Edge Therapeutics, Inc. (NASDAQ:EDGE) Files An 8-K Results of Operations and Financial Condition

Edge Therapeutics, Inc. (NASDAQ:EDGE) Files An 8-K Results of Operations and Financial Condition
Item 2.02

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Results of Operations and Financial Condition

On February 21, 2019, Edge Therapeutics, Inc. issued a press release announcing its financial results for the full-year ended December 31, 2018. A copy of that press release and the financial schedules attached thereto is furnished herewith as Exhibit 99.1 to this Current Report on Form 8-K.

In accordance with General Instruction B.2 of Form 8-K, the information set forth in this Current Report on Form 8-K (including Exhibit 99.1) is deemed to be “furnished” and shall not be deemed to be “filed” for purposes of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). The information in this Item 2.02, as well as Exhibit 99.1, shall not be deemed incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Exchange Act regardless of any general incorporation language in such filing.

Item 9.01.

Financial Statements and Exhibits

Exhibit

Number

Description

99.1

Press release dated February 21, 2019 announcing financial results for the full-year ended December 31, 2018.

Edge Therapeutics, Inc. Exhibit
EX-99.1 2 ex99_1.htm EXHIBIT 99.1 Exhibit 99.1 Edge Therapeutics Announces Full Year 2018 Financial Results BERKELEY HEIGHTS,…
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About Edge Therapeutics, Inc. (NASDAQ:EDGE)

Edge Therapeutics, Inc. is a clinical-stage biotechnology company that discovers, develops and seeks to commercialize, hospital-based therapies capable of transforming treatment paradigms in the management of life-threatening neurological and other conditions. Edge is evaluating EG-1962, its lead product candidate, in the Phase 3 NEWTON 2 study in adult patients with aneurysmal subarachnoid hemorrhage (aSAH). This study will evaluate EG-1962’s ability to improve patient outcomes versus standard of care oral nimodipine after an aSAH resulting from a ruptured brain aneurysm. Edge’s product candidates utilize Precisa, a platform with a approach that seeks to enable targeted and sustained drug exposure at the site of injury, while potentially avoiding off-target side effects associated with systemic delivery. Edge is also using its Precisa development platform to develop additional product candidates targeting other acute, serious conditions where limited or no current therapies exist.

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