Genovis AB Half-Yearly report January – June 2025
12 augusti, 08:00
12 augusti, 08:00
Strong organic growth and doubled operating profit in the enzyme business
April – June 2025
January – June 2025
*Previous year excluding the divested antibody business. The antibody business was divested on August 19, 2024.
** Previous year including the divested antibody business
***Earnings per share are calculated by dividing profit by the weighted average number of shares during the year. There is no dilutive effect.
Message from the CEO
We maintained strong momentum in the second quarter, delivering 28% organic growth. Adjusted for the divested antibody business, EBIT doubled compared with the same period last year, despite currency headwinds from the strengthened Swedish krona.
The organic growth was strong across all our main geographic markets: North America, Europe, and Asia. Sales growth in the Chinese market continued its positive trend during the second quarter, and Europe posted strong sales growth compared with the previous year. Despite uncertainties around tariffs, government research funding, and questions related to the FDA, sales in the US showed continued robust development.
Growth during the quarter was primarily driven by large pharmaceutical companies, while smaller biotech companies continued to face a challenging venture capital market, which limits their activity levels.
During the quarter, growth was relatively evenly distributed across our product portfolio. Enzymes for analysis showed strong sales growth, and our offerings in antibody conjugation and ADCs (Antibody Drug Conjugates) remain strong drivers of our business. Our service business, which has grown strongly in recent quarters, also showed solid growth and continued healthy inflow of new projects.
The macroeconomic environment remains characterized by increased uncertainty, including new trade tariffs. This creates volatility in the markets and affects investment appetite broadly, including in the Life Science sector. At the same time, there are industry-specific challenges, such as cuts in NIH research funding and turbulence within the FDA. While the short-term market for us as a supplier to the research and pharmaceutical industries is more difficult to assess, we continue to see strong underlying drivers. The global need for new medicines and better health is growing, and we are well-positioned to contribute with innovation to this development.
Our ambitions for continued growth through a broader product portfolio, commercial sharpness, and strong customer relationships remain unchanged. We have a strong financial position with good liquidity and cash flows, which gives us room to invest in future growth – both organically and inorganically.
At the beginning of the third quarter, we also executed two important inorganic growth initiatives: the acquisition of SEQURNA and an expanded licensing agreement with Thermo Fisher Scientific. Through the acquisition of SEQURNA, we secure access to critical innovation and a promising product pipeline to further strengthen our position in the rapidly growing RNA analysis market. Through the licensing agreement with Thermo Fisher Scientific, we can now support our customers throughout the entire development chain for ADCs – from early research all the way to commercial manufacturing – thereby creating new value in a rapidly growing market. These steps further strengthen our strategic position and broaden our market presence. Despite a turbulent financial climate influenced by macroeconomic and geopolitical uncertainty, we continue to see opportunities to act with a long-term, value-creating approach. Our strategy remains unchanged.
Finally, I would like to extend a sincere thank you to all my colleagues at Genovis. In a time when the world around us is changing rapidly, you demonstrate outstanding commitment and the ability to stay focused on what matters most – our customers. With customer-focused innovation as our guiding principle, you contribute every day to developing tools that help our customers create the medicines of the future.
Contacts
Fredrik Olsson, CEO
Tel: +46 (0)70-276 46 56 fredrik.olsson@genovis.com
About Us
Headquartered in Kävlinge, Sweden, Genovis offers customers in the biopharmaceutical and research industries tools that facilitate and save time in the development of new treatment methods and diagnostics. Genovis enzyme products, known as SmartEnzymes, are used by scientists all over the world and the innovative product formats facilitate development and quality control of biological drugs. The Group consists of Genovis AB and the wholly owned subsidiary Genovis Inc. (US). Genovis shares are listed on Nasdaq First North Growth Market and DNB Carnegie Investment Bank AB is the Company’s Certified Adviser.
This is a translation of the Swedish original. In the event of any discrepancy between this translation and the Swedish original, the Swedish version shall prevail.
This information is information that Genovis is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact persons set out above, at 2025-08-12 08:00 CEST.
Attachments
Genovis Interim Report January June 2025
12 augusti, 08:00
Strong organic growth and doubled operating profit in the enzyme business
April – June 2025
January – June 2025
*Previous year excluding the divested antibody business. The antibody business was divested on August 19, 2024.
** Previous year including the divested antibody business
***Earnings per share are calculated by dividing profit by the weighted average number of shares during the year. There is no dilutive effect.
Message from the CEO
We maintained strong momentum in the second quarter, delivering 28% organic growth. Adjusted for the divested antibody business, EBIT doubled compared with the same period last year, despite currency headwinds from the strengthened Swedish krona.
The organic growth was strong across all our main geographic markets: North America, Europe, and Asia. Sales growth in the Chinese market continued its positive trend during the second quarter, and Europe posted strong sales growth compared with the previous year. Despite uncertainties around tariffs, government research funding, and questions related to the FDA, sales in the US showed continued robust development.
Growth during the quarter was primarily driven by large pharmaceutical companies, while smaller biotech companies continued to face a challenging venture capital market, which limits their activity levels.
During the quarter, growth was relatively evenly distributed across our product portfolio. Enzymes for analysis showed strong sales growth, and our offerings in antibody conjugation and ADCs (Antibody Drug Conjugates) remain strong drivers of our business. Our service business, which has grown strongly in recent quarters, also showed solid growth and continued healthy inflow of new projects.
The macroeconomic environment remains characterized by increased uncertainty, including new trade tariffs. This creates volatility in the markets and affects investment appetite broadly, including in the Life Science sector. At the same time, there are industry-specific challenges, such as cuts in NIH research funding and turbulence within the FDA. While the short-term market for us as a supplier to the research and pharmaceutical industries is more difficult to assess, we continue to see strong underlying drivers. The global need for new medicines and better health is growing, and we are well-positioned to contribute with innovation to this development.
Our ambitions for continued growth through a broader product portfolio, commercial sharpness, and strong customer relationships remain unchanged. We have a strong financial position with good liquidity and cash flows, which gives us room to invest in future growth – both organically and inorganically.
At the beginning of the third quarter, we also executed two important inorganic growth initiatives: the acquisition of SEQURNA and an expanded licensing agreement with Thermo Fisher Scientific. Through the acquisition of SEQURNA, we secure access to critical innovation and a promising product pipeline to further strengthen our position in the rapidly growing RNA analysis market. Through the licensing agreement with Thermo Fisher Scientific, we can now support our customers throughout the entire development chain for ADCs – from early research all the way to commercial manufacturing – thereby creating new value in a rapidly growing market. These steps further strengthen our strategic position and broaden our market presence. Despite a turbulent financial climate influenced by macroeconomic and geopolitical uncertainty, we continue to see opportunities to act with a long-term, value-creating approach. Our strategy remains unchanged.
Finally, I would like to extend a sincere thank you to all my colleagues at Genovis. In a time when the world around us is changing rapidly, you demonstrate outstanding commitment and the ability to stay focused on what matters most – our customers. With customer-focused innovation as our guiding principle, you contribute every day to developing tools that help our customers create the medicines of the future.
Contacts
Fredrik Olsson, CEO
Tel: +46 (0)70-276 46 56 fredrik.olsson@genovis.com
About Us
Headquartered in Kävlinge, Sweden, Genovis offers customers in the biopharmaceutical and research industries tools that facilitate and save time in the development of new treatment methods and diagnostics. Genovis enzyme products, known as SmartEnzymes, are used by scientists all over the world and the innovative product formats facilitate development and quality control of biological drugs. The Group consists of Genovis AB and the wholly owned subsidiary Genovis Inc. (US). Genovis shares are listed on Nasdaq First North Growth Market and DNB Carnegie Investment Bank AB is the Company’s Certified Adviser.
This is a translation of the Swedish original. In the event of any discrepancy between this translation and the Swedish original, the Swedish version shall prevail.
This information is information that Genovis is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact persons set out above, at 2025-08-12 08:00 CEST.
Attachments
Genovis Interim Report January June 2025
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