A Real World Study Evaluating the Long-Term Quality of Life of Tildrakizumab in Adult Patients With Psoriasis

Sun Pharma

Status and phase

Completed

Phase 4

Conditions

Psoriasis

Treatments

Drug: Injections of tildrakizumab

Study type

Interventional

Funder types

Industry

Identifiers

NCT03718299

TIL2018-1

Details and patient eligibility

About

This is a Phase 4 multicenter, uncontrolled open-label study design. There will be a total of 10 study visits at Screening, Baseline, Week 4, Week 8, Week 12, Week 16, Week 28, Week 40, Week 52 and Week 64, with subjects receiving tildrakizumab injections at Week 0, Week 4, Week 16, Week 28, Week 40, and Week 52. The total study duration will be approximately 64 weeks, excluding a screening period.

Enrollment

55 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subjects are non-immunocompromised males or females 18 years of age or older.
Subjects have ≥3% total body surface area plaque psoriasis.
Subjects are candidates for phototherapy or systemic therapy.
Subject must be diagnosed at least 6 months prior to entering the study.
Females must be surgically sterile, postmenopausal for >5 years, or using a highly effective form of birth control (<1% failure rate), for at least 30 days prior to test article exposure, with a negative serum pregnancy test.

Exclusion criteria

Subject is pregnant, lactating, or is planning to become pregnant during the study.
Subject is younger than 18 years of age.
Subjects with uncontrolled mental illness or active suicidal ideations based on baseline mental health questionnaire of choice.
Subject is known, or suspected of being unable to comply with the study protocol, in the opinion of the investigator.
Subject is currently enrolled in an investigational drug or device study.