DeğerQ4, 24Q1, 25Q2, 25Q3, 25Q4, 25Q1, 26Q2, 26TTMSatış/genel/idari giderler1.64 M2.46 M2.38 M1.75 M2.33 M1.69 M1.56 M7.33 MAraştırma ve geliştirme4.48 M4.43 M4.01 M3.74 M3.7 M3.68 M3.77 M14.89 MFaaliyet karı-6.12 M-6.89 M-6.39 M-5.49 M-6.03 M-5.37 M-5.33 M-22.22 MFaaliyet Dışı Gelir, Toplam185.48 K-9 5410-3 77160.94 K-12.85 K-22.26 K22.06 KFaiz gideri (aktifleştirilmiş faizler düşüldükten sonra)—170 K———88 K117 K—Faaliyet Dışı Gelir (Faiz Giderleri Hariç)00000-88 K-117 K-205 KOlağandışı gelirler/giderler185.48 K-9 5410-3 77160.94 K-12.85 K-22.26 K22.06 KVergi öncesi kar-5.93 M-6.9 M-6.39 M-5.49 M-5.97 M-5.38 M-5.35 M-22.19 MKazançlardaki özsermayeler————————Vergiler————————Kontrol gücü olmayan/azınlık payı————————Vergi sonrası diğer gelirler/giderler135-1351 0462 059—-2 301-19.55 K—Durdurulan faaliyetler öncesi net kar-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-5.47 M-22.7 MDurdurulan faaliyetler————————Net kar-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-5.47 M-22.7 MSeyreltme ayarlaması————————İmtiyazlı temettüler————————Adi hisse senedi sahiplerine düşen seyreltilmiş net kar-6.77 M-7.07 M-6.57 M-5.66 M-6.1 M-5.47 M-5.47 M-22.7 MTemel hisse başına kazanç (Temel EPS)————————Seyreltilmiş hisse başına kazanç (Seyreltilmiş EPS)-2.72-3.3-2.4-1.360.67-0.68-0.67-2.04Dolaşımdaki ortalama adi hisse senedi sayısı————————Dolaşımdaki seyreltilmiş hisse senedi sayısı1.8 M2.18 M2.82 M4.15 M4.06 M8.02 M8.14 M—FAVÖK—-7.06 M-6.57 M-5.65 M-6.13 M-5.45 M-5.44 M-22.68 MFVÖK—-7.06 M-6.57 M-5.66 M-6.16 M-5.46 M-5.44 M-22.72 MGelir maliyeti————————Satılan malların diğer maliyeti————————Amortisman ve itfa (nakit akışı)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.