Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects With Moderate to Severe Plaque Psoriasis
Status: | Completed |
---|---|
Conditions: | Psoriasis |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 6/10/2017 |
Start Date: | April 2015 |
End Date: | January 2017 |
A Phase 1b Open Label, Randomized Study Evaluating the Absorption and Systemic Pharmacokinetics and HPA Axis Suppression Potential of Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects With Moderate to Severe Plaque Psoriasis
Suppression Potential of Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects
with Moderate to Severe Plaque Psoriasis.
with Moderate to Severe Plaque Psoriasis.
A Phase 1b Open-Label, Randomized Study Evaluating the Absorption and Systemic
Pharmacokinetics and HPA Axis Suppression Potential of Topically Applied IDP-118 Lotion and
HP Monad Lotion in Subjects with Moderate to Severe Plaque Psoriasis.
Pharmacokinetics and HPA Axis Suppression Potential of Topically Applied IDP-118 Lotion and
HP Monad Lotion in Subjects with Moderate to Severe Plaque Psoriasis.
Inclusion Criteria:
- Male or Female of any race, at least 18 years old of age (inclusive)
- Freely provides both written and oral informed consent.
- Has a clinical diagnosis of psoriasis at the Baseline visit with an Investigator's
Global Assessment Score of 3 or 4. The face, scalp ,axillae, and intertriginous areas
are to be excluded in this calculation.
- Has an area of plaque psoriasis for topical treatment that involves a BSA of at least
20%.
- The willing and able to avoid prolonged exposure of the treatment area to ultraviolet
radiation (natural and artificial) for the duration of the study.
Key Exclusion Criteria:
- Has spontaneously improving or rapidly deteriorating plaque psoriasis or postural
psoriasis, as determined by the investigator.
- Presents with psoriasis that was treated with prescription medication and failed to
respond to presents).
- Has a history of adrenal disease.
- Presents with any other concurrent skin conditions that could interfere with the
evaluation of the treatment areas, as determined by the investigator.
- Is pregnant, nursing, or planning pregnancy during the study period.
We found this trial at
12
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