Adtralza Европейски съюз - малтийски - EMA (European Medicines Agency)

adtralza

leo pharma a/s - tralokinumab - dermatite, atopika - preparazzjonijiet oħra dermatoloġiċi - adtralza is indicated for the treatment of moderate to severe atopic dermatitis in adult and adolescent patients 12 years and older who are candidates for systemic therapy.

Ontilyv Европейски съюз - малтийски - EMA (European Medicines Agency)

ontilyv

bial portela & companhia s.a. - opicapone - marda ta 'parkinson - mediċini kontra l-parkinson - ontilyv is indicated as adjunctive therapy to preparations of levodopa/ dopa decarboxylase inhibitors (ddci) in adult patients with parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.

Vyepti Европейски съюз - малтийски - EMA (European Medicines Agency)

vyepti

h. lundbeck a/s - eptinezumab - disturbi fl-emigranja - analġeżiċi - vyepti is indicated for the prophylaxis of migraine in adults who have at least 4 migraine days per month.

Nulibry Европейски съюз - малтийски - EMA (European Medicines Agency)

nulibry

tmc pharma (eu) limited - fosdenopterin hydrobromide dihydrate - metal metabolism, inborn errors - oħra tal-passaġġ alimentari u tal-metaboliżmu-prodotti, - nulibry is indicated for the treatment of patients with molybdenum cofactor deficiency (mocd) type a.

Tecvayli Европейски съюз - малтийски - EMA (European Medicines Agency)

tecvayli

janssen-cilag international n.v. - teclistamab - majloma multipla - aġenti antineoplastiċi - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Omvoh Европейски съюз - малтийски - EMA (European Medicines Agency)

omvoh

eli lilly nederland b.v. - mirikizumab - kolite, ulċerattiva - immunosoppressanti - omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.