On September 14, 2020 Ipsen (Euronext: IPN; ADR: IPSEY) reported that novel clinical trial and real-world evidence data across a variety of tumor types and oncology therapeutic settings, will be the subject of multiple oral and poster presentations at the European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) 2020 Congress, taking place virtually 19–21 September 2020 (Press release, Ipsen, SEP 14, 2020, View Source [SID1234565058]). Results from these 17 abstracts reflect Ipsen’s commitment to oncology research and mission to provide treatment options tailored to patients with significant unmet needs. The impact of this progress is highlighted by the selection of three abstracts for proffered paper presentations, with one featuring in the ESMO (Free ESMO Whitepaper) Presidential Symposium.
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"The breadth of oncology research we’re presenting at ESMO (Free ESMO Whitepaper) this year highlights our commitment to prioritize the development of innovative treatment options that enhance patient care," said Prof. Dr. Steven Hildemann, Executive Vice President, Chief Medical Officer, Head of Global Medical Affairs and Patient Safety, Ipsen. "The positive results from the pivotal Phase III CheckMate -9ER trial are just one example of our successful partnership strategy to catalyze and broaden our progress in delivering potential new or improved options in cancers with significant unmet needs."
Highlights from key data on Ipsen medicines to be presented during the ESMO (Free ESMO Whitepaper) 2020 Congress include:
Superior survival and response rates in previously untreated patients with advanced clear cell renal cell carcinoma (aRCC) with Cabometyx (cabozantinib) in combination with Opdivo (nivolumab) versus sunitinib.
Real-world evidence on Cabometyx (cabozantinib) from the CABOREAL study in non-clear cell metastatic renal cell carcinoma and sarcomatoid renal cell carcinoma, and from an interim analysis of the European CASSIOPE study in aRCC after VEGF-targeted therapy.1
Results from the Phase II CLARINET FORTE trial detailing the efficacy and safety of increasing the frequency of Somatuline Autogel (lanreotide) dosing in progressive pancreatic and midgut neuroendocrine tumors (NETs).1
Aligned with the virtual format of the ESMO (Free ESMO Whitepaper) 2020 Congress, Ipsen is launching a new virtual congress platform, which will include a virtual press office to support media in accessing further information and insights around Ipsen’s data and contribution to the ESMO (Free ESMO Whitepaper) 2020 scientific program, the company’s mission to advance oncology research, and its commitment to address patients’ unmet needs.
The virtual congress platform is available here and the virtual press office is available here. To receive a recording of the virtual media briefing and receive exclusive media content, please register your interest here: View Source
Follow Ipsen on Twitter via @IpsenGroup and keep up to date with ESMO (Free ESMO Whitepaper) 2020 Congress news and updates by using the hashtag #ESMO20.
Overview of presentations featuring Ipsen medicines in development at the ESMO (Free ESMO Whitepaper) 2020 Congress:
Medicine
Abstract title
Presentation number/timing
(CEST)
Cabometyx
(cabozantinib)
Nivolumab + cabozantinib vs sunitinib in first-line treatment for
advanced renal cell carcinoma: first results from the randomized phase 3 CheckMate -9ER trial
Presentation number: 696O
Date/time: 19 September, 19:34 – 19:46
Cabozantinib in elderly patients: results from a subanalysis
of the CABOREAL study
Presentation number: 722P
Date/time: 17 September, on-demand
Cabozantinib in non-clear cell metastatic renal cell carcinoma
and sarcomatoid renal cell carcinoma: real-world data from the CABOREAL study
Presentation number: 732P
Date/time: 17 September, on-demand
CaboPoint: a phase II study of second-line cabozantinib in patients with metastatic
renal cell carcinoma (RCC)
Presentation number: 804TiP
Date/time: 17 September, on-demand
Interim analysis of CASSIOPE, a real-world study of cabozantinib for the treatment of
advanced renal cell carcinoma (aRCC) after VEGF-targeted therapy in Europe
Presentation number: 741P
Date/time: 17 September, on-demand
Clinical outcomes stratified by Charlson Comorbidity Index (CCI) score from a retrospective study of patients
with advanced renal cell carcinoma (aRCC) who received cabozantinib as part of
the UK Managed Access Program (MAP)
Presentation number: 1645P
Date/time: 17 September, on-demand
Cabozantinib (C) in combination with atezolizumab (A) in non-clear cell renal cell carcinoma (nccRCC):
results from cohort 10 of the COSMIC-021 study
Presentation number: 709P
Date/time: 17 September, on-demand
Cabozantinib (C) in combination with atezolizumab (A) as first-line therapy for
advanced clear cell renal cell carcinoma (ccRCC): results from the COSMIC-021 study
Presentation number: 702O
Date/time: 21 September, 17:04–17:16
Onivyde
(liposomal irinotecan)
RESILIENT part 1: pharmacokinetics of second-line (2L) liposomal irinotecan
in patients with small cell lung cancer (SCLC)
Presentation number: 1793P
Date/time: 17 September, on-demand
First-line (1L) liposomal irinotecan + 5 fluorouracil/leucovorin (5-FU/LV) + oxaliplatin (OX)
in patients with locally advanced or metastatic pancreatic ductal adenocarcinoma (mPDAC):
exploratory subgroup analyses of survival by changes in CA 19-9 levels
Presentation number: 1529P
Date/time: 17 September, on-demand
Multivariable analysis of real-world clinical outcomes associated with dose reductions (DRs)
for patients (pts) with metastatic pancreatic ductal adenocarcinoma (mPDAC)
treated with liposomal irinotecan
Presentation number: 1534P
Date/time: 17 September, on-demand
Real-world treatment patterns and effectiveness of liposomal irinotecan in a NAPOLI1-based
regimen among patients with metastatic pancreatic ductal adenocarcinoma (mPDAC):
a multi-academic center chart review
Presentation number: 1555P
Date/time: 17 September, on-demand
Clinical pathway implications and real-world characteristics and outcomes for
patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) treated with first line category 1
National Comprehensive Cancer Network (NCCN) regimens
Presentation number: 1564P
Date/time: 17 September, on-demand
Decapeptyl
(triptorelin pamoate)
Efficacy of triptorelin after radical prostatectomy in patients with high-risk prostate cancer
Presentation number: 664P
Date/time: 17 September, on-demand
Somatuline
(lanreotide)
Efficacy and safety of lanreotide autogel (LAN) 120 mg every 14 days in progressive pancreatic or
midgut neuroendocrine tumours (NETs): CLARINET FORTE study results
Presentation Number: 1162MO
Date/time: 18 September, on-demand
Lanreotide autogel (LAN) and temozolomide (TMZ) combination therapy in progressive thoracic
neuroendocrine tumours (TNETs): ATLANT study results
Presentation number: 1161MO
Date/time: 18 September, on-demand
Satoreotide tetraxetan
An international open-label study on safety and efficacy of 177Lu-satoreotide tetraxetan in somatostatin
receptor positive neuroendocrine tumours (NETs): an Interim Analysis
Presentation number: 1160O
Date/time: 20 September, 14:37–14:49
About renal cell carcinoma
There are over 400,000 new cases of kidney cancer diagnosed worldwide each year.2 Of these, renal cell carcinoma (RCC) is the most common type of kidney cancer, accounting for approximately 90% of cases.3,4 It is twice as common in men, and male patients account for over two thirds of deaths.2 If 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.5,6
About NETs
Neuroendocrine tumors, or NETs, are a group of uncommon tumors that develop in the cells of the neuroendocrine system, throughout the body.7,8 NETs occur in both men and women, in general aged 50 to 60 years old, although they can affect anyone of any age.9
The three main areas where NETs are found in the body are the gastrointestinal tract, the pancreas and the lungs.8,10
Gastrointestinal NETs (GI-NETs) are found in the gastrointestinal tract or digestive system and are the most common type of NETs.10
Pancreatic NETs (panNETs) are formed in the islet cells of the pancreas and include several uncommon types of NETs.10
Lung NETs are less common than other types, accounting for about one quarter of NETs.10
The symptoms of NETs are often not distinct and difficult to identify, and can sometimes take between five to seven years to fully diagnose.11 The number of people being newly diagnosed with NETs overall is believed to be rising.12 This is mainly due to increased awareness of the condition and diagnostic testing.12 NETs are now the fastest growing class of cancers worldwide, accounting for around 2% of all cancers at any time.12
About pancreatic cancer
Pancreatic cancer occurs when cells in the pancreas grow uncontrollably from a malignant tumor. It is the seventh leading cause of cancer death globally and the 12th most common cancer,13,14 and has the lowest survival rate of the most common cancers.15,16 As there are often no symptoms, or symptoms may be non-specific in the early stages,17 it is most commonly diagnosed at an incurable stage.18 Around 80% of pancreatic cancer patients are diagnosed with metastatic disease and for these the average survival is less than a year.19
About the CheckMate -9ER trial
CheckMate -9ER is an open-label, randomized, multi-national Phase III trial evaluating the treatment of patients with previously untreated advanced or metastatic RCC. Patients were randomized 1:1 to Opdivo and Cabometyx or sunitinib. The primary endpoint is progression-free survival (PFS). Secondary endpoints include overall survival (OS) and objective response rate (ORR). The primary efficacy analysis compared the doublet combination versus sunitinib in 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.
About CLARINET FORTE
CLARINET FORTE is a prospective single-arm, open-label, exploratory, international Phase II study to explore the efficacy and safety of a reduced lanreotide autogel dosing interval (120 mg every 14 days) in patients with metastatic or locally advanced unresectable pancreatic neuroendocrine tumors (G1/2 panNETs) or midgut NETs, with centrally-accessed progression within the last two years while on a standard lanreotide autogel regimen (120 mg every 28 days) for more than 24 weeks.
About Ipsen Products
This press release mentions investigational uses of Ipsen products. Product indications and approvals for use vary by jurisdiction; please see SmPC/PI for full indications and safety information, including Boxed Warnings.
About Cabometyx (cabozantinib)
Cabometyx is currently approved in 54 countries, including in the European Union, the U.S., the U.K., Norway, Iceland, Australia, 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 and Panama 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, Jordan, Russian Federation, Turkey, United Arab Emirates, Saudi Arabia, Israel, Mexico, Chile and Panama for previously untreated intermediate- or poor-risk advanced RCC; and in the European Union, the U.S., the U.K., Norway, Iceland, Canada, Australia, Switzerland, Saudi Arabia, Serbia, Israel, Taiwan, Hong Kong, South Korea, Singapore, Jordan, Russian Federation, Turkey, United Arab Emirates, and Panama for HCC in adults who have previously been treated with sorafenib.
The detailed recommendations for the use of Cabometyx are described in the Summary of Product Characteristics (SmPC) and in the U.S. Prescribing Information (PI).
Cabometyx is 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 outside of the U.S. and Japan.
About Somatuline (lanreotide)
Somatuline Autogel/Depot is made of the active substance lanreotide, which is a long-acting somatostatin analogue that inhibits the secretion of growth hormone and certain hormones secreted by the digestive system. The main indications of Somatuline and Somatuline Autogel are:20
The treatment of individuals with acromegaly when the circulating levels of Growth Hormone (GH) and/or Insulin-like Growth Factor-1 (IGF-1) remain abnormal after surgery and/or radiotherapy, or in patients who otherwise require medical treatment.
The treatment of grade 1 and a subset of grade 2 (Ki-67 index up to 10%) gastroenteropancreatic neuroendocrine tumors (GEP-NETs) of midgut, pancreatic or unknown origin where hindgut sites of origin have been excluded, in adult patients with unresectable locally advanced or metastatic disease.
The treatment of symptoms associated with neuroendocrine (particularly carcinoid) tumors.
The detailed recommendations for the use of Somatuline Autogel are described in the Summary of Product Characteristics (SmPC) and in the U.S. Prescribing Information (PI).
About Decapeptyl
Decapeptyl (triptorelin pamoate) is an agonist analogue of the natural gonadotropin-releasing hormone (GnRH), currently available in three sustained-release formulations (1, 3 and 6 months). First registered in France in 1986, triptorelin is currently marketed by Ipsen under a license agreement from Debiopharm Group in more than 80 countries, being the market leader in many territories worldwide.
The detailed recommendations for the use of Decapeptyl are described in the Summary of Product Characteristics (SmPC).
About Onivyde (irinotecan liposome injection)
Onivyde is an encapsulated formulation of irinotecan available as a 43 mg/10 mL single dose vial. This liposomal form is designed to increase length of tumor exposure to both irinotecan and its active metabolite, SN- 38. Onivyde is approved by the U.S. FDA in combination with fluorouracil (5-FU) and leucovorin (LV) for the treatment of patients with metastatic adenocarcinoma of the pancreas after disease progression following gemcitabine-based therapy.
In 2017 Ipsen completed the acquisition from Merrimack Pharmaceuticals of Onivyde and gained exclusive commercialization rights for the current and potential future indications for Onivyde in the U.S.21 Servier is responsible for the development and commercialization of Onivyde outside of the U.S. and Taiwan under an exclusive licensing agreement with Ipsen Biopharm Ltd.
Onivyde is approved by the U.S. FDA in combination with fluorouracil (5-FU) and leucovorin (LV) for the treatment of patients with metastatic adenocarcinoma of the pancreas after disease progression following gemcitabine-based therapy.
Servier is an international pharmaceutical company governed by a non-profit foundation, with its headquarters in France (Suresnes). More information: www.servier.com/en/.
The detailed recommendations for the use of Onivyde are described in the Summary of Product Characteristics (SmPC) and in the U.S. Prescribing Information (PI).