8-K
0001672619false00016726192023-11-092023-11-09

 

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): November 09, 2023

 

 

Enliven Therapeutics, Inc.

(Exact name of registrant as specified in its charter)

 

 

Delaware

001-39247

81-1523849

(State or other jurisdiction
of incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

6200 Lookout Road

 

Boulder, Colorado

 

80301

(Address of principal executive offices)

 

(Zip Code)

 

Registrant’s telephone number, including area code: 720 647-8519

 

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 $0.001 per share

 

ELVN

 

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.

 

 


Item 2.02 Results of Operations and Financial Condition.

On November 9, 2023, Enliven Therapeutics, Inc. (the “Company”) issued a press release announcing its financial results for the quarter ended September 30, 2023. The full text of the press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

 

All of the information furnished in this Item 2.02 and Item 9.01 (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, and shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit Number

 

Exhibit Description

99.1

 

Press Release issued on November 9, 2023

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 hereunto duly authorized.

 

 

 

Enliven Therapeutics, Inc.

 

 

 

 

Date:

November 9, 2023

By:

/s/ Samuel Kintz

 

 

Name:

Samuel Kintz

 

 

Title:

President and Chief Executive Officer

 


EX-99.1

 

https://cdn.kscope.io/c69e8878a9846d5950ba26647d574ef2-img107523686_0.jpg 

Enliven Therapeutics Reports Third Quarter 2023 Financial Results and Provides a Business Update

Company on track to deliver initial proof of concept data for ELVN-001 and ELVN-002 in 2024

 

Strong balance sheet, closing the quarter with $263 million in cash, cash equivalents and marketable securities, which is expected to provide cash runway into early 2026

BOULDER, Colo., November 9, 2023 (GLOBE NEWSWIRE) -- Enliven Therapeutics, Inc. (Enliven) (Nasdaq: ELVN), a clinical-stage precision oncology company focused on the discovery and development of next-generation small molecule kinase inhibitors, today reported financial results for the third quarter ended September 30, 2023, and provided a business update.

“We made significant progress this past quarter,” said Sam Kintz, MBA, Enliven’s Co-founder and Chief Executive Officer. “Both of our parallel lead programs are advancing in their respective Phase 1 trials, and there continues to be strong patient demand for both trials. Our team is laser-focused on continuing to execute, and we look forward to sharing initial data for these programs next year.”

 

Recent Business Highlights and Upcoming Milestones

 

Research and Development Highlights

 

ELVN-001 and ELVN-002: Patient enrollment continues to progress and Enliven expects to report initial proof of concept data in 2024 for the Phase 1 clinical trials evaluating ELVN-001 in adults with chronic myeloid leukemia (CML) (NCT05304377) and ELVN-002 in patients with solid tumors with HER2 alterations (NCT05650879).

Pipeline: The Company continues to advance its early-stage pipeline. It has completed IND enabling studies for its third program, has an additional program in lead optimization and has multiple efforts ongoing in target validation and lead identification. In the near-term, the Company plans to remain focused on progressing ELVN-001 and ELVN-002 and will prioritize taking full advantage of the development opportunities related to these programs before initiating a potential clinical trial for a third program. The Company intends to provide additional detail and guidance on its pipeline in the first half of 2024.


 

 

 

 


 

Third Quarter 2023 Financial Results

Cash Position: As of September 30, 2023, the Company had cash, cash equivalents and marketable securities totaling $263.5 million.

Research and development (R&D) expenses: R&D expenses were $19.6 million for the third quarter of 2023, compared to $7.8 million for the third quarter of 2022.

General and administrative (G&A) expenses: G&A expenses for the third quarter of 2023 were $4.6 million, compared to $3.1 million for the third quarter of 2022.

Net Loss: Enliven reported a net loss of $20.8 million for the third quarter of 2023, compared to a net loss of $10.6 million for the third quarter of 2022.

About Enliven Therapeutics

Enliven Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and development of small molecule inhibitors to help patients with cancer not only live longer, but better. Enliven aims to address existing and emerging unmet needs with a precision oncology approach that improves survival and enhances overall patient well-being. Enliven’s discovery process combines deep insights in clinically validated biological targets and differentiated chemistry to design potentially first-in-class or best-in-class therapies. Enliven is based in Boulder, Colorado.

Forward-Looking Statements

This press release contains forward-looking statements (including within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended )concerning Enliven and other matters. These statements may discuss goals, intentions and expectations as to future plans, trends, events, results of operations or financial condition, or otherwise, based on current beliefs of the management of Enliven, as well as assumptions made by, and information currently available to, management of Enliven. Forward-looking statements generally include statements that are predictive in nature and depend upon or refer to future events or conditions, and include words such as “may,” “will,” “should,” “would,” “expect,” “anticipate,” “plan,” “likely,” “believe,” “estimate,” “project,” “intend,” and other similar expressions or the negative or plural of these words, or other similar expressions that are predictions or indicate future events or prospects, although not all forward-looking statements contain these words. Statements that are not historical facts are forward-looking statements. Forward-looking statements in this press release include, but are not limited to, statements regarding the potential of, and plans and expectations regarding, Enliven’s programs, including ELVN-001, ELVN-002, Enliven’s third program and its early-stage discovery programs; Enliven’s pipeline of product candidates; the expected timing of initial results for ELVN-001 and ELVN-002; statements relating to Enliven’s expected cash runway; the

 

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expected timing of disclosure of more information on Enliven’s pipeline; and statements by Enliven’s Co-founder, President and Chief Executive Officer. Forward-looking statements are based on current beliefs and assumptions that are subject to risks and uncertainties and are not guarantees of future performance. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, without limitation: the limited operating history of Enliven; the significant net losses incurred since its inception; the ability to advance product candidates through preclinical and clinical development; the ability to obtain regulatory approval for, and ultimately commercialize, product candidates; the outcome of preclinical testing and early clinical trials for product candidates and the potential that the outcome of preclinical testing and early clinical trials may not be predictive of the success of later clinical trials; Enliven’s limited resources; the risk of adverse events, toxicities or other undesirable side effects; potential delays or difficulties in the enrollment or maintenance of patients in clinical trials; the decision to develop or seek strategic collaborations to develop Enliven’s current or future product candidates in combination with other therapies and the cost of combination therapies; Enliven’s limited experience as a company in designing and conducting clinical trials; the ability to attract, hire, and retain highly skilled executive officers and employees; the ability of Enliven to protect its intellectual property and proprietary technologies; the scope of any patent protection Enliven obtains or the loss of any of Enliven’s patent protection; developments relating to Enliven’s competitors and its industry, including competing product candidates and therapies; reliance on third parties, including contract manufacturing organizations, contract research organizations and strategic partners; general market or macroeconomic conditions; Enliven’s ability to obtain additional capital to fund Enliven’s general corporate activities and to fund Enliven’s research and development; and other risks and uncertainties, including those more fully described in Enliven’s filings with the Securities and Exchange Commission (SEC), including additional risks which may be found in the section entitled “Risk Factors” in Enliven’s Annual and Quarterly Reports on Form 10-K and 10-Q filed with the SEC and in Enliven’s future reports to be filed with the SEC. Except as required by applicable law, Enliven undertakes no obligation to revise or update any forward-looking statement, or to make any other forward-looking statements, whether as a result of new information, future events or otherwise.

This press release contains hyperlinks to information that is not deemed to be incorporated by reference into this press release.

Contact:

Enliven Investors & Media:

Argot Partners

Enliven@argotpartners.com

 

 

 

 

 

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Enliven Therapeutics, Inc.

Selected Condensed Consolidated Financial Information

(in thousands, except per share data)

(unaudited)

 

Statements of Operations

 

 

Three Months Ended September 30,

 

 

Nine Months Ended September 30,

 

 

 

 

2023

 

 

2022

 

 

2023

 

 

2022

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

 

    Research and development

 

 

$

19,606

 

 

$

7,829

 

 

$

46,669

 

 

$

22,825

 

    General and administrative

 

 

 

4,642

 

 

 

3,105

 

 

 

14,131

 

 

 

5,803

 

Total operating expenses

 

 

 

24,248

 

 

 

10,934

 

 

 

60,800

 

 

 

28,628

 

Loss from operations

 

 

 

(24,248

)

 

 

(10,934

)

 

 

(60,800

)

 

 

(28,628

)

Other income (expense), net

 

 

 

3,479

 

 

 

380

 

 

 

8,586

 

 

 

516

 

Net loss

 

 

$

(20,769

)

 

$

(10,554

)

 

$

(52,214

)

 

$

(28,112

)

Net loss per share, basic and diluted

 

 

$

(0.51

)

 

$

(3.27

)

 

$

(1.55

)

 

$

(9.15

)

Weighted-average shares outstanding,
   basic and diluted

 

 

 

41,031

 

 

 

3,229

 

 

 

33,665

 

 

 

3,071

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance Sheets

 

 

 

 

 

 

September 30,

 

 

December 31,

 

 

 

 

 

 

 

 

2023

 

 

2022

 

Assets

 

 

 

 

 

 

 

Current assets:

 

 

 

 

 

 

 

    Cash, cash equivalents and marketable securities

 

 

$

263,478

 

 

$

75,536

 

    Prepaid expenses and other current assets

 

 

 

5,128

 

 

 

2,217

 

Total current assets

 

 

 

268,606

 

 

 

77,753

 

Property and equipment, net

 

 

 

806

 

 

 

890

 

Operating lease right-of-use assets

 

 

 

398

 

 

 

626

 

Deferred offering costs

 

 

 

563

 

 

 

3,975

 

Restricted cash

 

 

 

54

 

 

 

54

 

Other long-term assets

 

 

 

3,614

 

 

 

 

Total assets

 

 

$

274,041

 

 

$

83,298

 

Liabilities, Convertible Preferred Stock and Stockholders' Equity (Deficit)

 

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

 

 

    Accounts payable

 

 

$

1,493

 

 

$

3,438

 

    Accrued expenses and other current liabilities

 

 

 

10,586

 

 

 

6,277

 

Total current liabilities

 

 

 

12,079

 

 

 

9,715

 

Long-term liabilities

 

 

 

214

 

 

 

659

 

Total liabilities

 

 

 

12,293

 

 

 

10,374

 

Convertible preferred stock

 

 

 

 

 

 

149,749

 

Stockholders' equity (deficit)

 

 

 

261,748

 

 

 

(76,825

)

Total liabilities, convertible preferred stock and stockholders' equity (deficit)

 

 

$

274,041

 

 

$

83,298

 

 

 

 

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