Inventiva announces participation at several conferences in November 2021
Daix (France), Long Island City (New York, United States), November 29, 2021 – Inventiva (Euronext Paris and Nasdaq: IVA), a clinical-stage biopharmaceutical company focused on the development of oral small molecule therapies for the treatment of non-alcoholic steatohepatitis (NASH), mucopolysaccharidoses (MPS) and other diseases with significant unmet medical need, today announced that the Company’s leadership will participate in two upcoming conferences in November 2021.
The event details are as follows:
Conference n°1: Stifel Virtual Healthcare Conference 2021
Event type: Corporate presentation, one-on-one investor meetings
Date: Monday, November 15, 2021
Time: 2:40 – 3:10 pm (CET) / 8:40 – 9:10 am (ET)
Format: Virtual event
Live and replay link: https://wsw.com/webcast/stifel58/iva/1918080
Conference n°2: Jefferies 2021 London Healthcare Conference
Event type: Fireside chat
Date: Monday-Thursday, November 15-18, 2021
Format: Hybrid event
Replay link: https://wsw.com/webcast/jeff201/iva/1683648
The links to these events will also be available on Inventiva’s website in the “Investors – Investor Presentations” section.
À propos d’Inventiva
Inventiva est une société biopharmaceutique spécialisée dans le développement clinique de petites molécules administrées par voie orale pour le traitement de la NASH, des MPS et d’autres maladies avec un besoin médical non satisfait significatif.
Forte de son expertise et de son expérience significative dans le développement de composés ciblant les récepteurs nucléaires, les facteurs de transcription et la modulation épigénétique, Inventiva développe actuellement deux candidats médicaments, ainsi qu’un portefeuille important de plusieurs programmes en stade préclinique.
Lanifibranor, son candidat médicament le plus avancé, est actuellement en cours de développement pour le traitement de patients atteints de la NASH, une maladie hépatique chronique courante et progressive, pour laquelle il n’existe actuellement aucun traitement approuvé. En 2020, Inventiva a publié des résultats positifs de son étude clinique de Phase IIb évaluant lanifibranor pour le traitement des patients atteints de la NASH et a obtenu les statuts de « Breakthrough Therapy » et de « Fast Track » pour lanifibranor dans le traitement de la NASH. Lanifibranor est actuellement en cours d’évaluation dans le cadre d’une étude clinique pivot de Phase III.
Odiparcil est le second candidat médicament au stade clinique que Inventiva développe pour le traitement de patients souffrant d'un sous-type de MPS, un groupe de maladies génétiques rares. A la fin de l’année 2019, Inventiva a publié des résultats positifs de son étude clinique de Phase IIa évaluant odiparcil pour le traitement des patients adultes atteints de la MPS VI et a obtenu le statut de « Fast Track » dans la MPS VI pour odiparcil en octobre 2020.
En parallèle, Inventiva est en cours de sélection d’un candidat médicament en oncologie pour son programme dans la voie de signalisation Hippo. Par ailleurs, la Société a conclu un partenariat stratégique avec AbbVie dans le domaine des maladies auto-immunes. AbbVie a démarré le développement clinique d’ABBV-157, un candidat médicament pour le traitement de la forme modérée à sévère du psoriasis, issu de sa collaboration avec Inventiva. Ce partenariat permet le versement à Inventiva de paiements d'étapes en fonction de l’atteinte d’objectifs précliniques, cliniques, réglementaires et commerciaux ainsi que des redevances sur les ventes des produits développés dans le cadre de ce partenariat.
La Société dispose d’une équipe scientifique d'environ 70 personnes dotée d’une forte expertise en biologie, chimie médicinale et computationnelle, pharmacocinétique et pharmacologie ainsi qu’en développement clinique. Par ailleurs, Inventiva dispose d'une chimiothèque d’environ 240.000 molécules, dont environ 60% sont la propriété de la Société, ainsi que de ses propres laboratoires et équipements.
Inventiva est une société cotée sur le compartiment C du marché réglementé d'Euronext Paris (Euronext Paris : IVA – ISIN : FR0013233012) et sur le marché Nasdaq Global Market aux États-Unis (symbole : IVA). www.inventivapharma.com
Contacts
| Inventiva Pascaline Clerc VP Global External Affairs media@inventivapharma.com +1 240 620 9175 | Brunswick Group Laurence Frost / Tristan Roquet Montegon / Aude Lepreux Relations médias inventiva@brunswickgroup.com +33 1 53 96 83 83 | Westwicke, an ICR Company Patricia L. Bank Relations investisseurs patti.bank@westwicke.com +1 415 513-1284 |
Attachment
To view this piece of content from www.globenewswire.com, please give your consent at the top of this page.To view this piece of content from ml-eu.globenewswire.com, please give your consent at the top of this page.
About GlobeNewswire by notified
GlobeNewswire by notifiedGlobeNewswire by notified is one of the world's largest newswire distribution networks, specializing in the delivery of corporate press releases financial disclosures and multimedia content to the media, investment community, individual investors and the general public.
Subscribe to releases from GlobeNewswire by notified
Subscribe to all the latest releases from GlobeNewswire by notified by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from GlobeNewswire by notified
Galapagos increases share capital through subscription right exercises3.12.2021 22:01:00 CET | Press release
Mechelen, Belgium; 3 December 2021, 22.01 CET; regulated information – Galapagos NV (Euronext & NASDAQ: GLPG) announces a share capital increase arising from subscription right exercises. Galapagos issued 22,600 new ordinary shares on 3 December 2021, for a total capital increase (including issuance premium) of €578,700.00. Pursuant to the subscription right exercise program of Galapagos’ management board, members of the management board automatically are committed to exercise a minimum number of subscription rights, subject to certain conditions. In accordance with the rules of this program, one management board member exercised 5,000 subscription rights. In accordance with Belgian transparency legislation1, Galapagos notes that its total share capital currently amounts to €354,582,005.11, the total number of securities conferring voting rights amounts to 65,552,721, which is also the total number of voting rights (the “denominator”), and all securities conferring voting rights and al
Sampo plc’s share buybacks 03/12/20213.12.2021 21:30:00 CET | Press release
SAMPO PLC STOCK EXCHANGE RELEASE 03/12/2021 at 10:30 pm Sampo plc’s share buybacks 03/12/2021 On 03/12/2021 Sampo plc (business code 0142213-3, LEI 743700UF3RL386WIDA22) has acquired its own A shares (ISIN code FI0009003305) as follows: Sampo plc’s share buybacksAggregated daily volume (in number of shares)Daily weighted average price of the purchased shares*Market (MIC Code)23,68743.29AQEU27,42643.28CEUX4,32043.37TQEX72,59243.31XHELTOTAL128,02543.30 *rounded to two decimals On 1 October 2021, Sampo announced a share buyback programme of up to a maximum of EUR 750 million in compliance with the Market Abuse Regulation (EU) 596/2014 (MAR) and the Commission Delegated Regulation (EU) 2016/1052. The programme, which started on 4 October 2021, is based on the authorization granted by Sampo's Annual General Meeting on 19 May 2021. After the disclosed transactions, the company owns in total 6,263,553 Sampo A shares representing 1.13 per cent of the total number of shares in Sampo plc. Detail
Projekt Öyfjellet försenat – beräknas färdigställas under första kvartalet 20223.12.2021 21:15:00 CET | Pressemelding
Hässleholm den 3 december 2021 I delårsrapporten för det tredje kvartalet, som offentliggjordes den 18 november 2021, kommunicerade Eolus att det finns risk för försening i färdigställandet av det norska 400 MW projektet Öyfjellet. Baserat på uppdaterad information om byggprocessen beräknar Eolus nu att vindparken färdigställs under det första kvartalet 2022. Per idag, den 3 december 2021, har samtliga 72 turbiner färdigmonterats. 34 turbiner har börjat generera el. Huvudskälen till förseningen är utmanande väderförhållanden, vilket har påverkat installationsarbetet, samt Covid-19 relaterade orsaker som begränsat både resemöjligheterna för personal och lett till leveransförseningar avseende komponenter. Förseningen kommer att ha en negativ påverkan på Eolus projektmarginal. För ytterligare information kontakta: Per Witalisson, VD, telefon +46 (0)70-265 16 15 Johan Hammarqvist, kommunikationschef, telefon +46 (0)720-50 59 11 Kort om Eolus Eolus Vind är en av Nordens ledande projektörer
Project Øyfjellet delayed - new estimated completion in the first quarter of 20223.12.2021 21:15:00 CET | Press release
Hässleholm, Sweden, December 3rd, 2021 In the interim report for the third quarter, released on November 18, 2021, Eolus communicated a risk of delay in the completion of the 400 MW Norwegian wind project Øyfjellet. Based on updated information of the construction progress, Eolus now estimates that the wind farm will be completed during the first quarter of 2022. As of today, December 3, 2021, construction of all 72 turbines have been completed. First electricity production has been achieved by 34 turbines. The main reasons for the delay are challenging weather conditions which has effected the progress of the installations and Covid-19 related issues which has restricted both travel possibilities for personnel and led to delays in delivery of components. The delay is expected to have a negative impact on Eolus’ profit margin for the construction of the project. For further information contact: Per Witalisson, CEO, +46 70-265 16 15 Johan Hammarqvist, Head of Communications, +46 720 50
ING reports outcome of 2021 EU-wide Transparency Exercise and Risk Assessment Report3.12.2021 18:12:26 CET | Press release
ING reports outcome of 2021 EU-wide Transparency Exercise and Risk Assessment Report ING notes the announcements made today by the European Banking Authority (EBA) and the European Central Bank (ECB) regarding the information of the 2021 EU-wide Transparency Exercise and Risk Assessment Report. Background EU‐wide Transparency Exercise The EBA Board of Supervisors approved the package for the EU‐wide Transparency Exercise, which since 2016 is performed on an annual basis and published along with the Risk Assessment Report (RAR). The annual transparency exercise is based solely on regulatory reporting data (COREP/FINREP) on the form and scope to assure a sufficient and appropriate level of information to market participants. The templates were centrally filled in by the EBA and sent afterwards for verification by banks and supervisors. The outcome of the exercise related to ING Group can be found in the annexes on the EBA website. Note for editors For further information on ING, please v
KBC Group: KBC report on the 2021 EBA Transparency Exercise3.12.2021 18:10:00 CET | Press release
Press Release Outside trading hours - Regulated information* Brussels, 3 December 2021 – after trading hours KBC report on the 2021 EBA Transparency Exercise KBC notes the announcements made today by the European Banking Authority (EBA) and the European Central Bank (ECB) regarding the publication of the EU-wide Transparency Exercise. The information of this 2021 EU-wide Transparency Exercise refers to the reported data as of 30 September 2020, 31 December 2020, 31 March 2021 and 30 June 2021. The templates, published on a bank-by-bank basis, are the following: Key MetricsLeverage ratioCapitalRisk exposure amountsP<otal Assets: fair value and impairment distributionLiabilitiesMarket RiskCredit RiskGeneral governments exposuresPerforming and Non-Performing ExposuresForborne ExposuresLoans and advances to non-financial corporationsCovid-19 The data collection relies on the standard information reported by the banks to the EBA on a regular basis through the supervisory reporting framewo
Changes in the Board of Directors3.12.2021 17:40:00 CET | Press release
Basel, 3 December 2021 - Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that at its December meeting the Board of Directors of Roche Holding Ltd has approved first proposals to the Annual General Meeting (AGM) scheduled for 15 March 2022. Mr Paul Bulcke, who has been serving on the Board of Directors since 2011, has decided not to stand for re-election at the AGM in 2022, following almost eleven years of tenure. The Board of Directors proposes Dr Jemilah Mahmood, currently the Special Advisor on Public Health to Malaysia’s prime minister, for election to the Board of Directors at the AGM 2022. “As a member of the Board and of the Audit Committee, Paul Bulcke has made significant contributions to Roche’s success,” said Roche Chairman Christoph Franz. “On behalf of the Board of Directors, I would like to extend our sincere thanks to Paul Bulcke who gave great support to Roche with his enormous leadership experience and his strong entrepreneurial thinking.” Christoph Franz added: “I a