Aldeyra Therapeutics Reports Full-Year 2019 Financial Results and Provides Updates on Anticipated Clinical Milestones
- INVIGORATE Phase 3 Trial of Reproxalap in Allergic Conjunctivitis Expected to be Completed in Second Half of 2020
- Based on Achievement of Symptom Endpoint in Two Clinical Trials, Subsequent Development Plans for Reproxalap in Dry Eye Disease Pending FDA Feedback, Expected in the Second Half of 2020
- GUARD Phase 3 Trial of ADX-2191 in Proliferative Vitreoretinopathy Initiated
- Strategic Prioritization of Late-Stage Ocular Pipeline Expected to Extend Company’s Cash Runway Through the End of 2021
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Management to Host Conference Call at
8:00 a.m. ET Today
“2019 was a year of continued momentum for our lead programs, as we reported statistically significant and clinical relevant data that underscored the potential of reproxalap as a first-line therapy in allergic conjunctivitis and dry eye disease, conditions that in the aggregate affect more than one billion people worldwide,” stated
Recent Highlights and Upcoming Milestones
- Allergic Conjunctivitis: Aldeyra expects to complete the INVIGORATE Phase 3 clinical trial of topical ocular reproxalap in the second half of 2020. In 2019, Aldeyra announced achievement of the primary endpoint of the Phase 3 ALLEVIATE Trial in allergic conjunctivitis, as well as statistically significant reductions in ocular itching and redness in an allergen chamber clinical trial.
-
Dry Eye Disease: Based on the achievement of symptom endpoints in two well-controlled clinical trials, Aldeyra plans to meet with the
U.S. Food and Drug Administration (FDA) prior to initiating Part 2 of the RENEW Trial, and plans to provide an update on future development in dry eye disease following FDA feedback, expected in the second half of 2020. - Proliferative Vitreoretinopathy (PVR): Aldeyra is currently enrolling patients in the GUARD Phase 3 Trial of ADX-2191, a novel anti-inflammatory and anti-proliferative agent for the prevention of PVR, a rare sight-threatening condition with no approved treatment. The GUARD Trial is a two-part, multi-center, randomized, controlled, adaptive clinical trial evaluating the efficacy of intravitreal injections of ADX-2191 versus standard-of-care for the prevention of PVR. The trial will compare recurrent retinal detachment rates over a 24-week period following surgical repair of retinal detachment due to PVR or open globe injury. Enrollment is currently expected to be completed in 2021.
- Systemic Autoimmune Disease: A single and multiple ascending dose Phase 1 clinical trial has been completed for ADX-629, a novel orally administered RASP inhibitor in development for the treatment of systemic autoimmune disease and potentially other serious medical conditions. Top-line results are expected in the second quarter of this year. Initiation of Phase 2 clinical testing is planned for the second half of 2020.
Strategic Prioritization of Late-Stage Programs in Ocular Disease
In a separate news release issued earlier today, Aldeyra announced strategic prioritization of late-stage ocular disease programs in allergic conjunctivitis, dry eye disease, and proliferative vitreoretinopathy. In conjunction with the strategic prioritization, Aldeyra appointed ophthalmology drug development expert
Aldeyra has elected to place on hold its clinical development of topical dermal reproxalap for the treatment of ichthyosis associated with Sjogren-Larsson Syndrome and ADX-1612 for the treatment of post-transplant lymphoproliferative disorder. The initiatives to prioritize the portfolio are expected to extend the company's cash runway through the end of 2021.
Year Ended
Aldeyra reported a net loss of
Research and development expenses were approximately
Acquired in-process research and development expenses were
General and administrative expenses were approximately
Total operating expenses were approximately
Cash, cash equivalents, and marketable securities were
Conference Call & Webcast Information
Aldeyra will host a conference call today at
A live webcast of the conference call will also be available on the Investors Relations section of the
About Reproxalap
Reproxalap is a novel, small-molecule immune-modulating covalent inhibitor of RASP (reactive aldehyde species), which are elevated in ocular and systemic inflammatory disease, and lead to activation of intracellular inflammatory factors, including NF-kB, inflammasomes, and Scavenger Receptor A. Reproxalap’s mechanism of action has been validated with the demonstration of statistically significant and clinically relevant activity in multiple physiologically distinct late-phase clinical indications. Topical ocular reproxalap has now been studied in more than 1,100 patients with no observed safety concerns reported; mild instillation site irritation is the most commonly reported adverse event in clinical trials.
About ADX-2191
ADX-2191, an intravitreal formulation of methotrexate, has received orphan drug and fast track designations from the FDA for the prevention of PVR. The observed clinical activity of ADX-2191 in patients with PVR is believed to be the result of down-regulation of aberrant retinal cell proliferation and activity, thereby leading to reduced retinal scarring that is characteristic of PVR. Aldeyra retains an exclusive license to certain patents related to the use of ADX-2191 for the prevention of PVR.
About
Safe Harbor Statement
This release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding Aldeyra's strategy, future operations, future financial position and cash runway, projected costs and expenses, prospects, plans, and objectives and Aldeyra's plans and expectations for its product candidates, including plans relating to current or future clinical development and its strategic prioritization. Aldeyra intends such forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995. In some cases, you can identify forward-looking statements by terms such as, but not limited to, "may," "might," "will," "objective," "intend," "should," "could," "can," "would," "expect," "believe," "anticipate," "project," "on track," "scheduled," "target," "design," "estimate," "predict," "potential," "aim," "plan" or the negative of these terms, and similar expressions intended to identify forward-looking statements. Such forward-looking statements are based upon current expectations that involve risks, changes in circumstances, assumptions and uncertainties. Aldeyra is at an early stage of development and may not ever have any products that generate significant revenue. All of Aldeyra's development timelines may be subject to adjustment depending on recruitment rate, regulatory review, preclinical and clinical results, and other factors that could delay the initiation or completion of clinical trials. Important factors that could cause actual results to differ materially from those reflected in Aldeyra's forward-looking statements include, among others, the timing of enrollment, commencement and completion of Aldeyra's clinical trials, the timing and success of preclinical studies and clinical trials conducted by Aldeyra and its development partners; updated or refined data based on Aldeyra's continuing review and quality control analysis of clinical data, Aldeyra's ability to design clinical trials with protocols and endpoints acceptable to applicable regulatory authorities; delay in or failure to obtain regulatory approval of Aldeyra's product candidates; the ability to maintain regulatory approval of Aldeyra's product candidates, and the labeling for any approved products; the risk that prior results, such as signals of safety, activity or durability of effect, observed from preclinical or clinical trials, will not be replicated or will not continue in ongoing or future studies or clinical trials involving Aldeyra's product candidates; the scope, progress, expansion, and costs of developing and commercializing Aldeyra's product candidates; uncertainty as to Aldeyra’s ability to commercialize (alone or with others) Aldeyra's product candidates following regulatory approval, if any; the size and growth of the potential markets and pricing for Aldeyra's product candidates and the ability to serve those markets; Aldeyra's expectations regarding Aldeyra's expenses and revenue, the sufficiency or use of Aldeyra's cash resources and needs for additional financing; political, economic, legal, and social risks that may affect Aldeyra’s business or the global economy; the rate and degree of market acceptance of any of Aldeyra's product candidates; Aldeyra's expectations regarding competition; Aldeyra's anticipated growth strategies; Aldeyra's ability to attract or retain key personnel; Aldeyra’s limited sales and marketing infrastructure; Aldeyra's ability to establish and maintain development partnerships; Aldeyra’s ability to successfully integrate acquisitions into its business; Aldeyra's expectations regarding federal, state and foreign regulatory requirements; regulatory developments in
In addition to the risks described above and in Aldeyra's other filings with the
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| CONSOLIDATED BALANCE SHEETS | |||||||||
|
|
2019 |
|
|
2018 |
|
||||
| ASSETS | |||||||||
| Current assets: | |||||||||
| Cash and cash equivalents |
$ |
16,425,830 |
|
$ |
3,357,472 |
|
|||
| Cash equivalent- reverse repurchase agreements |
|
28,000,000 |
|
|
44,000,000 |
|
|||
| Marketable securities |
|
28,938,545 |
|
|
46,242,220 |
|
|||
| Prepaid expenses and other current assets |
|
1,804,450 |
|
|
1,169,594 |
|
|||
| Total current assets |
|
75,168,825 |
|
|
94,769,286 |
|
|||
| Deferred offering costs | — |
|
86,644 |
|
|||||
| Property and equipment, net |
|
148,449 |
|
|
235,225 |
|
|||
| Right-of-use assets |
|
201,007 |
|
— | |||||
| Total assets |
$ |
75,518,281 |
|
$ |
95,091,155 |
|
|||
| LIABILITIES AND STOCKHOLDERS' EQUITY | |||||||||
| Current liabilities: | |||||||||
| Accounts payable |
$ |
808,302 |
|
$ |
3,051,678 |
|
|||
| Accrued expenses |
|
11,873,122 |
|
|
5,421,498 |
|
|||
| Current portion of operating lease liabilities |
|
226,328 |
|
— | |||||
| Total current liabilities |
|
12,907,752 |
|
|
8,473,176 |
|
|||
| Long-term debt |
|
14,528,212 |
|
— | |||||
| Total liabilities |
|
27,435,964 |
|
|
8,473,176 |
|
|||
| Commitments and contingencies | |||||||||
| Stockholders' equity: | |||||||||
| Preferred stock, |
|||||||||
| outstanding | — | — | |||||||
| Common stock, voting, |
|||||||||
| and 26,244,435 shares issued and outstanding, respectively |
|
28,657 |
|
|
26,244 |
|
|||
| Additional paid-in capital |
|
247,409,793 |
|
|
225,136,127 |
|
|||
| Accumulated other comprehensive income (loss) |
|
5,866 |
|
|
(9,224 |
) |
|||
| Accumulated deficit |
|
(199,361,999 |
) |
|
(138,535,168 |
) |
|||
| Total stockholders’ equity |
|
48,082,317 |
|
|
86,617,979 |
|
|||
| Total liabilities and stockholders’ equity |
$ |
75,518,281 |
|
$ |
95,091,155 |
|
|||
| CONSOLIDATED STATEMENT OF OPERATIONS | ||||||||
| Years ended |
||||||||
|
|
2019 |
|
|
2018 |
|
|||
| Operating expenses: | ||||||||
| Research and development |
$ |
44,351,851 |
|
$ |
29,823,007 |
|
||
| Acquired in-process research and development |
|
6,567,754 |
|
— | ||||
| General and administrative |
|
12,154,702 |
|
|
9,876,144 |
|
||
| Loss from operations |
|
(63,074,307 |
) |
|
(39,699,151 |
) |
||
| Other income (expense): | ||||||||
| Interest income |
|
1,541,349 |
|
|
952,698 |
|
||
| Interest expense |
|
(603,846 |
) |
|
(146,792 |
) |
||
|
Total other income (expense), net |
|
937,503 |
|
|
805,906 |
|
||
| Loss before income taxes |
|
(62,136,804 |
) |
|
(38,893,245 |
) |
||
| Income tax benefit |
|
1,309,973 |
|
— | ||||
| Net loss |
$ |
(60,826,831 |
) |
$ |
(38,893,245 |
) |
||
| Net loss per share - basic and diluted |
$ |
(2.24 |
) |
$ |
(1.79 |
) |
||
| Weighted average common shares outstanding - basic and diluted |
|
27,111,840 |
|
|
21,685,642 |
|
||
View source version on businesswire.com: https://www.businesswire.com/news/home/20200312005181/en/
Corporate Contact:
Tel: 781-761-4904 ext. 218
dmcmullin@aldeyra.com
Investor & Media Contact:
Tel: 617-542-5300
ALDX@investorrelations.com
Source: