ValorQ4, 24Q1, 25Q2, 25Q3, 25Q4, 25Q1, 26TTMGastos comerciales, generales y administrativos1.64 M2.46 M2.38 M1.75 M2.33 M1.69 M8.15 MInvestigación y desarrollo4.48 M4.43 M4.01 M3.74 M3.7 M3.68 M15.13 MBeneficio operativo-6.12 M-6.89 M-6.39 M-5.49 M-6.03 M-5.37 M-23.29 MTotal de ingresos no operativos185.48 K-9 5410-3 77160.94 K-12.85 K44.31 KGastos por intereses, netos de intereses capitalizados—————88 K—Ingresos no operativos, una vez deducidos los gastos por intereses00000-88 K-88 KIngresos/gastos extraordinarios185.48 K-9 5410-3 77160.94 K-12.85 K44.31 KBeneficio antes de impuestos-5.93 M-6.9 M-6.39 M-5.49 M-5.97 M-5.38 M-23.24 MParticipación en los beneficios———————Impuestos———————Participación minoritaria———————Otros ingresos/gastos después de impuestos135-1351 046——-2 301—Beneficio neto antes de actividades interrumpidas-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-23.81 MOperaciones suspendidas———————Beneficio neto-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-23.81 MAjuste por dilución———————Dividendos de las acciones preferentes———————Beneficio neto diluido atribuible a los accionistas-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-23.81 MBeneficio básico por acción———————Beneficio por acción diluido-2.72-3.3-2.4-1.360.74-0.68-3.7Número medio de acciones ordinarias———————Acciones diluidas1.8 M2.18 M2.82 M4.15 M4.06 M8.02 M19.04 MEBITDA—-7.06 M-6.57 M-5.65 M-6.13 M-5.45 M-23.81 MEBIT—-7.06 M-6.57 M-5.66 M-6.16 M-5.46 M-23.85 MCosto de los ingresos———————Otros costes de producción———————Amortización y depreciación (flujo de caja)32 K8 0007 0007 00027 K5 00046 K
Cel-Sci Corporation
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.