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Human medicine European public assessment report (EPAR): Zevalin
ibritumomab tiuxetan, Lymphoma, Follicular
Date of authorisation: 16/01/2004, Revision: 21, Authorisedfor the public Zevalin ibritumomabtiuxetan This is a summary of the … of the active substance ibritumomabtiuxetan. What is Zevalin used for … Authorised ibritumomabtiuxetan Overview This is a summary … -
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Human medicine European public assessment report (EPAR): Gazyvaro
Obinutuzumab, Leukemia, Lymphocytic, Chronic, B-Cell
Date of authorisation: 22/07/2014,
, 
, Revision: 7, Authorised
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Human medicine European public assessment report (EPAR): Carmustine Obvius
carmustine, Hodgkin Disease, Lymphoma, Non-Hodgkin
Date of authorisation: 18/07/2018,
, Revision: 1, Authorised
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Human medicine European public assessment report (EPAR): Lympreva
dasiprotimut-t, Lymphoma, Non-Hodgkin
Date of refusal: 03/07/2015,, Refused
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Human medicine European public assessment report (EPAR): Yttriga
yttrium [90Y] chloride, Radionuclide Imaging
Date of authorisation: 19/01/2006, Revision: 9, AuthorisedHodgin’s lymphoma ([90Y] ibritumomabtiuxetan, Zevalin). Radio-immunoconjugates … -
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Referral: Levact
bendamustine, associated names: Ribomustin, Article 29(4) referrals
Status: European Commission final decision, opinion/position date: 18/03/2010, EC decision date: 07/07/2010,