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Cash and cash equivalents of €12.3 million as of June 30, 2026, a 2.4-fold increase compared to December 31, 2025 (€5.1 million), following the €15 million capital increase completed in May. Shareholders’ equity returned to positive territory at €3.0 million (compared to −€4.9 million as of December 31, 2025), and adjusted net financial debt was more than halved to €7.8 million (from €17.4 million). BARDA revenue totaled €2.5 million (€6.6 million in H1 2025), as H1 2025 saw a concentration of v
The Executive Board is expanded to five members: Olivier Lacombe, Didier Morin and Lionel Seltz join Patrick Alexandre and Isabelle LiebschutzA leadership team covering the entire value chain: pharmaceutical development, industrial operations, quality and regulatory affairs, finance and corporateCROSSJECT US strengthens its regulatory leadership with the appointment of David Pudwill as Vice President, Regulatory & Scientific Affairs DIJON, FRANCE, September 25, 2026 – 07h30 (CEST) – CROSSJECT (I
CROSSJECT and BARDA have consolidated the clinical development plan for the pediatric indication of ZEPIZURE®, in alignment with the FDA guidance$4.7 million in additional, non-dilutive funding, to cover the planned activities — total BARDA funding for ZEPIZURE® development now $48.0 millionContract period of performance extended through June 21, 2030 The EUA pathway for the adult indication is unaffected: the scope, content and data package of the EUA dossier remain unchanged DIJON, France — Se
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