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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): November 13, 2024
MERSANA THERAPEUTICS, INC.
(Exact name of registrant as specified in its
charter)
Delaware |
|
001-38129 |
|
04-3562403 |
(State or other jurisdiction
of incorporation) |
|
(Commission
File Number) |
|
(IRS Employer
Identification No.) |
840
Memorial Drive Cambridge,
Massachusetts |
|
02139 |
(Address of Principal Executive Offices)
|
|
(Zip
Code) |
Registrant’s telephone number, including
area code: (617) 498-0020
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, $0.0001 par value |
MRSN |
The Nasdaq Stock Market LLC |
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 13, 2024,
Mersana Therapeutics, Inc. (the “Company”) issued a press release announcing business updates and financial results for the
fiscal quarter ended September 30, 2024. A copy of the press release is being furnished as Exhibit 99.1 to this Current Report on Form
8-K.
The information furnished
in this Item 2.02, 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, nor shall such information
be deemed incorporated by reference in any filing by the Company with the Securities and Exchange Commission (the “SEC”) under
the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, regardless of any general incorporation
language contained in such filing, except as expressly set forth by specific reference in such a filing.
Item 7.01 |
Regulation FD Disclosure. |
On November 13, 2024,
the Company posted an updated corporate presentation on the Company’s website. To access
the presentation, investors should visit the “Events & Presentations” page under the “Investors &
Media” section of the Company’s website at ir.mersana.com.
The information furnished
under this Item 7.01 shall not be deemed “filed” for purposes of Section 18 of the Exchange Act, or otherwise subject
to the liabilities of that section, nor shall such information be deemed incorporated by reference in any filing by the Company with the
SEC under the Securities Act or the Exchange Act, regardless of any general incorporation language contained in such filing, except as
expressly set forth by specific reference in such a filing.
Item 9.01. | Financial Statements and Exhibits. |
(d) Exhibits
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.
|
MERSANA THERAPEUTICS, INC. |
|
|
|
Date: November 13, 2024 |
By: |
/s/ Brian DeSchuytner |
|
|
Brian DeSchuytner |
|
|
Senior Vice President, Chief Operating Officer and Chief Financial Officer |
Exhibit 99.1
Mersana Therapeutics Provides Business Update
and Announces
Third Quarter 2024 Financial Results
| - | Plan to announce initial clinical data for XMT-1660 at a company event by the end of 2024 |
| - | Dose escalation advancing in Phase 1 clinical trial of XMT-2056 |
| - | Conference call today at 8:00 a.m. ET |
CAMBRIDGE, Mass., November 13, 2024 – Mersana Therapeutics,
Inc. (NASDAQ: MRSN), a clinical-stage biopharmaceutical company focused on discovering and developing a pipeline of antibody-drug conjugates
(ADCs) targeting cancers in areas of high unmet medical need, today provided a business update and reported financial results for the
third quarter ended September 30, 2024.
“During
the third quarter of 2024, our team continued its strong execution as we advanced the dose escalation portions of our Phase 1 clinical
trials of XMT-1660 and XMT-2056, made further progress in our collaborations and maintained the strength of our balance sheet,”
said Martin Huber, M.D., President and Chief Executive Officer of Mersana Therapeutics. “In multiple presentations over the
course of the past year, we shared data demonstrating the potential for Dolasynthen ADCs to generate anti-tumor activity and avoid many
of the toxicities that have limited other ADC platforms. We are looking forward to presenting initial XMT-1660 clinical data later this
year. We also are finalizing plans to begin the expansion portion of our trial, with an initial focus on patients with triple-negative
breast cancer who have previously been treated with at least one topoisomerase-1 ADC.”
Recent Accomplishments, Strategic Priorities and Expected Milestones
XMT-1660:
Mersana continues to advance its Phase 1 clinical trial of XMT-1660, the company’s lead Dolasynthen ADC candidate targeting B7-H4.
The dose escalation portion of the trial is ongoing, with the company having recently escalated to a dose of 115 milligrams per meter
squared administered every four weeks. A maximum tolerated dose has not yet been established. Approximately 75 percent of the patients
that have been enrolled in the trial to date have triple-negative breast cancer (TNBC) or hormone receptor-positive breast cancer (HR+BC).
Among the enrolled patients with TNBC, approximately 90 percent have received a prior topoisomerase-1 (topo-1) ADC, and among the enrolled
patients with HR+BC, approximately half have received a prior topo-1 ADC. Last week at World ADC 2024, Mersana presented new preclinical
data demonstrating XMT-1660’s anti-tumor activity following topo-1 treatment. By the end of 2024, Mersana plans both to share initial
safety, tolerability, efficacy and biomarker data from its Phase 1 dose escalation and backfill cohorts at a company event and to initiate
the expansion portion of the trial in patients with TNBC who have previously been treated with at least one topo-1 ADC.
XMT-2056:
Mersana continues to escalate dosing in its Phase 1 clinical trial of XMT-2056, the company’s lead Immunosynthen ADC candidate targeting
a novel HER2 epitope. GSK plc has an exclusive global license option to co-develop and commercialize XMT-2056. At the Society for Immunotherapy
of Cancer (SITC) 2024 Annual Meeting last week, Mersana presented new preclinical data demonstrating XMT-2056’s ability to activate
STING signaling and inhibit tumor growth at very low doses.
Collaborations:
Mersana continues to advance its Johnson & Johnson and Merck KGaA, Darmstadt, Germany collaborations. The collaboration with Merck
KGaA, Darmstadt, Germany focuses on discovering novel Immunosynthen ADCs for up to two targets. The collaboration with Johnson & Johnson
focuses on discovering novel Dolasynthen ADCs for up to three targets. In the third quarter of 2024, Mersana achieved and received payment
for an $8 million development milestone under the Johnson & Johnson collaboration and achieved a $1 million development milestone
under the Merck KGaA, Darmstadt, Germany collaboration, for which payment was received in the fourth quarter of 2024.
Third Quarter 2024 Financial Results
| · | Cash, cash equivalents and marketable securities as of September 30, 2024,
were $155.2 million. Mersana continues to expect that its capital resources will be sufficient to support its current operating plan commitments
into 2026. |
| · | Net cash used in operating activities for the third quarter of 2024 was $8.6
million, which reflects the impact of the aforementioned $8 million milestone payment and a $3.5 million payment for manufacturing
activities from Johnson & Johnson. |
| · | Collaboration revenue for the third quarter of 2024 was $12.6 million, compared
to $7.7 million for the same period in 2023. The year-over-year change was primarily related to an increase in revenue recognized under
Mersana’s collaboration and license agreements with Johnson & Johnson and Merck KGaA, Darmstadt, Germany. |
| · | Research and development (R&D) expenses for the third quarter of 2024
were $14.8 million, compared to $30.5 million for the same period in 2023. Included in the third quarter of 2024 R&D expenses were
$2.3 million in non-cash stock-based compensation expenses. The year-over-year decline in R&D expenses was primarily related to reduced
costs associated with manufacturing and clinical development activities for UpRi, a discontinued ADC candidate, and reduced employee compensation
expense following the company’s restructuring in 2023. |
| · | General and administrative (G&A) expenses for the third quarter of 2024
were $9.9 million, compared to $12.9 million during the same period in 2023. Included in the third quarter
of 2024 G&A expenses were $1.7 million in non-cash stock-based compensation expenses. The year-over-year decline in G&A expenses
was primarily related to reduced consulting and professional services fees and reduced employee compensation expense following the aforementioned
restructuring. |
| · | Net loss for the third quarter of 2024 was $11.5 million, or $0.09 per share,
compared to a net loss of $41.7 million, or $0.35 per share, for the same period in 2023. |
Conference Call Reminder
Mersana will host a conference call today at 8:00 a.m. ET to discuss
business updates and its financial results for the third quarter of 2024. To access the call, please dial 833-255-2826 (domestic) or 412-317-0689
(international). A live webcast of the presentation will be available on the Investors & Media section of the Mersana website at www.mersana.com,
and a replay of the webcast will be available in the same location following the conference call for approximately 90 days.
About Mersana Therapeutics
Mersana Therapeutics
is a clinical-stage biopharmaceutical company focused on the development of novel antibody-drug conjugates (ADCs) and driven by the knowledge
that patients are waiting for new treatment options. The company has developed proprietary cytotoxic (Dolasynthen) and immunostimulatory
(Immunosynthen) ADC platforms that are generating a pipeline of wholly-owned and partnered product candidates with the potential to treat
a range of cancers. Its pipeline includes XMT-1660, a Dolasynthen ADC targeting B7-H4, and XMT-2056, an Immunosynthen ADC targeting a
novel epitope of human epidermal growth factor receptor 2 (HER2). Mersana routinely posts information that may be useful to investors
on the “Investors & Media” section of its website at www.mersana.com.
Forward-Looking Statements
This press release contains “forward-looking” statements
and information within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by words
such as “aims,” “anticipates,” “believes,” “could,” “estimates,” “expects,”
“forecasts,” “goal,” “intends,” “may,” “plans,” “possible,” “potential,”
“seeks,” “will” and variations of these words or similar expressions, although not all forward-looking statements
contain these words. Forward-looking statements in this press release include, but are not limited to, statements concerning Mersana’s
plans regarding the clinical development of XMT-1660 and XMT-2056, including with respect to the progress and design of the clinical trials
of these product candidates; Mersana’s planned data presentations, including with respect to its Phase 1 clinical trial of XMT-1660;
Mersana’s cash runway; Mersana’s collaborations with third parties; and the development and potential of Mersana’s product
candidates, platforms, technology and pipeline of ADC candidates. Mersana may not actually achieve the plans, intentions or expectations
disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results
or events could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result
of various factors, including, among other things, uncertainties inherent in research and development, in the advancement, progression
and completion of clinical trials and in the clinical development of Mersana’s product candidates, including XMT-1660 and XMT-2056;
the risk that Mersana may face delays in patient enrollment in its Phase 1 clinical trial of XMT-2056; the risk that Mersana may not realize
the intended benefits of its platforms, technology and collaborations; and other important factors, any of which could cause Mersana’s
actual results to differ from those contained in the forward-looking statements, that are described in greater detail in the section entitled
“Risk Factors” in Mersana’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (“SEC”)
on August 13, 2024, as well as in other filings Mersana may make with the SEC in the future. Any forward-looking statements contained
in this press release speak only as of the date hereof, and Mersana expressly disclaims any obligation to update any forward-looking statements
contained herein, whether because of any new information, future events, changed circumstances or otherwise, except as otherwise required
by law.
Mersana
Therapeutics, Inc.
Selected
Condensed Consolidated Balance Sheet Data
(in
thousands and unaudited)
| |
September 30,
2024 | | |
December 31,
2023 | |
Cash, cash equivalents and marketable securities | |
$ | 155,171 | | |
$ | 209,084 | |
Working capital(1) | |
| 92,256 | | |
| 150,420 | |
Total assets | |
| 169,530 | | |
| 226,060 | |
Total stockholders' equity | |
| 1,049 | | |
| 36,904 | |
(1) The company defines working capital as current assets less current liabilities.
Mersana Therapeutics, Inc.
Condensed Consolidated Statement of Operations
(in thousands, except share and per share data,
and unaudited)
| |
Three months ended | | |
Nine months ended | |
| |
September 30,
2024 | | |
September 30,
2023 | | |
September 30,
2024 | | |
September 30,
2023 | |
Collaboration revenue | |
$ | 12,598 | | |
$ | 7,698 | | |
$ | 24,136 | | |
$ | 26,154 | |
| |
| | | |
| | | |
| | | |
| | |
Operating expenses: | |
| | | |
| | | |
| | | |
| | |
Research and development | |
| 14,803 | | |
| 30,531 | | |
| 50,734 | | |
| 126,774 | |
General and administrative | |
| 9,864 | | |
| 12,894 | | |
| 31,927 | | |
| 49,409 | |
Restructuring expenses | |
| - | | |
| 8,214 | | |
| - | | |
| 8,214 | |
Total operating expenses | |
| 24,667 | | |
| 51,639 | | |
| 82,661 | | |
| 184,397 | |
Total other income, net | |
| 986 | | |
| 2,285 | | |
| 3,868 | | |
| 6,117 | |
Loss before income taxes | |
| (11,083 | ) | |
| (41,656 | ) | |
| (54,657 | ) | |
| (152,126 | ) |
Income tax expense | |
| (418 | ) | |
| - | | |
| (418 | ) | |
| - | |
Net loss | |
$ | (11,501 | ) | |
$ | (41,656 | ) | |
$ | (55,075 | ) | |
$ | (152,126 | ) |
Net loss per share — basic and diluted | |
$ | (0.09 | ) | |
$ | (0.35 | ) | |
$ | (0.45 | ) | |
$ | (1.33 | ) |
Weighted-average number of common shares — basic and diluted | |
| 122,721,918 | | |
| 120,521,985 | | |
| 122,197,585 | | |
| 114,595,910 | |
###
Contact:
Jason Fredette
617-498-0020
jason.fredette@mersana.com
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