Afamelanotide and Narrow-Band Ultraviolet B (NB-UVB) Light in the Treatment of Nonsegmental Vitiligo (NSV)

Exclusion Criteria

• •Fitzpatrick skin types I-II
• •Vitiligo involving the hands and feet only
• •Extensive leukotrichia, in the opinion of the Investigator
• •Vitiligo of more than 5 years duration
• •Previous treatment with NB-UVB within 6 months prior to the Screening Visit
• •Patient not responsive to previous NB-UVB treatment, defined as a patient who has undergone at least 30 NB-UVB sessions with no or minimal clinically relevant pigmentary response, in the opinion of the Investigator
• •Allergy to afamelanotide or the polymer contained in the implant or to lignocaine/lidocaine or other local anesthetic to be used during the administration of the implant
• •Previous treatment with topical immunomodulators (corticosteroids, calcineurin inhibitors) for vitiligo within 4 weeks prior to the Screening Visit
• •History of photosensitivity disorders
• •Claustrophobia
• •History of photosensitive lupus
• •Any active and/or unstable autoimmune disease judged to be clinically significant by the Investigator
• •History of melanoma or lentigo maligna
• •History of dysplastic nevus syndrome
• •Any malignant skin lesions
• •Any skin disease that may interfere with the study evaluation
• •Any evidence of organ dysfunction or deviation from normal in clinical or laboratory determinations judged to be clinically significant by the Investigator
• •History of systemic or psychiatric disease judged to be clinically significant by the Investigator and which may interfere with the study evaluation
• •Female who is pregnant (confirmed by positive β-HCG pregnancy test), are lactating
• •Female of child-bearing potential (pre-menopausal, not surgically sterile) not using adequate contraceptive measures (i.e. oral contraceptives, diaphragm plus spermicide, intrauterine device) during the trial and for a period of three months thereafter
• •Sexually active man with a partner of child-bearing potential not using barrier contraception during the trial and for a period of three months hereafter
• •Participation in a clinical trial for an investigational agent within 30 days prior to the Screening Visit
• •Use of any prior and concomitant therapy which may interfere with the objective of the study, including drugs that cause photosensitivity or skin pigmentation within 60 days prior to the Screening Visit
• •Subjects assessed as not suitable for the study in the opinion of the Investigator