Latest news with #GenSightBiologics
Business Wire
13-05-2025
- Business
- Business Wire
GenSight Biologics Announces Approval of All Resolutions Supported by the Board of Directors at the Combined General Meeting of May 13, 2025
PARIS--(BUSINESS WIRE)--Regulatory News: The Combined General Meeting of shareholders of GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders, took place on May 13, 2025, at 2:00 pm CEST at the Company's headquarters, 74 rue du Faubourg Saint-Antoine, 75012 Paris, France. The General Meeting was chaired by Laurence Rodriguez, Chief Executive Officer of the Company. All resolutions recommended by the Board of Directors and submitted to the Combined General Meeting were adopted, with the exception of Resolution A, which was rejected, in accordance with the recommendations of the Board. The quorum on first convening amounted to 56.51%. During the General Meeting, the Chief Executive Officer reviewed the key achievements of 2024, a year marked by careful cash management, strengthened financial structure with the participation of new investors and renewed support from historical shareholders, as well as the renegotiation of the Company's financial obligations. She also highlighted progress in manufacturing, including the optimization of GenSight's technology, preparation for technology transfer to a new manufacturing partner, and the successful mixing and pharmaceutical release of two active substance batches. On the regulatory and clinical fronts, the year saw the preparation of the Phase III RECOVER protocol, the planned submission of the Early Access Program (AAC) application in November 2024, and the continuation of strong scientific communication through international congresses and high-impact journal publications. Looking ahead to 2025, the Company will maintain strict spending discipline while actively pursuing refinancing opportunities. Strategic priorities include the finalization of the Phase III RECOVER protocol in alignment with health authorities, the submission of the LUMEVOQ ® registration dossier to the UK's Medicines and Healthcare products Regulatory Agency (MHRA), and the resumption of the Early Access Program in France through continued engagement with the French agency ANSM. On the manufacturing side, efforts will focus on successfully completing the technology transfer initiated at the end of 2024, optimizing LUMEVOQ ® production yields, and finalizing the quality control plan. In parallel, the Company will continue to explore strategic options through discussions already underway. The results of the vote by resolution and the videocast of the Annual General Meeting will be available on the Company's website in the Investors section ( About GenSight Biologics GenSight Biologics S.A. is a clinical-stage biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders. GenSight Biologics' pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence (MTS) and optogenetics, to help preserve or restore vision in patients suffering from blinding retinal diseases. GenSight Biologics' lead product candidate, GS010 (lenadogene nolparvovec) is in Phase III in Leber Hereditary Optic Neuropathy (LHON), a rare mitochondrial disease that leads to irreversible blindness in teens and young adults. Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to each eye by intravitreal injection to offer patients a sustainable functional visual recovery.
Yahoo
23-04-2025
- Business
- Yahoo
GenSight Biologics Annual General Meeting on May 13, 2025
Procedures for obtaining preparatory documents for the General Meeting PARIS, April 23, 2025--(BUSINESS WIRE)--Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders, announced that it will hold its Annual General Meeting on May 13, 2025, at 2:00 pm CEST at the Company's headquarters, 74 rue du Faubourg Saint-Antoine, 75012 Paris, France. The General Meeting will also be webcast live for shareholders on at the following link: The notice containing the agenda and draft resolutions was published in the French BALO on April 7, 2025. The notice confirming the time and place of the meeting was published in the French BALO and in a legal gazette on April 23, 2025. The preparatory documents for the General Meeting listed in Article R. 22-10-23 of the French Commercial Code are posted on the Company's website ( in the Investors, Documentation section. The preparatory documents for the General Meeting will also be made available to shareholders as of the convening of the meeting. It is specified that the full text of the documents intended to be presented to the Meeting, in accordance in particular with Articles L. 225-115 and R. 225-83 of the Commercial Code, are made available at the Company's headquarters. From the date of the convocation and until the fifth day inclusive before the meeting, any shareholder may ask the Company to send him the documents and information mentioned in Articles R. 225-81 and R. 225-83 of the Commercial Code, preferably by email to the following address: investor_relations@ Bearer shareholders must justify this status by sending an account registration certificate. About GenSight Biologics GenSight Biologics S.A. is a clinical-stage biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders. GenSight Biologics' pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence (MTS) and optogenetics, to help preserve or restore vision in patients suffering from blinding retinal diseases. GenSight Biologics' lead product candidate, GS010 (lenadogene nolparvovec) is in Phase III in Leber Hereditary Optic Neuropathy (LHON), a rare mitochondrial disease that leads to irreversible blindness in teens and young adults. Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to each eye by intravitreal injection to offer patients a sustainable functional visual recovery. View source version on Contacts GenSight Biologics Chief Financial OfficerJan Eryk Umiastowskijeumiastowski@ Sign in to access your portfolio
Associated Press
17-03-2025
- Business
- Associated Press
GenSight Biologics Announces LUMEVOQ® Scientific Updates at NANOS 2025
Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on discovering and developing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders, today announced that new scientific data and analyses on the gene therapy LUMEVOQ ® will be presented at the 51 st Annual Meeting of the North American Neuro-Ophthalmology Society (NANOS) in Tucson, Arizona, USA (March 15-20, 2025). Leading Leber Hereditary Optic Neuropathy (LHON) Key Opinion Leaders will share new data on predictive factors of response to LUMEVOQ ® treatment; on a comparison of the treatment outcomes from idebenone and LUMEVOQ ®; on real-world experience with LUMEVOQ ®; and on long-term outcomes from bilateral treatment with the gene therapy. Poster presentation: ' Predictive Factors of Improved Final Visual Outcome in Patients with Leber Hereditary Optic Neuropathy Treated with Lenadogene Nolparvovec Gene Therapy' Presenter: Robert C. Sergott, MD, Wills Eye Hospital, Philadelphia, USA Poster Number 209 Time: Monday, March 17th, 2025, 5:00 pm – 6:00 pm (MDT) Location: Arizona Ballroom 1-6 Poster presentation: 'Efficacy of Lenadogene Nolparvovec Gene Therapy Versus Idebenone: Two Matched Adjusted Indirect Comparisons' Presenter: Patrick Yu-Wai-Man, MD, PhD, University of Cambridge, Moorfields Eye Hospital, and the UCL Institute of Ophthalmology, UK Poster Number 186 Time: Monday, March 17th, 2025, 6:00 pm – 7:00 pm (MDT) Location: Arizona Ballroom 1-6 Poster presentation: ' Efficacy and Safety of Lenadogene Nolparvovec Gene Therapy for Leber Hereditary Optic Neuropathy in the Real-Life Setting ' Presenter: Mark L. Moster, MD, Wills Eye Hospital, Philadelphia, USA Poster Number 12 Time: Sunday, March 16th, 2025, 2:00 pm – 3:00 pm (MDT) Location: Arizona Ballroom 1-6 Platform presentation: 'Long-Term Outcomes of Bilateral Injection of Lenadogene Nolparvovec Gene Therapy for Leber Hereditary Optic Neuropathy' Presenter: Nancy J. Newman, MD, Emory University School of Medicine, Atlanta, USA Scientific Platform Session I Time: Monday, March 17th, 2025, 11:45 am – 12:00 pm (MDT) Location: Tucson Ballroom About GenSight Biologics GenSight Biologics S.A. is a clinical-stage biopharma company focused on discovering and developing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders. GenSight Biologics' pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence (MTS) and optogenetics, to help preserve or restore vision in patients suffering from blinding retinal diseases. GenSight Biologics' lead product candidate, GS010, is in Phase III trials in Leber Hereditary Optic Neuropathy (LHON), a rare mitochondrial disease that leads to irreversible blindness in teens and young adults. Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to each eye by intravitreal injection to offer patients a sustainable functional visual recovery. About Leber Hereditary Optic Neuropathy (LHON) Leber Hereditary Optic Neuropathy (LHON) is a rare maternally inherited mitochondrial genetic disease, characterized by the degeneration of retinal ganglion cells that results in brutal and irreversible vision loss that can lead to legal blindness, and mainly affects adolescents and young adults. LHON is associated with painless, sudden loss of central vision in the 1 st eye, with the 2 nd eye sequentially impaired. It is a symmetric disease with poor functional visual recovery. 97% of subjects have bilateral involvement at less than one year of onset of vision loss, and in 25% of cases, vision loss occurs in both eyes simultaneously. About LUMEVOQ ® (GS010; lenadogene nolparvovec) LUMEVOQ ® (GS010; lenadogene nolparvovec) targets Leber Hereditary Optic Neuropathy (LHON) by leveraging a mitochondrial targeting sequence (MTS) proprietary technology platform, arising from research conducted at the Institut de la Vision in Paris, which, when associated with the gene of interest, allows the platform to specifically address defects inside the mitochondria using an AAV vector (Adeno-Associated Virus). The gene of interest is transferred into the cell to be expressed and produces the functional protein, which will then be shuttled to the mitochondria through specific nucleotidic sequences in order to restore the missing or deficient mitochondrial function. 'LUMEVOQ' was accepted as the invented name for GS010 (lenadogene nolparvovec) by the European Medicines Agency (EMA) in October 2018. LUMEVOQ ® (GS010; lenadogene nolparvovec) has not been registered in any country at this stage. Chief Financial Officer Jan Eryk Umiastowski [email protected] Advisors Investor Relations Guillaume van Renterghem +41 (0)76 735 01 31 SOURCE: GenSight Biologics Copyright Business Wire 2025. PUB: 03/17/2025 02:30 AM/DISC: 03/17/2025 02:29 AM
Yahoo
17-03-2025
- Business
- Yahoo
GenSight Biologics Announces LUMEVOQ® Scientific Updates at NANOS 2025
PARIS, March 17, 2025--(BUSINESS WIRE)--Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on discovering and developing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders, today announced that new scientific data and analyses on the gene therapy LUMEVOQ® will be presented at the 51st Annual Meeting of the North American Neuro-Ophthalmology Society (NANOS) in Tucson, Arizona, USA (March 15-20, 2025). Leading Leber Hereditary Optic Neuropathy (LHON) Key Opinion Leaders will share new data on predictive factors of response to LUMEVOQ® treatment; on a comparison of the treatment outcomes from idebenone and LUMEVOQ®; on real-world experience with LUMEVOQ®; and on long-term outcomes from bilateral treatment with the gene therapy. Poster presentation: "Predictive Factors of Improved Final Visual Outcome in Patients with Leber Hereditary Optic Neuropathy Treated with Lenadogene Nolparvovec Gene Therapy" Presenter: Robert C. Sergott, MD, Wills Eye Hospital, Philadelphia, USA Poster Number 209 Time: Monday, March 17th, 2025, 5:00 pm – 6:00 pm (MDT) Location: Arizona Ballroom 1-6 Poster presentation: "Efficacy of Lenadogene Nolparvovec Gene Therapy Versus Idebenone: Two Matched Adjusted Indirect Comparisons" Presenter: Patrick Yu-Wai-Man, MD, PhD, University of Cambridge, Moorfields Eye Hospital, and the UCL Institute of Ophthalmology, UK Poster Number 186 Time: Monday, March 17th, 2025, 6:00 pm – 7:00 pm (MDT) Location: Arizona Ballroom 1-6 Poster presentation: "Efficacy and Safety of Lenadogene Nolparvovec Gene Therapy for Leber Hereditary Optic Neuropathy in the Real-Life Setting" Presenter: Mark L. Moster, MD, Wills Eye Hospital, Philadelphia, USA Poster Number 12 Time: Sunday, March 16th, 2025, 2:00 pm – 3:00 pm (MDT) Location: Arizona Ballroom 1-6 Platform presentation: "Long-Term Outcomes of Bilateral Injection of Lenadogene Nolparvovec Gene Therapy for Leber Hereditary Optic Neuropathy" Presenter: Nancy J. Newman, MD, Emory University School of Medicine, Atlanta, USA Scientific Platform Session I Time: Monday, March 17th, 2025, 11:45 am – 12:00 pm (MDT) Location: Tucson Ballroom About GenSight Biologics GenSight Biologics S.A. is a clinical-stage biopharma company focused on discovering and developing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders. GenSight Biologics' pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence (MTS) and optogenetics, to help preserve or restore vision in patients suffering from blinding retinal diseases. GenSight Biologics' lead product candidate, GS010, is in Phase III trials in Leber Hereditary Optic Neuropathy (LHON), a rare mitochondrial disease that leads to irreversible blindness in teens and young adults. Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to each eye by intravitreal injection to offer patients a sustainable functional visual recovery. About Leber Hereditary Optic Neuropathy (LHON) Leber Hereditary Optic Neuropathy (LHON) is a rare maternally inherited mitochondrial genetic disease, characterized by the degeneration of retinal ganglion cells that results in brutal and irreversible vision loss that can lead to legal blindness, and mainly affects adolescents and young adults. LHON is associated with painless, sudden loss of central vision in the 1st eye, with the 2nd eye sequentially impaired. It is a symmetric disease with poor functional visual recovery. 97% of subjects have bilateral involvement at less than one year of onset of vision loss, and in 25% of cases, vision loss occurs in both eyes simultaneously. About LUMEVOQ® (GS010; lenadogene nolparvovec) LUMEVOQ® (GS010; lenadogene nolparvovec) targets Leber Hereditary Optic Neuropathy (LHON) by leveraging a mitochondrial targeting sequence (MTS) proprietary technology platform, arising from research conducted at the Institut de la Vision in Paris, which, when associated with the gene of interest, allows the platform to specifically address defects inside the mitochondria using an AAV vector (Adeno-Associated Virus). The gene of interest is transferred into the cell to be expressed and produces the functional protein, which will then be shuttled to the mitochondria through specific nucleotidic sequences in order to restore the missing or deficient mitochondrial function. "LUMEVOQ" was accepted as the invented name for GS010 (lenadogene nolparvovec) by the European Medicines Agency (EMA) in October 2018. LUMEVOQ® (GS010; lenadogene nolparvovec) has not been registered in any country at this stage. View source version on Contacts GenSight Biologics Chief Financial OfficerJan Eryk Umiastowskijeumiastowski@ LifeSci Advisors Investor RelationsGuillaume van Renterghemgvanrenterghem@ +41 (0)76 735 01 31 Sign in to access your portfolio
Yahoo
07-03-2025
- Business
- Yahoo
GenSight Biologics Announces Financing Amounting to c. €0.9 Million from Existing Investors
PARIS, March 07, 2025--(BUSINESS WIRE)--Regulatory News: This press release is not being made in and copies of It may not be distributed or sent, directly or indirectly, into the United States, Canada, South Africa, Japan or Australia GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible) (the "Company"), a biopharma Company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders, announced today a new round of financing reserved to specialized investors and funded by the issuance of new shares with warrants attached, for a total gross amount of approximately €0.9 million (excluding the future net proceeds related to the exercise of the warrants) (the "Reserved Offering"). The subscription price for one ABSA is €0.2248 (the "Offering Price"). "This round of bridge financing, the third since the November submission of our dossier to ANSM to resume compassionate access (AAC) program in France, underscores the unwavering confidence of our long-standing investors in our innovative gene therapy program. Notwithstanding the extended time required to re-start the AAC, we remain steadfast in our mission." commented Jan Eryk Umiastowski, CFO of GenSight Biologics. "The support we have received, particularly the renewed commitment from our key stakeholders Bpifrance, Invus and Sofinnova, demonstrates the market's recognition of our potential. With the anticipated research tax credit and our projected cash runway post-AAC resumption, we are positioned to advance our critical therapeutic research and to progress on providing access to LUMEVOQ for patients." Business update The Company released its estimated annual results for 2024 on February 27, 2025, together with a business update1. Such estimated annual results for 2024 show, in particular, that (i) operating income decreased by 11.4% to € 2.6 million in FY 2024, (ii) net loss was € 14.0 million in FY 2024 compared to a loss of € 26.2 million in FY 2023 and (iii) cash and cash equivalents totaled €2.5 million as of December 31, 2024, compared to €2.1 million as of December 31, 2023. Since its last financial communication on February 27, 2025, the Company submitted to the French medicines safety agency (ANSM - Agence Nationale de Sécurité des Médicaments et produits de santé) on March 5, 2025, its responses to the follow-up questions on the compassionate access dossier for LUMEVOQ® , which were received on February 17, 2025. The Company expects to obtain the resumption of the French Compassionate Access Program (AAC) for LUMEVOQ® in April 2025. Use of Proceeds The Company intends to use the net proceeds from the Reserved Offering to finance only its general corporate needs in connection with the delay the Company has experienced in the resumption of the early access program, now expected in April 2025. Working Capital Statement To date, without taking into account the net proceeds of the Reserved Offering, the Company does not have sufficient net working capital to meet its obligations over the next twelve months but only until early April 2025, with the approximately €1.1 million Research Tax Credit (CIR) expected to be collected in March. As of February 28, 2025, the Company's available cash and cash equivalents amounted to €0.7million. Before completion of the Reserved Offering and without taking into account the potential indemnities generated by the resumption of AAC, the Company estimates that (i) its net cash requirement for the next twelve months is approximately €36 million, and (ii) it will need to raise approximately €0.5 million to supplement its working capital requirements and fund its operating expenses until the first payments connected to the potential resumption of the early access in France (AAC), which is expected in April 2025. Taking into account the expected net proceeds of the Reserved Offering for €0.9 million and the collection of approximately €1.1 million Research Tax Credit (CIR), the Company does not have sufficient net working capital to meet its obligations over the next 12 months but only until early May 2025, when the first payments from the potentially resumed AAC program are expected. With the potential indemnities generated by the resumption of AAC and the net proceeds of the Reserved Offering, the Company anticipates that it would have sufficient net working capital to meet its obligations over the next 12 months. In November 2026, the Company will have to pay the annual rebates on the 2025 AAC program which will amount to around 40% of the AAC indemnities generated over the year. Consequently, the Company will need to seek other sources of debt or equity financing or realize partnering or M&A opportunities, in order to supplement its working capital requirements and fund its operating expenses before the second half of 2026. Even though the Company believes in its ability to achieve its manufacturing objectives, to raise additional funds or to realize partnership or M&A opportunities, no assurance can be given at this time as to whether the Company will be able to achieve these objectives or to obtain funds at attractive terms and conditions. Terms of the Reserved Offering The Reserved Offering, for a total of €860,839 (share issue premium included), was carried out through the issuance of 3,829,355 ABSA (as defined below) via a capital increase without shareholders' preferential subscription rights reserved to a category of persons satisfying predefined characteristics2, pursuant to Article L. 225-138 of the French Commercial Code and in accordance with the 23rd resolution of the Company's combined general shareholders' meeting held on May 29, 2024 (the "General meeting"), through the issuance of new shares at a per value of €0.025 (the "New Shares"), to which are attached one warrant for one new share (the "Warrants" and together with the New Shares, the "ABSA" and the new shares of the Company resulting from the exercise of the Warrants, the "Warrants Shares"). Among Eligible Investors, the Reserved Offering was opened exclusively (i) in the European Union (including France) to "qualified investors" within the meaning of Article 2(e) of Regulation (EU) 2017/1129 of the European Parliament and of the Council of June 14, 2017, as amended (the "Prospectus Regulation") and (ii) outside the European Union to certain institutional and qualified investors on a private placement basis. The ABSA will be issued and the price per ABSA determined by the decision of the Chief Executive Officer of the Company dated March 6, 2025, pursuant to and within the limits of the sub-delegation of authority granted by the Company's Board of Directors held on February 26, 2025 and in accordance with the 23rd and 29th resolutions of the General Meeting, it being specified that, in accordance with Article L. 225-38 of the French Commercial Code and in application of the provisions of the Board of Directors' internal rules relating to conflicts of interest, Sofinnova Partners took no part in the deliberations nor in the vote relating to this decision. The Offering Price is €0.2248, equal the volume-weighted average price of the Company's shares on Euronext Paris during the last five trading sessions preceding its setting (i.e., February 28, March 3, 4, 5 and 6, 2025) (the "Reference Price") plus a premium of 0.6%. Taking into account the estimated theoretical value of 100% of a Warrant (i.e., €0.0417, the value of which was obtained using the Black & Scholes method with a volatility of 31%), this would represent a discount of 18.04% compared with the Reference Price, in accordance with the 23rd resolution of the General Meeting. Upon settlement of the Reserved Offering, the Warrants will be exercisable from December 31, 2025 until November 6, 2029. In no event, the Warrants will be exercisable before December 31, 2025. The exercise of a Warrant will give the right to subscribe to one (1) Warrant Share (the "Exercise Ratio"), it being specified that this Exercise Ratio may be adjusted following any transactions carried out by the Company on its share capital or reserves, as from the issuance date of the Warrants, in order to maintain the rights of the Warrants' holders. The exercise price of the Warrants will be equal to €0.2248, i.e., a premium of 0.6% to the Reference Price, payable at the time of exercise of the Warrants. Admission to Trading of the New Shares Settlement delivery of the Reserved Offering and the admission of the New Shares for trading on the regulated market of Euronext Paris are expected on March 12, 2025. The New Shares will be immediately fungible with the existing shares of the Company and will be traded on the same listing line under the ISIN Code FR0013183985. Application will be made for the Warrants to be admitted to Euroclear France. The Warrants will be detached from New Shares, and no application will be made for their admission on Euronext Paris. The Warrants Shares will be subject to periodic application for admission to trading until three business days following the Exercise Period, i.e., November 9, 2029 at the latest. Impact of the Reserved Offering on the share capital Following the settlement and delivery of the Reserved Offering, expected to occur on March 12, 2025, the Company's total share capital will be equal to €3,215,095 divided into 128,603,800 shares. For illustration purposes, the impact of the issuance of the New Shares and the Warrant Shares on the ownership of a shareholder holding 1% of the Company's share capital prior to the Reserved Offering and not subscribing to it, is as follows: Ownership interest (in %) On a non-diluted basis On a diluted basis(1) Prior to the issue of 3,829,355 New Shares 1.00% 0.64% Following the issue of 3,829,355 New Shares 0.97% 0.62% Following the issue of 3,829,355 New Shares and 3,829,355 Warrants Shares from the exercise of all the Warrants 0.94% 0.62% (1) The calculations are based on the assumption of the exercise of all the share warrants, founders share warrants, free shares and stock options outstanding at the date hereof, giving access to a maximum of 73,202,953 shares Impact of the Reserved Offering on Shareholders' Equity For illustration purposes, the impact of the issuance of the New Shares and the Warrant Shares on the Company's equity per share (calculation made on the basis of the Company's shareholders' equity at December 31, 2024) is as follows: Share of equity per share (in euros) On a non-diluted basis On a diluted basis(1) Prior to the issue of 3,829,355 New Shares -0.22 0.02 Following the issue of 3,829,355 New Shares -0.20 0.02 Following the issue of 3,829,355 New Shares and 3,829,355 Warrants Shares from the exercise of all the Warrants -0.19 0.02 (1) The calculations are based on the assumption of the exercise of all the share warrants, founders share warrants, free shares and stock options outstanding at the date hereof, giving access to a maximum of 73,202,953 shares Evolution of the Shareholding Structure following the Reserved Offering To the Company's knowledge, the breakdown in share ownership before and after the Reserved Offering is as follows: The shareholding structure of the Company before the Reserved Offering: Shareholders Shareholders (non-diluted) Shareholders (diluted) Number of shares and voting rights % of share capital and voting rights Number of shares and voting rights % of share capital and voting rights 5% Shareholders Sofinnova 29,023,594 23.26% 39,562,461 20.38% Invus 10,749,774 8.62% 21,730,085 11.19% UPMC 10,158,364 8.14% 12,487,477 6.43% ARMISTICE 2,647,122 2.12% 8,976,235 4.62% Heights 10,484,910 8.40% 47,177,226 24.30% Bpifrance 1,209,191 0.97% 1,209,191 0.62% Goldman Sachs Group, Inc 6,360,453 5.10% 6,360,453 3.28% Directors and Officers 167,002 0.13% 2,392,002 1.23% Employees 80,000 0.06% 548,000 0.28% Other shareholders (total) 53,894,035 43.20% 53,704,913 27.66% Total 124,774,445 100.00% 194,148,043 100.00% The shareholding structure of the Company following the settlement of the Reserved Offering: Shareholders Shareholders (non-diluted) Shareholders (diluted) Number of shares and voting rights % of share capital and voting rights Number of shares and voting rights % of share capital and voting rights 5% Shareholders Sofinnova 29,913,274 23.26% 41,341,821 20.49% Invus 12,799,774 9.95% 25,830,085 12.80% UPMC 10,158,364 7.90% 12,487,477 6.19% ARMISTICE 2,647,122 2.06% 8,976,235 4.45% Heights 10,484,910 8.15% 47,177,226 23.38% Bpifrance 2,098,866 1.63% 2,988,541 1.48% Goldman Sachs Group, Inc 6,360,453 4.95% 6,360,453 3.15% Directors and Officers 167,002 0.13% 2,392,002 1.18% Employees 80,000 0.06% 548,000 0.27% Other shareholders (total) 53,894,035 41.91% 53,704,913 26.61% Total 128,603,800 100.00% 201,806,753 100.00% The shareholding structure of the Company following the settlement of the Reserved Offering and the exercise of all the Warrants: Shareholders Shareholders (non-diluted) Shareholders (diluted) Number of shares and voting rights % of share capital and voting rights Number of shares and voting rights % of share capital and voting rights 5% Shareholders Sofinnova 30,802,954 23.26% 41,341,821 20.49% Invus 14,849,774 11.21% 25,830,085 12.80% UPMC 10,158,364 7.67% 12,487,477 6.19% ARMISTICE 2,647,122 2.00% 8,976,235 4.45% Heights 10,484,910 7.92% 47,177,226 23.38% Bpifrance 2,988,541 2.26% 2,988,541 1.48% Goldman Sachs Group, Inc 6,360,453 4.80% 6,360,453 3.15% Directors and Officers 167,002 0.12% 2,392,002 1.18% Employees 80,000 0.06% 548,000 0.27% Other shareholders (total) 53,894,035 40.70% 53,704,913 26.61% Total 132,433,155 100.00% 201,806,753 100,00% Sofinnova Partners, represented on the Company's Board of Directors and holding 23.26% of the share capital of the Company before the Reserved Offering, subscribes for 889,680 ABSA of the Company and will hold, after the completion of the Reserved Offering (excluding the exercise of the Warrants), 23.26% of the Company's share capital. After the exercise of all its Warrants, Sofinnova Partners will hold 23.26% of the Company's share capital. Invus holding 8.62% of the share capital of the Company before the Reserved Offering, subscribes for 2,050,000 ABSA of the Company and will hold, after the completion of the Reserved Offering (excluding the exercise of the Warrants), 9.95% of the Company's share capital. After the exercise of all its Warrants, Invus will hold 11.21% of the Company's share capital. Fonds Biothérapies Innovantes et Maladies Rares, managed by Bpifrance, holding 0.97% of the share capital of the Company before the Reserved Offering, subscribes for 889,675 ABSA of the Company and will hold, after the completion of the Reserved Offering (excluding the exercise of the Warrants), 1.63% of the Company's share capital. After the exercise of all its Warrants, Fonds Biothérapies Innovantes et Maladies Rares will hold 2.26% of the Company's share capital. No Prospectus The Reserved Offering is not subject to a prospectus requiring an approval from the French Financial Markets Authority (Autorité des Marchés Financiers, the "AMF") in accordance with Articles 1(4)(a) and 1(5)(a) and (b) of the Prospectus Regulation. Information available to the public and risk factors Detailed information regarding the Company, including its business, financial information, results, perspectives and related risk factors, is contained in the Company's 2023 Universal Registration Document filed with the AMF on April 17, 2024, under number D. 24-299 (the "2023 Universal Registration Document"), as amended by an amendment to the 2023 Universal Registration Document, which was filed with the AMF on May 7, 2024 (the "Amendment to the 2023 Universal Registration Document"). These documents, as well as other regulated information (including the half-year financial report of the Company for the six-month period ended June 30, 2024) and all of the Company's press releases (including the estimated full-year 2024 consolidated financial results press release), are available free of charge on the Company's website ( Attention is drawn to the risk factors related to the Company and its activities, presented in chapter 3 of its 2023 Universal Registration Document and in chapter 2 of the Amendment to the 2023 Universal Registration Document. About GenSight Biologics GenSight Biologics S.A. is a clinical-stage biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders. GenSight Biologics' pipeline leverages two core technology platforms, the Mitochondrial Targeting Sequence (MTS) and optogenetics, to help preserve or restore vision in patients suffering from blinding retinal diseases. GenSight Biologics' lead product candidate, LUMEVOQ® (GS010; lenadogene nolparvovec), is an investigational compound and has not been registered in any country at this stage, developed for the treatment of Leber Hereditary Optic Neuropathy (LHON), a rare mitochondrial disease affecting primarily teens and young adults that leads to irreversible blindness. Using its gene therapy-based approach, GenSight Biologics' product candidates are designed to be administered in a single treatment to each eye by intravitreal injection to offer patients a sustainable functional visual recovery. Disclaimer The distribution of this press release may be restricted by certain local laws. Recipients of this press release are required to inform themselves of any such restrictions and, if applicable, to observe them. This press release does not constitute an offer or a solicitation of an offer to purchase or subscribe for securities in France. This announcement is an advertisement and not a prospectus within the meaning of the Prospectus Regulation. Any decision to purchase securities must be made solely on the basis of publicly available information on the Company. In France, the Reserved Offering described above will be carried out exclusively within the framework of offering reserved in favor of a categories of beneficiaries as referred to in the 23rd resolution of the General Meeting. In respect of Member States of the European Economic Area (the "Member States"), no action has been or will be taken to permit a public offering of the securities requiring the publication of a prospectus in any of these Member States. Consequently, the securities can and will only be offered in any of the Member State (including France), to qualified investors as defined in Article 2(e) of the Prospectus Regulation. This document and the information contained herein do not constitute either an offer to sell or purchase, or the solicitation of an offer to sell or purchase, securities of the Company in any jurisdiction. No communication and no information in respect of the offering by the Company of its securities may be distributed to the public in any jurisdiction where registration or approval is required. No steps have been taken or will be taken in any jurisdiction where such steps would be required. The offering or subscription of securities may be subject to specific legal or regulatory restrictions in certain jurisdictions. This announcement does not, and shall not, in any circumstances, constitute a public offering nor an invitation to the public in connection with any offer. The distribution of this document may be restricted by law in certain jurisdictions. Persons into whose possession this document comes are required to inform themselves about and to observe any such restrictions. Not for release, directly or indirectly, in or into the United States, Canada, South Africa, Japan or Australia. This document (and the information contained herein) does not contain or constitute an offer of securities for sale, or solicitation of an offer to purchase securities, in the United States, Canada, South Africa, Japan or Australia or any other jurisdiction where such an offer or solicitation would be unlawful. The securities referred to herein have not been and will not be registered under the Securities Act, or under the securities laws of any state or other jurisdiction of the United States, and may not be offered or sold in the United States except pursuant to an exemption from, or in a transaction not subject to, the registration requirements of the Securities Act and in compliance with the securities laws of any state or any other jurisdiction of the United States. No public offering of the securities will be made in the United States. 1 2 (i) Natural or legal persons (including companies), investment companies, trusts, investment funds or other investment vehicles in whatever form, whether under French or foreign law, investing on a regular basis in the pharmaceutical, biotechnological, ophthalmological, neurodegenerative diseases or medical technologies sectors; and/or (ii) French or foreign companies, institutions or entities, whatever their form, exercising a significant part of their activity in these fields (such investors, being "Eligible Investors"). View source version on Contacts GenSight Biologics Chief Financial Officer Jan Eryk Umiastowskijeumiastowski@ LifeSci Advisors Investor Relations Guillaume van Renterghem gvanrenterghem@ +41 (0)76 735 01 31 Sign in to access your portfolio
