Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

janssen-cilag international nv - guselkumab - Ψωρίαση - Ανοσοκατασταλτικά - plaque psoriasis tremfya is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritis tremfya, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adult patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (dmard) therapy (see section 5.

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

sanofi winthrop industrie - dupilumab - dermatitis, atopic; prurigo; esophageal diseases; asthma; sinusitis - Παράγοντες για δερματίτιδα, εξαιρουμένων των κορτικοστεροειδών - atopic dermatitisadults and adolescentsdupixent is indicated for the treatment of moderate-to-severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. children 6 months to 11 years of agedupixent is indicated for the treatment of severe atopic dermatitis in children 6 months to 11 years old who are candidates for systemic therapy. asthmaadults and adolescentsdupixent is indicated in adults and adolescents 12 years and older as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), see section 5. 1, who are inadequately controlled with high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. children 6 to 11 years of agedupixent is indicated in children 6 to 11 years old as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils and/or raised fraction of exhaled nitric oxide (feno), who are inadequately controlled with medium to high dose inhaled corticosteroids (ics) plus another medicinal product for maintenance treatment. chronic rhinosinusitis with nasal polyposis (crswnp)dupixent is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adults with severe crswnp for whom therapy with systemic corticosteroids and/or surgery do not provide adequate disease control. prurigo nodularis (pn)dupixent is indicated for the treatment of adults with moderate-to-severe prurigo nodularis (pn) who are candidates for systemic therapy. eosinophilic esophagitis (eoe)dupixent is indicated for the treatment of eosinophilic esophagitis in adults and adolescents 12 years and older, weighing at least 40 kg, who are inadequately controlled by, are intolerant to, or who are not candidates for conventional medicinal therapy.

Ελλάδα - Ελληνικά - Εθνικός Οργανισμός Φαρμάκων

sanofi-aventis groupe, france 54 rue la boetie,, 75008, paris, - dupilumab - inj.so.pfs (ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ ΣΕ ΠΡΟΓΕΜΙΣΜΕΝΗ ΣΥΡΙΓΓΑ) - (150mg/ml) 300mg/2ml - dupilumab 600mg - dupilumab

Ευρωπαϊκή Ένωση - Ελληνικά - EMA (European Medicines Agency)

merck europe b.v. - avelumab - Νευροενδοκρινικοί όγκοι - Άλλοι αντινεοπλασματικοί παράγοντες, Μονοκλωνικά αντισώματα - Το bavencio ενδείκνυται ως μονοθεραπεία για τη θεραπεία ενηλίκων ασθενών με μεταστατικό καρκίνωμα κυττάρων merkel (mcc). bavencio σε συνδυασμό με axitinib ενδείκνυται για τη θεραπεία πρώτης γραμμής σε ενήλικες ασθενείς με προχωρημένο νεφροκυτταρικό καρκίνωμα (rcc). bavencio is indicated as monotherapy for the first‑line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (uc) who are progression-free following platinum‑based chemotherapy.