UTRECHT, The Netherlands and PHILADELPHIA, Aug. 20, 2024 (GLOBE NEWSWIRE) — LAVA Therapeutics N.V. (NASDAQ: LVTX, “LAVA,” “the Company”), a clinical-stage immuno-oncology company focused on developing its proprietary Gammabody® platform of bispecific gamma delta T cell engagers, today announced financial results for the second quarter ended June 30, 2024 and provided an update on recent corporate highlights.
“LAVA has continued to make progress in the Phase 1/2a study for LAVA-1207, our lead Gammabody® product candidate in mCRPC. Patients in the Phase 1/2a study are being treated with LAVA-1207 monotherapy at dose level 12,” said Stephen Hurly, President and Chief Executive Officer of LAVA. “In Q2 2024, we initiated dosing in the pembrolizumab combination arm and have dosed our first patients. We expect to release the next data for LAVA-1207 at a medical meeting later this year. We are also excited to start our clinical trial for LAVA-1266 for AML/MDS later this year.”
Portfolio Highlights:
LAVA-1207 – In Phase 1/2a (NCT05369000) – Next update planned for Q4 2024
Designed to mediate potent killing of prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC) cells
LAVA-1266 – Trial initiation activities underway
Designed to target CD123+ tumor cells for the treatment of hematological malignancies, including acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS)
Pfizer PF-08046052 – In Phase 1 (NCT05983133)
Potential first-in-class EGFR and bispecific gamma delta T cell-targeted therapy for solid tumors
Johnson and Johnson Innovative Medicine Collaboration – In Research
Discovery and development of novel bispecific gamma delta T cell engager for the treatment of blood cancer
Second Quarter 2024 Financial Results
We will transition from foreign private issuer to U.S. domestic filer status beginning on January 1, 2025 and expect to incur increased costs associated with being a U.S. domestic filer, including expenses related to financial reporting, preparation of financial statements in accordance with U.S. GAAP and compliance with U.S. federal proxy rules.
| LAVA Therapeutics N.V. Condensed Consolidated Interim Statements Loss and Comprehensive Loss (in thousands, except share and per share amounts) (unaudited) |
|||||||||||||||||
| Three Months Ended | For the Six Months Ended | ||||||||||||||||
| June 30, | June 30, | ||||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||||
| Revenue: | |||||||||||||||||
| Revenue from contracts with customers | $ | — | $ | 5,139 | $ | 6,992 | $ | 6,363 | |||||||||
| Cost of sales of goods | — | (2,361 | ) | — | (2,546 | ) | |||||||||||
| Cost of providing services | — | (27 | ) | — | (772 | ) | |||||||||||
| Gross profit | — | 2,751 | 6,992 | 3,045 | |||||||||||||
| Operating expenses: | |||||||||||||||||
| Research and development | (6,336 | ) | (12,599 | ) | (12,345 | ) | (22,542 | ) | |||||||||
| General and administrative | (3,025 | ) | (3,697 | ) | (5,960 | ) | (7,587 | ) | |||||||||
| Total operating expenses | (9,361 | ) | (16,296 | ) | (18,305 | ) | (30,129 | ) | |||||||||
| Operating loss | (9,361 | ) | (13,545 | ) | (11,313 | ) | (27,084 | ) | |||||||||
| Interest income, net | 811 | 698 | 1,621 | 1,315 | |||||||||||||
| Foreign currency exchange gain (loss), net | 339 | 244 | 997 | (703 | ) | ||||||||||||
| Total non-operating income | 1,150 | 942 | 2,618 | 612 | |||||||||||||
| Loss before income tax | (8,211 | ) | (12,603 | ) | (8,695 | ) | (26,472 | ) | |||||||||
| Income tax expense | (85 | ) | (97 | ) | (154 | ) | (168 | ) | |||||||||
| Loss for the period | $ | (8,296 | ) | $ | (12,700 | ) | $ | (8,849 | ) | $ | (26,640 | ) | |||||
| Items that may be reclassified to profit or loss | |||||||||||||||||
| Foreign currency translation adjustment | (329 | ) | (243 | ) | (1,392 | ) | 1,303 | ||||||||||
| Total comprehensive loss | $ | (8,625 | ) | $ | (12,943 | ) | $ | (10,241 | ) | $ | (25,337 | ) | |||||
| Loss per share: | |||||||||||||||||
| Loss per share, basic and diluted | $ | (0.31 | ) | $ | (0.48 | ) | $ | (0.33 | ) | $ | (1.01 | ) | |||||
| Weighted-average common shares outstanding, basic and diluted | 26,822,139 | 26,289,087 | 26,805,793 | 26,289,087 | |||||||||||||
| LAVA Therapeutics N.V. Condensed Consolidated Statements of Financial Position (in thousands) (unaudited) |
|||||||||
| June 30, | December 31, | ||||||||
| 2024 | 2023 | ||||||||
| Assets | |||||||||
| Non-current assets: | |||||||||
| Property and equipment, net | $ | 1,230 | $ | 1,602 | |||||
| Right-of-use assets | 737 | 892 | |||||||
| Other non-current assets and security deposits | 144 | 319 | |||||||
| Total non-current assets | 2,111 | 2,813 | |||||||
| Current assets: | |||||||||
| Receivables and other | 582 | 1,459 | |||||||
| Prepaid expenses and other current assets | 2,223 | 1,627 | |||||||
| VAT receivable | 568 | 240 | |||||||
| Investments | 51,714 | 51,340 | |||||||
| Cash and cash equivalents | 35,086 | 44,231 | |||||||
| Total current assets | 90,173 | 98,897 | |||||||
| Total assets | $ | 92,284 | $ | 101,710 | |||||
| Equity and Liabilities | |||||||||
| Equity: | |||||||||
| Share capital | $ | 3,716 | $ | 3,715 | |||||
| Equity-settled employee benefits reserve | 13,729 | 12,005 | |||||||
| Foreign currency translation reserve | (12,291 | ) | (10,899 | ) | |||||
| Additional paid-in capital | 194,448 | 194,424 | |||||||
| Accumulated deficit | (156,724 | ) | (148,067 | ) | |||||
| Total equity | 42,878 | 51,178 | |||||||
| Non-current liabilities: | |||||||||
| Deferred revenue | 35,000 | 35,000 | |||||||
| Lease liabilities | 295 | 591 | |||||||
| Total non-current liabilities | 35,295 | 35,591 | |||||||
| Current liabilities: | |||||||||
| Trade payables and other | 4,161 | 4,446 | |||||||
| Borrowings | 5,383 | 5,282 | |||||||
| Lease liabilities | 485 | 440 | |||||||
| Accrued expenses and other current liabilities | 4,082 | 4,773 | |||||||
| Total current liabilities | 14,111 | 14,941 | |||||||
| Total liabilities | 49,406 | 50,532 | |||||||
| Total equity and liabilities | $ | 92,284 | $ | 101,710 | |||||
About LAVA Therapeutics
LAVA Therapeutics N.V. is a clinical-stage immuno-oncology company focused on advancing its proprietary Gammabody® platform to develop a portfolio of bispecific gamma-delta T cell engagers for the potential treatment of solid tumors and hematologic malignancies. The Company utilizes bispecific antibodies engineered to selectively kill cancer cells by triggering Vγ9Vδ2 (Vgamma9 Vdelta2) T cell anti-tumor effector functions upon cross-linking to tumor-associated antigens.
A Phase 1/2a dose escalation study (NCT05369000) to evaluate the lead program, LAVA-1207, in patients with metastatic castration-resistant prostate cancer (mCRPC) is actively enrolling in Europe and the United States in a study evaluating monotherapy and with interleukin-2 (IL-2). The Company is expanding the Phase 1/2a study to include a combination arm with KEYTRUDA®(pembrolizumab) through a clinical collaboration with Merck & Co., Inc., Rahway, NJ, USA. The Company licensed PF-08046052 (formerly LAVA-1223) to Pfizer Inc. for clinical development and commercialization. The pipeline also includes several pre-clinical programs. For more information, please visit www.lavatherapeutics.com, and follow us on LinkedIn, X, and YouTube.
KEYTRUDA® is a registered trademark of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co. LLC, Rahway, NJ, USA
Gammabody® is a registered trademark of LAVA Therapeutics N.V.
LAVA’s Cautionary Note on Forward-Looking Statements
This press release contains forward-looking statements, including with respect to the Company’s anticipated growth and clinical development plans including the timing and results of clinical trials. Words such as “anticipate”, “believe”, “could”, “will”, “may”, “expect”, “should”, “plan”, “intend”, “estimate”, “potential”, “suggests”, and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on LAVA’s expectations and assumptions as of the date of this press release and are subject to various risks and uncertainties that may cause actual results to differ materially from these forward-looking statements. Forward-looking statements contained in this press release include but are not limited to statements relating to the therapeutic potential, development and potential uses of LAVA’s product candidates, the timing of initiation of clinical trials, including the expansion phase of the Phase 1/2a trial to evaluate LAVA-1207 in combination with KEYTRUDA® and the timing of initiating the Phase 1 trial of LAVA-1266, the timing of regulatory submissions, including an IND for LAVA-1266 in AML and MDS, LAVA’s cash runway and the sufficiency of resources to pursue development activities, availability of information regarding clinical development plans, progress and data from clinical trials, the ability of LAVA’s product candidates to treat various tumor targets, including CRC, NSCLC, PDAC and HNSCC, and improve patient outcomes and the sufficiency of resources to pursue development activities. Many factors, risks and uncertainties may cause differences between current expectations and actual results, including, among other things, the Company’s ability to leverage its initial programs to develop additional product candidates using our Gammabody® platform, and the failure of LAVA’s collaborators to support or advance collaborations or LAVA’s product candidates, the timing and results of LAVA’s research and development programs and preclinical and clinical trials, the possibility that clinical trials may fail to establish sufficient efficacy, the risk that adverse events or safety signals may occur, in clinical trials, the risk that results obtained in clinical trials to date may not be indicative of results obtained in ongoing or future trials, the risk that adverse regulatory actions or other setbacks could occur in clinical trials even after promising results in earlier clinical trials or preclinical studies, the Company’s ability to obtain regulatory approval for and commercialize its product candidates, and the risk that setbacks in development could occur as a result of the difficulty and uncertainty of pharmaceutical product development and other factors. There may be adverse effects on the Company’s business condition and results from general economic and market conditions and overall fluctuations in the United States and international equity markets, including as a result of inflation, heightened interest rates, recent and potential future pandemics and other health crises, and hostilities, including between Russia and Ukraine or the Israel-Hamas war. These and other risks are described in greater detail under the caption “Risk Factors” and included in LAVA’s filings with the Securities and Exchange Commission. LAVA assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.
CONTACTS
Investor Relations
ir@lavatherapeutics.com
LifeSci Advisors (IR/Media)
Joyce Allaire
Jallaire@lifesciadvisors.com
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