Marinus Pharmaceuticals
Oct 31, 2017

Marinus Pharmaceuticals Provides Business Update and Reports Third Quarter 2017 Financial Results

RADNOR, Pa., Oct. 31, 2017 (GLOBE NEWSWIRE) -- Marinus Pharmaceuticals, Inc. (Nasdaq:MRNS) (the "Company"), a biopharmaceutical company dedicated to the development of innovative therapeutics to treat epilepsy and neuropsychiatric disorders, today provided a business update and reported its financial results for the quarter ended September 30, 2017.

"We achieved an important milestone this quarter as we announced successful results from our clinical study in children with CDKL5 deficiency disorder, a rare, genetic epilepsy with no approved therapies," said Christopher M. Cashman, Chief Executive Officer of Marinus Pharmaceuticals.  "On the heels of this data, we raised capital to advance the development of ganaxolone into CDKL5 patients and extend our cash runway.  With a strong balance sheet in place, we are focused on quality execution of our clinical studies in postpartum depression, which will inform our later stage clinical development plans for this important underserved patient population."

Clinical Programs Update

CDKL5 Deficiency Disorder (CDD)

Postpartum Depression (PPD)

Status Epilepticus (SE)

Financial Update

At September 30, 2017, the Company had cash, cash equivalents and investment balances of $62.9 million.  The Company believes that its cash, cash equivalents and investments as of September 30, 2017 are adequate to fund operations into 2020.

Research and development expenses decreased to $2.6 million and $9.0 million for the three and nine months ended September 30, 2017, respectively, as compared to $4.8 million and $17.6 million for the same periods in the prior year.  The decreases were primarily due to a decrease of $1.8 million and $9.3 million for the three- and nine-month periods ended September 30, respectively, associated with our drug-resistant focal onset seizures program, which discontinued in June 2016.  Additionally, we sold $0.4 million in state research and development tax credits which we used to offset research and development expenses.  The decrease was partially offset by an increase of $0.9 million for the nine-month period ended September 30, associated with our IV programs in PPD, for which a Phase 2 clinical trial was initiated in June 2017, and SE, for which we are initiating a Phase 2 clinical trial. 

General and administrative expenses were $1.6 million and $5.1 million for the three and nine months ended September 30, 2017 as compared to similar expense amounts of $1.5 million and $4.7 million for the same periods in the prior year.

Cash used in operating activities decreased to $14.3 million for the nine months ended September 30, 2017 compared to $18.7 million for the same period a year ago. The decrease was driven primarily by a decrease in our net loss of $8.5 million, partially offset by a decrease in the change in operating assets and liabilities of $4.1 million.  The net decrease in the change in operating assets and liabilities was primarily due to upfront payments for planned clinical trials in our IV program, payment of corporate insurance premiums and the timing of payment obligations related to our drug supply in 2016. 

Readers are referred to, and encouraged to read in its entirety, the Company's Quarterly Report on Form 10-Q for the quarter ended September 30, 2017 to be filed with the Securities and Exchange Commission, which includes further detail on the Company's business plans and operations, financial condition and results of operations.

About Marinus Pharmaceuticals

Marinus Pharmaceuticals, Inc. is a biopharmaceutical company dedicated to the development of ganaxolone, which offers a new mechanism of action, demonstrated efficacy and safety, and convenient dosing to improve the lives of patients suffering from epilepsy and neuropsychiatric disorders. Ganaxolone is a positive allosteric modulator of GABAA that acts on a well-characterized target in the brain known to have both anti-seizure and anti-anxiety effects. Ganaxolone is being developed in three different dose forms (IV, capsule and liquid) intended to maximize therapeutic reach to adult and pediatric patient populations in both acute and chronic care settings. Marinus is currently evaluating ganaxolone in women with postpartum depression and preparing to initiate studies in children with CDKL5 deficiency disorder and patients with status epilepticus, both of which are orphan indications. For more information visit www.marinuspharma.com. Please follow us on Twitter: @MarinusPharma.

Forward-Looking Statements

To the extent that statements contained in this press release are not descriptions of historical facts regarding Marinus, they are forward-looking statements reflecting the current beliefs and expectations of management made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.  Words such as "may", "will", "expect", "anticipate", "estimate", "intend", "believe", and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements.  Examples of forward-looking statements contained in this press release include, among others, statements regarding our interpretation of preclinical studies, development plans for our product candidate, including the development of dose forms, the clinical trial testing schedule and milestones, the ability to complete enrollment in our clinical trials, interpretation of scientific basis for ganaxolone use, timing for availability and release of data, the safety, potential efficacy and therapeutic potential of our product candidate and our expectation regarding the sufficiency of our working capital. Forward-looking statements in this release involve substantial risks and uncertainties that could cause our clinical development programs, future results, performance or achievements to differ significantly from those expressed or implied by the forward-looking statements.  Such risks and uncertainties include, among others, the uncertainties inherent in the conduct of future clinical trials, the timing of the clinical trials, enrollment in clinical trials, availability of data from ongoing clinical trials, expectations for regulatory approvals, the attainment of clinical trial results that will be supportive of regulatory approvals, and other matters, including the development of formulations of ganaxolone, and the availability or potential availability of alternative products or treatments for conditions targeted by the Company that could affect the availability or commercial potential of our drug candidates.  Marinus undertakes no obligation to update or revise any forward-looking statements.  For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to the business of the Company in general, see filings Marinus has made with the Securities and Exchange Commission.          
           
CONTACT:   
   Lisa M. Caperelli
   Executive Director, Investor & Strategic Relations
   Marinus Pharmaceuticals, Inc.
   484-801-4674
   lcaperelli@marinuspharma.com



Marinus Pharmaceuticals, Inc.
Selected Financial Data (in thousands, except share and per share amounts)
(unaudited)
   
  September 30,
2017
 December 31,
2016
     
   
ASSETS  
Cash and cash equivalents$37,530$26,178
Investments 25,373 3,922
Other assets 1,754 1,347
Total assets$64,657$31,447
LIABILITIES AND STOCKHOLDERS' EQUITY  
Total current liabilities$2,430$8,084
Notes payable, long-term portion  1,743
Other long term liabilities 127 141
  Total liabilities 2,557 9,968
  Total stockholders' equity 62,100 21,479
Total liabilities and stockholders' equity$64,657$31,447


              
  Three Months Ended September 30,  Nine Months Ended September 30,  
  2017  2016  2017  2016  
              
Expenses:             
Research and development $ 2,642  $ 4,840  $ 9,032  $ 17,593  
General and administrative   1,571    1,529    5,074    4,719  
Loss from operations   (4,213)   (6,369)   (14,106)   (22,312) 
Interest income   45    36    116    93  
Interest expense   (3)   (118)   (159)   (365) 
Other income (expense)   1    (13)   (11)   (44) 
Net loss $ (4,170) $ (6,464) $ (14,160) $ (22,628) 
Per share information:             
Net loss per share of common stock—basic and diluted $ (0.15) $ (0.33) $ (0.60) $ (1.16) 
Basic and diluted weighted average shares outstanding   28,666,656    19,509,220    23,531,745    19,494,424