{"id":36199,"date":"2021-02-26T08:00:00","date_gmt":"2021-02-26T07:00:00","guid":{"rendered":"https:\/\/www.ipsen.com\/press-releases\/ipsen-receives-positive-chmp-opinion-recommending-cabometyx-in-combination-with-opdivo-as-first-line-treatment-for-patients-living-with-advanced-renal-cell-carcinoma\/"},"modified":"2024-07-23T13:28:51","modified_gmt":"2024-07-23T11:28:51","slug":"ipsen-receives-positive-chmp-opinion-recommending-cabometyx-in-combination-with-opdivo-as-first-line-treatment-for-patients-living-with-advanced-renal-cell-carcinoma","status":"publish","type":"press_release","link":"https:\/\/www.ipsen.com\/press-releases\/ipsen-receives-positive-chmp-opinion-recommending-cabometyx-in-combination-with-opdivo-as-first-line-treatment-for-patients-living-with-advanced-renal-cell-carcinoma\/","title":{"rendered":"Ipsen receives positive CHMP opinion recommending Cabometyx\u00ae in combination with Opdivo\u00ae as first-line treatment for patients living with advanced renal cell carcinoma"},"content":{"rendered":"<ul>\n<li style=\"margin-bottom:3px\">Recommendation based on the Phase III CheckMate -9ER trial, in which Cabometyx\u00ae\u00a0(cabozantinib) in combination with Opdivo\u00ae\u00a0(nivolumab) doubled progression-free survival and significantly improved overall survival and response rates1<\/li>\n<li style=\"margin-bottom:3px\">Cabometyx\u00ae\u00a0in combination with Opdivo\u00ae\u00a0showed consistent efficacy benefits across key subgroups of patients1<\/li>\n<\/ul>\n<ul>\n<li style=\"margin-bottom:3px\">Patients treated with Cabometyx\u00ae\u00a0in combination with Opdivo\u00ae\u00a0reported significantly better health-related quality of life and a lower rate of discontinuation versus sunitinib2,3<\/li>\n<\/ul>\n<p><b>PARIS, FRANCE, 26 February 2021\u00a0<\/b><b>\u2013\u00a0<\/b>Ipsen (Euronext: IPN; ADR: IPSEY) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended approval for Cabometyx\u00ae\u00a0(cabozantinib) in combination with Bristol Myers Squibb\u2019s Opdivo\u00ae\u00a0(nivolumab) for the first-line treatment of advanced renal cell carcinoma (aRCC). The European Commission, which has the authority to approve medicines for the European Union (E.U.), will now review the CHMP recommendation and a final decision on the application in the E.U. is expected in the coming months.<\/p>\n<p>\u201cAdvanced renal cell carcinoma is a disease that significantly impacts the lives of people around the world. We\u2019re proud to be able to share that the CHMP has confirmed a positive recommendation for Cabometyx\u00ae\u00a0in combination with Opdivo\u00ae, bringing this impactful new treatment option one step closer for patients,\u201d said Howard Mayer, Executive Vice President and Head of Research and Development, Ipsen. \u201cAt Ipsen, we are committed to progressing treatment for cancers which have an urgent need for additional therapeutic options and this recommendation marks an important milestone in achieving this.\u201d<\/p>\n<p>The CHMP adopted the positive opinion based on results from the pivotal Phase III CheckMate -9ER trial, which demonstrated significant and clinically meaningful improvements in progression-free survival (PFS), overall survival (OS) and objective response rate (ORR) compared to sunitinib, with consistent efficacy benefits observed across key subgroups of patients.1\u00a0Cabometyx\u00ae\u00a0combined with Opdivo\u00ae\u00a0was well tolerated and reflected the known safety profiles of the immunotherapy and tyrosine kinase inhibitor (TKI) components in first-line advanced RCC.1\u00a0The full data from the CheckMate -9ER trial were presented during a Presidential Symposium at the European Society for Medical Oncology (ESMO) Virtual Congress 2020. At the recent American Society of Clinical Oncology 2021 Genitourinary Cancers Symposium (ASCO GU), additional data from the CheckMate -9ER trial were also presented, highlighting sustained superior efficacy with a longer duration of follow-up as well as significantly improved health-related quality of life outcomes for the combination versus sunitinib.2,3<\/p>\n<p>Ipsen and its partners have shared the CheckMate -9ER data with regulatory authorities around the world. \u00a0The combination of Cabometyx\u00ae\u00a0and Opdivo\u00ae\u00a0was approved by the U.S. Food and Drug Administration (FDA) as first-line treatment for patients living with advanced renal cell carcinoma in January 2021.<\/p>\n<p>\u201cToday\u2019s news is welcomed by physicians treating people living with advanced renal cell carcinoma,\u201d said Dr. Cristina Su\u00e1rez, Medical Oncologist at the Vall d\u00b4Hebron University Hospital, Barcelona, Spain, and a lead investigator on the Phase III CheckMate -9ER trial. \u201cThe positive CHMP opinion brings us one step closer to the promise of a new approach that combines improved treatment outcomes, a favorable tolerability profile and superior health-related quality of life for patients.\u201d<\/p>\n<p><b>About renal cell carcinoma<\/b><br \/>There are over 400,000 new cases of kidney cancer diagnosed worldwide each year.4\u00a0Of these, renal cell carcinoma (RCC) is the most common type of kidney cancer, accounting for approximately 90% of cases.5,6\u00a0It is twice as common in men, and male patients account for over two thirds of deaths.4\u00a0If detected in the early stages, the five-year survival rate is high, but for patients with advanced or late-stage metastatic RCC the survival rate is much lower, around 12%, with no identified cure for this disease.7,8<\/p>\n<p><b>About the CheckMate -9ER trial<\/b><br \/>CheckMate -9ER is an open-label, randomized, multi-national Phase III trial evaluating patients with previously untreated advanced or metastatic RCC. A total of 651 patients (23% favorable risk, 58% intermediate risk, 20% poor risk; 25% PD-L1 \u22651%) were randomized to Cabometyx\u00ae\u00a0plus Opdivo\u00ae\u00a0(n= 323) versus sunitinib (n= 328). The primary endpoint is progression-free survival (PFS). Secondary endpoints include overall survival (OS) and objective response rate (ORR). The primary efficacy analysis is comparing the doublet combination versus sunitinib in all randomized patients. The trial is sponsored by Bristol Myers Squibb and Ono Pharmaceutical Co and co-funded by Exelixis, Ipsen and Takeda Pharmaceutical Company Limited.<\/p>\n<p><b>About Cabometyx<\/b><b>\u00ae<\/b><b>\u00a0(cabozantinib)<\/b><br \/>Cabometyx\u00ae\u00a0is currently approved in 57 countries, including\u00a0 in the European Union, the U.K., Norway, Iceland, Australia, New Zealand, Switzerland, South Korea, Canada, Brazil, Taiwan, Hong-Kong, Singapore, Macau, Jordan, Lebanon, Russian Federation, Ukraine, Turkey, United Arab Emirates, Saudi Arabia, Serbia, Israel, Mexico, Chile, Peru, Panama, Guatemala, Dominican Republic, Ecuador and Thailand for the treatment of advanced RCC in adults who have received prior VEGF-targeted therapy; in the European Union, the U.K., Norway, Iceland, Canada, Australia, Brazil, Taiwan, Hong Kong, Singapore, Lebanon, Jordan, Russian Federation, Ukraine, Turkey, United Arab Emirates, Saudi Arabia, Israel, Mexico, Chile, Peru, Panama, Guatemala, Dominican Republic, Ecuador and Thailand for previously untreated intermediate- or poor-risk advanced RCC; and in the European Union, the U.K., Norway, Iceland, Canada, Australia, Switzerland, Saudi Arabia, Serbia, Israel, Taiwan, Hong Kong, South Korea, Singapore, Jordan, Russian Federation, Ukraine, Turkey, Lebanon, United Arab Emirates, Peru, Panama, Guatemala, Chile, Dominican Republic, Ecuador and Thailand \u00a0for HCC in adults who have previously been treated with sorafenib.<\/p>\n<p>The detailed recommendations for the use of Cabometyx\u00ae\u00a0are described in the\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=ebQJ0RgOGU66lhwjSgnHk932_g6DMG3Kfa1mYmV3apeFGEzZd15oq-Ecwb5ANQZaJ0bHDZC-sqM_-LnVeHwu633xH04Byl5yX72JlQ7ixERllnZ3e2QHivKLv2bE7Rh7rTDR1w6xMMdogmHVux3r34oqu2EV2LH-6NDTKJhSG9w=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>Summary of Product Characteristics (SmPC)<\/b><\/a>\u00a0and in the\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=HcQX9ZcNe5hEXZGWe7Yn8CAFYgA3_Vhu7EczTMrWxTcKm6cW8sZB306TMkPo7-AKZb--xy3DBKKRB6tdv1x_LoPbmFPV6P7_-A4qILwkX58_JjWI9_kpRB-CnUeZp1EsfQvey_Ue0Ff9ijt3IuCcQA==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>U.S. Prescribing Information (PI)<\/b><\/a>.<\/p>\n<p>Cabometyx\u00ae\u00a0is marketed by Exelixis, Inc. in the United States and by Takeda Pharmaceutical Company Limited in Japan. Ipsen has exclusive rights for the commercialization and further clinical development of Cabometyx\u00ae\u00a0outside of the U.S. and Japan. Cabometyx\u00ae\u00a0is a registered trademark of Exelixis, Inc.<\/p>\n<p><b>About Ipsen\u00a0<\/b><br \/>Ipsen is a global mid-size biopharmaceutical company with a focus on transformative medicines in Oncology, Rare Disease and Neuroscience. Ipsen also has a well-established Consumer Healthcare business. With total sales over \u20ac2.5 billion in 2020, Ipsen sells more than 20 drugs in over 115 countries, with a direct commercial presence in more than 30 countries. Ipsen\u2019s R&amp;D is focused on its innovative and differentiated technological platforms located in the heart of the leading biotechnological and life sciences hubs (Paris-Saclay, France; Oxford, UK; Cambridge, US; Shanghai, China). The Group has about 5,700 employees worldwide. Ipsen is listed in Paris (Euronext: IPN) and in the United States through a Sponsored Level I American Depositary Receipt program (ADR: IPSEY). For more information on Ipsen, visit\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=IupqRC1VDl8F6AEz58qkKQCLwXZrKIKqeXfFYesp79WARZYTSCaOuqdOaIbVckkBMeFr2wUhTgKzMQE57EyMnlOmSU-ubjHdEdZ-9my6y38=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>www.ipsen.com.fr<\/b><\/a><\/p>\n<p>Opdivo\u00ae\u00a0is a registered trademark of Bristol-Myers Squibb Company.<\/p>\n<p><b>Ipsen\u2014Cautionary Note Regarding Forward-Looking Statements<\/b><br \/>The forward-looking statements, objectives and targets contained herein are based on the Group\u2019s management strategy, current views and assumptions. Such statements involve known and unknown risks and uncertainties that may cause actual results, performance or events to differ materially from those anticipated herein. All of the above risks could affect the Group\u2019s future ability to achieve its financial targets, which were set assuming reasonable macroeconomic conditions based on the information available today. Use of the words \u201cbelieves\u201d, \u201canticipates\u201d and \u201cexpects\u201d and similar expressions are intended to identify forward-looking statements, including the Group\u2019s expectations regarding future events, including regulatory filings and determinations. Moreover, the targets described in this document were prepared without taking into account external growth assumptions and potential future acquisitions, which may alter these parameters. These objectives are based on data and assumptions regarded as reasonable by the Group. These targets depend on conditions or facts likely to happen in the future, and not exclusively on historical data. Actual results may depart significantly from these targets given the occurrence of certain risks and uncertainties, notably the fact that a promising product in early development phase or clinical trial may end up never being launched on the market or reaching its commercial targets, notably for regulatory or competition reasons and also taking into consideration assessment delays of certain clinical trials in light of the ongoing COVID-19 pandemic. The Group must face or might face competition from generic products that might translate into a loss of market share. Furthermore, the Research and Development process involves several stages each of which involves the substantial risk that the Group may fail to achieve its objectives and be forced to abandon its efforts with regards to a product in which it has invested significant sums. Therefore, the Group cannot be certain that favorable results obtained during pre-clinical trials will be confirmed subsequently during clinical trials, or that the results of clinical trials will be sufficient to demonstrate the safe and effective nature of the product concerned. There can be no guarantees a product will receive the necessary regulatory approvals or that the product will prove to be commercially successful. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements. Other risks and uncertainties include but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and health care legislation; global trends toward health care cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the Group\u2019s ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the Group\u2019s patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and\/or regulatory actions. The Group also depends on third parties to develop and market some of its products which could potentially generate substantial royalties; these partners could behave in such ways which could cause damage to the Group\u2019s activities and financial results. The Group cannot be certain that its partners will fulfil their obligations. It might be unable to obtain any benefit from those agreements. A default by any of the Group\u2019s partners could generate lower revenues than expected. Such situations could have a negative impact on the Group\u2019s business, financial position or performance. The Group expressly disclaims any obligation or undertaking to update or revise any forward-looking statements, targets or estimates contained in this press release to reflect any change in events, conditions, assumptions or circumstances on which any such statements are based, unless so required by applicable law. The Group\u2019s business is subject to the risk factors outlined in its registration documents filed with the French Autorit\u00e9 des March\u00e9s Financiers. The risks and uncertainties set out are not exhaustive and the reader is advised to refer to the Group\u2019s 2018 Registration Document available on its website (<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=IupqRC1VDl8F6AEz58qkKa_Ovc5TuM1BrwDWZRst2Af97Wd3Gpje4Qe_BRGY1St6VoD4uGQQO8RQMRvIlJKEPg==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>www.ipsen.com<\/b><\/a>).<\/p>\n<p><b><u>For further information:<\/u><\/b><\/p>\n<p><\/p>\n<table style=\"border-collapse: collapse;width:715.422px;border-collapse:collapse\">\n<tr>\n<td><b>Media<\/b><\/p>\n<p>Giovanni Asta<\/p>\n<p>Head of Global Franchises Communication\/Global Head of Institutional Affairs, Patient Advocacy &amp; Communication\/Italy<\/p>\n<p>+39 335 744 07 34<\/p>\n<p><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=FF_-8knmg9PJiQw_cCt57CMHSKObhqtp3yXwLSpLdqUXAyuQlSzi17IDsgli-cbWrUx2_ATtxa-WHH_2AKjHzNBCEsRc3JHMN_y8lFEt38Q=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>giovanni.asta@ipsen.com<\/b><\/a><\/p>\n<p>\u00a0<\/p>\n<p><b>Media and Financial Community<\/b><\/p>\n<p>Ipsen Global Communications<\/p>\n<p><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=6fIxK6lPO4vfHLhM4PjbIMR599W5aktoZkemhivlP6V2vaw4Uum2HCJXyuYXIzlbG5SUbwUoaFThU5Oa4uPsxBg8e1Q9yfLpaDoFYXGH4Meo13vZiMSMfwu2WWIuy01U\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>global@communication.ipsen.info<\/b><\/a><\/p>\n<p><b>\u00a0<\/b><\/td>\n<td>\u00a0<\/p>\n<p>\u00a0<\/p>\n<p>\u00a0<\/p>\n<p>\u00a0<\/p>\n<p>\u00a0<\/td>\n<td>\u00a0<\/p>\n<p>\u00a0<\/p>\n<p>\u00a0<\/td>\n<\/tr>\n<\/table>\n<p><\/p>\n<p><b>References<\/b><\/p>\n<ol>\n<li style=\"margin-bottom:3px\">Choueiri TK et al. Nivolumab + cabozantinib vs sunitinib in first-line treatment for advanced renal cell carcinoma: First results from the randomized phase III CheckMate 9ER trial. European Society for Medical Oncology. 2020; 31:4, DOI:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fCrK1q93nscCi0-tVr5zSzSPXWXrLRqIQGlgqH4X2mprRWyFsf_7RwCkOzE3DYLUUkJpUSgrgv2SVW3CUPhhJNIaY8jXNEIiGQ48BXy5zSn25zB13ypv3TuYstyMNfejcAewUGIcsVjO7-swOZjN--0e9mZhpiTLnUccMJUo81o=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>https:\/\/doi.org\/10.1016\/j.annonc.2020.08.2257<\/b><\/a><\/li>\n<li style=\"margin-bottom:3px\">Motzer et al., ASCO-GU 2021. Nivolumab + cabozantinib (NIVO+CABO) vs sunitinib (SUN) as first-line therapy for advanced renal cell carcinoma (aRCC): extended follow-up and outcomes in the sarcomatoid subgroup of CheckMate -9ER.<\/li>\n<li style=\"margin-bottom:3px\">Cella et al., ASCO-GU 2021. Patient-reported outcomes (PROs) of patients (pts) with advanced renal cell carcinoma (aRCC) treated with first-line (1L) nivolumab plus cabozantinib (NIVO+CABO) vs sunitinib (SUN): the randomized phase 3 CheckMate -9ER trial.<\/li>\n<li style=\"margin-bottom:3px\">Kidney Cancer Factsheet. GLOBOCAN 2018. Accessed: February 2021. Available:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fCrK1q93nscCi0-tVr5zS-TQmDw13R2-lDwiRgkkf29n-Hhr_ALw_uO2KdyfyvxvG_sjd0LrI4l13dAz25_jaeNTxb656are01eQ2vgrb59iF-BAYbk9v_hnxjuyMLjONxLcjb7bagbUFxBTlMSyCokukm7GVS51kex0IIieSmtWMCt0LcUkZOTk3bsJ1PY_SX37nUQIfLbO5kCTjwsSshW2U4Xmqzl7jPqdrgB1UDtZMoMGjW03l1vEWmhf6gDh\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>https:\/\/gco.iarc.fr\/today\/data\/factsheets\/cancers\/29-Kidney-fact-sheet.pdf<\/b><\/a>.<\/li>\n<li style=\"margin-bottom:3px\">Kidney Cancer. Mayo Clinic. Accessed: February 2021. Available:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fCrK1q93nscCi0-tVr5zSypzxpKPezfcxk1UBnDLgE7EBZJ7sskRkcHYQ0V5ascTanDgmDwiZJkda19BA3LmT57Ue67Z6DJ5IdrEw_l9LLNXMhPwYw-eIBvdqwKByqJGn4YHOPrpeGujbbleE11WWCX1-IAyvXX814evbm_itNfXfXx4ryKpOwiOfqW6NNz_WiezcyvFxZL8YfjyHWmmloYNtxI9LmuZKIAwmNcHJJACr2XBbSMvaB3Fi9BpNTVKtOQAODOvhmi-ukfEV8FtUQ==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>https:\/\/www.mayoclinic.org\/diseases-conditions\/kidney-cancer\/symptoms-causes\/syc-20352664<\/b><\/a>.<\/li>\n<li style=\"margin-bottom:3px\">Infographic: Kidney Cancer. Mayo Clinic. Accessed: February 2021. Available:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fCrK1q93nscCi0-tVr5zSypzxpKPezfcxk1UBnDLgE7EBZJ7sskRkcHYQ0V5ascTanDgmDwiZJkda19BA3LmT4s1Qu2qFXoqH9ONcOacvd5DD8tLwqan9YGt5mPi9DBMgxuADQ3vnVlicK8XSYJjIbdk5s4Bqw4EA_WU4cAdz7UzaIXhRrhDcBQxIDWvZRLCPaMqhsPV5J-jxYYPb49tmRukVQnxG4D_dg5UVYv-rV4sds8rZuQPY913HOHEtFaYEO2qHsPF5LzcTMmJF7YFtBDIjXK6arlEeGJVx3wjX7HRiHtt3_yw_K2biux6Z4MjPdvXLp4lWJU3_fR8Y87ijg==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>https:\/\/www.mayoclinic.org\/diseases-conditions\/kidney-cancer\/multimedia\/kidney-cancer-infographic\/ifg-20441505<\/b><\/a>.<\/li>\n<li style=\"margin-bottom:3px\">Survival rates for kidney cancer. American Cancer Society. Accessed: February 2021. Available:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fCrK1q93nscCi0-tVr5zSx9xn02uOZchO47lWms-I5-sQpjWlRiHDLni3eYJlEMgQDllYm1F17-1PKTd7NQ_qoYr5oHhVuWra9b__859vKbCF_OUNt4jUTRi5WSDV-XeMAwMlW0eMhFiNaWQrybeH32q1xHpcd6wPEhOCa7MxMDRj8cO4nIrlEPKEmFhUa03BH3zGAVFzKH42nbQZGmLoILYkWegRSIsG-qOoX2-W9KqoCDMnRKdhmUAiNpWLfl8X7C6j6B4BgMQmOT86w06XDtbJPXWlRA_8mswDGdciIU=\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>https:\/\/www.cancer.org\/cancer\/kidney-cancer\/detection-diagnosis-staging\/survival-rates.html<\/b><\/a>.<\/li>\n<li style=\"margin-bottom:3px\">Orlin, I et al. Renal cell carcinomas epidemiology in the era of widespread imaging. Journal of Clinical Oncology. 2019; 37:15. DOI:\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fCrK1q93nscCi0-tVr5zS01TkXEN3YCic5ZR4LYW4nHWE0LSgEzfYRQjBy7YmWH9Nxhr8oMKH6_c0lLGcZC3VtEQSE5g3zux0gqDJXsHFS31CTlVMlyCwff1XfpdvkYn24PtFv1OHBX0wBOOLv_qF-B7GrWogFNS6cjcHXJ22rXUHVIdOQIwOCJxgQCkG3yPDvdMqE3P7KC_F8nI37CZSQ==\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\"><b>https:\/\/ascopubs.org\/doi\/10.1200\/JCO.2019.37.15_suppl.e13083<\/b><\/a>.<\/li>\n<\/ol>\n<p id=\"gnw_attachments_section-header\">\n    <strong>Attachment<\/strong>\n<\/p>\n<ul id=\"gnw_attachments_section-items\">\n<li>\n        <a target=\"_blank\" href=\"https:\/\/www.globenewswire.com\/Tracker?data=20k6ql85SCDwYa4N12q5u8jSs4wD0OkoCoKgcFtz2tHAcv-yrvcP4bDc5K8L1QrAOoBAXI1Dwjf0R5xEEGnaN8hG2PRDcUVUgXTCrgNvmliS_mu0y-A73wNcxYGyqF1TPzvmBiOf4jeccYo14nYwMK33KfZZEvaqknVJC7WP4S48j_iozQdTqV7eZfYSIK_l\" title=\"Ipsen-CHMP-release-26-February-2021\" rel=\"nofollow noopener\">Ipsen-CHMP-release-26-February-2021<\/a>\n      <\/li>\n<\/ul>\n<p><img src='https:\/\/ml-eu.globenewswire.com\/media\/ZWUzNWUzMTQtMWM5Yi00YzZiLTg4MDUtYzMyMmM3MzQ5MTc3LTEwMTA5NDM=\/tiny\/Ipsen-SA.png' \/><\/p>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":1,"template":"","categories":[1763,1767,149],"tags":[],"class_list":["post-36199","press_release","type-press_release","status-publish","hentry","category-corporate-pressrelease","category-oncology-pressrelease","category-pressrelease","entry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.5 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Ipsen receives positive CHMP opinion recommending Cabometyx\u00ae in combination with Opdivo\u00ae as first-line treatment for patients living with advanced renal cell carcinoma<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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