Genmab — Marts 2025
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Fra Løntoft "- Det var en lidt netruller, om J&J ville udnytte den her option til at fortsætte udviklingen af Hexabody mod knoglemarvskræft, konstaterer senioranalytikeren.
Samtidig gør han det klart, at han ikke selv havde indregnet et positiv tilbagemelding fra partneren. Og det tror han heller ikke, at mange af hans analytikerkolleger havde. Derfor ville det formentlig have været en større overraskelse for markedet, hvis J&J havde valgt at gå videre med midlet, end at de nu vælger at droppe
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et partnerskab.
- I givet fald har det været indregnet med en lav værdiansættelse, som afspejler meget få data for Hexabody-CD38 og en lav sandsynlighed, som også er ud fra den betragtning, at der var større "upside" end "downside" fra et investorperspektiv, siger Søren Løntoft Hansen."
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Preliminary data submitted by Genmab to J&J, inclusive of 88 patients who received a study treatment and 84 patients who were response evaluable (42 in each arm), demonstrated an overall response rate (ORR) of 55% (95% CI: 39%, 70%) in the HexaBoby-CD38 IV arm vs. 52% in the daratumumab SC arm (95% CI: 36%, 68%); very good partial response (VGPR) or better rate was 29% vs. 17%; and complete response (CR) or better rate was 7% vs. 2%.
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TEAEs leading to death included one patient in the HexaBody-CD38 IV arm and two patients in the daratumumab SC arm; none of these deaths was related to the study treatment. Follow-up is ongoing and more mature data will be presented at a future medical conference.
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Gad vide, hvor stor opbakning Jan.v.d.W efterhånden har hos de større aktionærer?
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