Genmab — Januar 2025
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Ledelsen siger selv "Q1", så hvordan og andre har opfundet 1.03 fremstår lidt tåget.
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Korrekt og intet om, at det er 1. marts
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Winkel siger også, at data er leveret af flere omgange men altså ikke om, at deadline skulle være "1. marts" men "Q1"
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repeat- from Genmab A/S Virtual R&D Update and ASH Data Review Dec 11, 2024: . Let's start with HexaBody-CD38. Here, I will reiterate what I said already during our third quarter results call. We are well on track to submit a data package to J&J by the end of this month. The optimum period of 60 days is expected to start in the beginning of January, which means that we anticipate a decision from J&J no later than the first quarter of 2025.
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JPMorgan- So can you confirm the data has now gone to J&J? Their clock has already started, is that where we are?
Jan Van De Winkel, Genmab A/S - President, Chief Executive Officer [2]
Absolutely. JNJ has access to all the data and the data room. We loaded it up in different batches, but it's all there. clock has started and the decision as per the contract, James must come in Q1 at the latest.
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Gentogen 12:54, ja det sagde Novod efter ASH. Det er det samme som at sige at selv om data er gode så vil de hellere se om en af fuglene på taget eller en fremtidig bi-specifik måske kan noget mere. Men det er efter min mening en slap analyse og ville være et kæmpe sats. Det eneste jeg kan se er at JnJ har låst Erzo og Gmab i MM så om de opter ud, og gmab må ligge Erzo i MM i skuffe kan JnJ altid senere komme tilbage hvis der ikke kommer nogle bi-specific der kan noget mere.
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Jeg så omtalt på yahoo, at JNJ risikerede dårligere kredit rating pga seneste M&A. Hvis de forhandler dybere kunne det jo være en fusion, hvor vi får nogle JNJ aktier. Mener de har en stor stak liggende fra deres fission for godt et år siden. Genmabs sælgerne står også og mangler stoffer
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some more quotes from JPM interview- So I think the mix is actually quite ideal when you have both access to immuno-oncology molecules and different types of ADCs. You can actually come to combination regimens, which are completely chemo-free and potentially much better treatments for different types of cancer.
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So what we intend to do is to actually explore them broadly. We have also other immuno-oncology antibodies right now. We have an HexaBody-OX40 in dose escalation with fantastic preclinical data you'll probably see going forward a mix of immune checkpoint targeted molecules together with and likely combinations also in clinical trials.
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