Genmab's Q2 2025: Unraveling Contradictions in Rina-S, EPKINLY Launch, and HexaBody-OX40 Development Strategies
Generado por agente de IAAinvest Earnings Call Digest
domingo, 10 de agosto de 2025, 11:37 am ET1 min de lectura
GMAB--
Rina-S development strategy, launch strategy for EPKINLY, and development of HexaBody-OX40 are the key contradictions discussed in GenmabGMAB-- A/S's latest 2025Q2 earnings call.
Revenue Growth and Product Performance:
- Genmab A/S reported a 19% increase in total revenue for the first half of 2025, fueled by increased recurring revenue.
- The growth was driven by the performance of products like EPKINLY and Tivdak, as well as strong royalties from DARZALEX and Kesimpta.
Operating Profit Improvement:
- Genmab saw a 56% growth in operating profit during the first half of 2025, despite strategic investments in high-impact programs.
- This improvement was attributed to disciplined capital allocation, with a focus on late-stage pipeline development and commercialization execution.
Regulatory Milestones and Pipeline Advancements:
- Genmab achieved significant regulatory milestones, including the submission of an sBLA for epcoritamab in second-line follicular lymphoma and the first disclosure for single-agent Rina-S in advanced endometrial cancer.
- These advancements were part of a strategic plan to broaden the reach of key programs and accelerate clinical development.
Commercialization Success:
- Sales of EPKINLY and Tivdak grew by 60% year-over-year in the first half of 2025, accounting for 31% of the total revenue growth.
- The success was driven by strong market penetration, positive physician feedback, and strategic expansions into new markets.

Revenue Growth and Product Performance:
- Genmab A/S reported a 19% increase in total revenue for the first half of 2025, fueled by increased recurring revenue.
- The growth was driven by the performance of products like EPKINLY and Tivdak, as well as strong royalties from DARZALEX and Kesimpta.
Operating Profit Improvement:
- Genmab saw a 56% growth in operating profit during the first half of 2025, despite strategic investments in high-impact programs.
- This improvement was attributed to disciplined capital allocation, with a focus on late-stage pipeline development and commercialization execution.
Regulatory Milestones and Pipeline Advancements:
- Genmab achieved significant regulatory milestones, including the submission of an sBLA for epcoritamab in second-line follicular lymphoma and the first disclosure for single-agent Rina-S in advanced endometrial cancer.
- These advancements were part of a strategic plan to broaden the reach of key programs and accelerate clinical development.
Commercialization Success:
- Sales of EPKINLY and Tivdak grew by 60% year-over-year in the first half of 2025, accounting for 31% of the total revenue growth.
- The success was driven by strong market penetration, positive physician feedback, and strategic expansions into new markets.

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