Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.14M 1.06M 957K 1.79M 122M 1.82M 12.72M 5.03M 63.59M 4.8M 4.69M 201M P/E 2023 *
-
P/E 2024 * -
Enterprise Value 1.28M 1.14M 1.06M 957K 1.79M 122M 1.82M 12.72M 5.03M 63.59M 4.8M 4.69M 201M 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
64.8
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%-.--%-.--%-45.50% 1.39M
-3.10%-3.43%+36.29%+67.69% 65.28B
+0.10%0.00%+9.79%+77.48% 54.57B
-0.05%+1.38%+9.51%+101.40% 53.59B
+0.58%+2.47%+26.23%+52.53% 45.03B
-2.32%-5.54%+15.14%+113.08% 42.17B
+0.77%-5.04%+221.85%+902.90% 39.42B
-0.74%-4.84%+14.53%+44.45% 32.71B
-2.70%-7.34%+23.17%+0.36% 24.01B
+1.21%+15.33%+60.48%+49.53% 26.5B
Average -0.68%+1.36%+41.70%+136.39% 38.33B
Weighted average by Cap. -0.78%+1.72%+43.34%+155.45%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -11.01M -10.19M -9.23M -17.27M -1.17B -17.55M -123M -48.5M -613M -46.23M -45.24M -1.94B -
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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