BerandaCVM • NYSEAMERICAN
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CEL-SCI Corp
$2,38
Setelah Jam Perdagangan Normal:(3,36%)-0,080
$2,30
Tutup: 6 Jun, 19.12.42 GMT-4 · USD · NYSEAMERICAN · Pernyataan Penyangkalan
Tutup sebelumnya
$2,36
Rentang hari
$2,25 - $2,40
Rentang tahun
$1,98 - $66,60
Kapitalisasi pasar
12,22Â jt USD
Volume Rata-Rata
234,30Â rb
Rasio P/E
-
Hasil dividen
-
Berita pasar
Keuangan
Laporan Pendapatan
Pendapatan
Laba bersih
(USD) | Mar 2025info | Perubahan Y/Y |
---|---|---|
Pendapatan | — | — |
Biaya operasional | 2,38Â jt | -2,76% |
Laba bersih | -6,57Â jt | 9,28% |
Margin laba bersih | — | — |
Penghasilan per saham | — | — |
EBITDA | -5,42Â jt | 10,89% |
Tarif pajak efektif | — | — |
Neraca
Total aset
Total liabilitas
(USD) | Mar 2025info | Perubahan Y/Y |
---|---|---|
Investasi tunai jangka pdk | 1,93Â jt | -63,73% |
Total aset | 21,81Â jt | -27,43% |
Total liabilitas | 13,81Â jt | -12,28% |
Total ekuitas | 8,00 jt | — |
Saham yang beredar | 3,03 jt | — |
Harga terhadap nilai buku | 0,83 | — |
Tingkat pengembalian aset | -67,30% | — |
Tingkat pengembalian modal | -78,12% | — |
Arus Kas
Perubahan kas bersih
(USD) | Mar 2025info | Perubahan Y/Y |
---|---|---|
Laba bersih | -6,57Â jt | 9,28% |
Kas dari operasi | -4,37Â jt | 3,49% |
Kas dari investasi | 0,00 | — |
Kas dari pembiayaan | 1,68Â jt | -74,53% |
Perubahan kas bersih | -2,69Â jt | -230,08% |
Arus kas bebas | -2,22Â jt | -5,78% |
Tentang
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
Didirikan
Mar 1983
Kantor pusat
Situs
Karyawan
43