MindMed Reports Third Quarter 2022 Financial Results and Business Highlights
Mind Medicine (MindMed) Inc. (NASDAQ: MNMD) reported its Q3 2022 financial results, highlighting a net loss of $16.5 million, an improvement from $17.2 million in Q3 2021. The company has cash reserves of $154.5 million, sufficient to fund operations into 2025. MindMed has initiated a Phase 2b trial for MM-120 in patients with Generalized Anxiety Disorder, expecting topline results in late 2023. Additionally, it has made strides in clinical programs for MM-402 and reduced overall cash expenditures, raising $60 million to support ongoing developments.
- Cash and cash equivalents of $154.5 million expected to fund operations into first half of 2025.
- Initiated Phase 2b trial for MM-120 with expected topline results in late 2023.
- Reduced cash expenditures and raised approximately $60 million to enhance financial stability.
- Net loss of $16.5 million for Q3 2022, though improved from $17.2 million in Q3 2021.
- R&D expenses increased to $27.3 million for the nine months ended September 30, 2022.
– Initiated Phase 2b dose-optimization trial in patients with Generalized Anxiety Disorder, with first patients dosed in Q3 2022 and key clinical readout expected in late 2023 –
– Advanced IND-enabling studies for MM-402 and initiated Phase 1 investigator-initiated trial in Q3 2022 –
– Cash and cash equivalents of
– Company to host conference call today at 8:30 AM ET –
NEW YORK, Nov. 10, 2022 /PRNewswire/ -- Mind Medicine (MindMed) Inc. (NASDAQ: MNMD), (NEO: MMED), (the "Company" or "MindMed"), a clinical stage biopharmaceutical company developing novel products to treat brain health disorders, today reported its financial results for the quarter ended September 30, 2022.
"We are pleased with the progress made in the third quarter as we continue executing on our core development programs, MM-120 and MM-402, and accelerating preparations for Phase 3 studies – all with the goal of bringing our treatments to market as efficiently as possible for the benefit of both patients and shareholders. During the quarter, we initiated enrollment in the largest well-controlled clinical trial of LSD, a 200-patient Phase 2b trial in patients diagnosed with Generalized Anxiety Disorder (GAD). We expect a readout of that data in the late half of 2023. Additionally, we continue our efforts to bring MM-402 into human clinical studies," said Robert Barrow, Chief Executive Officer and Director of MindMed. "Throughout the third quarter, we have taken meaningful steps to reduce our cash expenditures and we further bolstered our balance sheet by raising approximately
The Company enhanced and strengthened its financial resources with approximately
MM-120 (LSD D-tartrate): a proprietary, pharmaceutically optimized form of lysergic acid diethylamide (LSD) that is primarily being developed for the treatment of generalized anxiety disorder (GAD).
- In August 2022, the Company initiated patient dosing in the Phase 2b dose-optimization study of MM-120 for the treatment of GAD. Patient enrollment is currently ongoing and topline results are expected in the late half of 2023.
- In September 2022, results from a Phase 2 placebo-controlled investigator-initiated clinical trial of LSD in the treatment of anxiety disorders (LSD-Assist Study) were published in the peer-reviewed scientific journal Biological Psychiatry. Topline results in 46 patients with clinically significant anxiety demonstrated the significant, rapid, durable, and beneficial effects of LSD and its potential to safely mitigate symptoms of anxiety and depression.
- Enrollment is ongoing for Study MMED007, a Phase 2a proof-of-concept trial for the treatment of ADHD. The study is designed to assess the safety and efficacy of repeated low-dose MM-120 administration. The Company expects topline results in the late half of 2023.
- The Company continues to prioritize and focus its current development efforts and resources on MM-120 in psychiatric indications. MindMed currently owns and retains all clinical data and manufacturing rights for MM-120 and is aggressively protecting and expanding its intellectual property portfolio.
MM-402 or R(-)-MDMA: a synthetic R-enantiomer of 3,4-Methylenedioxymethamphetamine
(MDMA) that the Company is developing for the treatment of core symptoms of autism spectrum disorder.
- IND-enabling studies are currently ongoing and initiation of a Phase 1 clinical trial of MM-402 is planned in 2023.
- A Phase 1 pharmacokinetic/pharmacodynamic investigator-initiated trial of R(-)-MDMA, S(+)-MDMA and R/S-MDMA in healthy volunteers is currently underway through the Company's collaboration with the University Hospital Basel in Switzerland.
Cash Balance. As of September 30, 2022, MindMed had cash and cash equivalents totaling
Net Cash in Operating Activities. The net cash used in operating activities was
Research and Development (R&D). R&D expenses were
General and Administrative (G&A). G&A expenses were
Net Loss. The net loss for the three months ended September 30, 2022 was
MindMed management will host a conference call at 8:30 AM ET today to provide a corporate update and review the company's third quarter 2022 financial results. Individuals may participate via telephone by dialing (888) 999-3182 (domestic) or (848) 280-6330 (international) and using conference ID 8072033. The webcast can be accessed on MindMed's Investor Resources webpage. The webcast will be archived on the company's website for at least 30 days after the conference call.
MindMed is a clinical stage biopharmaceutical company developing novel products to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative drug candidates, with and without acute perceptual effects, targeting the serotonin, dopamine and acetylcholine systems.
MindMed trades on NASDAQ under the symbol MNMD and on the Canadian NEO Exchange under the symbol MMED.
Certain statements in this news release related to the Company constitute "forward-looking information" within the meaning of applicable securities laws and are prospective in nature. Forward-looking information is not based on historical facts, but rather on current expectations and projections about future events and are therefore subject to risks and uncertainties which could cause actual results to differ materially from the future results expressed or implied by the forward-looking statements. These statements generally can be identified by the use of forward-looking words such as "will", "may", "should", "could", "intend", "estimate", "plan", "anticipate", "expect", "believe", "potential" or "continue", or the negative thereof or similar variations. Forward-looking information in this news release include, but are not limited to, statements regarding anticipated upcoming milestones and studies, results and timing of clinical studies, and the availability of cash and cash equivalents. There are numerous risks and uncertainties that could cause actual results and the Company's plans and objectives to differ materially from those expressed in the forward-looking information, including history of negative cash flows; limited operating history; incurrence of future losses; availability of additional capital; lack of product revenue; compliance with laws and regulations; difficulty associated with research and development; risks associated with clinical trials or studies; heightened regulatory scrutiny; early stage product development; clinical trial risks; regulatory approval processes; novelty of the psychedelic inspired medicines industry; as well as those risk factors discussed or referred to herein and the risks described in the Company's Annual Report on Form 10-K for the fiscal year ended December 31, 2021 and its Quarterly Report on Form 10-Q for the period ended June 30, 2022 under headings such as "Special Note Regarding Forward-Looking Statements," and "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" and other filings and furnishings made by the Company with the securities regulatory authorities in all provinces and territories of Canada which are available under the Company's profile on SEDAR at www.sedar.com and with the U.S. Securities and Exchange Commission on EDGAR at www.sec.gov. Except as required by law, the Company undertakes no duty or obligation to update any forward-looking statements contained in this release as a result of new information, future events, changes in expectations or otherwise.
For Media: media@mindmed.co
For Investors: ir@mindmed.co
Mind Medicine (MindMed) Inc. | ||||||||||||||||
Condensed Consolidated Statements of Operations and Comprehensive Loss | ||||||||||||||||
(Unaudited) | ||||||||||||||||
(In thousands, except share and per share amounts) | ||||||||||||||||
Three Months | Nine Months | |||||||||||||||
2022 | 2021 | 2022 | 2021 | |||||||||||||
Operating expenses: | ||||||||||||||||
Research and development | $ | 7,772 | $ | 9,019 | $ | 27,339 | $ | 23,906 | ||||||||
General and administrative | 9,211 | 8,208 | 25,092 | 52,390 | ||||||||||||
Total operating expenses | 16,983 | 17,227 | 52,431 | 76,296 | ||||||||||||
Loss from operations | (16,983) | (17,227) | (52,431) | (76,296) | ||||||||||||
Other income/(expense): | ||||||||||||||||
Interest income/(expense), net | 360 | (64) | 443 | (220) | ||||||||||||
Foreign exchange gain/(loss), net | 138 | (40) | 94 | 94 | ||||||||||||
Other income | — | 135 | 1 | 215 | ||||||||||||
Total other income | 498 | 31 | 538 | 89 | ||||||||||||
Loss before income taxes | (16,485) | (17,196) | (51,893) | (76,207) | ||||||||||||
Income taxes | — | — | — | — | ||||||||||||
Net loss | (16,485) | (17,196) | (51,893) | (76,207) | ||||||||||||
Other comprehensive gain/(loss): | ||||||||||||||||
(Loss)/gain on foreign currency translation | (107) | (383) | (303) | 380 | ||||||||||||
Comprehensive loss | $ | (16,592) | $ | (17,579) | $ | (52,196) | $ | (75,827) | ||||||||
Net loss per common share, basic and diluted | $ | (0.56) | $ | (0.61) | $ | (1.82) | $ | (2.81) | ||||||||
Weighted-average common shares, basic and diluted | 29,296,333 | 28,013,809 | 28,566,161 | 27,124,297 |
Mind Medicine (MindMed) Inc. | |||||||||
Condensed Consolidated Balance Sheets | |||||||||
(In thousands, except share amounts) | |||||||||
September 30, 2022 | December 31, 2021 | ||||||||
(unaudited) | |||||||||
Assets | |||||||||
Current assets: | |||||||||
Cash and cash equivalents | $ | 154,519 | $ | 133,539 | |||||
Prepaid and other current assets | 1,826 | 3,676 | |||||||
Right of use asset | 165 | — | |||||||
Total current assets | 156,510 | 137,215 | |||||||
Goodwill | 19,918 | 19,918 | |||||||
Intangible assets, net | 4,479 | 6,869 | |||||||
Total assets | $ | 180,907 | $ | 164,002 | |||||
Liabilities and Shareholders' Equity | |||||||||
Current liabilities: | |||||||||
Accounts payable | $ | 824 | $ | 4,178 | |||||
Accrued expenses | 7,467 | $ | 6,230 | ||||||
2022 USD Financing Warrants | 17,747 | — | |||||||
Total current liabilities | 26,038 | 10,408 | |||||||
Other liabilities, long-term | 1,276 | 1,930 | |||||||
Total liabilities | 27,314 | 12,338 | |||||||
Shareholders' Equity: | |||||||||
Common shares, no par value, unlimited authorized as of September 30, 2022 and December 31, 2021; 37,541,115 and 28,126,414 issued and outstanding as of September 30, 2022 and December 31, 2021, respectively | — | — | |||||||
Additional paid-in capital | 342,415 | 288,290 | |||||||
Accumulated other comprehensive (loss)/income | 743 | 1,046 | |||||||
Accumulated deficit | (189,565) | (137,672) | |||||||
Total shareholders' equity | 153,593 | 151,664 | |||||||
Total liabilities and shareholders' equity | $ | 180,907 | $ | 164,002 |
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SOURCE Mind Medicine (MindMed) Inc.
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