TuisCVM ā¢ NYSEAMERICAN
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CEL-SCI Corp
Vorige sluiting
$0,62
Dagwisseling
$0,60 - $0,62
Jaarwisseling
$0,54 - $3,23
Markkapitalisasie
35,46Ā m USD
Gemiddelde volume
426,03Ā k
P/V-verhouding
-
Dividend-opbrengs
-
Marknuus
.INX
0,29%
Finansieel
Inkomstestaat
Inkomste
Netto inkomste
(USD) | Jun. 2024info | J/J-verandering |
---|---|---|
Inkomste | ā | ā |
Bedryfskoste | 1,97Ā m | -19,84% |
Netto inkomste | -7,52Ā m | 10,17% |
Netto winsgrens | ā | ā |
Wins per aandeel | ā | ā |
EBITDA | -5,69Ā m | 20,98% |
Effektiewe belastingkoers | ā | ā |
Balansstaat
Totale bates
Totale aanspreeklikheid
(USD) | Jun. 2024info | J/J-verandering |
---|---|---|
Kontant en korttermynbeleggings | 435,78Ā k | -91,55% |
Totale bates | 24,07Ā m | -25,53% |
Totale aanspreeklikheid | 15,60Ā m | -11,03% |
Totale ekwiteit | 8,47Ā m | ā |
Uitstaande aandele | 61,49Ā m | ā |
Prys om te bespreek | 3,85 | ā |
Opbrengs op bates | -61,63% | ā |
Opbrengs op kapitaal | -70,15% | ā |
Kontantvloei
Netto kontantverandering
(USD) | Jun. 2024info | J/J-verandering |
---|---|---|
Netto inkomste | -7,52Ā m | 10,17% |
Kontant van bedrywe | -4,58Ā m | 19,19% |
Kontant van beleggings | -23,47Ā k | 88,08% |
Kontant van finansiering | -322,30Ā k | -133,87% |
Netto kontantverandering | -4,92Ā m | -0,27% |
Beskikbare kontantvloei | -1,94Ā m | 32,46% |
Meer oor
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
Gestig
Mrt. 1983
Hoofkwartier
Webwerf
Werknemers
43