Efficacy and Safety of Ingenol Mebutate Gel for Actinic Keratosis Applied on Large Area on Face, Scalp or Chest
| Status: | Completed |
|---|---|
| Conditions: | Dermatology |
| Therapuetic Areas: | Dermatology / Plastic Surgery |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 10/5/2018 |
| Start Date: | April 2015 |
| End Date: | March 2017 |
Efficacy and Safety of Ingenol Mebutate Gel in Field Treatment of Actinic Keratosis on Full Face, Balding Scalp or Approximately 250 cm2 on the Chest
The objective of the trial is to investigate efficacy and safety of ingenol mebutate gel for
actinic keratosis applied to large treatment areas once daily for three consecutive days on
face, scalp or chest.
actinic keratosis applied to large treatment areas once daily for three consecutive days on
face, scalp or chest.
Inclusion Criteria:
Subjects with 5 to 20 clinically typical, visible and discrete, actinic keratosis (AKs)
non-hyperkeratotic and non-hypertrophic AKs within a selected treatment area of sun-damaged
skin on either:
- The full face
- The full balding scalp
- A contiguous area of approximately 250 cm2 on the chest
Exclusion Criteria:
- Location of the treatment area (full face, full balding scalp or chest) within 5 cm of
an incompletely healed wound or within 5 cm of a suspected basal cell carcinoma (BCC)
or squamous cell carcinoma (SCC).
- Previously assigned treatment in this clinical trial or previously participated in a
clinical trial in the LEO clinical programme on ingenol mebutate gel for larger
treatment areas.
- Treatment with ingenol mebutate gel in the selected treatment area within the last 12
months.
- Lesions in the treatment area that have: atypical clinical appearance (e.g. cutaneous
horn) and/or, recalcitrant disease (e.g., did not respond to cryotherapy on two
previous occasions).
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