BRIDGEWATER, N.J.--(BUSINESS WIRE)-- CorMedix Inc. (“CorMedix”) (NYSE Amex: CRMD), a pharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of Cardiorenal disease, today announced its results for the quarter ended June 30, 2010.
Second Quarter 2010 Highlights:
- Added to Russell Microcap® Index
- Dosed First Patient in Phase II Clinical Trial of CRMD001
- Additional United States Patent Issued for Neutrolin® (CRMD003) to Prevent Catheter Related Bloodstream Infections (“CRBI”) and Clotting in Hemodialysis Catheters
Financial Results for the Three and Six-Month Periods Ended June 30, 2010
The net loss for the three months ended June 30, 2010 was $1.2 million, or $0.10 per diluted share, compared to a net loss of $1.2 million, or $1.42 per diluted share, for the first quarter in 2009. The net loss remained flat over the comparable periods as an increase of $0.6 million in total operating expenses was offset by a decrease of $0.6 million in interest expense. The increase in total operating expenses ($1.2 million in the second quarter of 2010 compared to $0.6 million in the second quarter of 2009) consisted of an increase of $0.3 million in research and development (“R&D”) expense and an increase of $0.3 million in general and administrative (“G&A”) expense. The increase in R&D expense during the second quarter of 2010 compared to the second quarter of 2009 was attributable to clinical development costs associated with CorMedix’s Phase II clinical trial of CRMD001 (a proprietary formulation of deferiprone), which commenced in June 2010, higher manufacturing costs for CRMD003 (Neutrolin®) in connection with CorMedix’s preparation for an Investigational Device Exemption submission by the end of 2010 and stock-based compensation expense related to a portion of the options granted to employees in connection with CorMedix’s IPO in March 2010. The increase in G&A expense over the same periods was primarily due to higher stock-based compensation expense related to a portion of the options granted to employees and directors in connection with the IPO and the increased costs of operating as a publicly-traded company following the IPO. The decrease in interest expense ($0 in the second quarter of 2010 compared to $0.6 million in the second quarter of 2009) was attributable to the conversion of all of CorMedix’s outstanding notes upon the completion of the IPO.
The net loss for the six months ended June 30, 2010 was $8.0 million, or $1.20 per diluted share, compared to a net loss of $2.3 million, or $2.78 per diluted share, for the six months ended June 30, 2009. The increase in net loss was primarily attributable to increases of $3.6 million in total operating expenses and $2.0 million in interest expense for the first half of 2010 compared to the first half of 2009. The increase in total operating expenses consisted of a $3.2 million increase in R&D expense as a result of anti-dilution stock issuances to licensors in connection with the conversion of all our outstanding convertible debt upon the closing of the IPO, increased clinical development and manufacturing costs and stock-based compensation costs, as described above, and an increase in G&A expense of $0.6 million resulting from higher stock-based compensation expense and the increased costs of operating as a publicly-traded company following the IPO. The increase in interest expense of $2.0 million was due to the amortization and write-off of deferred financing costs and debt discounts upon the completion of the IPO and beneficial conversion charges related to the debt conversion in connection with the IPO.
At June 30, 2010, CorMedix had cash and cash equivalents of $10.6 million, as compared to $1.5 million at December 31, 2009. CorMedix believes its currently available cash and cash equivalents will be sufficient to meet its planned clinical development and operating requirements through the end of the first quarter of 2012. The increase in cash and cash equivalents was attributed to the completion of the $12.5 million IPO in March 2010, which provided proceeds to the Company of approximately $10.4 million, net of underwriting discounts, commissions and offering expenses of approximately $2.1 million.
Commenting on the quarter, John C. Houghton, CorMedix’s president and chief executive officer, remarked, “CorMedix has made significant progress during the second quarter of 2010. We are very pleased to have begun patient dosing in our Phase II study of CRMD001, as well as being added to the Russell Microcap® Index.”
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CORMEDIX INC. (A Development Stage Company)
CONDENSED STATEMENTS OF OPERATIONS (Unaudited) |
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For the Three Months Ended June 30, 2010 |
For the Three Months Ended June 30, 2009 |
For the Six Months Ended June 30, 2010 |
For the Six Months Ended June 30, 2009 |
Cumulative Period from July 28, 2006 (inception) Through June 30, 2010 |
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| OPERATING EXPENSES | |||||||||||||||
| Research and development | $ | 560,690 | $ | 291,189 | $ | 3,657,351 | $ | 524,033 | $ | 16,201,800 | |||||
| General and administrative | 617,775 | 341,438 | 1,264,618 | 746,767 | 6,040,810 | ||||||||||
| Total Operating Expenses | 1,178,465 | 632,627 | 4,921,969 | 1,270,800 | 22,242,610 | ||||||||||
| LOSS FROM OPERATIONS | (1,178,465 | ) | (632,627 | ) | (4,921,969 | ) | (1,270,800 | ) | (22,242,610 | ) | |||||
| OTHER INCOME (EXPENSE) | |||||||||||||||
| Interest income | 5,683 | 587 | 5,711 | 2,083 | 94,574 | ||||||||||
| Interest expense, including amortization and write-off of deferred financing costs and debt discounts | - | (562,287 | ) | (3,093,763 | ) | (1,076,011 | ) | (11,193,028 | ) | ||||||
| NET LOSS | $ | (1,172,782 | ) | $ | (1,194,327 | ) | $ | (8,010,021 | ) | $ | (2,344,728 | ) | $ | (33,341,064 | ) |
| NET LOSS PER SHARE – BASIC AND DILUTED | $ | (0.10 | ) | $ | (1.42 | ) | $ | (1.20 | ) | $ | (2.78 | ) | |||
| WEIGHTED AVERAGE SHARES OUTSTANDING – BASIC AND DILUTED | 11,408,288 |
842,149 |
6,676,840 | 842,149 | |||||||||||
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CONDENSED BALANCE SHEET INFORMATION: |
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| June 30, 2010
(Unaudited) |
*December 31, 2009 |
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| Assets | ||||||||
| Cash and cash equivalents | $ | 10,585,717 | $ | 1,505,179 | ||||
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Total Assets |
$ | 10,990,758 | $ | 2,225,652 | ||||
| Deficit accumulated during the development stage | $ | (33,341,064 | ) | $ | (25,331,043 | ) | ||
| Total Stockholders’ Equity (Deficiency) | $ | 9,819,583 | $ | (14,708,899 | ) | |||
*Condensed from audited financial statements
About CorMedix
CorMedix Inc. is a pharmaceutical company that seeks to in-license, develop and commercialize therapeutic products for the prevention and treatment of cardiac and renal dysfunction, also known as cardiorenal disease. CorMedix’s goal is to treat kidney disease by reducing the commonly associated cardiovascular and metabolic complications, in effect, treating the kidney to treat the heart. CorMedix currently has several product candidates in development, including its two most advanced product candidates: CRMD-003 (Neutrolin®) for the prevention of central venous catheter infection and clotting in hemodialysis; and CRMD-001 (a proprietary formulation of deferiprone) for the prevention of contrast-induced nephropathy in high-risk patients with chronic kidney disease. Please see www.cormedix.com for additional information.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to risks and uncertainties. All statements, other than statements of historical facts, regarding management’s expectations, beliefs, goals, plans or CorMedix’s prospects, future financial position, future revenues and projected costs should be considered forward-looking. Readers are cautioned that actual results may differ materially from projections or estimates due to a variety of important factors, including the outcome of clinical trials of CorMedix’s drug candidates and whether they demonstrate these candidates’ safety and effectiveness; the risks and uncertainties associated with: obtaining additional financing to support CorMedix’s research and development and clinical activities and operations; obtaining regulatory approvals to conduct clinical trials and to commercialize CorMedix’s drug candidates; CorMedix’s ability to enter into and maintain collaborations with third parties for its drug development programs; CorMedix’s dependence on its collaborations and its license relationships; achieving milestones under CorMedix’s collaborations; CorMedix’s dependence on preclinical and clinical investigators, preclinical and clinical research organizations, manufacturers and consultants; protecting the intellectual property developed by or licensed to CorMedix; and CorMedix’s ability to maintain listing on NYSE Amex. These and other risks are described in greater detail in CorMedix’s filings with the Securities and Exchange Commission. CorMedix may not actually achieve the goals or plans described in its forward-looking statements, and investors should not place undue reliance on these statements. CorMedix disclaims any intent or obligation to update any forward-looking statements as a result of developments occurring after the date of this press release.
CONTACT:
CorMedix Inc.
Brian Lenz, 908-517-9486
Chief Financial Officer
or
Investor Relations:
BPC Financial Marketing
John Baldissera, 800-368-1217
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