BerandaCVM • NYSEAMERICAN
add
CEL-SCI Corp
$3,52
Setelah Jam Perdagangan Normal:(3,69%)+0,13
$3,65
Tutup: 12 Mar, 19.56.24 GMT-4 · USD · NYSEAMERICAN · Pernyataan Penyangkalan
Tutup sebelumnya
$3,70
Rentang hari
$3,52 - $3,96
Rentang tahun
$1,98 - $13,48
Kapitalisasi pasar
29,77Â jt USD
Volume Rata-Rata
51,44Â rb
Rasio P/E
-
Hasil dividen
-
Berita pasar
Keuangan
Laporan Laba Rugi
Pendapatan
Penghasilan bersih
| (USD) | Des 2025info | Perubahan Y/Y |
|---|---|---|
Pendapatan | — | — |
Biaya operasional | 1,69Â jt | -31,33% |
Penghasilan bersih | -5,47Â jt | 22,67% |
Margin laba bersih | — | — |
Penghasilan per saham | — | — |
EBITDA | -4,40Â jt | 25,33% |
Tarif pajak efektif | — | — |
Neraca
Total aset
Total liabilitas
| (USD) | Des 2025info | Perubahan Y/Y |
|---|---|---|
Investasi tunai jangka pdk | 6,28Â jt | 35,98% |
Total aset | 22,89Â jt | -10,91% |
Total liabilitas | 11,76Â jt | -18,31% |
Total ekuitas | 11,14 jt | — |
Saham yang beredar | 8,09 jt | — |
Harga terhadap nilai buku | 2,68 | — |
Tingkat pengembalian aset | -52,58% | — |
Tingkat pengembalian modal | -58,89% | — |
Arus Kas
Perubahan kas bersih
| (USD) | Des 2025info | Perubahan Y/Y |
|---|---|---|
Penghasilan bersih | -5,47Â jt | 22,67% |
Kas dari operasi | -4,02Â jt | 2,85% |
Kas dari investasi | — | — |
Kas dari pembiayaan | -653,77Â rb | -116,15% |
Perubahan kas bersih | -4,68Â jt | -3.669,11% |
Arus kas bebas | -2,16Â jt | -53,48% |
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