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Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.11M 1.03M 966K 1.81M 121M 1.82M 12.24M 4.74M 59.35M 4.8M 4.69M 206M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.11M 1.03M 966K 1.81M 121M 1.82M 12.24M 4.74M 59.35M 4.8M 4.69M 206M EV / Sales 2023 *
-
EV / Sales 2024 * -
Free-Float
86.62%
Yield 2023 *
-
Yield 2024 * -
3 years 0.36
Extreme 0.36
3.16
5 years 0.36
Extreme 0.36
109
10 years 0.36
Extreme 0.36
257.8
Manager TitleAgeSince
Corporate Officer/Principal - 2021-10-31
Director TitleAgeSince
Director/Board Member 56 2025-01-03
Change 5-day change 1-year change 3-year change Capi.($)
-3.20%-.--% - - 1.39M
+1.44%+1.71%-10.63%-9.16% 43.13B
+3.31%+5.93%+308.19%+562.02% 34.65B
+2.84%+2.14%+6.87%+34.93% 30.03B
-1.70%-7.54%+8.51%-22.34% 28B
-1.90%-1.56%+11.62%+19.80% 24.45B
-0.14%+5.86% - - 14.34B
+0.68%-1.53%+52.04%+107.47% 13.14B
-0.57%-2.43%+5.18%+4.20% 12.53B
-0.26%+1.15%+100.27%+80.69% 12.25B
Average +0.05%+0.73%+60.26%+97.20% 23.61B
Weighted average by Cap. +0.77%+1.27%+65.22%+113.23%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.74M -9.95M -9.31M -17.46M -1.16B -17.57M -118M -45.73M -572M -46.23M -45.24M -1.99B -
Net Debt - -
Logo NeuBase Therapeutics, Inc.
NeuBase Therapeutics, Inc. is a United States-based preclinical-stage biotechnology company. It is developing a modular peptide-nucleic acid (PNA) antisense oligo (PATrOL) platform to address genetic diseases, with a single, cohesive approach. The Company’s programs are NT-0100 in HD, NT-0200 in myotonic dystrophy type 1 (DM1) and NT-0300 in KRAS-driven cancers. The NT-0100 program is a PATrOL-enabled therapeutic program being developed to target the mutant expansion in the HD DNA or RNA. The NT-0200 program is a PATrOL-enabled therapeutic program being developed to target the mutant expansion in the DM1 disease RNA. The NT-0300 program is a PATrOL-enabled therapeutic program being developed to target the mutated KRAS gene. It uses its platform to address diseases which have a genetic source, with an initial focus on gene silencing in DM1, Huntington’s disease (HD), and oncology and in gene editing applications.
Employees
37
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