Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.12M 1.05M 962K 1.8M 122M 1.84M 12.43M 4.86M 60.56M 4.8M 4.69M 209M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.12M 1.05M 962K 1.8M 122M 1.84M 12.43M 4.86M 60.56M 4.8M 4.69M 209M 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
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
+0.47%+6.53%+0.59%+14.33% 48.95B
+1.90%+24.70%+27.25%+9.47% 40.75B
-1.60%-1.15%+388.84%+603.70% 38.46B
-0.98%+2.28%+7.02%+45.34% 36.38B
+1.47%+5.82%+5.76%+43.52% 28.45B
-0.94%+0.05% - - 16.62B
+2.44%+10.76%+30.59%+129.56% 16.33B
-1.14%+6.52%-3.80%-29.33% 13.65B
+0.23%+4.05%+4.12%+9.94% 13.56B
Average -0.14%+5.79%+57.55%+103.32% 28.13B
Weighted average by Cap. +0.22%+6.92%+71.95%+122.80%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.82M -10.1M -9.27M -17.35M -1.18B -17.78M -120M -46.85M -584M -46.24M -45.24M -2.02B -
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