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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02932878
Other study ID # DSXS 1503a
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date September 2, 2016
Est. completion date October 16, 2017

Study information

Verified date November 2018
Source Taro Pharmaceuticals USA
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

An Open Label, Safety Study to Assess the Potential for Adrenal Suppression Following Treatment with DSXS (Taro Pharmaceuticals U.S.A., Inc.) in Patients with Plaque Psoriasis


Description:

To evaluate the potential of DSXS to suppress HPA axis function in patients with mild to moderate plaque psoriasis.

To evaluate the efficacy parameters and adverse event (AE) profile of DSXS administered to patients with mild to moderate plaque psoriasis.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date October 16, 2017
Est. primary completion date April 10, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Years to 18 Years
Eligibility Inclusion Criteria:

- Male or non pregnant, non lactating females

Exclusion Criteria:

- Patients under 2 years of age

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
DSXS topical
topical treatment

Locations

Country Name City State
United States Taro Pharmaceuticals USA Inc. Hawthorne New York

Sponsors (1)

Lead Sponsor Collaborator
Taro Pharmaceuticals USA

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of Patients in the Study With HPA Axis Suppression Hypothalamic Pituitary Adrenal (HPA) Axis Response to Cosyntropin 28 Days
See also
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