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Ipsen (IPSEY) is a global biopharmaceutical leader focused on transformative therapies in oncology, rare diseases, and neuroscience. This page provides investors and industry professionals with verified updates on Ipsen’s strategic initiatives, research breakthroughs, and regulatory milestones.
Access comprehensive coverage of earnings reports, R&D developments, and strategic partnerships driving innovation in targeted therapies. Our curated news collection ensures timely insights into Ipsen’s clinical trials, regulatory submissions, and global market activities.
Key updates include advancements in RNA modulation technologies, T cell-based therapies, and international collaborations. Bookmark this page to monitor Ipsen’s progress in addressing complex medical challenges through its balanced approach to internal research and external innovation.
Ipsen announced that the European Commission has approved Cabometyx in combination with Opdivo for the first-line treatment of advanced renal cell carcinoma (aRCC). This marks Cabometyx's first European approval for use with another therapy and its third indication for renal cell carcinoma. The decision is based on results from the Phase III CheckMate -9ER trial, demonstrating significant improvements in median progression-free survival, overall survival, and objective response rate compared to sunitinib. The approval applies across all EU member states.
Fusion Pharmaceuticals has announced an agreement to acquire Ipsen's IPN-1087, a small molecule targeting neurotensin receptor 1 (NTSR1) in solid tumors. This acquisition aims to develop FPI-2059, an alpha-emitting radiopharmaceutical designed to target tumors overexpressing NTSR1. Fusion will issue 400,000 shares to Ipsen upon closing and up to €67.5 million in development milestones. Ipsen will receive royalties on future net sales and further milestone payments totaling €350 million.
The acquisition is set to diversify Fusion's pipeline, potentially advancing treatments for colorectal cancer and pancreatic ductal adenocarcinoma.
Ipsen (Euronext: IPN; ADR: IPSEY) announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended approval for Cabometyx® in combination with Opdivo® for treating advanced renal cell carcinoma (aRCC). The European Commission will review this recommendation, with a final decision expected soon. This follows successful results from the Phase III CheckMate -9ER trial, showing significant improvements in progression-free survival and overall survival compared to sunitinib.
Ipsen announced nine abstracts focused on neuroendocrine tumors (NETs) during the ENETS Conference, including data from the CLARINET FORTE study. This study showed no deterioration in patients' quality of life (QoL) when treated with lanreotide autogel. Pharmacokinetic data confirmed proportional increases with higher dosing without additional safety concerns. Additionally, an economic model indicated potential healthcare savings in the UK by increasing independent home administration of lanreotide, reducing nurse visits and costs by 16.4%.
Ipsen reported its 2020 financial results, achieving €2.592 million in sales, a 3.0% increase at constant currency. Specialty Care sales grew by 5.9%, while Consumer Healthcare declined by 21.3% due to COVID-19. Core Operating margin improved to 32.0%, with a net profit of €610.5 million, reflecting an 8.4% increase. Free Cash Flow rose significantly to €646.4 million, aided by operational efficiencies. The company set a 2021 sales growth guidance of over 4.0% and proposed a dividend of €1.00 per share. Ipsen emphasizes its ongoing focus on oncology and external innovations.
Ipsen (Euronext: IPN; ADR: IPSEY) announced it will present new data at the ASCO GU Symposium from February 11-13, 2021. The focus will be on ten abstracts related to genitourinary cancers, highlighting treatment advancements. Key findings include extended data from the CheckMate -9ER trial demonstrating that cabozantinib combined with nivolumab may improve survival for advanced renal cell carcinoma (RCC) patients. Significant real-world evidence also suggests cabozantinib offers higher response rates compared to other TKIs in metastatic RCC cases.
Ipsen has appointed Gwenan White as Executive Vice President, Communications and Public Affairs, effective March 2021. She will oversee global communications and report to CEO David Loew, contributing to the company's strategy, Focus. Together. For patients & society. White has extensive experience in communications from her previous role at Novartis and will strengthen Ipsen’s global stakeholder relationships. This leadership change aims to enhance the visibility of Ipsen's innovative medicines and align communications with strategic goals.
Ipsen announced analyses of Phase III clinical trial data for Dysport® (abobotulinumtoxinA), presented at the TOXINS 2021 conference. The studies focus on treatment intervals across five patient populations, showing significant long durations of response. Results indicated that a substantial percentage of patients did not require retreatment within 12-16 weeks: CD (72.6-81.5%), ALL (20.1-32.0%), AUL (24.0-36.9%), PLL (72.8-93.8%), and PUL (19.6-67.0%). Safety outcomes were consistent with expectations. Ipsen aims to enhance understanding of spasticity and dystonia treatment outcomes.