Item 7.01 Regulation FD Disclosure.

On April 1, 2020, NeuBase Therapeutics, Inc. (the "Company"), updated its corporate presentation materials to include information from its webcasted conference call held on March 31, 2020 and the target milestones of its two lead programs utilizing its PATrOL™ platform: the NT0100 Program focused on the treatment of Huntington's Disease and the NT0200 Program focused on the treatment of Myotonic Dystrophy Type 1. A copy of the updated corporate presentation materials referred to in this Item 7.01 of Current Report on Form 8-K (this "Current Report") is furnished herewith as Exhibit 99.1 to this Current Report and incorporated herein by reference.


Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995

This Current Report contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act. These forward-looking statements include, among other things, statements regarding the Company's target milestones for its two lead programs. These views involve risks and uncertainties that are difficult to predict and, accordingly, our actual results may differ materially from the results discussed in our forward-looking statements.

Our forward-looking statements contained herein speak only as of the date of this Current Report. Factors or events that we cannot predict, including those described in the risk factors contained in our filings with the U.S. Securities and Exchange Commission, may cause our actual results to differ from those expressed in forward-looking statements. The Company may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements, and you should not place undue reliance on these forward-looking statements. Because such statements deal with future events and are based on the Company's current expectations, they are subject to various risks and uncertainties and actual results, performance or achievements of the Company could differ materially from those described in or implied by the statements in this Current Report, including: the Company's plans to develop and commercialize its product candidates; the Company's plans to commence clinical trials in Huntington's disease and myotonic dystrophy type 1 and to potentially expand the pipeline into other indications; the utility of the preclinical data generated in existing studies performed by the Company in determining the results of potential future clinical trials and of the potential benefits of the PATrOL™ platform technology; the timing of initiation of the Company's planned clinical trials; the timing of the availability of data from the Company's clinical trials; the timing of any planned investigational new drug application or new drug application; the Company's plans to research, develop and commercialize its current and potential future product candidates; the clinical utility, potential benefits and market acceptance of the Company's current and potential future product candidates; the Company's commercialization, marketing and manufacturing capabilities and strategy; global health conditions, including the impact of COVID-19; the Company's ability to protect its intellectual property position; and the requirement for additional capital to continue to advance these product candidates, which may not be available on favorable terms or at all, as well as those risk factors in our filings with the U.S. Securities and Exchange Commission. Except as otherwise required by law, the Company disclaims any intention or obligation to update or revise any forward-looking statements, which speak only as of the date hereof, whether as a result of new information, future events or circumstances or otherwise.

Item 9.01 Financial Statements and Exhibits.





(d) Exhibits



Exhibit No.   Description
  99.1          Corporate Presentation Materials.

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