Vaccinex Reports First Quarter 2024 Financial Results and Provides Corporate Update
Vaccinex has announced its first quarter 2024 financial results and updates on the SIGNAL-AD Phase 2a study for Alzheimer’s disease treatment using pepinemab. The last patient visit is scheduled for early June 2024, with data analysis by early July. Key highlights include the study's potential to slow neurodegenerative disease progression, funded partly by $4.75 million from the Alzheimer's Drug Discovery Foundation, and $0.75 million from the Alzheimer's Association. Financial highlights feature cash equivalents of $3.0 million, reductions in R&D expenses to $3.4 million, and a net loss decrease to $3.9 million. However, Nasdaq has flagged the company for non-compliance with equity standards. In response, Vaccinex has submitted a compliance plan.
- Completion of the SIGNAL-AD Phase 2a study by early June 2024 with data analysis by early July.
- Pepinemab shows potential to slow or halt Alzheimer's disease progression.
- Funding support of $4.75 million from the Alzheimer's Drug Discovery Foundation and $0.75 million from the Alzheimer's Association.
- Cash and marketable securities increased to $3.0 million as of March 31, 2024, compared to $1.5 million on December 31, 2023.
- Reduction in R&D expenses from $3.8 million in Q1 2023 to $3.4 million in Q1 2024.
- Decrease in net loss from $5.0 million in Q1 2023 to $3.9 million in Q1 2024.
- Stockholders’ equity improved to $2.7 million by March 31, 2024, resolving previous deficits.
- Nasdaq non-compliance notice due to equity falling below $2.5 million.
- General and administrative expenses increased slightly from $1.7 million in Q1 2023 to $1.8 million in Q1 2024.
- Comprehensive loss per share was $(2.94) for the quarter.
- Persistent financial instability indicated by the need for private placements and public offerings to raise capital.
- Company's future compliance with Nasdaq listing standards remains uncertain despite submitted plan.
Vaccinex's financial results for Q1 2024 show improved
Retail investors should be cautious: while the financial influx helps stabilize Vaccinex momentarily, consistent net losses indicate continued financial risk. The company must demonstrate the ability to generate revenue or secure further funding to maintain operations long-term.
Additionally, the reverse stock split (1-for-14) should be noted, often a strategy to meet listing requirements rather than an indicator of fundamental strength.
The SIGNAL-AD Phase 2a study evaluating pepinemab offers potential breakthroughs in Alzheimer’s disease (AD) treatment. Progressing to the final patient visits in early June 2024 and subsequent data analysis in July, the study could impact the neurodegenerative disease market significantly if positive outcomes are evident.
Pepinemab targets SEMA4D-induced astrocyte activation, a novel mechanism differing from traditional anti-Aβ amyloid therapies. Given the limitations of current treatments and pepinemab’s capacity to modulate astrocyte behavior without triggering amyloid-related imaging abnormalities (ARIA), it provides a compelling alternative or adjunctive approach.
Investors should watch for detailed results, as success in this trial could lead to substantial advancements in AD care, positioning Vaccinex as a key player in the space. However, it's important to be mindful of potential setbacks typical in clinical trials.
Pepinemab’s potential extends beyond AD to other neurodegenerative diseases like Huntington’s Disease (HD). Previous data suggesting cognitive benefits in HD patients underscore the broader therapeutic promise of the drug. This cross-disease applicability could amplify its market impact, offering patients across multiple diseases a novel treatment approach.
Understanding the mechanisms—blocking SEMA4D to prevent astrocyte-induced neurotoxicity—could transform not just AD treatment but also the general approach to neuroinflammation in neurodegenerative diseases. Such innovation could attract further research interest and partnerships, enhancing Vaccinex's market position.
Last patient last visit in randomized, double-blind, SIGNAL-AD Phase 2a study of pepinemab treatment for Alzheimer’s Disease is scheduled for early June 2024
ROCHESTER, N.Y., May 15, 2024 (GLOBE NEWSWIRE) -- Vaccinex, Inc. (Nasdaq: VCNX), a clinical-stage biotechnology company pioneering a differentiated approach to treating neurodegenerative disease and cancer through the inhibition of Semaphorin 4D (SEMA4D), today announced financial results for the first quarter ended March 31, 2024, and provided a corporate update on its key program for Alzheimer’s disease.
Treatment with pepinemab believed to halt or slow progression of neurodegenerative disease:
Vaccinex expects to complete the planned 12-months of treatment of the last patients enrolled in its randomized, double-blind, Phase 2a SIGNAL-AD trial of pepinemab anti-SEMA4D antibody for mild Alzheimer’s disease (NCT04381468) in early June 2024. Database lock will follow by early July to enable final analysis of the major study outcomes.
Of interest to investors:
- Vaccinex’s lead product, pepinemab, is designed to block astrocyte activation that is otherwise triggered by SEMA4D upregulation on stressed or damaged neurons in the brain during progression of Alzheimer’s Disease (AD) and Huntington’s Disease (HD).
- Astrocytes, which are key brain cells that support the health and function of neurons, express high affinity receptors for SEMA4D and undergo substantial changes in morphology and gene expression when SEMA4D binds to these receptors. As a result, they switch from normal supportive functions to neurotoxic inflammatory activity that is believed to accelerate and aggravate progression of neurodegenerative diseases.
- The Company’s hypothesis, which is being tested in the SIGNAL-AD study, is that treating with pepinemab antibody can block signaling by SEMA4D and prevent some or all damaging consequences of astrocyte activation.
- The Company has previously reported that antibody blockade of SEMA4D appears to protect and restore healthy astrocyte functions and, by some measures, also appears to slow or prevent cognitive decline in Huntington’s disease.
- The Company believes that the prevalence of AD (6 million people diagnosed with AD in the US alone) and current concerns about the limitations of treatment with anti-Aβ amyloid antibodies could make pepinemab, if approved, attractive as a potential alternative treatment or possibly for use in combination with anti-Aβ to enhance the benefit to patients. Pepinemab has, to date, been well-tolerated in clinical trials that enrolled a total of more than 600 patients, with no evidence of amyloid-related imaging abnormalities (ARIA).
Of further interest to the medical and research communities:
- Deposition of Aβ amyloid in the brain is recognized as the earliest event in the pathologic cascade for AD. However, the observation that many elderly, cognitively normal subjects also evidence deposition of Aβ amyloid in their brains suggests that this is not of itself sufficient for disease progression and that a sequence of subsequent events, including astrocyte activation and formation of toxic tau tangles in neurons, is required. Others have recently shown that Aβ deposition in combination with astrocyte activation is associated with increased plasma levels of phosphorylated tau peptide (p-tau 217).
- Key outcomes of the SIGNAL-AD study will include impact of pepinemab treatment on brain metabolic activity, an important biomarker of clinical progression in AD, together with other biomarkers of disease progression including plasma levels of glial fibrillary acidic protein (GFAP) released by reactive astrocytes, and phosphorylated tau peptide. Exploratory evaluation of treatment effects on cognitive decline will employ several validated cognitive scales. Topline data will be presented at a major Alzheimer’s medical conference.
- The SIGNAL-AD study was funded in part by two investments from the Alzheimer’s Drug Discovery Foundation (ADDF) for a total of
$4.75 million , and by an$0.75 million grant from the Alzheimer’s Association.
Financial Results for the Quarter Ended March 31, 2024:
Cash and Cash Equivalents and Marketable Securities. Cash and cash equivalents and marketable securities on March 31, 2024, were
On February 8, 2024, and March 28, 2024, the Company completed private placements of common stock with accompanying warrants to purchase common stock to certain investors, including entities controlled by Albert D. Friedberg, the chairman of the Company’s board of directors and Maurice Zauderer, the Company’s President and CEO, for gross proceeds of
Research and Development Expenses. Research and development expenses for the quarter ended March 31, 2024, were
General and Administrative Expenses. General and administrative expenses for the quarter ended March 31, 2024, were
Comprehensive loss/Net loss per share. The Comprehensive Loss and Net loss per share for the quarter ended March 31, 2024, were
Total Stockholders’ Equity. Stockholders’ Equity as of March 31, 2024, was
Financial tables are included below. The Company effected a 1-for-14 reverse stock split on February 20 2024. All share and share amounts have been retroactively restated to give effect to the reverse stock split. For further details on Vaccinex’s financials and the reverse stock split, please refer to its Form 10K filed April 1, 2024, with the SEC.
About Pepinemab
Pepinemab is a humanized IgG4 monoclonal antibody designed to block SEMA4D, which can trigger collapse of the actin cytoskeleton and loss of homeostatic functions of astrocytes and other glial cells in the brain and dendritic cells in immune tissue. Over 600 patients have been treated or enrolled in clinical trials of pepinemab in different indications and pepinemab appears to be well-tolerated with a favorable safety profile.
About Vaccinex Inc.
Vaccinex, Inc. is pioneering a differentiated approach to treating slowly progressive neurodegenerative diseases and cancer through the inhibition of semaphorin 4D (SEMA4D). The Company’s lead drug candidate, pepinemab, blocks SEMA4D, a potent biological effector that it believes triggers damaging inflammation in chronic diseases of the brain and prevents immune infiltration into tumors. Pepinemab is being studied as a monotherapy in the Phase 1/2a SIGNAL-AD study in Alzheimer’s Disease, with ongoing exploration of potential Phase 3 development in Huntington’s disease. In oncology, pepinemab is being evaluated in combination with KEYTRUDA® in the Phase 1b/2 KEYNOTE-B84 study in recurrent or metastatic head and neck cancer (HNSCC) and in combination with BAVENCIO® in a Phase 1b/2 study in patients with metastatic pancreatic adenocarcinoma (PDAC). The oncology clinical program also includes several investigator-sponsored studies in solid tumors including breast cancer and melanoma.
Vaccinex has global commercial and development rights to pepinemab and is the sponsor of the KEYNOTE-B84 study which is being performed in collaboration with Merck Sharp & Dohme Corp, a subsidiary of Merck and Co, Inc. Kenilworth, NJ, USA. Additional information about the study is available at: clinicaltrials.gov.
KEYTRUDA is a registered trademark of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co. Inc., Kenilworth, NJ, USA. BAVENCIO®/avelumab is provided by Merck KGaA, Darmstadt, Germany, previously as part of an alliance between the healthcare business of Merck KGaA, Darmstadt, Germany and Pfizer.
Forward Looking Statements
To the extent that statements contained in this press release are not descriptions of historical facts regarding Vaccinex, Inc. (“Vaccinex,” “we,” “us,” or “our”), they are forward-looking statements reflecting management’s current beliefs and expectations. Such statements include, but are not limited to, statements about expectations and objectives with respect to the results and timing of the SIGNAL-AD clinical trial; expectations with respect to compliance with Nasdaq listing standards; our plans, expectations and objectives with respect to the results and timing of the KEYNOTE-B84 clinical trial; the use and potential benefits of pepinemab in R/M HNSCC, lung cancer, metastatic pancreatic adenocarcinoma (PDAC) and other indications; the potential for benefits as compared to single agent KEYTRUDA® or BAVENCIO®; expectations with respect to the collaboration of Merck, the potential to initiate a Phase 3 trial in Huntington’s disease; and other statements identified by words such as “anticipate,” “believe,” “schedule,” “being,” “will,” “appears,” “expect,” “ongoing,” “potential,” “suggest”, and similar expressions or their negatives (as well as other words and expressions referencing future events, conditions, or circumstances). Forward-looking statements involve substantial risks and uncertainties that could cause the outcome of our research and pre-clinical development programs, clinical development programs, future results, performance, or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, uncertainties inherent in the execution, cost and completion of preclinical studies and clinical trials, that interim and preliminary data may not be predictive of final results and does not ensure success in later clinical trials, uncertainties related to regulatory approval, risks related to our dependence on our lead product candidate pepinemab, the possible delisting of our common stock from Nasdaq if the Company is unable to regain compliance with the Nasdaq listing standards, and other matters that could affect our development plans or the commercial potential of our product candidates. Except as required by law, the Company assumes no obligation to update these forward-looking statements. For a further discussion of these and other factors that could cause future results to differ materially from any forward-looking statement, see the section titled “Risk Factors” in our periodic reports filed with the Securities and Exchange Commission and the other risks and uncertainties described in the Company’s annual year-end Form 10-K and subsequent filings with the SEC.
Investor Contact
Elizabeth Evans, PhD
Chief Operating Officer, Vaccinex, Inc.
(585) 271-2700
eevans@vaccinex.com
VACCINEX, INC.
Condensed Balance Sheets (Unaudited)
(in thousands, except share and per share data)
| As of March 31, 2024 | As of December 31, 2023 | |||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 2,972 | $ | 1,535 | ||||
| Accounts receivable | 2,775 | 961 | ||||||
| Prepaid expenses and other current assets | 1,312 | 853 | ||||||
| Derivative asset | 95 | - | ||||||
| Total current assets | 7,154 | 3,349 | ||||||
| Property and equipment, net | 110 | 136 | ||||||
| Operating lease right-of-use asset | 103 | 146 | ||||||
| TOTAL ASSETS | $ | 7,367 | $ | 3,631 | ||||
| LIABILITIES AND STOCKHOLDERS’ EQUITY | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 2,329 | $ | 2,039 | ||||
| Accrued expenses | 1,880 | 1,242 | ||||||
| Deferred revenue | 59 | 63 | ||||||
| Current portion of long-term debt | 76 | 75 | ||||||
| Operating lease liability | 103 | 146 | ||||||
| Warrant liability | 259 | 2,351 | ||||||
| Total current liabilities | 4,706 | 5,916 | ||||||
| Long-term debt | 6 | 26 | ||||||
| TOTAL LIABILITIES | 4,712 | 5,942 | ||||||
| Commitments and contingencies (Note 6) | ||||||||
| Stockholders’ equity (deficit): | ||||||||
| Convertible preferred stock (Series A), par value of | 1,236 | - | ||||||
| Common stock, par value of as of March 31, 2024, and December 31, 2023; 1,584,305 and 892,622 shares issued as of March 31, 2024 and December 31, 2023, respectively; 1,584,300 and 892,617 shares outstanding as of March 31, 2024 and December 31, 2023, respectively | 1 | - | ||||||
| Additional paid-in capital | 345,253 | 337,627 | ||||||
| Treasury stock, at cost; 5 shares of common stock as of March 31, 2024, and December 31, 2023, respectively | (11 | ) | (11 | ) | ||||
| Accumulated deficit | (343,824 | ) | (339,927 | ) | ||||
| TOTAL STOCKHOLDERS’ EQUITY/(DEFICIT) | 2,655 | (2,311 | ) | |||||
| TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY | $ | 7,367 | $ | 3,631 | ||||
VACCINEX, INC.
Condensed Statements of Operations and Comprehensive Loss (Unaudited)
(in thousands, except share and per share data)
| Three Months Ended March 31, | ||||||||
| 2024 | 2023 | |||||||
| Revenue | $ | 104 | $ | 550 | ||||
| Costs and expenses: | ||||||||
| Research and development | 3,383 | 3,812 | ||||||
| General and administrative | 1,795 | 1,724 | ||||||
| Total costs and expenses | 5,178 | 5,536 | ||||||
| Loss from operations | (5,074 | ) | (4,986 | ) | ||||
| Financing costs - warrant liabilities | (28 | ) | - | |||||
| Change in fair value of warrant liabilities | 1,206 | - | ||||||
| Other income (expense), net | (1 | ) | 24 | |||||
| Loss before provision for income taxes | (3,897 | ) | (4,962 | ) | ||||
| Provision for income taxes | - | - | ||||||
| Net loss attributable to Vaccinex, Inc. common stockholders | $ | (3,897 | ) | $ | (4,962 | ) | ||
| Comprehensive loss | $ | (3,897 | ) | $ | (4,962 | ) | ||
| Net loss per share attributable to Vaccinex, Inc. common stockholders, basic and diluted | $ | (2.94 | ) | $ | (20.89 | ) | ||
| Weighted-average shares used in computing net loss per share attributable to Vaccinex, Inc. common stockholders, basic and diluted | 1,327,257 | 237,527 | ||||||
FAQ
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