Genmab — August 2024
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Regulatory review of the New Drug Application (NDA) for TEPEZZA in Japan and multiple additional geographies continues.
A Phase 3 study of TEPEZZA in Japan continues to enroll patients with chronic or low clinical activity score TED.
A Phase 3 study evaluating the subcutaneous route of administration of TEPEZZA is enrolling patients with TED. -
Today, Exelixis announced it will discontinue the development of XB002, the company’s tissue factor (TF)-targeting ADC, as part of its portfolio prioritization efforts. Based on available data, the compound is unlikely to improve upon tisotumab vedotin or other competitor TF-targeting ADCs currently in development. https://ir.exelixis.com/news-releases/news-release-details/exelixis-announces-second-quarter-2024-financial-results-and
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Burde Genmab aktien egentlig ikke have steget, ovenpå udmeldingen at Biontech trak sig fra Gen1046?.... Er klar over at det selvfølgelig giver usikkerhed, når en partner trækker sig for et stof .Men at Genmab ikke går ud og søger ny aftale, eller selv overvejer at trække stikket fortæller jo også en hel del. - Tværtimod vælger Genmab selv at stå for udgifterne på et dyrt fase 3 forsøg. Hvilket må tolkes til at Genmab tror selv meget på stoffet, - og så må det jo egentlig være en gave at stå med
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Enig med Solsen i at havde BioNtech set et kæmpe potentiale, så kunne de også finde midlerne. De har trods alt deres egne NSCLC programmer, som de har valgt at fortsætte. Spørgsmålet er, hvor de mener det halter? Om det er sandsynligheden for at Fase 3 fejler. Det er primært (udelukkende) på varigheden Gen1046 skiller sig ud. Eller om det er manglende potentiale for best in class. Så længe Genmab holder fast i deres princip om best in class, så er jeg fortrøstningsfuld.
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