Axsome Therapeutics Reports Second Quarter 2022 Financial Results and Provides Business Update
Company to host conference call today at
“We are very pleased to report our first commercial sales following the closing of the Sunosi acquisition in the second quarter. The rest of the year promises to continue to be eventful with the pending FDA action on our NDA for AXS-05 in major depressive disorder, and a Type A FDA meeting to discuss our planned resubmission of the NDA for AXS-07 in migraine, both anticipated this quarter,” said
Axsome is committed to developing and delivering medicines that meaningfully improve the lives of patients living with CNS disorders. The Company is advancing a broad portfolio of differentiated, patent-protected, CNS products and product candidates.
Sunosi (solriamfetol) is Axsome’s dual-acting dopamine and norepinephrine reuptake inhibitor shown to improve wakefulness in adults living with excessive daytime sleepiness (EDS) due to narcolepsy or obstructive sleep apnea (OSA).
- Axsome completed its
U.S.acquisition of Sunosi from Jazz Pharmaceuticals on May 9, 2022. The ex- U.S.transaction is now expected to close in the fourth quarter of 2022.
- Axsome generated approximately
$8.8 millionin U.S.net sales of Sunosi from May 9 to June 30, 2022.
Axsome is advancing a portfolio of differentiated, patent-protected, CNS product candidates with five in active clinical development.
AXS-05 (dextromethorphan-bupropion) is Axsome’s novel, oral, investigational NMDA receptor antagonist with multimodal activity being developed for the following indications: major depressive disorder (MDD), Alzheimer’s disease (AD) agitation, and smoking cessation. AXS-05 has been granted
- Depression: Axsome’s New Drug Application (NDA) for AXS-05 for the treatment of MDD was granted Priority Review and is currently under review by the FDA. The Company previously disclosed that it had entered into labeling discussions with the FDA on the NDA. Based on this interaction, the Company anticipates potential FDA action on the NDA in the third quarter of 2022.
- Alzheimer’s Disease Agitation: Axsome has amended the relapse criteria for the ACCORD Phase 3 randomized withdrawal study of AXS-05 in AD agitation, informed by results of an analysis requested by the FDA of data from the previously completed positive ADVANCE-1 trial. To generate additional data to support the efficacy of AXS-05 in this indication, Axsome is initiating a new randomized, placebo-controlled parallel group trial (ADVANCE-2) this quarter. Concurrent with the initiation of ADVANCE-2, the Company is concluding the ACCORD randomized withdrawal trial. Topline results from ACCORD are now anticipated in the fourth quarter of 2022.
- Smoking Cessation: Axsome plans to proceed to a pivotal Phase 2/3 trial in this indication. The Company intends to provide information on the timing of initiation of this study in 2022.
AXS-07 (MoSEIC™ meloxicam-rizatriptan) is Axsome’s novel, oral, rapidly absorbed, multi-mechanistic, investigational medicine for the acute treatment of migraine.
- Migraine: Following the previously disclosed Complete Response Letter to the Company’s NDA for AXS-07 for the acute treatment of migraine, Axsome recently submitted for a Type A meeting with the FDA to discuss the Company’s approach to its planned resubmission of the NDA. The Company anticipates that this meeting will occur in the third quarter of 2022.
AXS-12 (reboxetine) is Axsome’s novel, oral, potent, and highly selective norepinephrine reuptake inhibitor for the treatment of narcolepsy. AXS-12 has been granted FDA Orphan Drug designation for the treatment of narcolepsy.
- Narcolepsy: Axsome is conducting the SYMPHONY study, a Phase 3 randomized, multicenter, double-blind, placebo-controlled, parallel-group trial of AXS-12 in the treatment of narcolepsy. Enrollment in the trial is progressing and topline results are anticipated in the first half of 2023.
AXS-14 (esreboxetine) is Axsome’s novel, oral, potent, and highly selective norepinephrine reuptake inhibitor for the management of fibromyalgia. Esreboxetine, the SS-enantiomer of reboxetine, is more potent and selective than racemic reboxetine.
- Fibromyalgia: Manufacturing and other activities related to the planned submission of an NDA for AXS-14 for the management of fibromyalgia are ongoing. The Company expects to submit the NDA in 2023. AXS-14 has previously met the primary endpoints and demonstrated positive and statistically significant results in a Phase 3 and in a Phase 2 trial for the management of fibromyalgia.
Solriamfetol is Axsome’s dual-acting dopamine and norepinephrine reuptake inhibitor in development for the treatment of attention deficit hyperactivity disorder (ADHD).
- ADHD: Axsome announced its plans to develop solriamfetol for the treatment of ADHD. The Company anticipates initiating a Phase 2/3 multi-center, randomized, double-blind, placebo-controlled trial to evaluate the efficacy and safety of solriamfetol in adults with ADHD in the fourth quarter of this year.
- Regulatory and Commercial:
- AXS-05 for MDD, FDA action on NDA (3Q 2022)
- AXS-05 for MDD, commercial launch, if approved (4Q 2022)
- AXS-07 for migraine, Type A meeting (3Q 2022)
- AXS-07 for migraine, NDA resubmission
- AXS-14 for fibromyalgia, NDA submission (2023)
- Clinical Trial Readouts:
- Phase 3 ACCORD trial of AXS-05 for Alzheimer’s disease agitation, topline data (4Q 2022)
- Phase 3 SYMPHONY trial of AXS-12 in narcolepsy, topline data (1H 2023)
- Clinical Trial Initiations:
- Phase 3 ADVANCE-2 trial of AXS-05 for Alzheimer’s disease agitation (3Q 2022)
- Phase 2/3 trial of solriamfetol for ADHD in adults (4Q 2022)
Second Quarter 2022 Financial Results
- Revenue: The Company recorded
U.S.net sales of Sunosi from the May 9, 2022acquisition date through the end of the second quarter 2022 of approximately $8.8 million. No net product sales were reported for the 2021 comparable period.
- Research and development (R&D) expenses: R&D expenses were
$15.8 millionfor the three months ended June 30, 2022and $14.5 millionfor the comparable period in 2021. The increase was driven by personnel expense and costs associated with ongoing clinical trials.
- Selling, general, and administrative (SG&A) expenses: SG&A expenses were
$31.2 millionfor the three months ended June 30, 2022and $16.3 millionfor the comparable period in 2021. The increase was primarily related to commercial activities for Sunosi, pre-commercial activities for our late-stage pipeline assets, and personnel expense, along with an increase in non-cash stock compensation expense.
- Net loss: Net loss was
$41.4 million, or $(1.06)per share, for the three months ended June 30, 2022compared to a net loss of $32.3 million, or $(0.86)per share, for the comparable period in 2021. The net loss for the current period included $10.2 millionof non-cash stock compensation expense compared to $5.5 millionin the comparable period in 2021.
- Cash: At
June 30, 2022, Axsome had $73.4 millionof cash compared to $86.5 millionat December 31, 2021. Including proceeds from recent use of the Company’s at-the-market equity facility and proceeds from operations, Axsome’s pro-forma cash balance is $102 million.
- Shares outstanding: At
June 30, 2022, Axsome had 39,914,411 shares of common stock outstanding.
- Acquisition of Sunosi: The preliminary accounting of the acquisition of Sunosi is included in our Q2 2022 financial statements. To date, we have performed a preliminary fair value analysis of the business combination. The final determination of these fair values will be completed within one year from the acquisition date.
- Axsome believes that its current cash, along with the remaining committed capital from the
$300 millionterm loan facility, is sufficient to fund anticipated operations into 2024, based on the current operating plan, which includes the commercialization of Sunosi and potential launch of AXS-05 in MDD.
- Axsome expects that its operating expenses will increase year over year as it continues to build out the commercial function and further advance its pipeline.
Conference Call Information
Axsome will host a conference call and webcast today at
Forward Looking Statements
Certain matters discussed in this press release are "forward-looking statements". We may, in some cases, use terms such as "predicts," "believes," "potential," "continue," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should" or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. In particular, the Company's statements regarding trends and potential future results are examples of such forward-looking statements. The forward-looking statements include risks and uncertainties, including, but not limited to, the continued commercial success of our Sunosi® product and the success of our efforts to obtain any additional indication(s) with respect to Sunosi®; the success, timing and cost of our ongoing clinical trials and anticipated clinical trials for our current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including our ability to fully fund our disclosed clinical trials, which assumes no material changes to our currently projected expenses), futility analyses and receipt of interim results, which are not necessarily indicative of the final results of our ongoing clinical trials, and the number or type of studies or nature of results necessary to support the filing of a new drug application ("NDA") for any of our current product candidates; our ability to fund additional clinical trials to continue the advancement of our product candidates; the timing of and our ability to obtain and maintain
Selected Consolidated Financial Data
Statements of Operations Information:
|Three Months||Six Months Ended|
|Product sales, net||$||8,819,786||$||—||$||8,819,786||$||—|
|Cost of product sales||982,836||—||982,836||—|
|Research and development||15,792,202||14,503,326||28,377,343||31,099,014|
|Selling, general and administrative||31,160,140||16,344,361||56,863,871||27,592,734|
|Gain in fair value of contingent consideration||(860,000||)||—||(860,000||)||—|
|Intangible asset amortization||925,650||—||925,650||—|
|Total operating expenses||48,000,828||30,847,687||86,289,700||58,691,748|
|Loss from operations||(39,181,042||)||(30,847,687||)||(77,469,914||)||(58,691,748||)|
|Interest income (expense)||(2,257,474||)||(1,436,522||)||(3,600,913||)||(2,852,431||)|
|Net loss per common share, basic and diluted||$||(1.06||)||$||(0.86||)||$||(2.09||)||$||(1.64||)|
|Weighted average common shares outstanding, basic and diluted||39,081,100||37,595,069||38,704,227||37,512,716|
Balance Sheet Information:
|Cash and cash equivalents||$||73,394,640||$||86,472,854|
|Accounts receivables, net||16,167,927||—|
|Prepaid and other current assets||4,091,369||45,286|
|Total current assets||103,977,682||86,518,140|
|Intangible asset, net||62,874,350||—|
|Accrued expenses and other current liabilities||17,189,442||9,915,855|
|Contingent consideration, current||5,950,000||—|
|Total current liabilities||42,570,403||23,065,184|
|Contingent consideration, non-current||29,330,407||—|
|Loan payable, long-term||93,458,824||49,089,522|
Chief Operating Officer
Source: Axsome Therapeutics, Inc.