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Actinic Keratosis clinical trials

View clinical trials related to Actinic Keratosis.

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NCT ID: NCT02120898 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participants With Actinic Keratoses

Start date: October 10, 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study it so compare the safety and efficacy profiles of a generic imiquimod 2.5% cream to the reference listed Zyclara® (imiquimod) cream in the treatment of actinic keratosis (AK).

NCT ID: NCT02120456 Completed - Actinic Keratosis Clinical Trials

Safety and Efficacy of Escalating Doses of LEO 43204 Applied Once Daily for Two Consecutive Days on Approximately 250 cm2 on Trunk and Extremities in Subjects With Actinic Keratosis

Start date: May 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Part 1: To identify Maximum Tolerated Dose (MTD) levels of LEO 43204 after once daily treatment for two consecutive days Part 2: To evaluate the efficacy of LEO 43204 in two doses after once daily treatment for two consecutive days compared to vehicle

NCT ID: NCT02100813 Completed - Actinic Keratosis Clinical Trials

Safety and Efficacy of Doses of LEO 43204 Once Daily for Two Consecutive Days on Full Balding Scalp in Subjects With Actinic Keratosis

Start date: May 2014
Phase: Phase 1/Phase 2
Study type: Interventional

To identify the Maximum Tolerated Dose levels of LEO 43204 after once daily treatment for two consecutive days and to evaluate efficacy of LEO 43204 in two doses after once daily treatment for two consecutive days compared to vehicle

NCT ID: NCT02090465 Completed - Actinic Keratosis Clinical Trials

Assessment of Treatment Success and Quality of Life in Patients With Actinic Keratoses Under Therapy With Ingenol Mebutate in a Period of 8 Weeks

Start date: July 2013
Phase:
Study type: Observational

Assessment of treatment success and quality of life in patients with actinic keratoses under therapy with Ingenol Mebutate (Picato) in a period of 8 weeks.

NCT ID: NCT02085395 Completed - Actinic Keratosis Clinical Trials

Clinical Study Assessment of SR-T100 Topical Gel Against Actinic Keratosis

AK
Start date: November 2007
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy of SR-T100 gel by observing the lesion size (length x width x height) of human cutaneous squamous cell carcinoma in situ (Actinic Keratosis and Bowen's Disease) reduced at least 75%.

NCT ID: NCT02029066 Completed - Actinic Keratosis Clinical Trials

Pharmacokinetic Study of Solamargine in Patients With Actinic Keratosis

Start date: November 2013
Phase: Phase 1
Study type: Interventional

This study is designed to evaluate the pharmacokinetics of solamargine of SR-T100 gel. As safety parameters, adverse events, and vital signs (blood pressure, heart rate, and body temperature) will be recorded.

NCT ID: NCT02019355 Completed - Actinic Keratosis Clinical Trials

Actinic Keratosis Study

AK
Start date: October 2013
Phase: Phase 0
Study type: Interventional

The main purpose of this study is to determine the effectiveness of a new combination therapy for actinic keratosis. This study investigates a new indication for an FDA-approved topical medication, calcipotriol, for treatment of actinic keratosis, including how well it works and how safe it is when used in combination with the standard of care medication (5-fluorouracil) for the skin condition.

NCT ID: NCT01998984 Completed - Actinic Keratosis Clinical Trials

Efficacy and Safety of Ingenol Mebutate Gel 0.06% When Applied Once Daily for 2, 3 or 4 Consecutive Days to a Treatment Area of Approximately 250 cm2 on Trunk and Extremities in Subjects With Actinic Keratosis

Start date: January 2014
Phase: Phase 2
Study type: Interventional

This is a randomised, double-blind, parallel groups, vehicle controlled, 8-week phase 2 trial. The objective is to evaluate efficacy of ingenol mebutate gel 0.06 % after once daily treatment for 2, 3 or 4 consecutive days compared to vehicle gel

NCT ID: NCT01966120 Completed - Actinic Keratosis Clinical Trials

Safety and Efficacy Study for the Field-directed Treatment of Actinic Keratosis (AK) With Photodynamic Therapy (PDT)

Start date: October 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of BF-200 ALA (Ameluz) versus placebo in the field-directed treatment of mild to moderate actinic keratosis with photodynamic therapy (PDT) when using the BF-RhodoLED lamp.

NCT ID: NCT01962987 Completed - Actinic Keratosis Clinical Trials

A Study Comparing Diclofenac Sodium Gel 3% to Solaraze® (Diclofenac Sodium) Gel 3% in the Treatment of Actinic Keratosis

Start date: March 2013
Phase: Phase 3
Study type: Interventional

To compare the relative efficacy and safety of the test formulation diclofenac sodium gel 3% (Actavis) to the marketed formulation Solaraze® (diclofenac sodium) Gel 3% (Fougera Pharms) in the treatment of the actinic keratosis