-85 who have 4-8 mild to moderate actinic keratosis (AK) spots on one arm. Participants must be in good health, avoid sunbathing or tanning, and agree to use effective birth control if needed. They should not use other skin products on the treatment area before visits.

Inclusion Criteria

I am between 18 and 85 years old and not pregnant.
I agree to not use any skin products in the treatment area 8 hours before clinic visits.
I have 4-8 mild to moderate skin lesions on my arm.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive Levulan application followed by blue light exposure for up to 2 PDT sessions depending on lesion clearance

12 weeks
Multiple visits for PDT sessions and assessments

Follow-up

Participants are monitored for safety, effectiveness, and recurrence of lesions after treatment

12 weeks
Visits at Weeks 12, 20, and 24 for assessments

What Are the Treatments Tested in This Trial?

Interventions

  • Reformulated Levulan Kerastick

Trial Overview

The study tests a new version of Levulan Kerastick (aminolevulinic acid gel) plus blue light therapy versus a placebo gel with blue light. Patients are randomly assigned to either group and may receive up to two treatments depending on how well their AK spots clear.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: LevulanExperimental Treatment2 Interventions
Group II: VehiclePlacebo Group2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Sun Pharmaceutical Industries, Inc.

Lead Sponsor

Citations

NCT07144345 | Study of Reformulated Levulan Kerastick ...

This Phase 3, randomized, multi-center, evaluator-blind, vehicle-controlled study evaluates the efficacy and safety of reformulated Levulan Kerastick ...

Review of photodynamic therapy in actinic keratosis and basal ...

The main advantages of topical PDT are that the method is non-invasive and effective, and generally gives a good cosmetic outcome. The application of ALA or MAL ...

3.

levulanhcp.com

levulanhcp.com/efficacy

proven results to treat actinic keratosis (ak)

LEVULAN KERASTICK + BLU-U blue light is proven to destroy AKs without scarring or dyschromia of the skin.1,2,4,11. No scarring was reported in clinical trials1, ...

The Role and Effectiveness of Photodynamic Therapy on ...

Several RCT studies have shown the effectiveness, complete response to treated lesions, and cosmetic outcomes using MAL-PDT and BF-200 ALA. BF-200 ALA has been ...

Study Details | NCT05359419 | Comparison of Two Modes ...

This study will be a prospective clinical trial performed in a single center, with 20 adult subjects presenting 4-17 clinically confirmed, mild to moderate AKs.

6.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/37134239/

A Meta-Analysis Update of Randomized Controlled Trials

Compared with other methods, PDT is significantly more effective for AK with excellent cosmetic results and reversible adverse effects.

Tolerability of Photodynamic Therapy Using 10% 5- ...

Based on this retrospective observational case series, PDT with ALA gel appears to be safe for treating patients with AKs covering surface areas 75 to 300cm 2.