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WKN: A2ANGZ | ISIN: FR0013183985 | Ticker-Symbol: G49N
Frankfurt
17.04.26 | 09:13
0,065 Euro
-13,68 % -0,010
Branche
Biotechnologie
Aktienmarkt
Sonstige
1-Jahres-Chart
GENSIGHT BIOLOGICS SA Chart 1 Jahr
5-Tage-Chart
GENSIGHT BIOLOGICS SA 5-Tage-Chart
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0,0790,08418.04.

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MiGenSight Biologics Announces the Filing of its 2025 Universal Registration Document253Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal...
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07.04.GenSight Biologics Reports Cash Position and Revenue from Early Access Program as of March 31, 2026345Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal...
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03.04.GenSight Biologics Confirms Definitive Full-Year 2025 Consolidated Financial Results Are in Line with Estimates507Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal...
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27.03.GenSight Biologics Reports Estimated Full-Year Consolidated Financial Results for 20252972025 was a turning point with key regulatory milestones providing a solid foundation for 2026. Cash runway is projected to extend through December 2026. Preparation of the Phase...
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20.03.The 15-20 National Hospital and GenSight Biologics Announce the First Treatments in the French Named Patient Early Access Program (AAC) for GS010/LUMEVOQ312The first group of patients in the GS010 AAC program were treated at the 15-20 National Hospital in Paris on March 19. The REVISE dose-ranging study is proceeding according to the planned...
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18.03.GenSight Biologics Announces the Closing of its Nearly €1.7 Million Fundraising389Regulatory News: NOT FOR DISTRIBUTION, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, CANADA, AUSTRALIA, JAPAN AND SOUTH AFRICA GenSight Biologics (the "Company") (Euronext: SIGHT...
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10.03.GenSight Biologics: €1.7 Million Raised Through Share And Warrant Financing To Extend Cash Runway1
09.03.GenSight Biologics Provides Updates about GS010/LUMEVOQ Early Access Programs and the Ongoing REVISE Study317Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal...
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18.02.GenSight Biologics S.A.: GenSight Biologics Bolsters Regulatory Leadership in US and Europe with Two Senior Appointments354Regulatory News: GenSight Biologics ("GenSight Biologics" or the "Company") (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing...
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10.02.GenSight Biologics S.A.: The 15-20 National Hospital and GenSight Biologics Announce the Treatment of the First Patient in the GS010/LUMEVOQ REVISE Study421First of 14 planned patients for the dose-ranging study approved by the ANSM in December 2025 Clinical study marks continuing partnership between the 15-20 Hospital and GenSight Biologics...
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29.01.GenSight Biologics S.A.: GenSight Biologics Announces the Results of its Extraordinary General Meeting of January 28, 2026900Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal...
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08.01.GenSight Biologics Reports Cash Position as of December 31, 2025, and Provides Business Updates439Cash position amounted to €2.4 million as of December 31, 2025 Successful closing of fundraising worth nearly €2.9 million on January 7, 2026 Payments for early access treatments...
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07.01.GenSight Biologics Announces Closing of Fundraising Worth Nearly EUR 2.9 Million390Regulatory News: NOT FOR DISTRIBUTION, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, CANADA, AUSTRALIA, JAPAN AND SOUTH AFRICA GenSight Biologics (the "Company") (Euronext: SIGHT...
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29.12.25GenSight Biologics Announces Successful Fundraising Amounting to Nearly €2.9 Million447Regulatory News: NOT FOR DISTRIBUTION, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, CANADA, AUSTRALIA, JAPAN AND SOUTH AFRICA GenSight Biologics ("GenSight" or the "Company") (Euronext:...
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22.12.25GenSight Biologics S.A.: GenSight Biologics Announces Regulatory Authorization for Early Access Treatment with GS010/LUMEVOQ in Israel527Israel's Ministry of Health authorizes individual patients early access treatment with GS010/LUMEVOQ, a candidate gene therapy for the treatment of ND4-LHON. Bilateral injection expected...
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22.12.25GenSight Biologics S.A.: GenSight Biologics Announces the Granting of Compassionate Use Authorization (CUA/AAC) for GS010/LUMEVOQ in France541French medicines agency ANSM has granted authorization for named patient early access program for GS010/LUMEVOQ, a gene therapy indicated for the treatment of ND4-LHON. Regulatory News: GenSight...
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02.12.25GenSight Biologics Announces Regulatory Approval for GS010/LUMEVOQ REVISE Dose-Ranging Study in France399French medicines agency ANSM and Ethics Committee authorize the dose-ranging study investigating two doses of candidate product for the treatment of ND4-LHON. Approval of the study protocol...
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13.11.25GenSight Biologics Announces Closing of Fundraising Worth Nearly EUR 2 Million505Regulatory News: NOT FOR DISTRIBUTION, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, CANADA, AUSTRALIA, JAPAN AND SOUTH AFRICA GenSight Biologics (the "Company") (Euronext: SIGHT...
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10.11.25GenSight Biologics S.A.: GenSight Biologics Announces Successful Fundraising Amounting to Nearly €2 Million354Regulatory News: NOT FOR DISTRIBUTION, DIRECTLY OR INDIRECTLY, IN THE UNITED STATES OF AMERICA, CANADA, AUSTRALIA, JAPAN AND SOUTH AFRICA GenSight Biologics ("GenSight" or the "Company") (Euronext:...
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30.10.25GenSight Biologics Announces Regulatory Authorizations for Individual Patient Expanded Access Treatment with GS010/LUMEVOQ in the US575FDA authorization and Institutional Review Board (IRB) approval followed by QP release for expanded access treatment of one patient in the US Treatment scheduled in November 2025 at the...
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