GenSight Biologics secures a €35 million credit facility from the European Investment Bank to support the launch of LUMEVOQ® in Europe
Paris, France, November 4, 2022 7:30am CET – 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, today announced that it has entered into a €35 million credit facility agreement with the European Investment Bank (“EIB”), supported by the European Fund for Strategic Investment (EFSI).
The Company plans to use the facility toward the development of its pipeline in the field of gene therapy for the treatment of neurodegenerative retinal diseases and disorders of the central nervous system and, in particular, LUMEVOQ® until its possible marketing in Europe, planned for the end of 2023.
The €35 million facility is divided into three tranches: €8 million for the first tranche (“Tranche A”), €12 million for the second tranche (“Tranche B”) and €15 million for the third tranche (“Tranche C”). The disbursement of each tranches, including the first disbursement of Tranche A, is subject to certain conditions which, as of the date of this press release, remain to be satisfied.
The disbursement of Tranche A is subject to, among other things:
- the execution of a warrant agreement (see hereafter) to be entered into with the EIB, issue of the warrants relating to Tranche A
- the full repayment of the outstanding financing with Kreos, [1]
- the successful manufacturing of one engineering batch of LUMEVOQ® (condition satisfied on September 19, 2022), [2]
- the decision by the Company to launch the validation batches (PPQ) manufacturing campaign, and
- a cash injection of €10 million, in the form of equity, convertible bonds (to the extent that their repayment would be subordinated to the EIB’s debt under the terms of a subordination agreement to be concluded) or license revenues.
- the full drawdown of Tranche A,
- the issue of the warrants relating to Tranche B,
- the successful manufacturing campaign of several PPQ batches of LUMEVOQ®, and
- the submission of responses to the Day 120 List of Questions to the European Medicines Agency (EMA) (condition satisfied in October 2022),[3]
- the full drawdown of Tranche B,
- the issue of the warrants relating to Tranche C,
- a cash injection of at least €20 million (in addition to the aforementioned €10 million), in the form of equity, convertible bonds (to the extent that their repayment would be subordinated to the EIB’s debt under the terms of a subordination agreement to be concluded) or license revenues,
- the obtaining of EMA marketing authorization for LUMEVOQ® in Europe, and
- a condition related to early access for patients.