Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.12M 1.03M 950K 1.79M 123M 1.83M 12.32M 4.84M 60.23M 4.8M 4.69M 207M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.12M 1.03M 950K 1.79M 123M 1.83M 12.32M 4.84M 60.23M 4.8M 4.69M 207M 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
-1.29%-2.54%-0.35%+4.30% 49.7B
+3.90%-2.60%+384.79%+598.27% 38.09B
-1.70%+3.03%+11.77%+58.93% 35.29B
-2.01%-1.30%+30.02%-6.71% 35.13B
+0.06%+1.56%+4.41%+27.42% 27.22B
+0.46%-5.24% - - 16.14B
-0.04%+0.42%+70.80%+121.10% 15.36B
+1.12%+2.15%+16.24%+19.12% 13.89B
0.00%+0.73%+18.02%-30.96% 13.02B
Average -0.27%-0.57%+66.96%+98.93% 27.09B
Weighted average by Cap. -0.09%-0.64%+78.08%+119.96%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.77M -9.94M -9.16M -17.27M -1.19B -17.65M -119M -46.66M -581M -46.25M -45.23M -2B -
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