Valeur202020212022202320242025TTMFrais de vente, généraux et administratifs11.7 M13.09 M10.71 M9 M8.19 M8.92 M7.33 MRecherche et développement17.84 M23.11 M25.36 M22.47 M18.16 M15.89 M14.89 MRésultat d'exploitation-28.99 M-36.19 M-36.06 M-31.48 M-26.35 M-24.81 M-22.22 MTotal des produits hors exploitation-86.71 K1.02 M76.97 K-42.81 K177.68 K47.63 K22.06 KCharges d'intérêts, nettes des intérêts capitalisés1.2 M——675.42 K745.67 K649 K—Résultat hors exploitation, hors charges d'intérêts-1.33 M1.03 M-30.18 K-675.42 K-745.67 K-649 K-205 KRevenus/dépenses exceptionnels38.76 K-8 213107.15 K-42.81 K177.68 K47.63 K22.06 KRésultat avant impôts-30.26 M-35.17 M-35.99 M-31.52 M-26.17 M-24.76 M-22.19 MPart des actionnaires dans le résultat———————Impôts———————Intérêts ne donnant pas le contrôle / intérêts minoritaires———————Autres produits/charges après impôts——-54.47 K-15.29 K-4 873——Résultat net avant activités abandonnées-30.26 M-36.36 M-36.7 M-32.19 M-27.58 M-25.41 M-22.7 MActivités abandonnées———————Résultat net-30.26 M-36.36 M-36.7 M-32.19 M-27.58 M-25.41 M-22.7 MAjustement de dilution———————Dividendes privilégiés———————Résultat net dilué revenant aux actionnaires ordinaires-30.28 M-37.8 M-37.63 M-32.37 M-27.58 M-25.41 M-22.7 MBénéfice par action de base (BPA de base)—-27-26.1————Bénéfice par action dilué (BPA dilué)-24.69-27.9-26.1—-15.3-6.27-2.04Nombre moyen d'actions de base en circulation1.23 M1.36 M1.44 M————Nombre d'actions en circulation après dilution1.23 M1.36 M1.44 M—1.8 M4.06 M—EBITDA-28.83 M-36.9 M-35.17 M——-23.4 M-22.68 MEBIT-30.93 M-37.34 M-37.14 M——-25.46 M-22.72 MCoût des ventes———————Autres coûts des ventes———————Amortissements (flux de trésorerie)2.1 M447 K1.98 M2.11 M2.13 M2.06 M45 K
Cel-Sci Corporation Common Stock
Cel-Sci Corporation, is a biotechnology company that tests drugs for the treatment of cancer, autoimmune and infectious diseases through the research and development of immunotherapy products.
Cel-Sci's main product is the drug Multikine, an immunotherapeutic agent designed to fight cancer by stimulating the body's immune system. Multikine is currently in Phase III of Clinical Trials with the Food and Drug Administration. Multikine has also been referred to as Leukocyte Interleukin Injection. Multikine was in Phase II testing of patients with head and neck cancer in the early 2000s, in which it demonstrated tumor-reducing ability. In January 2007, the US cleared the Phase 3 trial and Multikine was designated as an orphan drug by the FDA for neoadjuvant therapy of patients with squamous cell carcinoma of the head and neck. A total of 928 patients were enrolled in the head and neck cancer drug trial at that time. Subsequently, in June 2021, the company announced that the study missed its primary endpoint.