News und Analysen
Valbiotis presents its 2024 financial communication calendar
Valbiotis sets out its commercial and clinical roadmap for 2024
Valbiotis announces the success of its €15 M capital increase
Valbiotis announces the launch of a capital increase
Valbiotis announces the availability of an amendment to the Universal Registration Document
Valbiotis announces that it has received Food and Drug Administration (FDA) approval for New Dietary Ingredient (NDI) status
Valbiotis announces the success of the TOTUM•63 mode of action clinical study, against prediabetes and the early stages of type 2 diabetes
VALBIOTIS SA: the Phase II/III REVERSE-IT study selected for an oral presentation at the 2023 EASD congress, the main European learned society for diabetes
Valbiotis publishes its financial report for the first half of 2023 and confirms its strategic roadmap
VALBIOTIS SA: Valbiotis presents the full results of the Phase II/III REVERSE-IT study: impressive efficacy of TOTUM•63 against prediabetes and the early stages of type 2 diabetes
Valbiotis announces its roadmap and strategic priorities on the eve of key milestones for its portfolio of innovative active substances
Valbiotis announces the appointment of Charlotte JEZEQUEL as Director of Human Relations and Executive Committee member
GenSight Biologics Announces Presentation of LUMEVOQ® Efficacy and Safety Data from Early Access Programs for ND4-LHON Patients at NANOS 2023
Regulatory News:
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Figure 1: Global evolution of mean BCVA over two
GenSight Biologics Confirms Sustained Efficacy and Safety of Bilateral LUMEVOQ® Injections at 3-Year Follow-Up of REFLECT Phase III Trial
Regulatory News:
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Graph 1: Evolution of Best-Corrected Visual Acuity
GenSight Biologics Announces Publication of Indirect Comparison of LUMEVOQ® Versus Natural History in ND4-LHON Patients in Peer-Reviewed Journal Ophthalmology and Therapy
Regulatory News:
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Figure 1: from Indirect Comparison of Lenadogene
GenSight Biologics reports 5 years’ data showing sustained efficacy and safety following one-time treatment with LUMEVOQ®
Regulatory News:
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Figure 1. Evolution of BCVA In LUMEVOQ®-treated
Transgene’s Board of Directors Strengthens Its Governance and Proposes the Appointment of Dr. Alessandro Riva as Independent Chairman
Regulatory News:
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Dr. Alessandro Riva (Photo: Transgene)
Transgene
GenSight Biologics Reports Clinically Meaningful Vision Improvement is Maintained 4 Years After One-time Treatment with LUMEVOQ® Gene Therapy
Regulatory News:
This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20220123005091/en/
Figure 1. Evolution of BCVA In LUMEVOQ®-treated
GenSight Biologics Confirms Sustained Efficacy and Safety of Bilateral LUMEVOQ® Injections at 2-Year Follow-Up of REFLECT Phase III Trial
Regulatory News:
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Figure 1. Best-Corrected Visual Acuity (BCVA) Change
Sumitomo Pharma and Poxel Announce Topline Results from Post-Marketing Clinical Study on TWYMEEG® for the Treatment of Type 2 Diabetes in Japan
Regulatory News:
Sumitomo Pharma Co., Ltd. (Head Office: Osaka, Japan; Representative Director, President and CEO: Toru Kimura) and POXEL SA (Euronext : POXEL - FR0012432516), a clinical stage
EQS-News: Abivax Announces ABTECT Phase 3 Trial Achieves Key Enrollment Milestone
Sensorion Announces its Participation in Stifel's Biotech Summer Summit
Regulatory News:
Sensorion (FR0012596468 – ALSEN) a pioneering clinical-stage biotechnology company which specializes in the development of novel therapies to restore, treat and prevent within
Sartorius Stedim Biotech SA: DECLARATION RELATIVE TO THE NUMBER OF SHARES AND VOTING RIGHTS MAKING UP THE ISSUED CAPITAL