Previous close | 117.00 |
Open | 117.00 |
Bid | 0.00 x 0 |
Ask | 0.00 x 0 |
Day's range | 117.00 - 117.00 |
52-week range | 88.50 - 117.00 |
Volume | |
Avg. volume | 15 |
Market cap | 9.911B |
Beta (5Y monthly) | 0.72 |
PE ratio (TTM) | 15.31 |
EPS (TTM) | 7.64 |
Earnings date | N/A |
Forward dividend & yield | 1.28 (1.10%) |
Ex-dividend date | 02 Jun 2023 |
1y target est | N/A |
Aggregated presentation by day and by market Name of issuerIdentification code of issuer (Legal Entity Identifier) Day of transaction Identification code of financial instrumentAggregated daily volume (in number of shares) Daily weighted average price of the purchased shares * Market (MIC Code)IPSEN549300M6SGDPB4Z94P1101/06/2023FR0010259150284111,21AQEUIPSEN549300M6SGDPB4Z94P1101/06/2023FR0010259150690111,19CEUXIPSEN549300M6SGDPB4Z94P1101/06/2023FR001025915024111,26TQEXIPSEN549300M6SGDPB4Z94P110
REGULATED INFORMATION Ipsen initiates a share buy-back programto cover its free employee share-allocation plan Paris (France), 1 June 2023 - Ipsen (Euronext: IPN; ADR: IPSEY) has appointed an investment-services provider to purchase an aggregate number of Ipsen S.A. shares up to 350,000, or about 0.42% of the share capital, over a maximum period of six months. The shares purchased under this agreement will be allocated mainly to cover Ipsen’s free employee share-allocation plan. This program is
REGULATED INFORMATION COMBINED SHAREHOLDERS’ MEETING OF IPSEN S.A.HELD ON 31 MAY 2023 ALL THE RESOLUTIONS SUBMITTED TO THE SHAREHOLDERS’ VOTE HAVE BEEN APPROVED Paris (France), 31 May 2023 – The Combined Shareholders’ Meeting of IPSEN S.A. (Euronext: IPN; ADR: IPSEY) was held today at the Salons de l'Hôtel des Arts et Métiers, 9 bis, avenue d'Iéna, 75116 Paris (France), under the chairmanship of Mr. Marc de GARIDEL, Chairman of the Board of Directors and meeting Chairman, and in the presence of
REGULATED INFORMATION Description of the regulatory framework of the share repurchase programproposed by the Board of Directors to be approved at theCombined Shareholders’ Meeting on 31 May 2023(15th resolution) Boulogne-Billancourt (France), on 31 May 2023 - In accordance with the provisions of Article L.22-10-62 et seq. of the French Commercial Code, the European Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014, the Delegated Regulation No 2016/1052 of
Palovarotene is the first medicine to be submitted for regulatory approval for fibrodysplasia ossificans progressiva (FOP), an ultra-rare disease with an estimated prevalence of 1.36 per million individuals and around 900 people diagnosed worldwide.1,2FOP continuously and permanently causes abnormal bone formation,3 leading to progressive mobility loss and shortened life expectancyThere are currently no disease-modifying treatment options available in the E.U.Regulatory processes are continuing
The CRL is related to the U.S. FDA’s previous request for additional information on palovarotene clinical trial dataIpsen anticipates responding to the request in the first quarter of 2023 PARIS, FRANCE, 23 December 2022 – The U.S. Food and Drug Administration (FDA) issued a Complete Response Letter (CRL) regarding the New Drug Application for palovarotene, an investigational treatment for the reduction of new abnormal bone formation (heterotopic ossification) in people living with fibrodysplasi
Updated results to be presented at ASCO GU 2022 showed sustained efficacy and tumor shrinkage benefits with Cabometyx (cabozantinib) in combination with Opdivo (nivolumab) compared to sunitinib1People living with advanced renal cell carcinoma treated with the combination continued to report improvements in health-related quality of life2The safety profile at this longer follow-up in the CheckMate -9ER trial was consistent with that previously observed for Cabometyx and Opdivo1 PARIS, FRANCE, 15
New electronic autoinjector is designed to improve patient experience for people living with gastroenteropancreatic neuroendocrine tumors, carcinoid syndrome or acromegalyPerformance and safety studies ongoing, with first launches for the new device expected in 2024A fourth generation Somatuline® Autogel® / Somatuline® Depot device building on Ipsen’s 20 years’ heritage to date PARIS, FRANCE, 16 March 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) announced today it will invest in a new state-of-the-a
Ipsen delivers a strong sales performance in the first quarter of 2022 Paris (France), 27 April 2022 – Ipsen (Euronext: IPN; ADR: IPSEY), a global specialty-driven biopharmaceutical group, publishes its sales performance for the first quarter of 2022. Highlights A strong first-quarter total-sales performance, with growth of 9.6% at CER [1] (12.5% as reported) to €687.9m, driven by Decapeptyl® (triptorelin), Dysport® (botulinum toxin type A), Cabometyx® (cabozantinib) and Onivyde® (irinotecan lip
Paris (France), 16 February 2022 – Ipsen (Euronext: IPN; ADR: IPSEY), a global specialty-driven biopharmaceutical company, announced today the appointment of Catherine Abi-Habib as EVP Strategy, Transformation, and Digital, effective March 1st, 2022. Based in Boulogne-Billancourt, France, she will be reporting directly to David Loew, CEO, Ipsen, and serve on the Executive Leadership Team (ELT). She is replacing Dominique Bery, who after successfully leading the Strategy, Transformation and Digit
New data presented at ENETS 2022 showed patients treated with Somatuline® Autogel®/Somatline® Depot (lanreotide) pre-filled syringe reported less frequent injection-site pain lasting more than two days than those treated with octreotide long-acting release syringePeople living with gastroenteropancreatic neuroendocrine tumors enrolled on Somatuline® Autogel® patient support programs reported feeling in control and satisfied when administering at-home injections PARIS, France, 8 March 2022 – Ipse
PARIS, France, 24 January 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) today announced the Health Canada approval of Sohonos™ (palovarotene capsules), an oral selective retinoic-acid receptor gamma (RARγ) agonist indicated to reduce the formation of heterotopic ossification (HO; new bone formation) in adults and children aged 8 years and above for females and 10 years and above for males with fibrodysplasia ossificans progressiva (FOP).1 Sohonos is approved for the treatment of patients with FOP for
COSMIC-021 Phase Ib study is evaluating Cabometyx® (cabozantinib) in combination with atezolizumab in advanced solid tumors, including non-small cell lung cancerNew analyses from pivotal Phase III Checkmate -9ER trial further support the superior efficacy of Cabometyx and nivolumab over sunitinib in advanced renal cell carcinomaTwo new analyses from pivotal Phase III COSMIC-311 trial further support the potential of Cabometyx in radioactive iodine-refractory differentiated thyroid cancer PARIS,
Submission based on data from the pivotal international Phase III CONTENT clinical program, also recently published in European Urology1CONTENT showed that Dysport® decreased incontinence episodes, detrusor pressure and increased bladder capacity versus placebo, and improved quality of life1 PARIS, FRANCE, 9 June 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) today announced that Dysport® (abobotulinumtoxinA) has received positive opinion in Europe for the management of urinary incontinence (UI) in ad
Paris (France), 28 July 2022 – Ipsen (Euronext: IPN; ADR: IPSEY), a global specialty-driven biopharmaceutical company, presents its financial results for the first half of 2022: H1 2022 financial results Strong sales growth of 10.5% at CER1 (15.2% as reported)Core operating margin of 39.6%; IFRS operating margin of 35.7%Core consolidated net profit of €420m, growing by 19.9%. IFRS net profit up by 30.0% to €394mSolid cash-flow generation and strong balance sheet (€2m closing net debt) Strategic
At the primary analysis, the trial did not meet its primary endpoint of overall survival (OS)The safety profile was consistent with previously reported studies of Onivyde® (irinotecan liposomal injection)The clinical study results will be communicated with the regulatory agency PARIS, FRANCE, 03 August 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) announced today that the Phase III RESILIENT trial did not meet its primary endpoint of overall survival (OS) compared to topotecan. The trial is evaluatin
Multi-year collaboration will sustain Ipsen’s presence in oncology by leveraging Marengo’s novel discovery of TCR Vβ-targeted precision T cell activation approachIpsen to pay Marengo $45 million upfront with potential for additional milestone payments PARIS, FRANCE & CAMBRIDGE, MASSACHUSETTS, 01 August, 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) and Marengo Therapeutics, Inc. today announced a strategic partnership to advance two of Marengo’s preclinical STAR platform-generated candidates into the
PARIS, FRANCE, 12 August 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) today announced the closing of the definitive merger agreement under which Ipsen has acquired Epizyme, Inc. (Epizyme). Pursuant to the transaction, Ipsen acquires all outstanding shares of Epizyme for $1.45 per share plus a contingent value right (CVR) of $1.00 per share. Epizyme now operates as ‘an Ipsen company’ at deal close. As part of the transaction, Ipsen acquires Epizyme’s lead medicine, Tazverik® (tazemetostat), a first-i
Six abstracts to be presented demonstrating efficacy and tolerability of investigational Bylvay in select cholestatic liver diseasesNew data emphasizes the consistent benefit of Bylvay as an investigational drug in Alagille syndrome and an approved medicine in PFIC, with evidence of rapid, sustained, and significant improvements in pruritus and sleep, and reductions in serum bile acids (sBAs) Further data shows evidence of disease modification with longer-term native liver survival in PFIC patie
The trial did not meet its primary endpoint of overall survival (OS)The safety profile of the combination of cabozantinib and atezolizumab was consistent with the known safety profiles for each single agentThe clinical trial results will be presented at a future medical meeting PARIS, FRANCE, 8 December 2022 – Ipsen (Euronext: IPN; ADR: IPSEY) announced today that the CONTACT-01 study did not meet its primary endpoint of overall survival (OS) at the final analysis. CONTACT-01 is a phase III clin
Monthly information relative to the total number of voting rights and shares composing the share capital (in accordance with Article L.233-8 II of the French Commercial Code and Article 223-16 of the General Regulation of the Autorité des Marchés Financiers) Market: Euronext Paris ISIN Code: FR 0010259150LEI: 549300M6SGDPB4Z94P11 DateTotal number of shares composing the share capitalTotal number of voting rights (1)30 April 2023 83,814,526 Gross total* of voting rights: 132,089,350Net total** of
INFORMATION RELATING TO THE HOLDING OF THE COMBINED SHAREHOLDERS’ MEETING OF 31 MAY 2023 FORMALITIES FOR MAKING AVAILABLE AND CONSULTINGPREPARATORY DOCUMENTS TO THE MEETING Boulogne-Billancourt (France), 10 May 2023 – The Shareholders of the Company are invited to participate in the Combined Shareholders’ Meeting of Ipsen (Euronext: IPN; ADR: IPSEY) to be held on Wednesday 31 May 2023 at 3:00 p.m. (Paris time) at the Salons de l'Hôtel des Arts et Métiers, 9 bis avenue d'Iéna, 75116 Paris. The pr
Ipsen delivers robust sales growth in the first quarter of 2023 and confirms its full-year guidance Paris (France), 27 April 2023Ipsen (Euronext: IPN; ADR: IPSEY), a global specialty-driven biopharmaceutical company, today presents its sales performance for the first quarter of 2023. Q1 2023 Q1 2022 % change €m €m Actual CER1 Oncology 570.8 556.4 2.6% 1.1% Neuroscience 156.4 120.2 30.2% 24.4% Rare Disease 14.7 11.3 29.8% 29.0% Total Sales2 741.9 687.9 7.8% 5.7% Highlights Total-sales growth of 5
Ipsen appoints Sandra Silvestri as EVP, Chief Medical Officer and Head of Global Medical Affairs, Patient Safety and Patient Affairs PARIS, FRANCE, 24 April 2023 – Ipsen (Euronext: IPN; ADR: IPSEY), a global specialty-driven biopharmaceutical company, announced today the appointment of Sandra Silvestri, M.D., Ph.D., as EVP, Chief Medical Officer and Head of Global Medical Affairs, Patient Safety and Patient Affairs, effective 5 May 2023. She will serve on the Executive Leadership Team (ELT) and
Monthly information relative to the total number of voting rights and shares composing the share capital (in accordance with Article L.233-8 II of the French Commercial Code and Article 223-16 of the General Regulation of the Autorité des Marchés Financiers) Market: Euronext Paris ISIN Code: FR 0010259150LEI: 549300M6SGDPB4Z94P11 DateTotal number of shares composing the share capitalTotal number of voting rights (1)31 March 2023 83,814,526 Gross total* of voting rights: 132,092,083Net total** of