Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.15M 1.06M 960K 1.79M 122M 1.82M 12.67M 5.05M 63.68M 4.8M 4.69M 202M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.15M 1.06M 960K 1.79M 122M 1.82M 12.67M 5.05M 63.68M 4.8M 4.69M 202M EV / Sales 2023 *
-
EV / Sales 2024 * -
Free-Float
86.62%
Yield 2023 *
-
Yield 2024 * -
3 years 0.29
Extreme 0.2902
1.02
5 years 0.29
Extreme 0.2902
64.4
10 years 0.29
Extreme 0.2902
206
Manager TitleAgeSince
Corporate Officer/Principal - 2021-10-31
Director TitleAgeSince
Director/Board Member 56 2025-01-03
Date Insider Type Main position Quantity % Market Cap. Importance
9/14/23
Symetryx Corp.
SellCompany 282,445 11.9560%
9/7/23
Symetryx Corp.
SellCompany 207,075 8.7655%
9/1/23
Symetryx Corp.
BuyCompany 61,076 2.5854%
Change 5-day change 1-year change 3-year change Capi.($)
-0.58%-.--%-.--%-42.27% 1.39M
+0.65%-3.36%+36.98%+60.50% 63.48B
+1.76%+1.27%+11.82%+81.21% 54.55B
-0.94%+0.99%+10.45%+100.19% 53.59B
+2.76%+0.87%+27.92%+55.07% 44.75B
+2.00%-3.39%+17.83%+119.04% 41.62B
+1.34%-2.86%+224.43%+914.08% 39.91B
+0.64%-3.95%+11.15%+45.57% 32.47B
+29.06%+47.63%+107.12%+92.73% 26.7B
-2.55%-1.06%+22.42%-11.33% 23.36B
Average +3.34%-0.37%+47.01%+141.48% 38.04B
Weighted average by Cap. +2.80%+0.19%+47.96%+160.96%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -11.05M -10.22M -9.25M -17.29M -1.17B -17.5M -122M -48.65M -614M -46.22M -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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