HeimCVM • NYSEAMERICAN
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CEL-SCI Corp
0,60 $
Eftir lokun(1,43%)+0,0085
0,60 $
Lokað: 22. nóv., 17:44:22 GMT-5 · USD · NYSEAMERICAN · Lagalegir fyrirvarar
Við síðustu lokun
0,60 $
Dagbil
0,58 $ - 0,60 $
Árabil
0,54 $ - 3,23 $
Markaðsvirði
36,91 m. USD
Meðalmagn
424,90 þ.
V/H-hlutf.
-
A/V-hlutfall
-
Viðskiptafréttir
Fjármál
Rekstrarreikningur
Tekjur
Nettótekjur
(USD) | jún. 2024info | Breyting á/á |
---|---|---|
Tekjur | — | — |
Rekstrarkostnaður | 1,97 m. | -19,84% |
Nettótekjur | -7,52 m. | 10,17% |
Hagnaðarhlutfall | — | — |
Hagnaður á hvern hlut | — | — |
EBITDA | -5,69 m. | 20,98% |
Virkt skatthlutfall | — | — |
Efnahagsreikningur
Heildareignir
Heildarskuldir
(USD) | jún. 2024info | Breyting á/á |
---|---|---|
Reiðufé og skammtímafjárfestingar | 435,78 þ. | -91,55% |
Heildareignir | 24,07 m. | -25,53% |
Heildarskuldir | 15,60 m. | -11,03% |
Eigið fé alls | 8,47 m. | — |
Útistandandi hlutabréf | 61,49 m. | — |
Eiginfjárgengi | 3,78 | — |
Arðsemi eigna | -61,63% | — |
Ávöxtun eigin fjár | -70,15% | — |
Peningaflæði
Breyting á handbæru fé
(USD) | jún. 2024info | Breyting á/á |
---|---|---|
Nettótekjur | -7,52 m. | 10,17% |
Handbært fé frá rekstri | -4,58 m. | 19,19% |
Reiðufé frá fjárfestingum | -23,47 þ. | 88,08% |
Reiðufé frá fjármögnun | -322,30 þ. | -133,87% |
Breyting á handbæru fé | -4,92 m. | -0,27% |
Frjálst peningaflæði | -1,94 m. | 32,46% |
Um
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. Wikipedia
Stofnsett
mar. 1983
Höfuðstöðvar
Vefsvæði
Starfsfólk
43