REDWOOD CITY, Calif., Nov. 12, 2024 (GLOBE NEWSWIRE) -- Bolt Biotherapeutics (NASDAQ:BOLT), a clinical-stage biopharmaceutical company developing novel immunotherapies for the treatment of cancer, today reported financial results for the third quarter ended September 30, 2024, and provided a business update.
"During the third quarter, we continued to make progress with our two proprietary programs, BDC-3042 and BDC-4182," said Willie Quinn, Chief Executive Officer. "We have now completed the sixth dose level in the first-in-human clinical trial of BDC-3042, have opened the final cohort which will study a dose level of 10 mg/kg, and expect to provide a data update in the first half of 2025. We are particularly excited about our next-generation ISAC BDC-4182, which builds on the lessons we learned from our clinical experience with BDC-1001. We believe that BDC-4182's dramatic increase in potency and activity will potentially enable the treatment of patients whose tumors have lower claudin 18.2 expression and may provide even better anti-tumor activity than conventional ADCs. We presented some of the data that underlies this excitement at SITC, and the team is hard at work preparing for a clinical trial initiation of BDC-4182 in the second quarter next year."
Recent Highlights and Anticipated Milestones
Third Quarter 2024 Financial Results
About the Boltbody™ Immune-Stimulating Antibody Conjugate (ISAC) Platform
Bolt Biotherapeutics' Boltbody ISAC platform harnesses the precision of antibodies with the power of the innate and adaptive immune system to generate a productive anti-cancer response. Each Boltbody ISAC candidate comprises a tumor-targeting antibody, a non-cleavable linker, and a proprietary immune stimulant. The antibody is designed to target one or more markers on the surface of a tumor cell and the immune stimulant is designed to recruit and activate myeloid cells. Activated myeloid cells initiate a positive feedback loop by releasing cytokines and chemokines, chemical signals that attract other immune cells and lower the activation threshold for an immune response. This increases the population of activated immune system cells in the tumor microenvironment and promotes a robust immune response with the goal of generating durable therapeutic responses for patients with cancer.
About Bolt Biotherapeutics, Inc.
Bolt Biotherapeutics is a clinical-stage biopharmaceutical company developing novel immunotherapies for the treatment of cancer. Bolt Biotherapeutics' pipeline candidates are built on the Company's deep expertise in myeloid biology and cancer drug development. The Company's pipeline includes BDC-3042, a first-in-class agonist antibody that activates macrophages by targeting Dectin-2, and BDC-4182, a next-generation Boltbody™ Immune-Stimulating Antibody Conjugate (ISAC) clinical candidate targeting claudin 18.2. BDC-3042 is currently in a Phase 1 dose escalation trial that includes patients with any of seven different solid tumor types. BDC-4182 is supported by strong in vitro and in vivo data demonstrating potent anti-tumor activity, and activities are underway to support the initiation of clinical trials in 2025. Bolt Biotherapeutics is also developing additional Boltbody™ ISACs in strategic collaborations with leading biopharmaceutical companies. For more information, please visit https://www.boltbio.com/.
Forward-Looking Statements
This press release contains forward-looking statements about us and our industry that involve substantial risks and uncertainties and are based on our beliefs and assumptions and on information currently available to us. All statements other than statements of historical facts contained in this press release, including statements regarding the advancement and success of our BDC-3042 clinical trial, the potential initiation of clinical trials for BDC-4182, the anti-tumor potency, safety and tolerability, and characteristics of our product candidates, the initiation of future clinical trials, the potential value of collaborations, and the expected duration of our cash runway, are forward-looking statements. In some cases, you can identify forward-looking statements because they contain words such as "anticipate," "believe," "could," "estimate," "expect," "intend," "may," "on track," "plan," "potential," "predict," "project," "should," "will," or "would," or the negative of these words or other similar terms or expressions. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Forward-looking statements represent our current beliefs, estimates and assumptions only as of the date of this press release and information contained in this press release should not be relied upon as representing our estimates as of any subsequent date. These statements, and related risks, uncertainties, factors and assumptions, include, but are not limited to: the potential product candidates that we develop may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; clinical trials may not confirm any safety, potency or other product characteristics described or assumed in this press release; such product candidates may not be beneficial to patients or become commercialized; and our ability to maintain our current collaborations and establish further collaborations. These risks are not exhaustive. Except as required by law, we assume no obligation to update these forward-looking statements, or to update the reasons actual results could differ materially from those anticipated in the forward-looking statements, even if new information becomes available in the future. Further information on factors that could cause actual results to differ materially from the results anticipated by our forward-looking statements is included in the reports we have filed or will file with the Securities and Exchange Commission, including our Annual Report on Form 10-K for the year ended December 31, 2023. These filings, when available, are available on the investor relations section of our website at investors.boltbio.com and on the SEC's website at www.sec.gov.
Investor Relations and Media Contact:
Matthew DeYoung
Argot Partners
(212) 600-1902
boltbio@argotpartners.com
| BOLT BIOTHERAPEUTICS, INC. CONDENSED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS (Unaudited, in thousands, except share and per share amounts) | ||||||||||||||||
| Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||||
| 2024 | 2023 | 2024 | 2023 | |||||||||||||
| Collaboration revenue | $ | 1,141 | $ | 2,528 | $ | 7,690 | $ | 5,787 | ||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 13,785 | 14,951 | 45,747 | 45,220 | ||||||||||||
| General and administrative | 3,799 | 5,760 | 14,510 | 16,997 | ||||||||||||
| Restructuring charges | — | — | 3,565 | — | ||||||||||||
| Total operating expense | 17,584 | 20,711 | 63,822 | 62,217 | ||||||||||||
| Loss from operations | (16,443 | ) | (18,183 | ) | (56,132 | ) | (56,430 | ) | ||||||||
| Other income, net | ||||||||||||||||
| Interest income, net | 1,267 | 1,926 | 4,275 | 5,136 | ||||||||||||
| Other income | — | — | 4,675 | — | ||||||||||||
| Total other income, net | 1,267 | 1,926 | 8,950 | 5,136 | ||||||||||||
| Net loss | (15,176 | ) | (16,257 | ) | (47,182 | ) | (51,294 | ) | ||||||||
| Net unrealized gain on marketable securities | 249 | 55 | 168 | 745 | ||||||||||||
| Comprehensive loss | $ | (14,927 | ) | $ | (16,202 | ) | $ | (47,014 | ) | $ | (50,549 | ) | ||||
| Net loss per share, basic and diluted | $ | (0.40 | ) | $ | (0.43 | ) | $ | (1.24 | ) | $ | (1.36 | ) | ||||
| Weighted-average shares outstanding, basic and diluted | 38,250,982 | 37,868,480 | 38,149,830 | 37,768,308 | ||||||||||||
| BOLT BIOTHERAPEUTICS, INC. CONDENSED BALANCE SHEETS (Unaudited, in thousands) | ||||||||
| September 30, 2024 | December 31, 2023 | |||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 9,366 | $ | 10,810 | ||||
| Short-term investments | 44,432 | 91,379 | ||||||
| Restricted cash | 792 | — | ||||||
| Prepaid expenses and other current assets | 2,557 | 3,519 | ||||||
| Total current assets | 57,147 | 105,708 | ||||||
| Property and equipment, net | 3,565 | 4,957 | ||||||
| Operating lease right-of-use assets | 16,756 | 19,120 | ||||||
| Restricted cash, non-current | 981 | 1,765 | ||||||
| Long-term investments | 30,598 | 26,413 | ||||||
| Other assets | 287 | 1,821 | ||||||
| Total assets | $ | 109,334 | $ | 159,784 | ||||
| Liabilities and stockholders' equity | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 1,482 | $ | 2,987 | ||||
| Accrued expenses and other current liabilities | 11,806 | 12,486 | ||||||
| Deferred revenue | 1,971 | 2,201 | ||||||
| Operating lease liabilities | 2,824 | 2,782 | ||||||
| Total current liabilities | 18,083 | 20,456 | ||||||
| Operating lease liabilities, net of current portion | 15,353 | 17,437 | ||||||
| Deferred revenue, non-current | 3,867 | 9,107 | ||||||
| Other long-term liabilities | - | 43 | ||||||
| Total liabilities | 37,303 | 47,043 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders' equity: | ||||||||
| Preferred stock | — | — | ||||||
| Common stock | 1 | 1 | ||||||
| Additional paid-in capital | 483,292 | 476,988 | ||||||
| Accumulated other comprehensive gain | 205 | 37 | ||||||
| Accumulated deficit | (411,467 | ) | (364,285 | ) | ||||
| Total stockholders' equity: | 72,031 | 112,741 | ||||||
| Total liabilities and stockholders' equity | $ | 109,334 | $ | 159,784 | ||||
| BOLT BIOTHERAPEUTICS, INC. CONDENSED STATEMENTS OF CASH FLOWS (Unaudited, in thousands) | ||||||||
| Nine Months Ended September 30, | ||||||||
| 2024 | 2023 | |||||||
| CASH FLOWS FROM OPERATING ACTIVITIES: | ||||||||
| Net loss | $ | (47,182 | ) | $ | (51,294 | ) | ||
| Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||
| Depreciation and amortization | 1,355 | 1,387 | ||||||
| Stock-based compensation expense | 6,225 | 7,155 | ||||||
| Accretion of discount on marketable securities | (2,307 | ) | (3,299 | ) | ||||
| Gain on sale of fixed assets | (70 | ) | — | |||||
| Non-cash lease expense | 2,364 | 2,194 | ||||||
| Changes in operating assets and liabilities: | ||||||||
| Prepaid expenses and other assets | 2,496 | (2,198 | ) | |||||
| Accounts payable and accrued expenses | (2,185 | ) | (4,601 | ) | ||||
| Operating lease liabilities | (2,042 | ) | (1,754 | ) | ||||
| Deferred revenue | (5,470 | ) | (2,851 | ) | ||||
| Other long-term liabilities | (43 | ) | 1 | |||||
| Net cash used in operating activities | (46,859 | ) | (55,260 | ) | ||||
| CASH FLOWS FROM INVESTING ACTIVITIES: | ||||||||
| Purchase of property and equipment | (41 | ) | (200 | ) | ||||
| Proceeds from sales of property and equipment | 148 | — | ||||||
| Purchases of marketable securities | (75,602 | ) | (132,828 | ) | ||||
| Maturities of marketable securities | 120,839 | 188,257 | ||||||
| Net cash provided by investing activities | 45,344 | 55,229 | ||||||
| CASH FLOWS FROM FINANCING ACTIVITIES: | ||||||||
| Proceeds from issuance of common stock | 79 | 147 | ||||||
| Net cash provided by financing activities | 79 | 147 | ||||||
| Net (decrease) increase in cash | (1,436 | ) | 116 | |||||
| Cash, cash equivalents and restricted cash at beginning of year | 12,575 | 10,809 | ||||||
| Cash, cash equivalents and restricted cash at end of period | $ | 11,139 | $ | 10,925 | ||||
| Reconciliation of cash, cash equivalents and restricted cash: | ||||||||
| Cash and cash equivalents | $ | 9,366 | $ | 9,160 | ||||
| Restricted cash | 1,773 | 1,765 | ||||||
| Total cash, cash equivalents and restricted cash | $ | 11,139 | $ | 10,925 | ||||
