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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, DC 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): August 10, 2022

MaxCyte, Inc.

(Exact name of registrant as specified in its charter)

Delaware

    

001-40674

    

52-2210438

(State or other jurisdiction of
incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

9713 Key West Avenue, Suite 400

Rockville, Maryland 20850

(Address of principal executive offices, including zip code)

(301) 944-1700

(Registrant’s telephone number, including area code)

N/A

(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:

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, $0.01 par value

MXCT

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 account standards provided pursuant to Section 13(a) of the Exchange Act.

Item 2.02. Results of Operations and Financial Condition.

On August 10, 2022, MaxCyte, Inc. (the “Company”) issued a press release announcing its financial results for the quarter and six months ended June 30, 2022. This press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein by reference.

The information in this Current Report on Form 8-K, including Exhibit 99.1 attached hereto, is furnished and 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. The information contained herein and in the accompanying exhibit is not incorporated by reference in any filing of the Company under the Securities Act of 1933, as amended, or the Exchange Act, whether made before or after the date hereof and irrespective of any general incorporation language in any filings, except as 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, dated August 10, 2022

104

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

SIGNATURES

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

MaxCyte, Inc.

Dated: August 10, 2022

By:

/s/ Doug Doerfler

Doug Doerfler

President and Chief Executive Officer

Exhibit 99.1

A close-up of a logo

Description automatically generated with low confidence

MaxCyte Reports Second Quarter and Half-Year 2022 Financial Results

45% Year-Over-Year Core Business Revenue Growth in Second Quarter 2022

Raises 2022 Core Revenue Growth Guidance to Approximately 30%

ROCKVILLE, MD, August 10, 2022 — MaxCyte, Inc., (NASDAQ: MXCT; LSE: MXCT), a leading commercial cell-engineering company focused on providing enabling platform technologies to advance innovative cell-based research as well as next-generation cell therapeutic discovery, development and commercialization, today announced financial results for the second quarter and six months ended June 30, 2022.

Second Quarter and Recent Highlights

Total revenue of $9.6 million in the second quarter of 2022, an increase of 35% over the second quarter of 2021 driven by strong growth in the cell therapy market; core business revenues grew 45% led by revenue from cell therapy customers which increased 61%, with drug discovery revenues growing by 4%.
Raising 2022 revenue guidance for core business revenue growth to approximately 30%.
Expecting SPL Program-related revenue to be approximately $4 million for the full year.
Total cash, cash equivalents and short-term investments were $240.9 million as of June 30, 2022.
Signed the Company’s 17th SPL agreement in July 2022; LG Chem licensed the use of MaxCyte’s Flow Electroporation® ExPERT™ platform to advance cellular research and development of engineered cell-based therapies.

“We are pleased with these strong second quarter 2022 results, with 45% year-over-year core business revenue growth, highlighted by 61% growth in revenues from Cell Therapy customers. We remain encouraged by the ongoing growth of our SPL portfolio with the addition of LG Chem, our 17th SPL partner, and second SPL agreement signed in 2022, as well as the continued progress of our existing partnerships. Importantly, our LG Chem partnership broadens the reach of our SPL portfolio into Asia,” said Doug Doerfler, President and CEO of MaxCyte.

“Overall, our optimism about the potential for the development programs covered by our existing partners to generate growing revenue in both pre-clinical research and clinical progress remains high. Our ExPERT™ platform continues to be used to enable a broad range of cell types and approaches targeting a wide array of indications, and its adoption is increasing within the industry. We are making ongoing investments to drive revenue growth, support and expand the widening array of applications for our technology, while also strengthening our team and expanding our ability to support customers through in-house manufacturing and robust infrastructure. These investments should allow us to take advantage of expanding markets and support our partners as they move forward in development and commercialization.”

1


The following table provides details regarding the sources of our revenue for the periods presented.

Three Months Ended

Six Months Ended

June 30,

June 30,

    

2022

    

2021

%

2022

    

2021

%

(in thousands, except percentages)

 

  

 

  

 

  

 

  

 

Cell therapy

$

7,688

$

4,766

61%

$

15,104

$

9,494

59%

Drug discovery

 

1,916

 

1,838

4%

 

4,083

 

3,601

13%

Program-related

 

4

 

504

NM

 

2,008

 

508

295%

Total revenue

$

9,608

$

7,108

35%

$

21,195

$

13,603

56%

Second Quarter 2022 Financial Results

Total revenue for the second quarter of 2022 was $9.6 million, compared to $7.1 million in the second quarter of 2021, representing growth of 35%.

Core business revenue was $9.6 million, including 61% revenue growth from cell therapy customers and 4% from drug discovery customers, compared to core business revenue of $6.6 million in the same period last year.

We did not have any material SPL Program-related revenue in the second quarter of 2022, as compared to $0.5 million in the second quarter of 2021.

Gross profit for the second quarter of 2022 was $8.5 million (88% gross margin), compared to $6.3 million (89% gross margin) in the same period of the prior year.

Operating expenses for the second quarter of 2022 were $17.2 million, compared to operating expenses of $10.7 million in the second quarter of 2021. The overall increase in operating expenses was primarily driven by increased staff in field sales and science, manufacturing, and lab teams to support our customers’ and partners’ growth. The increase also included additional public company-related, stock-based compensation, and marketing expenses compared with the same period a year ago.

Second quarter 2022 net loss was $8.3 million compared to net loss of $4.4 million for the same period in 2021. EBITDA, a non-GAAP measure, was a loss of $8.2 million for the second quarter of 2022, compared to a loss of $4.1 million for the second quarter of the prior year. Stock-based compensation expense was $3.0 million for the second quarter versus $1.9 million for the same period in the prior year.

Total cash, cash equivalents and short-term investments were $240.9 million as of June 30, 2022.

First Half 2022 Financial Results

Total revenue for the first half of 2022 was $21.2 million, compared to $13.6 million in the first half of 2021, representing growth of 56%. Overall sales to the cell therapy (up 59%) and the drug discovery (up 13%) markets were sources of strength in the first half.

The Company recognized $2.0 million of program-related revenue in the first half of 2022, as compared to $0.5 million in program-related revenue in the first half of 2021.

Gross profit for the first half of 2022 was $19.0 million (90% gross margin), compared to $12.1 million (89% gross margin) in the same period of the prior year.

2


Operating expenses for the first half of 2022 were $31.9 million, compared to operating expenses of $22.9 million in the first half of 2021. The overall increase in operating expenses was primarily driven by increased staff in field sales and science, manufacturing, and lab teams to support our customers’ and partners’ growth. The increase also included additional stock-based compensation, public company-related, and marketing expenses compared with the same period a year ago.

First half 2022 net loss was $12.3 million compared to net loss of $11.5 million for the same period in 2021. EBITDA was a loss of $11.9 million for the first half of 2022, compared to a loss of $10.5 million for the same period of the prior year. Stock-based compensation expense was $5.4 million for the first half of 2022 versus $3.2 million for the same period in the prior year.

2022 Revenue Guidance

We expect core business revenue (instruments and disposables to cell therapy and drug discovery customers and excluding program-related revenue) in 2022 to grow approximately 30% compared to 2021. We continue to expect SPL Program-related revenue to be approximately $4 million in 2022.

Webcast and Conference Call Details

MaxCyte will host a conference call today, August 10, 2022, at 4:30 p.m. Eastern Time. Investors interested in listening to the conference call are required to register online. A live and archived webcast of the event will be available on the “Events” section of the MaxCyte website at https://investors.maxcyte.com/.

About MaxCyte

MaxCyte is a leading commercial cell-engineering company focused on providing enabling platform technologies to advance innovative cell-based research as well as next-generation cell therapeutic discovery, development and commercialization. Over the past 20 years, we have developed and commercialized our proprietary Flow Electroporation® technology, which facilitates complex engineering of a wide variety of cells. Our ExPERT™ platform, which is based on our Flow Electroporation technology, has been designed to support the rapidly expanding cell therapy market and can be utilized across the continuum of the high-growth cell therapy sector, from discovery and development through commercialization of next-generation, cell-based medicines. The ExPERT family of products includes: four instruments, the ATx™, STx™ GTx™ and VLx™; a portfolio of proprietary related processing assemblies or disposables; and software protocols, all supported by a robust worldwide intellectual property portfolio.

Non-GAAP Financial Measures

This press release contains EBITDA, which is a non-GAAP measure defined as earnings, before interest, tax, depreciation and amortization.  MaxCyte believes that EBITDA provides useful information to management and investors relating to its results of operations. The company’s management uses this non-GAAP measure to compare the company’s performance to that of prior periods for trend analyses, and for budgeting and planning purposes. The company believes that the use of EBITDA provides an additional tool for investors to use in evaluating ongoing operating results and trends and in comparing the company’s financial measures with other companies, many of which present similar non-GAAP financial measures to investors, and that it allows for greater transparency with respect to key metrics used by management in its financial and operational decision-making.

Management does not consider EBITDA in isolation or as an alternative to financial measures determined in accordance with GAAP. The principal limitation of EBITDA is that it excludes significant expenses that are required by GAAP to be recorded in the company’s financial statements. In order to compensate for these limitations, management presents

3


EBITDA together with GAAP results. Non-GAAP measures should be considered in addition to results prepared in accordance with GAAP, but should not be considered a substitute for, or superior to, GAAP results.  A reconciliation table of net loss, the most comparable GAAP financial measure, to EBITDA is included at the end of this release. MaxCyte urges investors to review the reconciliation and not to rely on any single financial measure to evaluate the company’s business.

Forward-Looking Statements

This press release contains "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995, including but not limited to, statements regarding our revenue guidance for the year ending December 31, 2022, and expectations regarding adoption of the ExPERT™ platform, expansion of and revenue from our SPL Programs and the progression of our customers’ programs into and through clinical trials. The words "may," “might,” "will," "could," "would," "should," "expect," "plan," "anticipate," "intend," "believe," “expect,” "estimate," “seek,” "predict," “future,” "project," "potential," "continue," "target" and similar words or expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Any forward-looking statements in this press release are based on management's current expectations and beliefs and are subject to a number of risks, uncertainties and important factors that may cause actual events or results to differ materially from those expressed or implied by any forward-looking statements contained in this press release, including, without limitation, risks associated with the impact of COVID-19 on our operations;  the timing of our customers’ ongoing and planned clinical trials; the adequacy of our cash resources and availability of financing on commercially reasonable terms; and general market and economic conditions may impact investor confidence in the biopharmaceutical industry affecting the amount of capital such investors provide to our current and potential partners resulting in decreased demand for our products. These and other risks and uncertainties are described in greater detail in the section entitled "Risk Factors" in our Annual Report on Form 10-K for the year ended December 31, 2021, filed with the Securities and Exchange Commission on March 22, 2022, as well as in discussions of potential risks, uncertainties, and other important factors in the other filings that we make with the Securities and Exchange Commission from time to time. These documents are available under the “SEC filings” page of the Investors section of our website at http://investors.maxcyte.com. Any forward-looking statements represent our views only as of the date of this press release and should not be relied upon as representing our views as of any subsequent date. We explicitly disclaim any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise. No representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.

4


MaxCyte Contacts:

US IR Adviser 

Gilmartin Group 

David Deuchler, CFA 

+1 415-937-5400 

ir@mazxcyte.com 

US Media Relations

Seismic

Valerie Enes

Nominated Adviser and Joint Corporate Broker 

Panmure Gordon 

Emma Earl / Freddy Crossley 

Corporate Broking 

Rupert Dearden 

+1 408-497-8568

+44 (0)20 7886 2500 

UK IR Adviser

Consilium Strategic Communications

Mary-Jane Elliott

Chris Welsh

 

+44 (0)203 709 5700

maxcyte@consilium-comms.com

5


MaxCyte, Inc.

Unaudited Consolidated Balance Sheets

June 30, 

December 31, 

    

2022

    

2021

(Unaudited)

 

Assets

 

Current assets:

 

  

 

  

Cash and cash equivalents

$

109,168,400

$

47,782,400

Short-term investments, at amortized cost

 

131,719,200

 

207,261,400

Accounts receivable

 

7,432,900

 

6,877,000

Accounts receivable – TIA*

475,600

Inventory

 

7,722,000

 

5,204,600

Prepaid expenses and other current assets

 

1,311,600

 

3,307,400

Total current assets

 

257,829,700

 

270,432,800

Property and equipment, net

20,596,100

 

7,681,200

Right of use asset - operating leases

 

10,430,300

 

5,689,300

Other assets

 

920,500

 

316,700

Total assets

$

289,776,600

$

284,120,000

Liabilities and stockholders’ equity

 

  

 

  

Current liabilities:

 

  

 

  

Accounts payable

$

$2,456,300

$

1,820,300

Accrued expenses and other

 

7,901,800

 

6,523,500

Operating lease liability, current

 

438,700

 

527,200

Deferred revenue, current portion

 

7,310,600

 

6,746,800

Total current liabilities

 

18,107,400

 

15,617,800

Operating lease liability, net of current portion

 

14,053,300

 

5,154,900

Other liabilities

 

393,000

 

450,200

Total liabilities

 

32,553,700

 

21,222,900

 

  

 

  

Stockholders’ equity

 

  

 

  

Preferred stock, $0.01 par value; 5,000,000 shares authorized and no shares issued and outstanding at June 30, 2022 and December 31, 2021

Common stock, $0.01 par value; 400,000,000 shares authorized, 101,661,288 and 101,202,705 shares issued and outstanding at June 30, 2022 and December 31, 2021, respectively

1,016,600

1,012,000

Additional paid-in capital

 

382,838,300

 

376,189,600

Accumulated deficit

 

(126,632,000)

 

(114,304,500)

Total stockholders’ equity

 

257,222,900

 

262,897,100

Total liabilities and stockholders’ equity

$

289,776,600

$

284,120,000

* Tenant improvement allowance (“TIA”)

6


MaxCyte, Inc.

Unaudited Consolidated Statements of Operations

    

Three Months Ended June 30, 

Six Months Ended June 30, 

2022

    

2021

    

2022

    

2021

Revenue

$

9,607,800

$

7,108,100

$

21,195,100

$

13,602,900

Cost of goods sold

 

1,120,400

 

784,500

 

2,183,000

 

1,477,600

Gross profit

 

8,487,400

 

6,323,600

 

19,012,100

 

12,125,300

Operating expenses:

 

  

 

  

 

  

 

  

Research and development

 

4,696,000

 

3,203,900

 

8,461,200

 

9,280,300

Sales and marketing

 

4,930,600

 

2,912,900

 

8,769,300

 

5,702,000

General and administrative

 

7,102,600

 

4,301,100

 

13,735,100

 

7,298,900

Depreciation and amortization

497,100

322,900

944,500

634,400

Total operating expenses

 

17,226,300

 

10,740,800

 

31,910,100

 

22,915,600

Operating loss

 

(8,738,900)

 

(4,417,200)

 

(12,898,000)

 

(10,790,300)

Other income (expense):

 

  

 

  

 

  

 

  

Interest and other expense

 

(13,200)

(755,500)

Interest income

 

478,700

8,600

570,500

18,400

Total other income (expense)

 

478,700

 

(4,600)

 

570,500

 

(737,100)

Net loss

$

(8,260,200)

$

(4,421,800)

$

(12,327,500)

$

(11,527,400)

Basic and diluted net loss per share

$

(0.08)

$

(0.05)

$

(0.12)

$

(0.14)

Weighted average shares outstanding, basic and diluted

 

101,427,430

 

84,706,516

 

101,547,583

 

82,865,526

7


MaxCyte, Inc.

Unaudited Consolidated Statements of Cash Flows

    

Six Months Ended June 30, 

2022

    

2021

    

Cash flows from operating activities:

 

  

 

  

 

Net loss

$

(12,327,500)

$

(11,527,400)

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

 

 

Depreciation and amortization

 

1,035,000

 

641,400

Net book value of consigned equipment sold

 

51,400

 

13,900

Loss on disposal of fixed assets

 

 

19,800

Fair value adjustment of liability classified warrant

 

 

358,200

Stock-based compensation

 

5,435,200

 

3,225,000

Amortization of discounts on short-term investments

 

(206,100)

 

1,900

Non-cash interest expense

 

 

5,400

Changes in operating assets and liabilities:

 

 

Accounts receivable

 

(555,900)

 

(547,300)

Accounts receivable - TIA

(475,600)

Inventory

 

(2,639,500)

 

(182,300)

Prepaid expense and other current assets

 

1,995,800

 

(342,700)

Right of use asset – operating leases

 

(4,741,000)

 

554,400

Right of use asset – finance lease

 

 

47,600

Other assets

 

(603,800)

 

(1,670,200)

Accounts payable, accrued expenses and other

 

939,900

 

(992,400)

Operating lease liability

 

8,809,900

 

(584,000)

Deferred revenue

 

563,800

 

1,911,800

Other liabilities

 

(57,200)

 

38,000

Net cash used in operating activities

 

(2,775,600)

 

(9,028,900)

Cash flows from investing activities:

 

  

 

  

Purchases of short-term investments

 

(131,547,700)

(35,963,100)

Maturities of short-term investments

 

207,296,000

16,000,000

Purchases of property and equipment

 

(12,804,800)

(1,271,100)

Proceeds from sale of equipment

4,600

Net cash provided by (used in) investing activities

 

62,943,500

 

(21,229,600)

Cash flows from financing activities:

 

  

 

  

Net proceeds from issuance of common stock

 

51,808,900

Principal payments on notes payable

 

(4,922,400)

Proceeds from exercise of stock options

 

1,218,100

2,089,300

Principal payments on finance leases

 

(49,300)

Net cash provided by financing activities

 

1,218,100

 

48,926,500

Net increase in cash and cash equivalents

 

61,386,000

 

18,668,000

Cash and cash equivalents, beginning of period

 

47,782,400

 

18,755,200

Cash and cash equivalents, end of period

$

109,168,400

$

37,423,200

8


Unaudited Reconciliation of Net Loss to EBITDA

Three Months Ended

Six Months Ended

June 30,

June 30,

2022

    

2021

    

2022

    

2021

(in thousands)

  

 

  

 

  

 

  

Net loss

$

(8,260)

$

(4,422)

$

(12,328)

$

(11,527)

Depreciation and amortization expense

548

333

1,035

641

Interest (income) expense, net

 

(479)

 

(6)

 

(571)

 

379

Income taxes

 

 

 

 

EBITDA

$

(8,191)

$

(4,095)

$

(11,864)

$

(10,507)

9