Genmab — Juni 2023
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SC dosing of amivantamab significantly improved IRR safety profile (16% vs 67% for IV) https://www.congresshub.com/Oncology/AM2023/Amivantamab/Minchom#interactive_pdf That should make this drug much much more tolerable
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another Hemophilia trial for Daratumumab ITI Using SCT800 Combining Daratumumab or SCT800 Alone in Hemophilia A Adolescents and Adults With High Titer Inhibitor https://www.clinicaltrials.gov/ct2/show/NCT05888870
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Janssen Presents Longer-Term Data for TECVAYLI
(teclistamab-cqyv) Showing a Duration of Response of 22 Months in Patients with Relapsed or Refractory Multiple Myeloma https://www.jnj.com/janssen-presents-longer-term-data-for-tecvayli-teclistamab-cqyv-showing-a-duration-of-response-of-22-months-in-patients-with-relapsed-or-refractory-multiple-myeloma -
J&J’s multiple myeloma combo produces déjà vu with 96% Carvykti-like response https://www.fiercebiotech.com/biotech/jjs-new-multiple-myeloma-combo-produces-deja-vu-96-carvykti-response
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https://www.bt.dk/udland/nyt-studie-overrasker-pille-halverer-risikoen-for-at-doe-af-lungekraeft Osimertinib vækker opsigt. Amivantamab går efter det marked (Tagrisso) i kombi med Lazertinib.
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Fireside Goldman Sachs - desværre ikke Jan, der deltager (link)
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longer term results of patients with DLBCL treated with epcoritamab+R-CHOP. The latest results support the preliminary data and this treatment induces high CMR rates with a manageable safety profile https://twitter.com/lymphomahub/status/1666142892270682128
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Dansk begejstring over FDA-godkendelse af epcoritamab: Det er et stort fremskridt
De amerikanske lægemiddelmyndigheder FDA har godkendt det bispecifikke antistof epcoritamab til behandling af patienter med relaps eller refraktært (r/r) storce
(haematologisktidsskrift.dk)
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Tak for den gode artikel, @Bulder. Den var til at forstå - selv for mig! Og det siger ikke så lidt
Jeg tør slet ikke tænke på, hvad der vi når op på, når superdara kommer.
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