Camcevi Unia Europejska - polski - EMA (European Medicines Agency)

camcevi

accord healthcare s.l.u. - leuprorelin mesilate - nowotwory stercza - terapia endokrynologiczna - camcevi is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

Sutent Unia Europejska - polski - EMA (European Medicines Agency)

sutent

pfizer limited - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - Środki przeciwnowotworowe - gastrointestinal stromal tumour (gist)sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib mesilate treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults. experience with sutent as first-line treatment is limited (see section 5.

Tagrisso Unia Europejska - polski - EMA (European Medicines Agency)

tagrisso

astrazeneca ab - osimertinib mesilate - rak, niedrobnokomórkowe płuca - inne leki przeciwnowotworowe, inhibitory białka kinazy - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Masivet Unia Europejska - polski - EMA (European Medicines Agency)

masivet

ab science s.a. - masitinib mesilate - Środki przeciwnowotworowe - psy - leczenie nieresekcyjnych nowotworów mastocytów u psów (stopień 2 lub 3) z potwierdzonym zmutowanym receptorem kinazy tyrozynowej c-kit.

Tafinlar Unia Europejska - polski - EMA (European Medicines Agency)

tafinlar

novartis europharm limited - dabrafenib mesilate - czerniak - Środki przeciwnowotworowe - melanomadabrafenib as monotherapy or in combination with trametinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 i 5. leczenie uzupełniające melanomadabrafenib w połączeniu z trametinib wskazany dla adjuvant leczenia dorosłych pacjentów z iii stadium czerniaka z brugh mutacja v600 daleko, po całkowitej resekcji. non-small cell lung cancer (nsclc)dabrafenib in combination with trametinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a braf v600 mutation.

Alsitek Unia Europejska - polski - EMA (European Medicines Agency)

alsitek

ab science - masitinib mesilate - amyotroficzne stwardnienie boczne - Środki przeciwnowotworowe - leczenie bocznego амиотрофического rozsianego.

Masipro Unia Europejska - polski - EMA (European Medicines Agency)

masipro

ab science - masitinib mesilate - mastocytoza - Środki przeciwnowotworowe - leczenie мастоцитоза.

Roclanda Unia Europejska - polski - EMA (European Medicines Agency)

roclanda

santen oy - latanoprost, netarsudil mesilate - glaucoma, open-angle; ocular hypertension - okulistyka - roclanda is indicated for the reduction of elevated intraocular pressure (iop) in adult patients with primary open-angle glaucoma or ocular hypertension for whom monotherapy with a prostaglandin or netarsudil provides insufficient iop reduction.