NANO. Ledelsen skjuler for mye for aksjonærene............
Arne Kolstad har fått dette nye studiet godkjent i forrige måned, som "gjemmes bort"............................
Title : Role of gene mutations and expressions for non-Hodgkin lymphoma (NHL) patients treated with 177Lu-lilotomab satetraxetan
https://helseforskning.etikkom.no/prosjekterirek/prosjektregister/prosjekt?p_document_id=1027580&p_parent_id=1047097&_ikbLanguageCode=n
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Her det det store fremskritt som ledelsen vet om, men de "publiserer" ikke dette heller. "Gjemmes" i patentpapirer
http://www.sumobrain.com/patents/wipo/Treatment-non-hodgkin-lymphoma-using/WO2018050851A1.html
https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2014195460&tab=NATIONALPHASE&maxRec=1000
......................................................Malene !
Title : Role of gene mutations and expressions for non-Hodgkin lymphoma (NHL) patients treated with 177Lu-lilotomab satetraxetan
https://helseforskning.etikkom.no/prosjekterirek/prosjektregister/prosjekt?p_document_id=1027580&p_parent_id=1047097&_ikbLanguageCode=n
--------------------------------------------------
Her det det store fremskritt som ledelsen vet om, men de "publiserer" ikke dette heller. "Gjemmes" i patentpapirer
http://www.sumobrain.com/patents/wipo/Treatment-non-hodgkin-lymphoma-using/WO2018050851A1.html
https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2014195460&tab=NATIONALPHASE&maxRec=1000
......................................................Malene !
blande
22.09.2018 kl 20:41
2051
Takk for interessant graving Frontmast, men hva er egentlig nytt og hva mener du de skjuler? Fint om du kan trekke noen konklusjoner også sammenfattet i korthet.
Merk dere nedenstående sitat fra en av linkene, metalliske isotoper (177 Lu) mot CD37 er altså tingen:
Previous studies thus show that CD37 is a potent target for both immunotherapy and RIT. The chloramine T method of 131 I-labeling was used in the early studies of CD37 RIT described above. 131 I labeled to antibodies with the iodogen or the chloramine T method are not being contained in the cells if the antigen-antibody complex is internalized. Inside the cells the nuclide is removed from the antibody by intracellular enzymes and diffuses out and away from the tumour cells. The same so-called dehalogenation has been shown with CD22 antibodies, which are also internalized. Metallic radionuclides labeled to antibodies with so-called chelators are however more stable and remain contained inside the cells to a much higher degree. By using metallic radionuclides internalizing antigens can be used for tumour targeting and tumour uptake may also be higher than for non-internalizing antibodies as well.
At the Norwegian Radium Hospital, an antibody (lilotomab also called HH1) was developed against CD37 in the 1980's. Lilotomab and the anti-CD20 antibody rituximab have been labeled with both 125 I and m In and measured cell bound activity after 4 days of incubation with a lymphoma cell line. The results show that the problem of catabolism of RIC can be circumvented by labeling with metallic nuclides such as m In or 177 Lu.
Merk dere nedenstående sitat fra en av linkene, metalliske isotoper (177 Lu) mot CD37 er altså tingen:
Previous studies thus show that CD37 is a potent target for both immunotherapy and RIT. The chloramine T method of 131 I-labeling was used in the early studies of CD37 RIT described above. 131 I labeled to antibodies with the iodogen or the chloramine T method are not being contained in the cells if the antigen-antibody complex is internalized. Inside the cells the nuclide is removed from the antibody by intracellular enzymes and diffuses out and away from the tumour cells. The same so-called dehalogenation has been shown with CD22 antibodies, which are also internalized. Metallic radionuclides labeled to antibodies with so-called chelators are however more stable and remain contained inside the cells to a much higher degree. By using metallic radionuclides internalizing antigens can be used for tumour targeting and tumour uptake may also be higher than for non-internalizing antibodies as well.
At the Norwegian Radium Hospital, an antibody (lilotomab also called HH1) was developed against CD37 in the 1980's. Lilotomab and the anti-CD20 antibody rituximab have been labeled with both 125 I and m In and measured cell bound activity after 4 days of incubation with a lymphoma cell line. The results show that the problem of catabolism of RIC can be circumvented by labeling with metallic nuclides such as m In or 177 Lu.
Redigert 22.09.2018 kl 21:33
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bravi
22.09.2018 kl 22:14
1932
Helt generelt kan man si at selskaper drøyer å melde dårlige nyheter så lenge som mulig. Gode nyheter meldes når de kommer. Hvis selskapet skjuler noe så er det i allefall ikke gode nyheter for å si det sånn.
Picosalax
22.09.2018 kl 22:18
1919
Dette er egentlig helt forbilledlig. Forskningsresultater skal presenteres i tidsskrifter og på kongresser slik Costa sa.
blande
25.09.2018 kl 13:52
1352
Frontmast:
Hørte ikke noe mer fra deg. Hva er egentlig viktig nytt i det du har funnet og hva mener du ledelsen skjuler, om noe i det hele tatt?
Hørte ikke noe mer fra deg. Hva er egentlig viktig nytt i det du har funnet og hva mener du ledelsen skjuler, om noe i det hele tatt?
Redigert 26.09.2018 kl 21:50
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