Valuation: NeuBase Therapeutics, Inc.

Market Cap 1.28M 1.11M 1.05M 957K 1.79M 122M 1.8M 12.55M 4.85M 62.19M 4.8M 4.69M 199M P/E 2023 *
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P/E 2024 * -
Enterprise Value 1.28M 1.11M 1.05M 957K 1.79M 122M 1.8M 12.55M 4.85M 62.19M 4.8M 4.69M 199M EV / Sales 2023 *
-
EV / Sales 2024 * -
Free-Float
86.62%
Yield 2023 *
-
Yield 2024 * -
3 years 0.29
Extreme 0.2902
1.1
5 years 0.29
Extreme 0.2902
70.8
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
9/14/23 A
Symetryx Corp.
SellCompany 282,445 11.9560%
9/7/23 A
Symetryx Corp.
SellCompany 207,075 8.7655%
9/1/23 A
Symetryx Corp.
BuyCompany 61,076 2.5854%
Change 5-day change 1-year change 3-year change Capi.($)
-0.58%-.--%-.--%-71.38% 1.39M
+1.23%+1.87%-0.15%+9.57% 45.91B
+0.23%+4.72%+44.32%+27.27% 44.25B
+0.52%-3.15%+349.53%+520.09% 41.99B
+1.55%+3.41%+6.40%+76.45% 39.58B
+1.75%-0.28%+12.42%+41.11% 31.08B
-0.20%+5.49%+23.57%+119.72% 17.21B
-3.49%-8.49% - - 16.27B
+2.92%+8.40%+22.46%+38.87% 14.96B
-2.45%+2.41%-3.16%-35.16% 13.42B
Average +0.15%+0.28%+50.60%+80.73% 26.47B
Weighted average by Cap. +0.58%+0.33%+72.35%+120.61%

Financials

2023 *2024 *
Net sales - -
Net income -12.32M -10.73M -10.15M -9.22M -17.23M -1.18B -17.32M -121M -46.76M -599M -46.27M -45.24M -1.92B -
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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