Phesgo Evropska unija - latvijščina - EMA (European Medicines Agency)

phesgo

roche registration gmbh - pertuzumab, trastuzumab - krūts audzējs - antineoplastiski līdzekļi - early breast cancer (ebc)phesgo is indicated for use in combination with chemotherapy in:the neoadjuvant treatment of adult patients with her2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrencethe adjuvant treatment of adult patients with her2-positive early breast cancer at high risk of recurrencemetastatic breast cancer (mbc)phesgo is indicated for use in combination with docetaxel in adult patients with her2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-her2 therapy or chemotherapy for their metastatic disease.

Pemazyre Evropska unija - latvijščina - EMA (European Medicines Agency)

pemazyre

incyte biosciences distribution b.v. - pemigatinib - cholangiocarcinoma - antineoplastiski līdzekļi - pemazyre monotherapy is indicated for the treatment of adults with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed  after at least one prior line of systemic therapy.

Imjudo Evropska unija - latvijščina - EMA (European Medicines Agency)

imjudo

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - antineoplastiski līdzekļi - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Tremelimumab AstraZeneca Evropska unija - latvijščina - EMA (European Medicines Agency)

tremelimumab astrazeneca

astrazeneca ab - tremelimumab - karcinoma, nesīkšūnu plaušas - antineoplastiski līdzekļi - tremelimumab astrazeneca in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Herwenda Evropska unija - latvijščina - EMA (European Medicines Agency)

herwenda

sandoz gmbh - trastuzumab - breast neoplasms; stomach neoplasms - antineoplastiski līdzekļi - treatment of metastatic and early breast cancer and metastatic gastric cancer (mgc).

Eribulin STADA 0,44 mg/ml šķīdums injekcijām Latvija - latvijščina - Zāļu valsts aģentūra

eribulin stada 0,44 mg/ml šķīdums injekcijām

stada arzneimittel ag, germany - eribulinum - Šķīdums injekcijām - 0,44 mg/ml