Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.13M 1.06M 963K 1.82M 123M 1.83M 12.76M 4.96M 62.8M 4.8M 4.69M 202M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.13M 1.06M 963K 1.82M 123M 1.83M 12.76M 4.96M 62.8M 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
70.8
10 years 0.29
Extreme 0.2902
206
Manager TitleAgeSince
Corporate Officer/Principal - 31/10/2021
Director TitleAgeSince
Director/Board Member 56 03/01/2025
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%-.--%-.--%-50.64% 1.39M
+4.16%+3.42%+49.37%+94.17% 74.31B
+2.76%-1.16%+23.05%+83.03% 56.95B
+0.24%-1.37%+4.08%+37.22% 48.3B
-3.76%-0.93%+327.90%+691.25% 44.51B
-2.30%-4.06%+25.82%+31.42% 43.8B
+0.31%-1.15%+5.50%+112.56% 41.12B
-0.11%+2.30%+9.19%+58.68% 31.07B
+4.51%+8.43%+37.27%+34.97% 28.97B
-1.96%-3.38%-9.25%-12.85% 24.53B
Average +0.33%-0.60%+47.29%+107.98% 39.36B
Weighted average by Cap. +0.77%-0.50%+56.58%+134.21%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.94M -10.24M -9.28M -17.5M -1.19B -17.64M -123M -47.82M -605M -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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