A Single Center Study to Evaluate the Effectiveness and Safety of ILUMYA in Combination With HALOG Ointment 0.1% for the Treatment of Moderate to Severe Plaque Psoriasis.

Who is this study for? Patients with moderate-to-severe plaque psoriasis
What treatments are being studied? Ilumya Injectable Product
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Patient with moderate-to-severe plaque psoriasis will receive Ilumya with or without Halog ointment.

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

• Male or female adult ≥ 18 years of age;

• Diagnosis of moderate-to-severe chronic plaque-type psoriasis as defined by

‣ BSA 10%

⁃ PGA ≥3

⁃ PASI ≥12

• Must be a candidate for phototherapy and/or systemic therapy

• Females of childbearing potential (FCBP) must have a negative serum pregnancy test at Screening and negative urine pregnancy test at 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.

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: 2020-04-06
Estimated Completion Date: 2021-03-01
Participants
Target number of participants: 25
Treatments
Experimental: Ilumya
Ilumya 100mg subcutaneous at weeks 0, 4 and 16.
Related Therapeutic Areas
Sponsors
Collaborators: Sun Pharmaceutical Industries Limited
Leads: Psoriasis Treatment Center of Central New Jersey

This content was sourced from clinicaltrials.gov