Agile Therapeutics Reports Second Quarter 2014 Financial Results
"The second quarter was an exciting time of growth and activity for Agile. We successfully completed our initial public offering in May, and now we are financially positioned to advance our lead product Twirla through the Phase 3 clinic," said
Second Quarter Financial Results
As of
For the second quarter of 2014,
Research and development expenses for both the second quarters of 2014 and 2013 were
General and administrative expenses for the second quarter of 2014 were
First Half Financial Results
For the six months ended
Research and development expenses for the six months ended
General and administrative expenses for the six months ended
Company Update
During the second quarter of 2014, the Company continued to advance its business in three key areas: initiating its confirmatory Phase 3 clinical trial of its product candidate Twirla, collaborating with Corium International (Corium), its third party manufacturer, to prepare clinical supply and plan the commercial scale up of manufacturing capabilities, and expanding its intellectual property portfolio.
The Company, in collaboration with Parexel International Corporation, its third party clinical research organization, made progress in the start-up of its confirmatory Phase 3 clinical trial, focusing on site selection and training activities. The Company also selected
The Company also continued to work closely with Corium to prepare clinical supply of its product candidate, Twirla, for the confirmatory Phase 3 clinical trial. The Company is currently planning the commercial scale up of manufacturing capabilities for Twirla, and is collaborating with Corium to continue the qualification and validation of equipment related to the expansion of Corium's commercial manufacturing capabilities. The Company expects to complete the validation and expansion by the end of 2016, in coordination with its planned commercialization activities. Corium is responsible for all aspects of Twirla manufacturing.
During the second quarter of 2014, the Company advanced its efforts to expand its intellectual property portfolio covering its Skinfusion® transdermal technology. In June, the Company announced that patent 8,747,888, a continuation of its prior patent 8,246,978, was issued in the U.S. and is intended to provide additional patent protection covering the transdermal contraceptive patch system for its product candidate Twirla. In July, the Company announced that it received a notice of allowance in the U.S. for additional claims covering dosing regimens using Twirla. The Company expects to list seven patents in the U.S.
About Agile
Forward Looking Statements
Certain information contained in this press release includes "forward-looking statements" related to the Company's projected cash position, timeline for its clinical trials, timeline for the qualification and validation of its commercial manufacturing process, and listing of patents in the U.S. FDA Orange Book. We may, in some cases use terms such as "predicts," "believes," "potential," "continue," "anticipates", "estimates," "expects," "plans," "intends," "may," "could," 'might," "will," "should" or other words that convey uncertainty of the future events or outcomes to identify these forward-looking statements. Our forward-looking statements are based on current expectations that involve risks, potential changes in circumstances, assumptions and uncertainties. Any or all of the forward-looking statements may turn out to be wrong, or be affected by inaccurate assumptions we might make
or by known or unknown risks and uncertainties. For example, our statements regarding our projected cash position could be affected by market factors, the inherent risks in our business, our ability to execute the Company's operational and budget plans, and unforeseen events in our clinical and manufacturing development plans; our statements about the timing and conduct of our clinical trial could be affected by the potential that we experience difficulty in identifying and initiating sites and enrolling subjects, we identify serious side effects or other safety issues, we do not have clinical supply of our product candidate that is adequate in amount and quality and supplied in a timely fashion, and the inherent risks of clinical development; our statements about the timeline for qualification and validation of our commercial manufacturing process could be affected by the potential that
installation of the new equipment is more difficult than anticipated, Corium experiences delays with their suppliers and other vendors, Corium's is unable to successfully manufacture product on a commercial scale according to our specifications and
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Balance Sheets | ||
(Unaudited) | ||
December 31, |
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2013 | 2014 | |
Assets | ||
Current assets: | ||
Cash and cash equivalents |
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Prepaid expenses and other current assets | 146,704 | 661,218 |
Total current assets | 2,266,350 | 54,155,240 |
Property and equipment, net of accumulated depreciation of |
11,963,079 | 11,964,777 |
Deferred financing costs, net | 157,499 | 132,985 |
Other assets | 18,208 | 18,208 |
Total assets |
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Liabilities, convertible preferred stock and stockholders' (deficit) equity | ||
Current liabilities: | ||
Accounts payable |
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Accrued expenses | 379,164 | 373,270 |
Loan payable, current portion | 5,105,407 | 2,151,653 |
Warrant liability | 644,478 | 452,157 |
Total current liabilities | 6,844,503 | 5,302,744 |
Loan payable, long‑term | 9,769,528 | 12,619,816 |
Commitment and contingencies | ||
Series A‑1, 8%, non‑cumulative convertible preferred stock, |
898,305 | ---- |
Series A‑2 convertible preferred stock, |
543,623 | ---- |
Series B, 8% non‑cumulative, convertible preferred stock, |
44,928,382 | ---- |
Series C, 12% non‑cumulative, convertible preferred stock, |
22,862,367 | ---- |
Stockholders' (deficit) equity: | ||
Preferred stock, |
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Common stock, |
88 | 1,860 |
Additional paid‑in capital | 46,872,723 | 169,540,281 |
Accumulated deficit | (118,314,383) | (121,193,491) |
Total stockholders' (deficit) equity | (71,441,572) | 48,348,650 |
Total liabilities, convertible preferred stock and stockholders' (deficit) equity |
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Agile Therapeutics, Inc. | ||||
Statements of Operations | ||||
(Unaudited) | ||||
Three Months Ended June 30, | Six Months Ended June 30, | |||
2013 | 2014 | 2013 | 2014 | |
Operating expenses: | ||||
Research and development | $ 2,425,741 | $ 2,390,857 | $ 5,497,454 | $ 3,785,180 |
General and administrative | 823,329 | 1,103,853 | 1,979,977 | 2,157,157 |
Total operating expenses | 3,249,070 | 3,494,710 | 7,477,431 | 5,942,337 |
Loss from operations | (3,249,070) | (3,494,710) | (7,477,431) | (5,942,337) |
Other income (expense) | ||||
Interest expense | (378,228) | (403,488) | (756,456) | (781,714) |
Interest income | 259 | 82 | 1,432 | 137 |
Change in fair value of warrants | 7,160 | 179,715 | 16,346 | 192,321 |
Loss before benefit from income taxes | (3,619,879) | (3,718,401) | (8,216,109) | (6,531,593) |
Benefit from income taxes | — | — | — | 3,652,485 |
Net loss | $ (3,619,879) | $ (3,718,401) | $ (8,216,109) | $ (2,879,108) |
Net loss per common share: | ||||
Basic and Diluted | $ (70.29) | $ (0.46) | $ (175.31) | $ (0.71) |
Weighted-average shares outstanding: | ||||
Basic and Diluted | 51,499 | 8,000,092 | 46,865 | 4,074,734 |
Unaudited pro forma net loss | $ (3,697,734) | $ (2,858,441) | ||
Unaudited pro forma net loss per share (1) | $ (0.28) | $ (0.26) | ||
Unaudited pro forma weighted average basic and diluted common shares outstanding (1) | 13,197,576 | 11,068,161 | ||
(1) Assumes the conversion of all outstanding shares of convertible preferred stock and convertible promissory notes into shares of common stock as of the beginning of the period or the date of issuance and related adjustment to eliminate interest expense on the promissory notes. |
CONTACT:Source:Mary Coleman (609) 683-1880
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