Purevax RCCh Európai Unió - magyar - EMA (European Medicines Agency)

purevax rcch

merial - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain) - immunológikumok a felidae, - macskák - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs and excretion;against chlamydophila felis infection to reduce clinical signs. a immunitásra való hajlamot 1 héttel a rhinotracheitis, calicivírus és chlamydophila felis komponensek. az immunitás időtartama az utolsó (újra) oltás után egy év.

Torisel Európai Unió - magyar - EMA (European Medicines Agency)

torisel

pfizer europe ma eeig - temszirolimusz - carcinoma, renal cell; lymphoma, mantle-cell - daganatellenes szerek - vese-sejt carcinomatorisel javallott az első-vonalbeli kezelésére felnőtt betegek speciális vese-sejtes carcinoma (rcc), akik legalább három, hat prognosztikai kockázati tényezők. mantle-sejt lymphomatorisel kezelésére javallt felnőtt betegek visszaesett és / vagy tűzálló mantle-sejtes lymphoma (mcl).

Bavencio Európai Unió - magyar - EMA (European Medicines Agency)

bavencio

merck europe b.v. - avelumab - neuroendokrin tumorok - egyéb daganatellenes szerek, monoklonális antitestek - a bavencio-t monoterápiaként említik metasztatikus merkel-sejtes karcinóma (mcc) felnőtt betegek kezelésére,. bavencio kombinálva axitinib javallott az első-vonalbeli kezelésére felnőtt betegek előrehaladott vesesejtes carcinoma (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.

Libtayo Európai Unió - magyar - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - karcinóma, squamous cell - daganatellenes szerek - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Sutent Európai Unió - magyar - EMA (European Medicines Agency)

sutent

pfizer limited - szunitinibbel - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - daganatellenes szerek - 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.

Sunitinib Accord Európai Unió - magyar - EMA (European Medicines Agency)

sunitinib accord

accord healthcare s.l.u. - szunitinibbel - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - daganatellenes szerek - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.