ValorQ4, 24Q1, 25Q2, 25Q3, 25Q4, 25Q1, 26Q2, 26TTMDespesas comerciais, gerais e administrativas1.64 M2.46 M2.38 M1.75 M2.33 M1.69 M1.56 M7.33 MPesquisa e desenvolvimento4.48 M4.43 M4.01 M3.74 M3.7 M3.68 M3.77 M14.89 MLucro operacional-6.12 M-6.89 M-6.39 M-5.49 M-6.03 M-5.37 M-5.33 M-22.22 MLucro não operacional, total185.48 K-9 5410-3 77160.94 K-12.85 K-22.26 K22.06 KDespesa com juros, líquida de juros capitalizados—170 K———88 K117 K—Receitas não operacionais, líquidas das despesas com juros00000-88 K-117 K-205 KReceitas/despesas incomuns185.48 K-9 5410-3 77160.94 K-12.85 K-22.26 K22.06 KLucro antes dos impostos-5.93 M-6.9 M-6.39 M-5.49 M-5.97 M-5.38 M-5.35 M-22.19 MParticipação no lucro————————Impostos————————Participação de minoritários————————Outras receitas/despesas após impostos135-1351 0462 059—-2 301-19.55 K—Lucro líquido antes das operações descontinuadas-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-5.47 M-22.7 MOperações descontinuadas————————Lucro líquido-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-5.47 M-22.7 MAjuste de diluição————————Dividendos de ações preferenciais————————Lucro líquido diluído disponível aos acionistas-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-5.47 M-22.7 MLucro básico por ação————————Lucro diluído por ação-2.72-3.3-2.4-1.360.67-0.68-0.67-2.04Número médio de ações básicas————————Ações diluídas1.8 M2.18 M2.82 M4.15 M4.06 M8.02 M8.14 M—EBITDA—-7.06 M-6.57 M-5.65 M-6.13 M-5.45 M-5.44 M-22.68 MEBIT—-7.06 M-6.57 M-5.66 M-6.16 M-5.46 M-5.44 M-22.72 MCusto da receita————————Outros componentes do custo————————Amortização e depreciação (fluxo de caixa)32 K8 0007 0007 00027 K5 0006 00045 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.