Unjoni Ewropea - Malti - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

genzyme europe b.v. - alemtuzumab - lewkimja, linfokitika, kronika, b-Ċellula - aġenti antineoplastiċi - mabcampath huwa indikat għall-kura ta 'pazjenti b'lewkimja limfoċitika kronika taċ-Ċellula b (bcll) li għalihom il-kemjoterapija kombinata ta' fludarabine mhijiex xierqa.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

amgen europe b.v. - adalimumab - arthritis, psoriatic; spondylitis, ankylosing; crohn disease; colitis, ulcerative; hidradenitis suppurativa; psoriasis; arthritis, rheumatoid - immunosoppressanti - jekk jogħġbok irreferi għas-sezzjoni 4. 1 tas-sommarju tal-karatteristiċi tal-prodott fid-dokument ta 'informazzjoni tal-prodott.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

baxter holding b.v. - doxorubicin hydrochloride - sarcoma, kaposi; multiple myeloma; ovarian neoplasms; breast neoplasms - aġenti antineoplastiċi - caelyx liposomali pegilat huwa indikat:bħala monoterapija għal pazjenti b'kanċer tas-sider metastatiku, fejn hemm żieda ta 'riskju kardijaċi;għall-kura avvanzata ta' l-ovarji f'nisa li jkunu fallew l-ewwel linja bbażata fuq il-platinu 'kors ta' kimoterapija;flimkien ma 'bortezomib għall-kura tal-mjeloma multipla progressiva f'pazjenti li rċevew mill-anqas terapija waħda qabel u li diġà għaddew jew li mhumiex tajbin għal trapjant tal-mudullun;għat-trattament tal-aids marbuta mal-sarkoma ta'kaposi (ks) f'pazjenti b'għadd ta' cd4 baxx (.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

teva b.v. - doxorubicin hydrochloride - neoplażmi tas-sider - aġenti antineoplastiċi - myocet doxorubicin, f'kombinazzjoni ma 'cyclophosphamide, huwa indikat għall-kura preferita ta' kanċer metastatiku tas-sider f'nisa adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

gilead sciences ireland uc - cobicistat - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (hiv-1) infected adults and adolescents aged 12 years and older:weighing at least 35 kg co‑administered with atazanavir orweighing at least 40 kg co‑administered with darunavir.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - doxorubicin hydrochloride - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - aġenti antineoplastiċi - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cobicistat, atazanavir - infezzjonijiet ta 'hiv - antivirali għal użu sistemiku - evotaz is indicated in combination with other antiretroviral medicinal products for the treatment of hiv-1 infected adults and adolescents (aged 12 years and older weighing at least 35 kg) without known mutations associated with resistance to atazanavir (see sections 4. 4 u 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

tlc biopharmaceuticals b.v. - doxorubicin hydrochloride - breast neoplasms; ovarian neoplasms - aġenti antineoplastiċi - it-trattament tal-kanċer tas-sider u kanċer tal-ovarji.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

regeneron ireland designated activity company (dac) - cemiplimab - karċinoma, Ċellula squamous - aġenti antineoplastiċi - 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.