Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.11M 1.04M 950K 1.79M 122M 1.82M 12.15M 4.77M 60.82M 4.8M 4.69M 202M P/E 2023 *
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P/E 2024 * -
Enterprise Value 1.28M 1.11M 1.04M 950K 1.79M 122M 1.82M 12.15M 4.77M 60.82M 4.8M 4.69M 202M 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
+2.01%+2.92%+5.24%+18.03% 48.7B
+0.26%+2.93%+439.43%+533.80% 42.05B
-1.53%-2.25%+30.95%+7.15% 38.26B
+0.69%+2.40%+10.48%+63.05% 37.5B
+2.47%+2.63%+14.71%+48.37% 31.44B
-0.47%+1.16%+35.93%+126.09% 16.33B
+2.31%-0.49% - - 16.47B
+0.80%+3.29%+7.15%+19.89% 13.98B
-1.43%-2.63%+3.70%-36.38% 12.43B
Average +0.18%+0.76%+68.45%+97.50% 28.57B
Weighted average by Cap. +0.68%+0.94%+89.35%+122.02%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.69M -10.01M -9.16M -17.28M -1.17B -17.51M -117M -45.95M -586M -46.24M -45.24M -1.95B -
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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