Tralokinumab for Dupilumab Failures

Inclusion Criteria

• •Male or female adult ≥ 18 years of age;
• •All participants must have prior treatment with dupilumab for atopic dermatitis meeting one of the following conditions:
• •* Participants who stopped dupilumab treatment due to non-response, partial response, loss of efficacy must have been previously treated with dupilumab for at least 12 weeks.
• •* Participants who stopped dupilumab treatment due to intolerance or AEs to the drug may enter the study with no required prior length of dupilumab treatment. AE's must be resolved prior to 1st tralokinumab dose.
• •Females of childbearing potential (FCBP) must have a 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.
• •Subject is a candidate for systemic therapy.
• •Subject must be in general good health 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.