Open Label Study, Evaluating Taltz in Combination With Enstilar (Calcipotriene and Betamethasone Dipropionate) Foam in Psoriasis Patients

Who is this study for? Patients with plaque psoriasis
What treatments are being studied? Enstilar
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Enstilar in combination with Taltz for plaque psoriasis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female adult ≥ 18 years of age;

• Diagnosis of chronic plaque-type

• Body Surface Area between 3%-8%.

• Patient has been treated with Taltz for a minimum of 24 weeks

• Females of childbearing potential (FCBP) must have a negative pregnancy test at Screening and Baseline. FCBP who engage in activity in which conception is possible must use one of the approved contraceptive options: hormonal contraception; intrauterine device (IUD); tubal ligation; or partner's vasectomy; Male or female condom diaphragm with spermicide, cervical cap with spermicide, or contraceptive sponge with spermicide.

• Subject must be in general good health (except for psoriasis) as judged by the Investigator, based on medical history, physical examination

• Able and willing to give written informed consent prior to performance of any study-related procedures.

Locations
United States
New Jersey
Psoriasis Treatment Center of Central New Jersey
RECRUITING
East Windsor
Contact Information
Primary
Jerry Bagel, MD
dreamacres1@aol.com
6094434500
Backup
Elise Nelson
enelson@windsordermatology.com
6094434500
Time Frame
Start Date: 2020-04-28
Estimated Completion Date: 2021-03-30
Participants
Target number of participants: 25
Treatments
Experimental: Enstilar
Enstilar foam
Related Therapeutic Areas
Sponsors
Collaborators: Eli Lilly and Company
Leads: Psoriasis Treatment Center of Central New Jersey

This content was sourced from clinicaltrials.gov