Axcella Health Reports First Quarter 2019 Financial Results and Provides Company Update
- Successfully completed initial public offering, raising
$71.4 million in gross proceeds - Presented data on AXA1665 and AXA1125 at two leading medical conferences
- Identified drug development path for AXA1665 following the FDA meeting in March
- Initiated two Non-IND, IRB-Approved Clinical Studies for AXA1665, AXA1125 and AXA1957
- Expanded leadership team and announced two patent issuances
CAMBRIDGE, Mass.,
“We are excited by the progress our organization has made across multiple fronts during the first quarter of 2019. We presented new data from both our AXA1665 program for Hepatic Encephalopathy and AXA1125 program in liver that we believe demonstrate the strength of our AXA development platform and potential of endogenous metabolic modulators. We also continued to strengthen our patent portfolio and made key senior level hires. All of these accomplishments successfully positioned Axcella to complete an initial public offering with gross proceeds of
Clinical Highlights
• In
- Increased basal (fasted) Fischer’s ratio, the molar ratio of branched chain amino acids to aromatic amino acids, which appears to have prognostic significance in subjects with cirrhosis and end-stage liver disease
- Decreased plasma ammonia area under the curve, suggesting that blood ammonia levels did not increase despite the administration of an added nitrogen load
- Tended to maintain a leaner (dry lean mass, lean body mass, and skeletal muscle mass) phenotype with the average Liver Frailty Index (LFI) score directionally moving toward less frailty compared to baseline
• In
- Lowered triglycerides in hepatocytes (metabolic node)
- Suppressed aerobic glycolysis while preserving total ATP levels; and reduced proinflammatory cytokines in macrophages (inflammation node)
- Reduced ProC3 protein secretion and other key fibrogenic markers, including reducing the activation and proliferation of stellate cells (fibrosis node)
- Multimodal effects were seen (or manifested) with AXA1125 consistently across cells, animal models, humans
• Following a meeting with the FDA in March, Axcella decided to pursue a drug development path for AXA1665. Under the planned IND, the initial indication would be for the treatment of HE
- A Phase IIb/III Clinical Trial is anticipated to launch in the second half of 2020 and could potentially serve as a registrational (pivotal) trial to support the submission of a New Drug Application, or NDA
• During the first quarter of 2019, Axcella initiated two Non-IND, IRB-Approved Clinical Studies
- Non-IND, IRB-Approved Clinical Study of AXA1665
- Non-IND, IRB-Approved Clinical Study of AXA1125 and AXA1957
Corporate Highlights
• In
• In
• In February and
Anticipated Milestones
• Initiate a Non-IND, IRB-Approved Clinical Study of AXA1957 in adolescent subjects with NAFLD in the second half of 2019
• Initiate a Non-IND, IRB-Approved Clinical Study of AXA4010 in subjects with sickle cell disease in the second half of 2019
• Report data from our Non-IND, IRB-Approved Clinical Study of AXA1665 in subjects with hepatic insufficiency in the first half of 2020
• Report data from our Non-IND, IRB-Approved Clinical Study of AXA1125 and AXA1957 in adult subjects with NAFLD in the second half of 2020
• Report data from our Non-IND, IRB-Approved Clinical Study of AXA1957 in adolescent subjects with NAFLD in the second half of 2020
• Report data from our Non-IND, IRB-Approved Clinical Study of AXA4010 in subjects with sickle cell disease in the second half of 2020
First Quarter 2019 Financial Results
For the first quarter ended
Total operating expenses for the quarter ended
Research and development expenses for the quarter ended
General and administrative expenses were
Cash and cash equivalents were
About
Axcella is designing and developing AXA Candidates, compositions of endogenous metabolic modulators, or EMMs, engineered in distinct ratios, designed to target and maximize the fundamental role that EMMs play in regulating multiple metabolic functions. Axcella’s AXA Candidates are generated from its proprietary, human-focused AXA Development Platform. Axcella believes its expertise and capabilities in EMMs position it to become a preeminent biotechnology company reprogramming metabolism to address a diverse set of complex diseases and support health. Axcella’s AXA Development Platform has already produced a pipeline of product candidates in programs targeting liver, muscle and blood. Axcella was founded by Flagship Pioneering.
About Non-IND, IRB-Approved Clinical Studies
Axcella conducts non-investigational new drug application (Non-IND),
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, statements regarding the development potential of our current AXA candidates, potential expansion into new therapeutic fields, the timing of our clinical studies and the timing of receipt of data from the same, our liquidity and our strategy, business plans and focus. The words “may,” “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “target” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management’s current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, those related to the breadth of our pipeline of product candidates, the strength of our proprietary product platform, the efficiency of our discovery and development approach, the clinical development and safety profile of our AXA Candidates and their therapeutic potential, whether and when, if at all, our AXA Candidates will receive approval from the U.S. Food and Drug Administration and for which, if any, indications, competition from other biotechnology companies, our liquidity, our ability to successfully develop our AXA Candidates through current and future milestones on the anticipated timeline, if at all, past results from Non-IND, IRB-Approved Clinical Studies not being representative of future results, and other risks identified in our SEC filings, including our final prospectus for our initial public offering, and subsequent filings with the SEC. We caution you not to place undue reliance on any forward-looking statements, which speak only as of the date they are made. We disclaim any obligation to publicly update or revise any such statements to reflect any change in expectations or in events, conditions or circumstances on which any such statements may be based, or that may affect the likelihood that actual results will differ from those set forth in the forward-looking statements. Any forward-looking statements contained in this press release represent our views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date. We explicitly disclaim any obligation to update any forward-looking statements.
Axcella Health Inc. | |||||||||||||
Condensed Consolidated Statements of Operations (Unaudited) | |||||||||||||
(in thousands, except share and per share data) | |||||||||||||
Three Months Ended March 31, | |||||||||||||
2019 | 2018 | ||||||||||||
Operating expenses: | |||||||||||||
Research and development | $ |
7,563 | $ |
5,455 | |||||||||
General and administrative | 3,468 | 2,136 | |||||||||||
Total operating expenses | 11,031 | 7,591 | |||||||||||
Loss from Operations | (11,031 | ) | (7,591 | ) | |||||||||
Other (expense) income | (542 | ) | (509 | ) | |||||||||
Net loss | $ |
(11,573 |
) | $ |
(8,100 |
) | |||||||
Net loss per share, basic and diluted | $ | (2.43 | ) | $ | (1.92 | ) | |||||||
Weighted average common shares outstanding, basic and diluted | 4,775,828 | 4,229,118 |
Axcella Health Inc. | |||||||||
Condensed Consolidated Balance Sheet Data (Unaudited) | |||||||||
(in thousands) | |||||||||
March 31, | December 31, | ||||||||
2019 | 2018 | ||||||||
Assets: | |||||||||
Cash and cash equivalents | $ | 66,769 | $ | 79,466 | |||||
Other assets | 4,149 | 2,378 | |||||||
Total assets | $ | 70,918 | $ | 81,844 | |||||
Liabilities and stockholders' (deficit) equity | |||||||||
Liabilities | $ | 33,253 | $ | 33,755 | |||||
Preferred stock | 197,888 | 197,842 | |||||||
Stockholders' (deficit) equity | (160,223 | ) | (149,753 | ) | |||||
Total liabilities and stockholders' equity | $ | 70,918 | $ | 81,844 |
Company Contact | Investor Contact |
Alison Williams | Lauren Stival |
awilliams@axcellahealth.com | ir@axcellahealth.com |
(857) 320-2204 | 212-698-8646 |
A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/181a24c7-a9e7-4ac6-b0ca-583d30e49532
Source: Axcella Health