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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): March 24, 2025

 

 

BOLT BIOTHERAPEUTICS, INC.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-39988

47-2804636

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

900 Chesapeake Drive

 

Redwood City, California

 

94063

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (650) 665-9295

 

Not Applicable

(Former Name or Former Address, if Changed Since Last Report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

☐Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
☐Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
☐Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
☐Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:


Title of each class

 

Trading
Symbol(s)

 


Name of each exchange on which registered

Common Stock, par value $0.00001 per share

 

BOLT

 

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§ 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§ 240.12b-2 of this chapter).

Emerging growth company ☒

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☒ On March 24, 2025, Bolt Biotherapeutics, Inc. (the “Company”) issued a press release announcing its financial results for the fourth and full year ended December 31, 2024 and a corporate update. A copy of the press release is furnished herewith as Exhibit 99.1 and incorporated herein by reference.

 


Item 2.02 Results of Operations and Financial Condition.

The information contained herein and the accompanying exhibit is furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended, nor shall it be deemed incorporated by reference in any filing with the Securities and Exchange Commission made by us, whether made before or after the date hereof, regardless of any general incorporation language in such filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

Exhibit No.

 

Description

 

 

99.1

 

Press Release dated March 24, 2025.

104

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

 


SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

 

 

 

Bolt Biotherapeutics, Inc.

 

 

 

 

Date:

March 24, 2025

By:

/s/ William P. Quinn

 

 

 

William P. Quinn
President, Chief Executive Officer and Chief Financial Officer

 


EX-99.1 2 bolt-ex99_1.htm EX-99.1 EX-99.1

 

Exhibit 99.1

img192637872_0.jpg

 

Bolt Biotherapeutics Reports Fourth Quarter and Full-Year 2024 Financial Results and Provides Business Update

 

BDC-4182 on track to start a clinical trial in gastric cancer in second quarter 2025
BDC-3042 Phase 1 clinical trial fully enrolled the highest dose cohort with no dose-limiting toxicities (DLTs), results will be reported in second quarter 2025
Cash balance of $70.2 million as of December 31, 2024 anticipated to fund key milestones through mid-2026

 

REDWOOD CITY, CA, Mar. 24, 2025 – 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 December 31, 2024, and provided a business update.


“2024 was a transformational year for Bolt as we focused the company on efficient development of the programs that could be most impactful for patients,” said Willie Quinn, Chief Executive Officer. “BDC-4182, our next-generation ISAC, is poised to enter the clinic in the second quarter. As the only ISAC targeting the validated tumor target claudin 18.2, we believe that BDC-4182 has the potential to offer a better option for patients with stomach and other claudin 18.2-expressing cancers. We are particularly excited about BDC-4182 as validation for our Boltbody ISAC approach. We’ve also completed enrollment and have cleared the DLT window for the highest dose level in the BDC-3042 Phase 1 dose escalation trial and will provide a data update next quarter at a medical meeting. BDC-3042 is our first-in-class dectin-2 agonist, and has potential across a broad range of solid tumors with high unmet medical need.”

 

Recent Highlights and Anticipated Milestones

Completed enrollment of the Phase 1 study of BDC-3042 in patients with advanced cancers. BDC-3042 is a proprietary agonist antibody that targets dectin-2, an immune-activating receptor expressed by tumor-associated macrophages (TAMs). This single-agent, dose-escalation Phase 1 clinical study is evaluating BDC-3042 in patients with metastatic or unresectable solid tumors including non-small cell lung cancer (NSCLC). BDC-3042 has been well tolerated with no dose-limiting toxicities (DLTs) and evidence of biological activity. Results from the trial will be presented at an upcoming medical meeting in the second quarter of 2025.
Finalizing preparations for first-in-human trial of BDC-4182 in patients with gastric cancer. BDC-4182 is a next-generation BoltbodyTM ISAC clinical candidate targeting claudin 18.2, a clinically validated target in oncology with expression in gastric/gastroesophageal junction cancer, pancreatic cancer, and other tumor types. BDC-4182 has advanced into IND-enabling activities, supported by in vitro and in vivo experiments demonstrating potent anti-tumor activity in multiple preclinical models. BDC-4182 was tolerated in non-human primates at the highest dose tested (12mg/kg) with an acceptable safety profile.

 

BDC-4182 outperformed cytotoxic claudin 18.2 ADCs, using MMAE or TOPO1, in syngeneic models. Key learnings were presented at SITC 2024 and the dose escalation trial is planned to start in Australia in the second quarter of 2025.
Collaborations with Genmab and Toray continue to progress. The Company continues to work with Genmab to discover and develop next-generation ISACs for the treatment of cancer. Genmab and the Company are working together to advance the collaboration’s first development candidate, and the collaboration also continues research and development on additional programs. The Toray collaboration combines the Company’s immunostimulatory linker-payloads with Toray antibodies targeting Caprin-1, a tumor-specific antigen that is strongly expressed on the cell membrane in multiple solid tumor types.
Cash, cash equivalents, and marketable securities were $70.2 million as of December 31, 2024. Cash on hand is expected to fund multiple milestones and operations through mid-2026.

 

Fourth Quarter and Full Year 2024 Financial Results

 

Collaboration Revenue – The Company recently reassessed its expected future performance obligations under the Genmab Agreement, and as a result reported no collaboration revenue for the quarter. Total collaboration revenue was $7.7 million for the fourth and full year ended December 31, 2024, respectively, compared to $2.1 million and $7.9 million for the same quarter and year in 2023,, respectively. Revenue in the comparative periods was generated from services performed under the R&D collaborations as we fulfill our performance obligations.

 

Research and Development (R&D) Expenses – R&D expenses were $11.7 million for the quarter and $57.5 million for the full year ended December 31, 2024, respectively, compared to $16.3 million and $61.5 million for the same quarter and year in 2023, respectively. The decrease between the comparable periods was mainly due to a decrease in salary and related expenses primarily as a result of the May 2024 restructuring partially offset by an increase in contract manufacturing expenses.

 

General and Administrative (G&A) Expenses – G&A expenses were $3.9 million for the quarter and $18.5 million for the full year ended December 31, 2024, respectively, compared to $5.5 million and $22.5 million for the same quarter and year in 2023, respectively. The decrease between the comparable periods was mainly due to a decrease in salary and related expenses primarily as a result of the May 2024 restructuring.

 

Loss from Operations – Loss from operations was $16.9 million for the quarter and $73.0 million for the full year ended December 31, 2024, respectively, compared to $19.8 million and $76.2 million for the same quarter and year in 2023, respectively.

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 the second quarter of 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 reporting of results 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, 2024. 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)

 

 

For The Three Months Ended December 31,

 

 

Years Ended December 31,

 

 

 

2024

 

 

2023

 

 

2024

 

 

2023

 

Collaboration revenue

 

$

 

 

$

2,089

 

 

$

7,690

 

 

$

7,876

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

 

11,722

 

 

 

16,322

 

 

 

57,469

 

 

 

61,542

 

General and administrative

 

 

3,947

 

 

 

5,533

 

 

 

18,457

 

 

 

22,530

 

Restructuring charges

 

 

(222

)

 

 

 

 

 

3,343

 

 

 

 

Impairment charges

 

 

1,469

 

 

 

 

 

 

1,469

 

 

 

 

Total operating expense

 

 

16,916

 

 

 

21,855

 

 

 

80,738

 

 

 

84,072

 

Loss from operations

 

 

(16,916

)

 

 

(19,766

)

 

 

(73,048

)

 

 

(76,196

)

Other income (expense), net:

 

 

 

 

 

 

 

 

 

 

 

 

Interest income, net

 

 

980

 

 

 

1,863

 

 

 

5,255

 

 

 

6,999

 

Other income, net

 

 

 

 

 

 

 

 

4,675

 

 

 

 

Total other income, net

 

 

980

 

 

 

1,863

 

 

 

9,930

 

 

 

6,999

 

Net loss

 

 

(15,936

)

 

 

(17,903

)

 

 

(63,118

)

 

 

(69,197

)

Net unrealized gain (loss) on marketable securities

 

 

(108

)

 

 

211

 

 

 

60

 

 

 

956

 

Comprehensive loss

 

$

(16,044

)

 

$

(17,692

)

 

$

(63,058

)

 

$

(68,241

)

Net loss per share, basic and diluted

 

$

(0.42

)

 

$

(0.47

)

 

$

(1.65

)

 

$

(1.83

)

Weighted-average shares outstanding, basic and diluted

 

 

38,285,490

 

 

 

37,941,587

 

 

 

38,183,931

 

 

 

37,811,984

 

 


 

BOLT BIOTHERAPEUTICS, INC.

CONDENSED BALANCE SHEETS

(Unaudited, in thousands)

 

 

December 31,

 

 

 

2024

 

 

2023

 

Assets

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

Cash and cash equivalents

 

$

7,205

 

 

$

10,810

 

Short-term investments

 

 

40,118

 

 

 

91,379

 

Restricted cash

 

 

784

 

 

 

-

 

Prepaid expenses and other current assets

 

 

2,707

 

 

 

3,519

 

Total current assets

 

 

50,814

 

 

 

105,708

 

Property and equipment, net

 

 

3,139

 

 

 

4,957

 

Operating lease right-of-use assets

 

 

21,756

 

 

 

19,120

 

Restricted cash, non-current

 

 

981

 

 

 

1,765

 

Long-term investments

 

 

22,880

 

 

 

26,413

 

Other assets

 

 

62

 

 

 

1,821

 

Total assets

 

$

99,632

 

 

$

159,784

 

 

 

 

 

 

 

 

Liabilities and stockholders' equity

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

Accounts payable

 

$

1,507

 

 

$

2,987

 

Accrued expenses and other current liabilities

 

 

9,083

 

 

 

12,486

 

Deferred revenue

 

 

3,015

 

 

 

2,201

 

Operating lease liabilities

 

 

2,251

 

 

 

2,782

 

Total current liabilities

 

 

15,856

 

 

 

20,456

 

Operating lease liabilities, net of current portion

 

 

22,958

 

 

 

17,437

 

Deferred revenue, non-current

 

 

3,620

 

 

 

9,107

 

Other long-term liabilities

 

 

-

 

 

 

43

 

Total liabilities

 

 

42,434

 

 

 

47,043

 

Commitments and contingencies

 

 

 

 

 

 

Stockholders' equity:

 

 

 

 

 

 

Common stock

 

 

 

 

 

 

Additional paid-in capital

 

 

484,504

 

 

 

476,989

 

Accumulated other comprehensive gain

 

 

97

 

 

 

37

 

Accumulated deficit

 

 

(427,403

)

 

 

(364,285

)

Total stockholders' equity

 

 

57,198

 

 

 

112,741

 

Total liabilities and stockholders' equity

 

$

99,632

 

 

$

159,784

 

 


 

BOLT BIOTHERAPEUTICS, INC.

CONDENSED STATEMENTS OF CASH FLOWS

(Unaudited, in thousands)

 

 

Years Ended December 31,

 

 

 

2024

 

 

2023

 

CASH FLOWS FROM OPERATING ACTIVITIES:

 

 

 

 

 

 

Net loss

 

$

(63,118

)

 

$

(69,197

)

Adjustments to reconcile net loss to net cash used in operating activities:

 

 

 

 

 

 

Depreciation and amortization

 

 

1,781

 

 

 

1,854

 

Stock-based compensation expense

 

 

7,407

 

 

 

9,223

 

Accretion of discount on marketable securities

 

 

(2,615

)

 

 

(4,493

)

Gain on sale of fixed assets

 

 

(70

)

 

 

 

Asset impairment

 

 

1,469

 

 

 

 

Non-cash lease expense

 

 

2,297

 

 

 

2,952

 

Changes in operating assets and liabilities:

 

 

 

 

 

 

Prepaid expenses and other assets

 

 

2,571

 

 

 

(454

)

Accounts payable and accrued expenses

 

 

(4,883

)

 

 

(3,413

)

Operating lease liabilities, net

 

 

(1,412

)

 

 

(2,392

)

Deferred revenue

 

 

(4,673

)

 

 

(3,606

)

Other long-term liabilities

 

 

(43

)

 

 

1

 

Net cash used in operating activities

 

 

(61,289

)

 

 

(69,525

)

CASH FLOWS FROM INVESTING ACTIVITIES:

 

 

 

 

 

 

Purchase of property and equipment

 

 

(41

)

 

 

(206

)

Proceeds from sales of property and equipment

 

 

148

 

 

 

 

Purchases of marketable securities

 

 

(88,855

)

 

 

(164,988

)

Maturities of marketable securities

 

 

146,324

 

 

 

236,232

 

Net cash provided by investing activities

 

 

57,576

 

 

 

71,038

 

CASH FLOWS FROM FINANCING ACTIVITIES:

 

 

 

 

 

 

Proceeds from issuance of common stock

 

 

108

 

 

 

253

 

Net cash provided by financing activities

 

 

108

 

 

 

253

 

NET (DECREASE) INCREASE IN CASH

 

 

(3,605

)

 

 

1,766

 

Cash, cash equivalents and restricted cash at beginning of year

 

 

12,575

 

 

 

10,809

 

Cash, cash equivalents and restricted cash at end of period

 

$

8,970

 

 

$

12,575

 

Reconciliation of cash, cash equivalents and restricted cash:

 

 

 

 

 

 

Cash and cash equivalents

 

$

7,205

 

 

$

10,810

 

Restricted cash

 

 

1,765

 

 

 

1,765

 

Total cash, cash equivalents and restricted cash

 

$

8,970

 

 

$

12,575

 

Supplemental schedule of non-cash investing and financing activities:

 

 

 

 

 

 

Purchases of property and equipment included in accounts payable and accrued liabilities

 

$

 

 

$

152

 

Right of use assets obtained in exchange for operating lease obligations

 

$

6,402

 

 

$