Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.14M 1.06M 966K 1.82M 123M 1.83M 12.83M 4.99M 62.81M 4.8M 4.69M 202M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.14M 1.06M 966K 1.82M 123M 1.83M 12.83M 4.99M 62.81M 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 - 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%-.--%-.--%-50.64% 1.39M
+4.16%+3.42%+49.37%+94.17% 74.16B
-0.37%-3.81%+19.75%+78.12% 57.39B
+1.63%-1.61%+3.83%+36.89% 47.64B
+0.50%+2.94%+344.62%+722.17% 44.29B
+3.05%-1.80%+28.78%+34.51% 42.5B
+1.00%-1.46%+5.17%+111.90% 40.71B
-0.54%+2.41%+9.31%+58.85% 30.97B
+1.56%+3.75%+31.34%+29.14% 28.53B
+0.76%-1.45%-7.44%-11.12% 24.34B
Average +1.12%-0.54%+48.47%+110.40% 39.05B
Weighted average by Cap. +1.55%-0.41%+58.06%+137.29%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.99M -10.24M -9.32M -17.54M -1.19B -17.67M -124M -48.12M -605M -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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