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Actinic Keratosis clinical trials

View clinical trials related to Actinic Keratosis.

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NCT ID: NCT00952783 Completed - Actinic Keratosis Clinical Trials

A Long Term Follow up Study of Patients Who Have Completed the PEP005-020 Study

Start date: July 2009
Phase: Phase 3
Study type: Observational

This study is designed to follow up patients, who have achieved complete clearance of AK lesions (lesion count of 0) at Day 57 in the PEP005-020 study, over a 12 month period to assess both recurrence of Actinic Keratosis (AK) lesions and long term safety in the selected treatment area.

NCT ID: NCT00926952 Completed - Actinic Keratosis Clinical Trials

Short Incubation Methylaminolevulinate Photodynamic Therapy Without Occlusion

Start date: July 2009
Phase: Phase 3
Study type: Interventional

Actinic keratoses on the face are often numerous and widespread. The application of Methylaminolevulinate (MAL) on individual lesions followed by the application of a plastic film on each lesion is difficult and takes time for subjects with many actinic keratoses. The waiting period of 3 hours between MAL cream application and red light exposure is also long for patients. The goal of this study is to evaluate the safety and efficacy of photodynamic therapy (PDT) with MAL with a shorter cream application time (90 minutes) and when MAL is applied on the entire face without the plastic film.

NCT ID: NCT00917306 Completed - Actinic Keratosis Clinical Trials

A Multi-center Study to Evaluate the Safety and Efficacy of PEP005 (Ingenol Mebutate) Gel, When Used to Treat Actinic Keratoses on Non-head Locations (Trunk and Extremities)

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The open label study is designed to assess the safety and efficacy of 0.05% PEP005 Gel when applied to an area of skin containing 4-8 AK lesions on non-head locations.

NCT ID: NCT00916006 Completed - Actinic Keratosis Clinical Trials

A Multi-center Study to Evaluate the Efficacy and Safety of PEP005 (Ingenol Mebutate) Gel, When Used to Treat Actinic Keratoses on the Head (Face or Scalp)

Start date: June 2009
Phase: Phase 3
Study type: Interventional

This Phase III study is designed to assess the efficacy and safety of PEP005 Gel, 0.015% when applied to an area of skin containing 4-8 AK lesions on the face or scalp.

NCT ID: NCT00915551 Completed - Actinic Keratosis Clinical Trials

A Multi-Center Study to Evaluate the Efficacy and Safety of PEP005 (Ingenol Mebutate) Gel, When Used to Treat Actinic Keratoses on the Head (Face or Scalp)

Start date: June 2009
Phase: Phase 3
Study type: Interventional

This Phase III study is designed to assess the efficacy and safety of PEP005 Gel, 0.015% when applied to an area of skin containing 4-8 AK lesions on the face or scalp.

NCT ID: NCT00894647 Completed - Actinic Keratosis Clinical Trials

Safety and Effectiveness Study of Actinic Keratosis Treatment Following Cryosurgery

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of imiquimod cream versus placebo cream when used after cryosurgery in the treatment of actinic keratoses (AKs).

NCT ID: NCT00859105 Completed - Actinic Keratosis Clinical Trials

A Randomized, Double-Blind, Parallel-Group, Vehicle-Controlled Therapeutic Equivalence Study of Three Imiquimod Cream 5% Treatments for Patients With Actinic Keratosis

Start date: February 2008
Phase: Phase 3
Study type: Interventional

Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Bio-equivalence Study

NCT ID: NCT00852137 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Pharmacokinetics of PEP005 (Ingenol Mebutate) Gel, 0.05%, When Applied in a Maximal Use Setting to the Dorsal Aspect of the Forearm in Patients With Actinic Keratosis

Start date: March 2009
Phase: Phase 2
Study type: Interventional

This Phase II study is designed to evaluate the pharmacokinetics of PEP005 (ingenol mebutate) Gel, 0.05% when applied in a maximal use setting to the dorsal aspect of the forearm in patients with actinic keratoses

NCT ID: NCT00850811 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Photoirritation Potential of PEP005 (Ingenol Mebutate) Gel, 0.01% in Healthy Volunteers

Start date: February 2009
Phase: Phase 1
Study type: Interventional

This Phase 1 study is designed to determine the photoirritation potential of PEP005 Gel, 0.01% when application is followed by light exposure.

NCT ID: NCT00850681 Completed - Actinic Keratosis Clinical Trials

A Study to Evaluate the Photoallergic Potential of PEP005 (Ingenol Mebutate) Gel, 0.01% in Healthy Volunteers

Start date: February 2009
Phase: Phase 1
Study type: Interventional

This Phase 1 study is designed to determine the photoallergic potential of PEP005 Gel, 0.01% and it's vehicle on normal skin.