Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.14M 1.04M 949K 1.79M 121M 1.84M 12.51M 5M 63.95M 4.8M 4.69M 202M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.14M 1.04M 949K 1.79M 121M 1.84M 12.51M 5M 63.95M 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
62.4
10 years 0.29
Extreme 0.2902
206
Manager TitleAgeSince
Corporate Officer/Principal - 01/11/2021
Director TitleAgeSince
Director/Board Member 56 04/01/2025
Date Insider Type Main position Quantity % Market Cap. Importance
14/09/23
Symetryx Corp.
SellCompany 282,445 11.9560%
07/09/23
Symetryx Corp.
SellCompany 207,075 8.7655%
01/09/23
Symetryx Corp.
BuyCompany 61,076 2.5854%
Change 5-day change 1-year change 3-year change Capi.($)
-0.58%-.--%-.--%-43.23% 1.39M
+3.80%+8.10%+63.78%+77.70% 69.4B
+0.07%+1.39%+12.75%+75.17% 57.24B
+1.63%+4.93%+24.89%+104.31% 57.62B
+0.41%-3.70%+26.06%+34.32% 43.65B
+2.51%+4.22%+20.49%+110.71% 44.03B
-11.04%-6.63%+199.38%+701.67% 38.08B
+7.50%+13.58%+29.07%+64.46% 36.31B
+1.59%-4.04%+97.66%+79.95% 32.61B
-2.30%+7.01%+36.00%-4.99% 25.47B
Average +0.37%+2.10%+51.01%+120.01% 40.44B
Weighted average by Cap. +0.83%+3.12%+52.86%+132.58%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.98M -10.04M -9.14M -17.23M -1.16B -17.7M -121M -48.22M -616M -46.23M -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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