Agile Therapeutics Reports Second Quarter 2019 Financial Results
FDA Assigned PDUFA (Prescription Drug User Fee Act) Goal Date is November 16, 2019
Cash Expected to
Second quarter 2019 and other recent corporate developments:
- Acceptance of New Drug Application (NDA) Resubmission of Twirla: The Company resubmitted its Twirla NDA on
May 16, 2019. The NDA resubmission was intended to be a complete response to the complete response letter the Company received from the U.S. Food and Drug Administration( FDA) in December 2017(2017 CRL) and included the results from a comparative wear study, which was recommended by the FDA, additional information on the Company’s manufacturing process, and other analyses responding to the 2017 CRL. The FDAinformed the Company that it considers the resubmission to be a complete, class 2 response to the CRL and established November 16, 2019as the Prescription Drug User Fee Act (PDUFA) goal date.
- Advisory Committee Meeting for Twirla NDA: In
June 2019, the Company announced that a meeting of the Bone, Reproductive and Urologic Drugs Advisory Committee of the FDAhas been scheduled for October 30, 2019to review the Company’s NDA for Twirla.
- Combined Safety Data from Three Phase 3 Studies Presented: A poster presenting the combined safety data from three Phase 3 studies of Twirla (AG200-15) was presented in an ePoster session at the 2019 Annual Clinical and Scientific Meeting of the
American Congress of Obstetricians and Gynecologists(ACOG). The poster, titled “Safety of AG200-15, an Investigational Transdermal Patch in Three Phase 3 Studies,” was presented by lead author Anita Nelson, M.D., Professor and Chair of Obstetrics and Gynecology, Western University of Health Sciencesand a Principle Investigator for SECURE, the pivotal Phase 3 study of Twirla (AG200-15)
“The second quarter of 2019 was a very productive quarter for the Company,” said
Second Quarter Financial Results
- Cash and cash equivalents: As of
June 30, 2019, Agile had $10.6 millionof cash and cash equivalents compared to $7.8 millionof cash and cash equivalents as of December 31, 2018. During the quarter ended June 30, 2019, the Company raised net proceeds of approximately $1.4 millionfrom the sale of 992,072 shares of common stock from its “at-the-market” equity offerings. The Company believes its cash and cash equivalents as of June 30, 2019will be sufficient to meet its projected operating requirements through the end of 2019. The Company will require additional capital to fund operating needs for 2020 and beyond, which will include, among other items, the completion of its commercial plan for Twirla, if approved, which primarily includes validation of the commercial manufacturing process and the commercial launch, and advancing the development of its other potential product candidates.
- Research and development (R&D) expenses: R&D expenses were
$1.8 millionfor the quarter ended June 30, 2019, compared to $2.4 millionfor the comparable period in 2018. The decrease in R&D expenses was primarily due to a decrease in manufacturing and commercialization expenses and a decrease in stock compensation expense. The reduction in manufacturing and commercialization expenses reflects reduced activity associated with the scale-up of the commercial manufacturing process which was implemented as a result of the receipt of the 2017 CRL. The decrease in stock compensation expense was primarily the result of a lower stock price associated with the January 2019stock option grants as compared to the January 2018stock option grants.
- General and administrative (G&A) expenses: G&A expenses were
$1.8 millionfor the quarter ended June 30, 2019, compared to $2.3 millionfor the comparable period in 2018. The decrease in G&A expenses was primarily due to decreased stock compensation expense primarily the result of a lower stock price associated with the January 2019stock option grants as compared to the January 2018stock option grants and the suspension of pre-commercialization activities as a result of the receipt of the 2017 CRL.
- Net loss: Net loss was
$3.5 million, or $0.08per share, for the quarter ended June 30, 2019, compared to a net loss of $5.3 million, or $0.16per share, for the quarter ended June 30, 2018.
- Shares Outstanding: At
June 30, 2019, Agile had 44,632,329 shares of common stock outstanding.
About Twirla® (AG200-15)
Twirla (ethinyl estradiol and levonorgestrel transdermal system) or AG200-15 is an investigational low-dose, once-weekly combined hormonal contraceptive (CHC) patch that contains the active ingredients ethinyl estradiol (EE), a type of estrogen, and levonorgestrel (LNG), a type of progestin. Twirla is designed to be applied once weekly for three weeks, followed by a week without a patch. The Company has completed its Phase 3 clinical trials of Twirla and is pursuing regulatory approval in the U.S.
Xulane® is a registered trademark of
Certain information contained in this press release includes “forward-looking statements”, within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, related to our regulatory submissions and projected cash position. We may, in some cases use terms such as “predicts,” “believes,” “potential,” “continue,” “anticipates,” “estimates,” “expects,” “plans,” “intends,” “may,” “could,” “might,” “likely,” “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 beliefs and expectations of our management team that involve risks, potential changes in circumstances, assumptions, and uncertainties, including statements regarding the approvability and subsequent availability of Twirla, the interpretation of data that supports the approval of Twirla, the timing of our advisory committee meeting and of the FDA’s review of the Twirla NDA, and the fact that our existing cash and cash equivalents likely will not be sufficient to fund our current and planned operations after the end of 2019, which raises substantial doubt about our ability to continue as a going concern, and which, in turn, may create negative reactions to the price of our common stock making it more difficult to obtain financing in the future, our expectations about Twirla and its NDA. 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. These forward looking statements are subject to risks and uncertainties including risks related to our available cash and our ability to obtain additional funding to fund our business plan without delay and to continue as a going concern, our ability to adequately respond to the deficiencies in the second Twirla CRL issued by the
Contact: Investor Relations -- 609-683-1880
|Agile Therapeutics, Inc.|
|Condensed Balance Sheets|
|June 30, 2019||December 31, 2018|
|Cash and cash equivalents||$||10,586||$||7,851|
|Total current assets||10,764||8,458|
|Property and equipment, net||13,906||13,916|
|Right of use and other assets||250||18|
|Liabilities and stockholders’ equity|
|Accounts payable and accrued expenses||$||1,607||$||2,218|
|Lease liability, current portion||167||-|
|Total current liabilities||1,774||2,218|
|Lease liability, long-term||82||-|
|Additional paid‑in capital||272,977||261,722|
|Total stockholders’ equity||23,064||20,174|
|Total liabilities and stockholders’ equity||$||24,920||$||22,392|
|Agile Therapeutics, Inc.|
|Condensed Statements of Operations|
|(in thousands, except share and per share amounts)|
|Three Months Ended
|Six Months Ended
|Research and development||$||1,779||$||2,413||$||4,660||$||6,372|
|General and administrative||1,768||2,318||3,594||5,404|
|Total operating expenses||3,547||5,147||8,254||12,192|
|Loss from operations||(3,547||)||(5,147||)||(8,254||)||(12,192||)|
|Other income (expense)|
|Change in fair value of warrants||—||22||—||29|
|Loss before benefit from income taxes||(3,484||)||(5,344||)||(8,153||)||(12,654||)|
|Benefit from income taxes||—||—||—||477|
|Net loss per share - basic and diluted||$||(0.08||)||$||(0.16||)||$||(0.20||)||$||(0.36||)|
|Weighted‑average shares outstanding – basic and diluted||43,776,549||34,277,601||40,560,259||34,253,515|
Source: Agile Therapeutics, Inc.