NeuBase Therapeutics, Inc. Share Price

Equities

O7P

US64132K2015

Biotechnology & Medical Research

Delayed Deutsche Boerse AG 11:33:16 13/05/2024 am IST 5-day change 1st Jan Change
0.3406 EUR -0.58% Intraday chart for NeuBase Therapeutics, Inc. -.--% -45.94%

Financials

Sales 2023 * - Sales 2024 * - Capitalization 12.78L 11.89L 11Cr
Net income 2023 * -1.2Cr -1.12Cr -100.21Cr Net income 2024 * - EV / Sales 2023 * -
Net cash position 2023 * - 0 0 Net cash position 2024 * - 0 0 EV / Sales 2024 * -
P/E ratio 2023 *
-
P/E ratio 2024 *
-
Employees 37
Yield 2023 *
-
Yield 2024 *
-
Free-Float 86.62%
More Fundamentals * Assessed data
Dynamic Chart
1 day-0.58%
1 month-7.75%
3 months-57.95%
6 months-51.34%
Current year-45.94%
More quotes
1 month
0.34
Extreme 0.3406
0.34
Current year
0.29
Extreme 0.2902
0.99
1 year
0.29
Extreme 0.2902
3.30
3 years
0.29
Extreme 0.2902
89.20
5 years
0.29
Extreme 0.2902
206.00
10 years
0.29
Extreme 0.2902
206.00
More quotes
Managers TitleAgeSince
Chief Executive Officer 54 10/22/10
Corporate Officer/Principal - -
Corporate Officer/Principal - 01/21/01
Members of the board TitleAgeSince
Chairman 56 12/19/12
Director/Board Member 63 12/19/12
Director/Board Member 57 11/21/11
More insiders
NeuBase Therapeutics, Inc. is a 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. It also focused on identifying and evaluating multiple indications for potential development.
More about the company