A1XEH4 Crossject SA

Crossject to report first-half 2024 financial results and host webcast on September 23, 2024

Crossject to report first-half 2024 financial results and host webcast on September 23, 2024

Dijon, France, 17 September, 2024 - Crossject (ISIN: FR0011716265; Euronext: ALCJ), a specialty pharma company developing medicines for emergency situations harnessing its award-winning needle-free auto-injector ZENEO®, will report its financial results for the six months ended June 30, 2024, as scheduled on Monday, September 23.

In addition, at 18:00 CET that day, CEO Patrick Alexandre will provide a commentary on the company’s strategic priorities during a webcast and be available for questions from the audience.

Marianne Svensson, Administrative & Finance Director, will also be present during the call. To register for the webcast, please use the following details:

A recording will be available after the event. The webcast will be held in French.

About Crossject

Crossject SA (Euronext: ALCJ; ) is an emerging specialty pharmaceuticals company developing medicines for emergency situations harnessing its award-winning needle-free auto-injector ZENEO® platform. Crossject is in advanced regulatory development for ZEPIZURE®, an epileptic rescue therapy, for which it has a $60 million contract* with the U.S. Biomedical Advanced Research and Development Authority (BARDA). The Company’s versatile ZENEO® platform is designed to enable patients or untrained caregivers to easily and instantly deliver a broad range of emergency medicines via intramuscular injection on bare skin or even through clothing. The Company’s other products in development include mainly solutions for allergic shocks and adrenal insufficiencies, as well as therapies and other emergency indications.

* Contract no: 75A50122C00031 with the Department of Health and Human Services; Administration for Strategic Preparedness and Response; Biomedical Research and Development Authority

For further information, please contact:

Investors

Natasha Drapeau

Cohesion Bureau

7





Media

Sophie Baumont

Cohesion Bureau

49

 

Attachment



EN
17/09/2024

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Crossject SA

 PRESS RELEASE

Information relative au nombre total de droits de vote et d’actions co...

Information relative au nombre total de droits de vote et d’actions composant le capital social Communiqué de Presse Dijon, le 20 novembre 2024  CROSSJECT (ISIN : FR0011716265 ; Mnémo : ALCJ), « specialty pharma » qui développe et commercialisera prochainement un portefeuille de médicaments dédiés aux situations d’urgence, publie conformément aux articles 223-16 du Règlement général de l’AMF et L.233-8 II du Code de commerce, le nombre total de droits de vote et d’actions composant son capital social au 31 octobre 2024. DateNombre d’actions Composant le capitalSocial (1)Nombre de droits d...

 PRESS RELEASE

Crossject’s ZENEO® Auto-Injector's usability further demonstrated in e...

Crossject’s ZENEO® Auto-Injector's usability further demonstrated in extreme HAZMAT conditions Crossject successfully completes a new U.S. summative human factors study to assess the usability of ZENEO® Midazolam, soon to be commercialized globally as ZEPIZURE®, under simulated chemical attack conditions.  Rigorous HAZMAT (Hazardous Materials) dry-run involved 75 participants, who deployed 375 ZENEO® Midazolam auto-injectors in challenging conditions, including while wearing protective suits, without any handling problem.Study underscores ZENEO® Midazolam’s usability in extreme, high-ri...

 PRESS RELEASE

Crossject annonce des progrès majeurs dans la fabrication de son trait...

Crossject annonce des progrès majeurs dans la fabrication de son traitement d’urgence ZEPIZURE®, pour la prise en charge des crises d’épilepsie, à l’approche du dépôt d’une demande d’autorisation d’utilisation d’urgence aux États-Unis. Le lot de produits annoncé en juillet a permis de recueillir davantage de données de stabilité, qui au premier trimestre 2025 soutiendront directement la stabilité requise de six  mois.Crossject prévoit de déposer une demande d’autorisation d’utilisation d’urgence (EUA) au début de l’année prochaine et anticipe une réponse positive de la FDA dans un délai cou...

 PRESS RELEASE

Crossject reports strong manufacturing progress with its epilepsy resc...

Crossject reports strong manufacturing progress with its epilepsy rescue therapy ZEPIZURE® ahead of filing U.S. Emergency Use Authorization Product batch announced in July yielded new regulatory stability data. These results will directly support the requested 6-month stability data in the first quarter of 2025Crossject expects to file for EUA early next year and to receive a positive FDA response shortly thereafterCrossject will manufacture additional product batches, including first commercial batches in early 2025, in anticipation of first BARDA deliveries later that year Dijon, Franc...

 PRESS RELEASE

Crossject : Information relative au nombre total de droits de vote et ...

Crossject : Information relative au nombre total de droits de vote et d'actions composant le capital social Communiqué de Presse Information relative au nombre total de droits de vote et d’actions composant le capital social Dijon, le 7 octobre 2024 CROSSJECT (ISIN : FR0011716265 ; Mnémo : ALCJ), « specialty pharma » qui développe et commercialisera prochainement un portefeuille de médicaments dédiés aux situations d’urgence, publie conformément aux articles 223-16 du Règlement général de l’AMF et L.233-8 II du Code de commerce, le nombre total de droits de vote et d’actions composant s...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch