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CEL-SCI Corp
0,60 $
Efter lukketid:(1,43 %)+0,0085
0,60 $
Lukket: 22. nov., 17.44.22 GMT-5 · USD · NYSEAMERICAN · Ansvarsfraskrivelse
Seneste lukkekurs
0,60 $
Dagsinterval
0,58 $ - 0,60 $
Årsinterval
0,54 $ - 3,23 $
Markedsværdi
36,91 mio. USD
Gns. volumen
424,90 t
P/E-værdi
-
Udbytteprocent
-
Markedsnyheder
Økonomi
Resultatopgørelse
Indtægt
Nettoindtægt
(USD) | jun. 2024info | År til år-ændring |
---|---|---|
Indtægt | — | — |
Driftsudgifter | 1,97 mio. | -19,84 % |
Nettoindtægt | -7,52 mio. | 10,17 % |
Overskudsgrad | — | — |
Earnings per share | — | — |
EBITDA | -5,69 mio. | 20,98 % |
Effektiv afgiftssats | — | — |
Årsbalance
Samlede aktiver
Samlede passiver
(USD) | jun. 2024info | År til år-ændring |
---|---|---|
Kontanter og korttidsinvesteringer | 435,78 t | -91,55 % |
Samlede aktiver | 24,07 mio. | -25,53 % |
Samlede passiver | 15,60 mio. | -11,03 % |
Samlet egenkapital | 8,47 mio. | — |
Shares outstanding | 61,49 mio. | — |
Kurs/indre værdi | 3,78 | — |
Afkast af aktiver | -61,63 % | — |
Afkast af kapital | -70,15 % | — |
Pengestrøm
Nettoændring i likviditet
(USD) | jun. 2024info | År til år-ændring |
---|---|---|
Nettoindtægt | -7,52 mio. | 10,17 % |
Pengestrøm fra drift | -4,58 mio. | 19,19 % |
Pengestrøm fra investering | -23,47 t | 88,08 % |
Pengestrøm fra finansiering | -322,30 t | -133,87 % |
Nettoændring i likviditet | -4,92 mio. | -0,27 % |
Fri pengestrøm | -1,94 mio. | 32,46 % |
Om
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
Grundlagt
mar. 1983
Hovedkvarter
Website
Ansatte
43