Recent Business Updates
- The GAIN Trial, the company’s Phase 2/3 study of COR388 versus placebo in patients with mild to moderate Alzheimer’s disease, is anticipated to continue on track in 2020. The trial is targeting an enrollment of 570 patients across 90 sites in the United States and Europe, with top-line results from the trial expected in the fourth quarter of 2021. In addition, the company is evaluating the feasibility of conducting an interim analysis, and plans to discuss this strategy with the U.S. Food and Drug Administration (FDA).
- In September, Cortexyme announced the start of screening in Europe for the GAIN Trial. Cortexyme expects to enroll subjects in five European countries; sites in the UK, Spain, France, and Poland are already active. An updated listing can be found on www.clinicaltrials.gov.
Advancing a New Understanding of Alzheimer’s Causation and Treatment
- Earlier this month, Cortexyme announced that research on COR388’s impact on ApoE in Alzheimer’s disease patients will be the subject of an oral presentation at the 12th Clinical Trials on Alzheimer’s (CTAD) conference, which is being held December 4-7, 2019, in San Diego. Michael Detke, M.D., Ph.D., Cortexyme’s chief medical officer, will deliver the presentation (abstract OC28) at 10:00 a.m. PST on Saturday, December 7th. Additionally, the company will host a lunch symposium on Thursday, December 5th, from 12:30-1:30 p.m. PST. More details, including registration info, are available here.
- In July, COR388 was the subject of a research abstract presented at the Alzheimer’s Association International Conference (AAIC) 2019 in Los Angeles. In a Developing Topics poster that was included in the AAIC press program, researchers highlighted the Phase 1b clinical development experience of COR388 and provided an overview of the design for the GAIN trial. AAIC is the largest international meeting dedicated to advancing dementia science.
- In June, Cortexyme expanded its Clinical Advisory Board (CAB) with four new key clinical and regulatory experts. The CAB includes leading experts on Alzheimer’s, neurodegenerative disorders, and central nervous system drug development. Cortexyme has benefited from the group’s insights as it advanced COR388 through Phase 1 testing and laid the groundwork for the GAIN trial. Recently, Cortexyme’s regulatory advisor David Hosford, M.D., Ph.D. rejoined the FDA Division of Neurology Products. Thomas Laughren, M.D., a consultant and previous Division Director at the FDA, will now be advising the company on regulatory matters.
- In May, Cortexyme completed a successful initial public offering, raising approximately $77.8 million after expenses.
Financial Results for the Quarter Ended September 30, 2019
Cash, Cash Equivalents and Marketable Securities: Cash, cash equivalents, and short and long-term marketable securities as of September 30, 2019, were $127.8 million. Cortexyme expects current cash, cash equivalents and marketable securities will be sufficient to fund its operating and capital expenditures through 2021 and the completion of the GAIN Trial.
Research and Development (R&D) Expenses: For the quarter ended September 30, 2019, R&D expenses were $8.3 million, including $0.6 million of stock-based compensation, compared to R&D expenses of $2.3 million for the quarter ended September 30, 2018. The increase was primarily due to costs related to the research and development of COR388, the GAIN Trial, and stock-based compensation.
General and Administrative (G&A) Expenses: For the quarter ended September 30, 2019, G&A expenses were $2.3 million, which included $0.3 million of stock-based compensation. This compared to G&A expenses of $0.6 million for the quarter ended September 30, 2018. The increase was primarily attributable to personnel-related expenses, professional and legal fees, and stock-based compensation.
Net Loss: For the quarter ended September 30, 2019, net loss was $9.9 million, or a loss of $0.37 per basic share.
About the GAIN Trial
The GAIN Trial is a Phase 2/3 randomized, double-blind, placebo-controlled study assessing the efficacy, safety, and tolerability of two dose levels of COR388 oral capsules in subjects with mild to moderate AD. The trial is currently enrolling subjects in the U.S. and Europe, and top-line results from the trial are anticipated in the fourth quarter of 2021. More information about the trial can be found at www.GAINtrial.com.
About Cortexyme, Inc.
Cortexyme (Nasdaq: CRTX) is a clinical stage biopharmaceutical company pioneering a novel, disease-modifying therapeutic approach to treat what it believes to be a key underlying cause of Alzheimer’s disease and other degenerative diseases. Cortexyme is targeting a specific, infectious pathogen found in the brain of Alzheimer’s patients and tied to neurodegeneration and neuroinflammation in animal models. The company’s lead investigational medicine, COR388, is the subject of the GAIN Trial, an ongoing Phase 2/3 clinical study in patients with mild to moderate Alzheimer’s. To learn more about Cortexyme, visit www.cortexyme.com or follow @Cortexyme on Twitter.
Statements in this press release contain “forward-looking statements” that are subject to substantial risks and uncertainties. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “expect,” “believe,” “will,” “may,” “should,” “estimate,” “project,” “outlook,” “forecast” or other similar words. Forward-looking statements are based on Cortexyme’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. Factors that could cause actual results to differ include, but are not limited to, the risks and uncertainties described in the section titled “Risk Factors” in the final prospectus related to Cortexyme’s initial public offering filed with the Securities and Exchange Commission on May 9, 2019 and Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on June 12, 2019. Forward-looking statements contained in this press release are made as of this date, and Cortexyme undertakes no duty to update such information except as required under applicable law.
|Cortexyme, Inc. Condensed Statements of Operations
(In thousands, except share and per share amounts)
|Three Months Ended September 30,||Nine Months Ended September 30,|
|Research and development||$||8,253||$||2,290||$||20,187||$||6,989|
|General and administrative||2,316||584||6,032||1,288|
|Total operating expenses||10,569||2,874||26,219||8,277|
|Loss from operations||(10,569)||(2,874)||(26,219)||(8,277)|
|Change in fair value of derivative liability||—||—||—||(206)|
|Other comprehensive income/ (loss):|
|Unrealized gain / (loss) on available for sales securities||16||(16)||145||(16)|
|Total comprehensive income/(loss)||(9,842)||(2,537)||(24,456)||(9,022)|
|Net loss per share – basic and diluted||(0.37)||(0.75)||(1.59)||(2.68)|
|Weighted average shares of common stock outstanding –
basic and diluted
|Cortexyme, Inc. Condensed Balance Sheets
(In thousands, except share and per share amounts)
|September 30, 2019||December 31, 2018|
|Cash and cash equivalents||$||44,740||$||24,872|
|Short term investments||75,730||46,844|
|Prepaid expenses and other current assets||3,649||868|
|Total current assets||124,369||72,584|
|Property and equipment, net||270||283|
|Long term investments||7,341||—|
|LIABILITIES AND STOCKHOLDERS’ EQUITY / (DEFICIT)|
|Accrued expenses and other current liabilities||3,832||962|
|Total current liabilities||6,127||1,457|
|Total stockholders’ equity / (deficit)||127,287||(32,626)|
|Total liabilities and stockholders’ equity / (deficit)||$||133,414||$||72,877|
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