Ero sivun ”Rituksimabi” versioiden välillä

Wikipediasta
Siirry navigaatioon Siirry hakuun
[katsottu versio][katsottu versio]
Poistettu sisältö Lisätty sisältö
Rivi 5: Rivi 5:
Rituksiimabin kehitti [[Biogen Idec|IDEC Pharmaceuticals]] tuotenimellä '''IDEC-C2B8'''.<ref>[http://www.sandiegometro.com/1999/apr/biotech.html "Why San Diego Has Biotech"], Fikes, Bradley J. ''San Diego Metropolitan,'' April 1999. Accessed June 20, 2008.</ref>
Rituksiimabin kehitti [[Biogen Idec|IDEC Pharmaceuticals]] tuotenimellä '''IDEC-C2B8'''.<ref>[http://www.sandiegometro.com/1999/apr/biotech.html "Why San Diego Has Biotech"], Fikes, Bradley J. ''San Diego Metropolitan,'' April 1999. Accessed June 20, 2008.</ref>


Based on its safety and effectiveness in [[clinical trial]]s,<ref>{{cite journal |author=Maloney DG, Grillo-López AJ, White CA, ''et al.'' |title=IDEC-C2B8 (Rituximab) anti-CD20 monoclonal antibody therapy in patients with relapsed low-grade non-Hodgkin's lymphoma |journal=Blood |volume=90 |issue=6 |pages=2188–95 |year=1997 |month=September |pmid=9310469 |doi= |url=http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=9310469}}</ref> rituximab was approved by the [[U.S. Food and Drug Administration]] in 1997 to treat B-cell [[non-Hodgkin lymphoma]]s resistant to other [[chemotherapy]] regimens.<ref>{{cite journal |author=Scott SD |title=Rituximab: a new therapeutic monoclonal antibody for non-Hodgkin's lymphoma |journal=Cancer Pract |volume=6 |issue=3 |pages=195–7 |year=1998 |pmid=9652253 |doi= 10.1046/j.1523-5394.1998.006003195.x|url=http://www.blackwell-synergy.com/openurl?genre=article&sid=nlm:pubmed&issn=1065-4704&date=1998&volume=6&issue=3&spage=195}}</ref> Rituximab, in combination with [[CHOP]] chemotherapy, is superior to CHOP alone in the treatment of [[diffuse large B-cell lymphoma]] and many other B-cell lymphomas.<ref>''Harrison's Principles of Internal Medicine'', Longo et al. ''McGraw Hill Medical'' 2011 page 931</ref> In 2010 it was approved by the [[European Commission]] for maintenance treatment after initial treatment of [[follicular lymphoma]].<ref>{{cite news |url=http://www.genengnews.com/gen-news-highlights/roche-gets-ec-nod-for-follicular-lymphoma-maintenance-therapy/81244149/ |title=Roche Gets EC Nod for Follicular Lymphoma Maintenance Therapy |date=October 29, 2010 }}</ref>
Perustuen [[Kliininen tutkimus| kliinisiin tutkimuksiin]],<ref>{{cite journal |author=Maloney DG, Grillo-López AJ, White CA, ''et al.'' |title=IDEC-C2B8 (Rituximab) anti-CD20 monoclonal antibody therapy in patients with relapsed low-grade non-Hodgkin's lymphoma |journal=Blood |volume=90 |issue=6 |pages=2188–95 |year=1997 |month=September |pmid=9310469 |doi= |url=http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=9310469}}</ref> rituksiimabi sai hyväksynnän USA:n [[FDA]]:lta vuonna 1997 to treat B-cell [[non-Hodgkin lymphoma]]s resistant to other [[chemotherapy]] regimens.<ref>{{cite journal |author=Scott SD |title=Rituximab: a new therapeutic monoclonal antibody for non-Hodgkin's lymphoma |journal=Cancer Pract |volume=6 |issue=3 |pages=195–7 |year=1998 |pmid=9652253 |doi= 10.1046/j.1523-5394.1998.006003195.x|url=http://www.blackwell-synergy.com/openurl?genre=article&sid=nlm:pubmed&issn=1065-4704&date=1998&volume=6&issue=3&spage=195}}</ref> Rituximab, in combination with [[CHOP]] chemotherapy, is superior to CHOP alone in the treatment of [[diffuse large B-cell lymphoma]] and many other B-cell lymphomas.<ref>''Harrison's Principles of Internal Medicine'', Longo et al. ''McGraw Hill Medical'' 2011 page 931</ref> In 2010 it was approved by the [[European Commission]] for maintenance treatment after initial treatment of [[follicular lymphoma]].<ref>{{cite news |url=http://www.genengnews.com/gen-news-highlights/roche-gets-ec-nod-for-follicular-lymphoma-maintenance-therapy/81244149/ |title=Roche Gets EC Nod for Follicular Lymphoma Maintenance Therapy |date=October 29, 2010 }}</ref>


Rituximab is currently co-marketed by [[Biogen Idec]] and [[Genentech]] in the U.S., by [[Hoffmann–La Roche]] in Canada and the [[European Union]], and by [[Chugai Pharmaceuticals]] and Zenyaku Kogyo in Japan.
Rituximab is currently co-marketed by [[Biogen Idec]] and [[Genentech]] in the U.S., by [[Hoffmann–La Roche]] in Canada and the [[European Union]], and by [[Chugai Pharmaceuticals]] and Zenyaku Kogyo in Japan.

Versio 19. syyskuuta 2012 kello 15.42

Rituximab (MabThera ja Rituxan) on kimeerinen monoklonaalinen vasta-aine lääke potilaille jotka ovat CD20-positiivisia. Rituximab tuhoaa B-soluja ja siksi käytetään hoidettaessa sairauksia joissa esiintyy poikkeavan runsaasti B-soluja, yliaktiivisia B-soluja tai toimintahäiriöisiä B-soluja. Näitä ovat monet Lymfooma, leukemia, elinsiirtojen hylkimis reaktiot ja muutamat autoimmuunisairaudet.


Historiaa

Rituksiimabin kehitti IDEC Pharmaceuticals tuotenimellä IDEC-C2B8.[1]

Perustuen kliinisiin tutkimuksiin,[2] rituksiimabi sai hyväksynnän USA:n FDA:lta vuonna 1997 to treat B-cell non-Hodgkin lymphomas resistant to other chemotherapy regimens.[3] Rituximab, in combination with CHOP chemotherapy, is superior to CHOP alone in the treatment of diffuse large B-cell lymphoma and many other B-cell lymphomas.[4] In 2010 it was approved by the European Commission for maintenance treatment after initial treatment of follicular lymphoma.[5]

Rituximab is currently co-marketed by Biogen Idec and Genentech in the U.S., by Hoffmann–La Roche in Canada and the European Union, and by Chugai Pharmaceuticals and Zenyaku Kogyo in Japan.

Lähteet

  1. "Why San Diego Has Biotech", Fikes, Bradley J. San Diego Metropolitan, April 1999. Accessed June 20, 2008.
  2. Maloney DG, Grillo-López AJ, White CA, et al. (September 1997). "IDEC-C2B8 (Rituximab) anti-CD20 monoclonal antibody therapy in patients with relapsed low-grade non-Hodgkin's lymphoma". Blood 90 (6): 2188–95. PMID 9310469. 
  3. Scott SD (1998). "Rituximab: a new therapeutic monoclonal antibody for non-Hodgkin's lymphoma". Cancer Pract 6 (3): 195–7. doi:10.1046/j.1523-5394.1998.006003195.x. PMID 9652253. 
  4. Harrison's Principles of Internal Medicine, Longo et al. McGraw Hill Medical 2011 page 931
  5. "Roche Gets EC Nod for Follicular Lymphoma Maintenance Therapy", October 29, 2010. 

Aiheesta muualla