Breaking News Bar

Business News and Information

Edge Therapeutics Reports Second Quarter 2017 Financial Results and Continued Operational Progress

BERKELEY HEIGHTS, N.J., Aug. 01, 2017 (GLOBE NEWSWIRE) -- Edge Therapeutics, Inc. (Nasdaq:EDGE), a clinical-stage biotechnology company developing novel hospital-based therapies for the management of acute, life-threatening conditions, today announced financial and operational results for the quarter ended June 30, 2017, and recent corporate progress.

“During the second quarter, we further advanced development of EG-1962 on multiple fronts and achieved important pre-commercial and regulatory progress for EG-1962,” said Brian A. Leuthner, Edge’s President and Chief Executive Officer. “NEWTON 2, our Phase 3 clinical study designed to support potential registrations throughout the world for EG-1962 as a treatment for aneurysmal subarachnoid hemorrhage (aSAH) delivered via external ventricular drain, is ongoing. We look forward to the study’s pre-planned futility analysis in late-2017, top-line efficacy results from the interim analysis in the first quarter of 2018 and, if needed, top-line results from the full study in late-2018. We are also evaluating alternative routes of administration to expand the population of aSAH patients who may benefit from EG-1962. This includes our ongoing controlled study of EG-1962 delivered directly into the basal cisterns of the brain in good-grade patients with ruptured brain aneurysms. In addition, during the quarter, we initiated development activities for lumbar administration of EG-1962. There remains a significant unmet need to improve outcomes in patients with aSAH, and we look forward to receiving EG-1962 data in the coming quarters.”

Second Quarter and Recent Key Achievements

  • Received from the European Medicines Agency a product-specific pediatric waiver for EG-1962 across all subsets of the pediatric population, which removes the requirement for pediatric clinical studies to support a marketing authorization application for EG-1962 in Europe.
  • Signed a supply agreement with Oakwood Laboratories for the commercial manufacturing of EG-1962 for initial product launch and thereafter.
  • Initiated a preclinical study of lumbar administration of EG-1962 in order to explore alternative routes of administration for aSAH patients, as well as to investigate EG-1962’s potential to address other serious conditions with high unmet need and few available treatment options.
  • Secured $18 million in gross proceeds from a registered direct offering of common stock at a purchase price of $10.00 per share, a price that exceeded the closing price of Edge common stock on the date of the purchase agreement.

Financial Results

Cash Position: Cash, cash equivalents and marketable securities as of June 30, 2017 were $108.7 million, compared with $106.4 million as of December 31, 2016.

Research & Development (R&D) Expenses:  R&D expenses were $9.0 million in the second quarter of 2017, compared to $6.0 million in the second quarter of 2016. The increase in R&D expense was primarily due to an increase in external expenses related to EG-1962 clinical development, personnel-related costs related to the NEWTON 2 study and other R&D expenses.

General & Administrative (G&A) Expenses: G&A expenses were $4.2 million for the three months ended June 30, 2017, compared to $3.3 million in the comparable period in 2016. The increase in G&A expense was largely due to increases in legal and professional fees, personnel-related costs, and other expenses.

Net Loss: Net loss was $13.5 million for the second quarter ended June 30, 2017, compared to net loss of $9.4 million for the comparable period in 2016.

Conference Call Details

Edge will host a conference call and webcast today, Tuesday, August 1, 2017 at 8:30 a.m. EDT. Please dial (877) 388-5691, or (562) 350-0788 for international callers, and reference participant code 53280120 approximately 15 minutes prior to the call. A replay of the call may be accessed through August 15, 2017 on the investor section of Edge’s website or by dialing (855) 859-2056, or (404) 537-3406 for international callers, and referencing participant code 53280120. A live webcast of the conference call will be available on the investor relations section of Edge’s website at

About Edge Therapeutics, Inc.
Edge Therapeutics, Inc. is a clinical-stage biotechnology company that discovers, develops and seeks to commercialize novel, hospital-based therapies capable of transforming treatment paradigms for the management of acute, life-threatening neurological and other conditions. EG-1962, Edge’s lead product candidate, has the potential to fundamentally improve patient outcomes and transform the management of aneurysmal subarachnoid hemorrhage, which is bleeding around the brain due to a ruptured brain aneurysm. Edge is evaluating EG-1962 in two clinical studies: a pivotal Phase 3 NEWTON 2 study of EG-1962 delivered via external ventricular drain, and a study of direct intracisternal administration of EG-1962. For additional information about Edge, please visit

Forward-Looking Statements
This press release and any statements of representatives of Edge Therapeutics, Inc. related thereto that are not historical in nature contain, or may contain, among other things, certain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements may include, without limitation, statements with respect to Edge’s plans, objectives, projections, expectations and intentions and other statements identified by words such as “projects," "may," "will," "could," "would," "should," "believes," "expects," "anticipates," "estimates," “seeks,” "intends," "plans," "potential" or similar expressions, including statements with respect to the potential effects of its products, the design of NEWTON 2 potentially supporting registration for EG-1962 throughout the world, the pre-planned futility analysis in late-2017, top-line efficacy results from the interim analysis in the first quarter of 2018 and, if needed, top-line results from the full study in late-2018. These statements are based upon the current beliefs and expectations of Edge’s management and are subject to significant risks and uncertainties. Actual results may differ significantly from those set forth in the forward-looking statements. These forward-looking statements involve certain risks and uncertainties that are subject to change based on various risk factors (many of which are beyond Edge's control) as described under the heading "Risk Factors" in Edge’s filings with the United States Securities and Exchange Commission.

Statements of Operations and Comprehensive Loss
 Three Months Ended June 30, Six Months Ended June 30,
 2017  2016  2017  2016 
Operating expenses:       
Research and development expenses$8,975,304  $5,975,306  $16,564,800  $11,322,069 
General and administrative expenses 4,173,384   3,288,889   8,375,226   6,974,486 
Total operating expenses 13,148,688   9,264,195   24,940,026   18,296,555 
Loss from operations (13,148,688)  (9,264,195)  (24,940,026)  (18,296,555)
Other income (expense):           
Interest income 168,974   49,376   265,233   92,190 
Interest expense (524,768)  (161,310)  (999,909)  (342,174)
Net loss and comprehensive loss (13,504,482)  (9,376,129)  (25,674,702)  (18,546,539)
Loss per share basic and diluted$(0.44) $(0.33) $(0.86) $(0.64)
Weighted average common shares outstanding basic and diluted 30,403,419   28,828,449   29,704,898   28,820,678 

Balance Sheets
 June 30, 2017 December 31, 2016
Current assets:   
Cash and cash equivalents$108,714,544  $106,398,919 
Prepaid expenses and other current assets 636,939   954,581 
Total current assets 109,351,483   107,353,500 
Property and equipment, net 3,491,619   3,418,077 
Other assets 142,870   142,870 
Total assets$112,985,972  $110,914,447 
Current liabilities:     
Accounts payable$4,350,153  $3,471,032 
Accrued expenses 4,154,019   3,213,715 
Short term debt 3,086,296   - 
Total current liabilities 11,590,468   6,684,747 
Noncurrent liability:     
Long term debt 17,127,131   14,953,143 
Preferred stock, 5,000,000  shares authorized at June 30, 2017 and December 31, 2016, 0 outstanding -   - 
Common stock, $0.00033 par value, 75,000,000 shares authorized at June 30, 2017 and December 31, 2016,
30,829,264 shares and 28,918,516 shares issued and outstanding at June 30, 2017 and December 31, 2016, respectively
 10,386   9,756 
Additional paid-in capital 211,021,245   190,341,769 
Accumulated deficit (126,763,258)  (101,074,968)
Total stockholders' equity 84,268,373   89,276,557 
Total liabilities and stockholders' equity$112,985,972  $110,914,447 


Investor and Media Contact:
Gregory Gin
Edge Therapeutics, Inc.
Tel: 1-800-208-EDGE (3343)

Data & News supplied by
Stock quotes supplied by Barchart
Quotes delayed at least 20 minutes.
By accessing this page, you agree to the following
Privacy Policy and Terms and Conditions.
bottom clear