2024/26/09 - 18:30 |
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ABIONYX Pharma announces its 2024 Half-Year financial results
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pdf
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2024/22/08 - 18:00 |
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ABIONYX Pharma provides an update on its business and cash position for the 1st half of 2024
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pdf
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2024/01/07 - 08:00 |
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ABIONYX carries out successfully a capital increase with cancellation of preferential subscription rights for the benefit of a category of persons through the issue of shares with warrants for an amount of c.€3.4 million
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2024/27/06 - 19:00 |
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ABIONYX Pharma announces unanimous approval of all resolutions put to the vote at its Combined General Meeting
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2024/19/06 - 19:30 |
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ABIONYX decides on a capital increase with cancellation of preferential subscription rights for the benefit of a category of persons through the issue of shares with warrants for an amount of c.€3.4 million
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2024/13/06 - 19:30 |
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ABIONYX Pharma has completed a successful pre-IND meeting with the FDA for CER-001 Phase 2b/3 Clinical Trial for Patients with Sepsis
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2024/16/05 - 18:00 |
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ABIONYX Pharma provides an update on its activity and cash position for the 1st quarter 2024
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pdf
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2024/02/05 - 18:00 |
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Availability of the Universal Registration Document for the year 2023
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pdf
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2024/14/03 - 18:00 |
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Bpifrance supports the development of CER-001 in ophthalmology with a nearly €1 million non-dilutive innovation grant
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pdf
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2024/11/03 - 07:30 |
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ABIONYX Pharma announces its 2023 full-year financial results
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pdf
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2024/07/03 - 19:00 |
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ABIONYX Pharma announces its financial calendar for the year 2024
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pdf
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2024/29/02 - 18:08 |
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ABIONYX Pharma provides an update on its activity and cash position for the 4th quarter 2023
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pdf
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2024/16/02 - 08:00 |
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Clarification about clinical results from the phase 3 of apoA-I study, CSL112
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pdf
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2024/15/02 - 18:00 |
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Clinical results of the Phase 3 AEGIS-II study: - Validation of ABIONYX Pharma's strategic repositioning in severe diseases with short apoA-I treatment - No safety or tolerability problems in 18,000 patients
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pdf
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2024/08/01 - 18:03 |
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ABIONYX Pharma appoints Rob Scott, MD, as Chief Medical Officer and Head of R&D
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2023/18/12 - 18:00 |
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ABIONYX Pharma successfully manufactures a third batch of recombinant human apoA-I CER-001 using a new, innovative and robust industrial bioprocess
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pdf
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2023/23/11 - 19:23 |
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ABIONYX Pharma presents preclinical results for CER-001 in Brain Fog, at the 1st International Scientific Congress on Brain-Kidney Interaction in Naples on November 23-24, 2023
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pdf
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2023/21/11 - 07:00 |
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ABIONYX Pharma announces new positive results in a uveitis model for the strategic development of the first class of biomedicines in ophthalmology based on its recombinant apoA-I
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pdf
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2023/16/11 - 18:00 |
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ABIONYX Pharma provides an update on its activity, its revenue and its cash position for the third quarter of 2023
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pdf
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2023/02/11 - 18:55 |
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Poster RACERS - CER-001, an Engineered High-Density Lipoprotein, shows beneficial pleiotropic effects in patients with sepsis in RACERS: a Phase 2a randomized clinical tria
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pdf
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2023/02/11 - 17:56 |
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ABIONYX Pharma RACERS study data in sepsis presented at the American Society of Nephrology (ASN) 2023 Annual Meeting "Kidney Week"
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pdf
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2023/16/10 - 07:00 |
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ABIONYX Pharma RACERS study in sepsis selected for Late-Breaking Clinical Results Poster Presentation at the American Society of Nephrology (ASN) 2023 Annual Meeting "Kidney Week"
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pdf
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2023/06/10 - 07:30 |
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ABIONYX Pharma completes a capital increase in favor of categories of persons
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pdf
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2023/26/09 - 20:00 |
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ABIONYX Pharma announces its 2023 Half-Year financial results
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pdf
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2023/12/09 - 20:00 |
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World Sepsis Day: ABIONYX Pharma confirms its commitment to sepsis, a global public health issue
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pdf
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2023/17/08 - 18:00 |
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ABIONYX Pharma provides an update on its business and cash position for the first half of 2023
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pdf
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2023/26/07 - 18:30 |
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ABIONYX Pharma successfully manufactures a second batch of recombinant human ApoA-I CER-001 using a new, innovative and robust industrial bioprocess
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pdf
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2023/13/07 - 07:30 |
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ABIONYX Pharma announces the appointment of Laurent Guerci as Chief Digital & Innovation Officer
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pdf
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2023/10/07 - 18:00 |
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ABIONYX Pharma announces a new Compassionate Access Authorization (CAA) for CER-001 in the rare disease LCAT deficiency or Norum disease in Europe
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pdf
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2023/29/06 - 18:00 |
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ABIONYX Pharma announces unanimous approval of all resolutions put to the vote at its Combined General Meeting
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pdf
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2023/29/05 - 20:15 |
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ABIONYX Pharma provides further details on the setting up of its equity-linked financing facility
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pdf
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2023/23/05 - 20:30 |
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ABIONYX Pharma accelerates its development by launching a new biomanufacturing campaign based on the recently announced robust innovative process supported by an equity-linked financing facility
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pdf
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2023/17/05 - 18:30 |
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ABIONYX Pharma provides an update on its activity and its cash position for the first quarter 2023
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pdf
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2023/10/05 - 18:30 |
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ABIONYX Pharma announces the successful manufacturing of the first batch of CER-001 with recombinant human ApoA-I using a new innovative and robust industrial bioprocess
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pdf
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2023/02/05 - 18:00 |
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Availability of the Universal Registration Document for the year 2022
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pdf
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2023/31/03 - 18:45 |
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ABIONYX Pharma announces its strategy in ophthalmology and new positive preclinical results for the deployment of two innovative technology platforms: apotherapy and biovectorization
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pdf
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2023/29/03 - 18:36 |
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ABIONYX Pharma announces its 2022 full-year financial results
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pdf
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2023/28/02 - 18:00 |
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ABIONYX Pharma provides an update on its activity and its cash position for the 4th quarter 2022
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pdf
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2023/03/02 - 19:30 |
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Press release
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pdf
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2023/16/01 - 12:00 |
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ABIONYX Pharma Reports Positive Results from Phase 2a Pilot Clinical Trial Evaluating CER-001 in the Treatment of Septic Patients at High Risk of Developing Acute Kidney Injury
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pdf
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2023/13/01 - 07:30 |
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ABIONYX Pharma announces its financial agenda for the year 2023
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pdf
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2022/17/11 - 18:30 |
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ABIONYX Pharma announces its cash position and provides an activity update on the 3rd quarter 2022
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pdf
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2022/04/10 - 18:00 |
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ABIONYX Announces Final Patient Enrollment in Phase 2a Clinical Trial with CER-001, Bio-HDL for the Treatment of Patients with Sepsis at High Risk of Developing Acute Kidney Injury
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pdf
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2022/29/09 - 18:30 |
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ABIONYX Pharma announces its 2022 half-year financial results
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pdf
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2022/18/08 - 17:45 |
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ABIONYX Pharma provides an update on its business and cash position for the first half of 2022
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pdf
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2022/04/07 - 17:45 |
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ABIONYX Pharma announces the reinitiation of coverage of its stock by TPICAP Midcap
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pdf
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2022/30/06 - 18:00 |
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Combined General Meeting of June 28, 2022
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pdf
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2022/19/05 - 18:00 |
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ABIONYX Pharma provides an update on its business and cash position for the first quarter of 2022
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pdf
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2022/29/04 - 18:00 |
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Availability of the Universal Registration Document for the year 2021
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pdf
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2022/28/04 - 18:00 |
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Annual results 2021
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pdf
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2022/07/04 - 07:30 |
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ABIONYX Pharma Reports Positive Interim Results from Phase 2a Clinical Trial Evaluating CER-001 in the Treatment of Septic Patients at High Risk of Developing Acute Kidney Injury
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pdf
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2022/29/03 - 17:45 |
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ABIONYX Pharma Receives FDA Orphan Drug Designation (ODD) for CER-001 for the Treatment of LCAT Deficiency Presenting as Kidney Dysfunction and/or Ophthalmologic Disease
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pdf
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2022/24/03 - 18:00 |
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ABIONYX announces positive clinical findings for CER-001 in treating COVID-19, published in Biomedecines, demonstrating that CER-001 limits inflammation effects
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pdf
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2022/24/02 - 18:00 |
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ABIONYX Pharma provides an update on its business and cash position for Q4 2021
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pdf
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2022/31/01 - 17:45 |
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ABIONYX Pharma announces its financial agenda for the year 2022
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pdf
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2022/03/01 - 18:00 |
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ABIONYX Pharma announces that the French Drug Safety Agency (Agence Nationale de Sécurité du Médicament or ANSM) has granted a Compassionate Access Authorization for the bio-HDL (CER-001) in COVID-19 disease
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pdf
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2021/06/12 - 07:30 |
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ABIONYX Pharma announces the completion of a contribution in kind to the company of 100% of the capital of IRIS Pharma Holding, fully compensated by the issue of new shares at a price of €3.60 per share to become a specialist of bioproducts in ophthalmolo
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pdf
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2021/02/12 - 07:30 |
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ABIONYX announces the success of its capital increase in cash by private placement at a price of €3.60 per share
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pdf
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2021/17/11 - 19:09 |
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ABIONYX announces the signing of an agreement for the contribution of 100% of the capital of IRIS Pharma Holding, fully remunerated by the issuance of new ABIONYX shares at a fixed price of 3.60 euros per share
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pdf
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2021/15/11 - 07:30 |
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ABIONYX Announces New Positive Clinical Results for CER-001 in kidney disease associated with LCAT deficiency Published in The Journal of Internal Medicine
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pdf
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2021/04/11 - 18:45 |
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ABIONYX Pharma announces its cash position and provides an activity update for the 3rd quarter 2021
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pdf
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2021/11/10 - 18:45 |
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ABIONYX Pharma initiates discussions with IRIS Pharma, a world leader in preclinical and clinical ophthalmology research, with a view to a possible strategic deal
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pdf
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2021/07/10 - 07:30 |
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ABIONYX Pharma announces positive preclinical results in a model of uveitis and launches the strategic development of the first class of biomedicines in ophthalmology based on its bio-HDL
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pdf
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2021/09/09 - 18:45 |
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ABIONYX Pharma announces its 2021 half year financial results and provides an update on its development activities
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pdf
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2021/05/08 - 19:00 |
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Gross cash position and business update for the first half of 2021
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pdf
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2021/28/07 - 07:30 |
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ABIONYX Pharma receives positive opinion from EMA within the framework of the Orphan Drug Designation process for CER-001 for the rare disease LCAT Deficiency
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pdf
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2021/16/06 - 18:00 |
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ABIONYX Pharma presents its “raison d'être” and states in its articles of association
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pdf
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2021/08/06 - 07:30 |
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ABIONYX Announces First Patient Enrolled in Phase 2a Clinical Study with CER-001, the Bio-HDL for the Treatment of septic patients at high risk of developing Acute Kidney Injury
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pdf
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2021/06/05 - 19:14 |
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Financial Highlights and business review for the first quarter of 2021
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pdf
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2021/27/04 - 18:00 |
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Availability of the Universal Registration Document for the year 2020
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pdf
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2021/26/04 - 18:00 |
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Convening of the 2021 Combined General Meeting
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pdf
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2021/25/03 - 07:54 |
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ABIONYX announces the signing of a strategic partnership with GTP Biologics (Fareva Group) and V-Nano (VBI Therapeutics group) for the bioproduction of the bio-HDL CER-001 in France
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pdf
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2021/02/03 - 07:34 |
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Positive Clinical Results From CER-001 in an ultrarare kidney disease Published in The Annals of Internal Medicine
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pdf
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2021/25/02 - 19:03 |
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Annual results 2020
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pdf
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2021/04/02 - 18:07 |
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ABIONYX Pharma provides an update on its cash position and the start of its clinical activities in Q4 2020
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pdf
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2021/25/01 - 08:00 |
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ABIONYX Pharma announces its financial agenda for the year 2021
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pdf
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2020/23/12 - 07:30 |
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ABIONYX initiates a Phase 2a clinical trial with CER-001 in septic patients at high risk of developing Acute Kidney Injury
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pdf
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2020/15/12 - 19:01 |
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Publication of pre-clinical data in the journal Metabolism demonstrating that CER-001 improves lipid profile and kidney function for an ultra-rare kidney disease
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pdf
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2020/25/11 - 19:03 |
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ABIONYX announces the observation of positive therapeutic signals in Temporary Authorizations for Use (ATUn) in France and Italy for an ultra-rare kidney disease
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pdf
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2020/22/10 - 18:21 |
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ABIONYX announces its cash position and provides an activity update for the 3rd quarter 2020
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pdf
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2020/14/10 - 19:24 |
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ABIONYX announces the success of a capital increase for the benefit of persons belonging to specific categories
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pdf
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2020/02/10 - 20:38 |
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ABIONYX clarifies its strategy and announces the launch of a capital increase for the benefit of persons belonging to specific categories
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pdf
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2020/10/09 - 18:37 |
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Availability of the half-year financial report 2020 (French)
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pdf
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2020/10/09 - 18:36 |
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2020 Half-year results
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pdf
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2020/23/07 - 18:05 |
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Gross cash position for the first semester of 2020
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pdf
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2020/27/04 - 17:50 |
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Availability of the Universal Registration Document for the year 2019
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pdf
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2020/23/04 - 20:17 |
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Gross cash position and business review for the first quarter of 2020
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pdf
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2020/10/03 - 19:19 |
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2019 annual results
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pdf
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2020/04/02 - 20:19 |
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Cash position and activity update for Q4 2019
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pdf
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2020/28/01 - 18:00 |
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ABIONYX Pharma announces its financial agenda for the year 2020
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pdf
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2020/08/01 - 08:00 |
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ABIONYX Pharma announces a named patient Temporary Authorization for Use (ATUn) for CER-001 in France
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pdf
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2020/03/01 - 14:48 |
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Resignation of a member of the Board of Directors
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pdf
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2019/24/10 - 18:00 |
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Cash position and activity update for Q3 2019
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pdf
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2019/13/09 - 08:00 |
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Message from the Board of Directors
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pdf
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2019/09/09 - 08:00 |
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Cyrille Tupin appointed CEO
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pdf
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2019/06/09 - 07:00 |
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2019 Half-year results
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pdf
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2019/27/08 - 18:30 |
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Change of name and stock symbol/mnemonic of ABIONYX Pharma shares (formerly CERENIS Therapeutics) as of August 29, 2019
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pdf
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2019/26/08 - 20:20 |
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ABIONYX Pharma announces appointment of a new member to the Board
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pdf
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2019/18/07 - 19:29 |
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CERENIS Therapeutics announces cash position and activity update for Q2 2019
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pdf
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2019/24/06 - 22:25 |
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Cerenis Therapeutics announces the results of the Annual Combined General Meeting of Shareholders
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pdf
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2019/14/06 - 19:59 |
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Cerenis announces the success of a capital increase for the benefit of persons belonging to specific categories
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pdf
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2019/13/06 - 21:00 |
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Cerenis announces the launch of a capital increase for the benefit of persons belonging to specific categories
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pdf
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2019/18/04 - 18:02 |
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Cash position and activity update for Q1 2019
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pdf
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2019/27/03 - 18:21 |
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Cerenis Therapeutics and H4Orphan Pharma enter into exclusive negotiations to consider a strategic merger
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pdf
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2019/24/01 - 19:12 |
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2018 Annual Results and clinical update
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pdf
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2019/23/01 - 18:15 |
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2019 Financial agenda
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pdf
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2018/20/12 - 19:35 |
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Results of the Phase I study of repeated and increasing doses to assess CER-209 in NASH/NAFLD
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pdf
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2018/19/12 - 06:21 |
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CERENIS Therapeutics’ Board of Directors appoints Richard Pasternak as CEO and Cyrille Tupin as Deputy CEO
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pdf
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2018/17/12 - 18:09 |
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Final results of TARGET PHASE II study demonstrate the ability of CER-001, an HDL mimetic, to target tumor in patients with esophageal cancer
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pdf
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2018/05/12 - 08:01 |
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CERENIS announces the results of TANGO, a Phase III clinical study evaluating CER-001 in patients with HDL deficiency
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pdf
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2018/21/11 - 08:02 |
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Statement following the evolution of the Cerenis share price
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pdf
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2018/25/10 - 18:02 |
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Cerenis Therapeutics - Announces its cash position for Q3 2018 and highlights the progress made over the period and key perspectives for the end of 2018
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pdf
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2018/22/10 - 18:07 |
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CERENIS to present new data validating HDL targeted drug delivery in the field of oncology and immuno-oncology at the 30th EORTC/NCI/AACR symposium
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pdf
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2018/10/09 - 07:02 |
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2018 Half-Year Results
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pdf
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2018/31/07 - 18:06 |
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Cerenis announces today the appointment of Barbara Yanni to its Board of Directors as an Independent Director
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pdf
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2018/26/07 - 07:48 |
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Cerenis announces financing from investment funds, management, its board of directors and its oncology scientific advisory board
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pdf
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2018/18/07 - 18:54 |
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Cash position and activity update for H1 2018 and key perspectives for the end of 2018
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pdf
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2018/25/06 - 18:53 |
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First results of TARGET PHASE II study demonstrate the ability of CER-001, an HDL mimetic, to target tumor in patients with esophageal cancer
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pdf
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2018/29/05 - 07:30 |
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CERENIS Therapeutics and University of North Texas Health Science Center announce a strategic initiative to develop new HDL-based pharmaceutical products
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pdf
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2018/07/05 - 17:55 |
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Cerenis to attend 2018 HDL Workshop (adjacent to ATVB|PVD Scientific Sessions)
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pdf
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2018/02/05 - 18:10 |
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Seasoned Scientific Experts and Strategic Pharmaceutical Industry Veterans Join Cerenis’ Scientific Advisory Board in Oncology
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pdf
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2018/23/04 - 22:19 |
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Publication of 2017 Registration Document
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pdf
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2018/19/04 - 19:01 |
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Cash position and activity update for Q1 2018
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pdf
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2018/07/03 - 19:25 |
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Approval to launch the Phase I Study of repeated and increasing doses to assess CER-209 in NASH/NAFLD
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pdf
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2018/01/02 - 19:32 |
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2017 Annual Results and Update on TANGO
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pdf
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2018/25/01 - 18:17 |
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Cash position and activity update for Q4 2017
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pdf
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2018/23/01 - 18:28 |
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2018 Financial Agenda
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pdf
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2017/22/11 - 08:14 |
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Cerenis - First patients enter TARGET study, recently initiated by Cerenis Therapeutics to evaluate HDL nanoparticles in patients with esophageal cancer
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pdf
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2017/08/11 - 07:52 |
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CERENIS Therapeutics acquires LYPRO Biosciences expanding its HDL strategy into immuno-oncology and chemotherapeutic drug delivery
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pdf
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2017/26/10 - 18:00 |
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Cash position and activity update for Q3 2017
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pdf
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2017/18/10 - 17:52 |
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Completion of patient enrollment in the Phase 3 study, TANGO, evaluating CER-001 in HDL genetic deficiency
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pdf
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2017/12/09 - 18:30 |
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2017 Half-Year Results
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pdf
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2017/04/09 - 18:01 |
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Cerenis Therapeutics announces participation at the 19th annual Rodman & Renshaw global investment conference in New York city, September 10-12, 2017
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pdf
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2017/20/07 - 18:20 |
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Cash position and activity update for H1 2017
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pdf
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2017/20/06 - 10:35 |
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Bpifrance supports the clinical development of CER-209 in NAFLD /NASH with a €0.75 million payment for innovation
|
pdf
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2017/07/06 - 19:10 |
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Positive results from the CER-209 Phase I Single Dose Tolerance study for NAFLD and NASH
|
pdf
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2017/28/04 - 20:41 |
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Publication of 2016 Registration Document
|
pdf
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2017/20/04 - 18:50 |
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Cash position and update on clinical developments for Q1 2017
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pdf
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2017/18/04 - 07:56 |
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Cerenis Therapeutics announces the initiation of the Phase 1 clinical study with CER-209 in NAFLD and NASH
|
pdf
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2017/20/03 - 07:58 |
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Cerenis Therapeutics announces that CARAT Phase 2 Study data on CER-001 have been presented at ACC annual meeting 2017
|
pdf
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2017/01/03 - 17:21 |
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Cerenis Therapeutics Announces Top line Results of CARAT Phase II Study
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pdf
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2017/17/02 - 18:02 |
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2016 Annual Results
|
pdf
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2017/03/02 - 17:58 |
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2017 Financial Calendar
|
pdf
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2017/19/01 - 19:07 |
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Clinical progress, cash position and revenue for Q4 2016
|
pdf
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2016/15/12 - 21:42 |
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Cerenis Therapeutics Receives FDA IND Approval to Begin Studies with CER-209 in NAFLD and NASH
|
pdf
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2016/08/11 - 07:09 |
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Cerenis Therapeutics Announces Last Patient Dosed in CARAT Phase II Study with CER-001 in Post-Acute Coronary Syndrome Patients
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pdf
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2016/07/11 - 09:15 |
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Cash position and revenue for Q3 2016
|
pdf
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2016/05/09 - 17:51 |
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2016 Half-Year Results - Solid cash position of €33 million and major scientific results
|
pdf
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2016/01/09 - 07:00 |
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Positive safety and tolerability profile of CER-001 presented at the European Society of Cardiology (ESC) Congress 2016
|
pdf
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2016/30/08 - 08:00 |
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Completion of patient enrolment in the CARAT study – meeting the clinical schedule
|
pdf
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2016/28/07 - 07:44 |
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Cash position and revenue for the first semester of 2016
|
pdf
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2016/02/06 - 07:44 |
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Publication of the LOCATION clinical study results in the renowned scientific journal of the European Atherosclerosis Society (EAS)
|
pdf
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2016/03/05 - 07:13 |
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Cash position and revenue for the 1st quarter of 2016
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pdf
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2016/18/04 - 18:06 |
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Cerenis Therapeutics announces the publication of an initiation of coverage report by PORTZAMPARC, within the framework of the share’s market coverage
|
pdf
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2016/08/03 - 18:18 |
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Cerenis Therapeutics announces its participation to the 28th ROTH Capital Partners annual conference
|
pdf
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2016/03/03 - 18:28 |
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Publication of an initiation of coverage report by KEPLER CHEUVREUX, within the framework of the share’s market coverage
|
pdf
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2016/01/03 - 19:01 |
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2015 annual results
|
pdf
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2016/25/02 - 07:50 |
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Cerenis Therapeutics featured prominently at the 25th Conference of the ASIAN PACIFIC ASSOCIATION FOR THE STUDY OF THE LIVER (APASL)
|
pdf
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2016/16/02 - 07:30 |
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Cash position and revenue for 2015
|
pdf
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2016/29/01 - 10:57 |
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Catalent Biologics And Cerenis Therapeutics Announce Phase III Trial Of CER-001 In Europe And North America Leveraging GPEx® Cell Line Technology
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www |
2016/26/01 - 20:15 |
|
2016 Financial calendar
|
pdf
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2015/17/12 - 19:45 |
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Cerenis Therapeutics admitted to the SRD (Defered Settlement Service) “Long-only”
|
pdf
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2015/10/12 - 07:27 |
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First patient enters Phase III TANGO clinical trial to evaluate efficacy to regress atherosclerosis and safety of CER-001 in patients with Familial Primary HypoAlphalipoproteinemia (FPHA)
|
pdf
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2015/23/11 - 18:29 |
|
Cerenis' flagship product named one of 2015's most promising cardiovascular projects at the American Therapeutic Area Partnerships conference
|
pdf
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2015/12/11 - 18:25 |
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Cash position and revenue for Q3 2015
|
pdf
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2015/10/11 - 07:41 |
|
New Data for CER-001 presented in key Oral Session at AMERICAN HEART ASSOCIATION (AHA) CONFERENCE 2015
|
pdf
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2015/03/11 - 08:08 |
|
CER-001: Analysis of clinical results to be presented at the American Heart Association Scientific Congress, on November 9, 2015 in Orlando, UNITED-STATES
|
pdf
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2015/17/09 - 08:01 |
|
Cerenis Therapeutics is joining the Euronext indexes CAC® Small, CAC® Mid & Small and CAC® All-Tradable
|
pdf
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2015/08/09 - 08:03 |
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First patients enter phase II CARAT trial to assess reduction in atherosclerotic plaque using CER-001 in post Acute Coronary Syndrome (ACS) patients
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2015/07/09 - 17:53 |
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Press release for the availability of preparatory documents for the shareholder meeting
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2015/04/09 - 07:54 |
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Publication of positive preclinical data in the world-renowned scientific journal PLOS ONE
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2015/25/08 - 18:12 |
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2015 Half-Year Results
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2015/21/07 - 07:53 |
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Revenue and cash position for H1 2015
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2015/15/07 - 02:00 |
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Cerenis Therapeutics announces the results of the LOCATION study
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2015/09/06 - 02:00 |
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Cerenis Therapeutics announces new Board members
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2015/26/05 - 17:27 |
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CERENIS THERAPEUTICS featured prominently at the INTERNATIONAL SYMPOSIUM ON ATHEROSCLEROSIS (IAS)
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2015/13/05 - 17:27 |
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Cash position and revenue for Q1 2015
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2015/25/03 - 16:27 |
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Outstanding success of Cerenis Therapeutics’ IPO with €53.4 million raised on Euronext Paris
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2015/12/03 - 16:27 |
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CERENIS THERAPEUTICS launches its IPO on the Euronext regulated market in Paris
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2015/09/02 - 16:27 |
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CERENIS THERAPEUTICS announces the appointment of a new Director of Clinical Research and new members to the Board
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2014/03/09 - 17:27 |
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CERENIS THERAPEUTICS receives EMA Orphan Drug Designations for CER-001 for the treatment of ApoA-I and ABCA-1 deficiencies
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2014/03/09 - 17:27 |
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CERENIS THERAPEUTICS appoints R. Pasternak as Chairman of Cerenis Board September 3, 2014
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2014/02/06 - 17:27 |
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CERENIS THERAPEUTICS reports two positive Phase II Studies for HDL mimetic CER-001 at EA
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