Annual Report
and Accounts 2020
Driving the next generation of cell-based therapies
2020 HIGHLIGHTS
MaxCyte® is advancing the next generation of cell-based therapies by unlocking the power of the human cell.
Revenue
(USD '000s)
20$26,169
19$21,621
18$16,667
17$13,985
16$12,270
Contents
Investment case | 4 |
Chairman and Chief Executive Officer's | |
joint review | 6 |
Focus on corporate social responsibility | 9 |
Life sciences | 10 |
Financial review | 14 |
Principal risks and uncertainties | 16 |
Governance | |
Leadership team | 18 |
Board of Directors | 20 |
Directors' report | 22 |
Corporate governance report | 23 |
Compensation report | 25 |
Directors' responsibilities | 27 |
Audit committee report | 28 |
Financial Statements | |
Report of independent registered | |
public accounting firm | 29 |
Balance sheets | 30 |
Statements of operations | 31 |
Consolidated statements of changes | |
in stockholders' equity | 32 |
Statements of cash flow | 33 |
Notes to financial statements | 34 |
AGM notice | 45 |
All financial amounts are in USD unless noted | |
otherwise. | |
d | MAXCYTE INC ANNUAL REPORT AND ACCOUNTS 2020 |
Revenue growth | Revenue growth |
from 2019 to 2020 | from 2016 to 2020 |
21% 23%
Five-year CAGR
MAXCYTE INC ANNUAL REPORT AND ACCOUNTS 2020
STRATEGIC REPORT Governance FINANCIAL STATEMENTS
Gross margin | Cumulative total | ||||||||||
instruments placed | |||||||||||
20 | 89.4% | 20 | 400+ | ||||||||
19 | 88.4% | 19 | 320+ | ||||||||
18 | 89.0% | 18 | 250+ | ||||||||
17 | 89.6% | 17 | 200+ | ||||||||
16 | 89.3% | 16 | 150+ | ||||||||
Gross funds raised
February 2021May302020
$55.3m $ .5m
Aggregate potential pre-commercial milestone payments from commercial agreements signed to date
>$950m
Operational highlights
- Expanded team of application scientists and increased number of collaborations to support use of MaxCyte technology in developing novel engineered next-generation cell therapies
- Significant commercial momentum in transformative therapies - three new strategic platform licences signed during 2020 with leading cell-therapy developers Allogene Therapeutics, Caribou Biosciences and novel therapy company APEIRON Biologics and a fourth strategic platform licence signed with Myeloid Therapeutics in January 2021
- Continued to introduce new processing assemblies within the ExPERT™ brand series of commercially‐oriented instruments and disposables to meet customer demands
- Bolstered the senior management team with several key appointments and a leadership promotion
- As announced in January 2021, MaxCyte is now focusing on out-licensing CARMA® platform manufacturing processes, pre-clinical and clinical data, and intellectual property (IP)
MAXCYTE INC ANNUAL REPORT AND ACCOUNTS 2020 | 1 |
AT A GLANCE
Technology is just the beginning
Our mission
We believe in the vast potential of next-generation cell therapies to have a meaningful impact on the millions of patients worldwide who, despite medical advancements, live with unmet medical needs across a variety of diseases. Our aim is to be the premier cell-engineering platform technology to support the development of advanced therapeutics.
Who we are
We are dedicated to advancing cell-engineering through application of our proprietary delivery platform and collaborative partnerships.
We are uniquely positioned at the centre
of next-generation cell therapy development, which aims to unlock the power of human cells to treat disease.
What we do
We help bring the promise of the next generation of cell therapies to life. Our Flow Electroporation® technology and ExPERT™ platform enable our partners to accelerate, streamline, and improve the drug discovery and development process from the early stages of research to commercialisation.
How we do it
The MaxCyte offering to partners is driven by ground-breaking technology, which allows customers to scale up from research to cGMP all in one platform - reducing clinical risk. Our talented and dedicated team of sales representatives and application scientists, of which 20 are in the field, works closely with our partners all along the development pathway to achieve clinical and commercial success. In addition, our FDA Master File and Technical Files, which have supported 30 clinical trials to date, help reduce our customers' regulatory risk.
Partnered programmes
Continued growth in total licensed programmes
Total strategic platform licences* | |||||||||||||||||
12 | |||||||||||||||||
2020 | 100+ | 140+ | |||||||||||||||
8 | |||||||||||||||||
2019 | 70+ | 100+ | |||||||||||||||
2018 | 3 | ||||||||||||||||
35+ | 70+ | Licensed for | |||||||||||||||
2017 | 1 | ||||||||||||||||
20+ | 50+ | clinical use | |||||||||||||||
0 | Total partnered | ||||||||||||||||
2016 | 15+ | 40+ | |||||||||||||||
programme | |||||||||||||||||
0 | 30 | 60 | 90 | 120 | 150 | ||||||||||||
licences |
* Between 1 January 2017 and 31 January 2021
2 | MAXCYTE INC ANNUAL REPORT AND ACCOUNTS 2020 |
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Disclaimer
MaxCyte Inc. published this content on 14 June 2021 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 16 June 2021 07:35:01 UTC.