Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.11M 1.05M 955K 1.79M 123M 1.8M 12.6M 4.86M 62.34M 4.8M 4.69M 201M P/E 2023 *
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P/E 2024 * -
Enterprise Value 1.28M 1.11M 1.05M 955K 1.79M 123M 1.8M 12.6M 4.86M 62.34M 4.8M 4.69M 201M EV / Sales 2023 *
-
EV / Sales 2024 * -
Free-Float
86.62%
Yield 2023 *
-
Yield 2024 * -
3 years 0.36
Extreme 0.36
1.51
5 years 0.36
Extreme 0.36
88
10 years 0.36
Extreme 0.36
257.8
Manager TitleAgeSince
Corporate Officer/Principal - 01/11/2021
Director TitleAgeSince
Director/Board Member 56 04/01/2025
Change 5-day change 1-year change 3-year change Capi.($)
-3.20%-.--% - - 1.39M
+0.11%+2.71%+0.44%+26.85% 46.28B
-1.12%+1.78%+42.30%+27.55% 43.85B
-3.04%-6.29%+338.56%+515.97% 40.93B
-0.74%+1.25%+4.92%+67.98% 39.89B
-0.50%+0.67%+10.29%+41.28% 29.5B
-0.46%+4.22%+22.81%+139.44% 17.09B
-0.97%-10.17% - - 15.55B
-0.57%+8.12%+22.19%+38.68% 15.22B
-3.14%+31.91%-11.79% - 14.05B
Average -1.36%+3.76%+53.72%+122.54% 29.15B
Weighted average by Cap. -1.10%+1.87%+68.04%+130.90%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.74M -10.14M -9.21M -17.25M -1.18B -17.33M -121M -46.88M -601M -46.27M -45.24M -1.93B -
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
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