Investor Presentation • Jan 5, 2023
Investor Presentation
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November 2022
The Company has prepared this presentation based on information available to it, including information derived from public sources that have not been independently verified. No representation or warranty, express or implied, is provided in relation to the fairness, accuracy, correctness, completeness or reliability of the information, opinions or conclusions expressed herein
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The Company does not undertake to update or modify the information included in this presentation to reflect events or any changes involving data editing, processing, or segmentation other than as provided herein or any amendments that may be implemented after the preparation of this presentation. Please also note that the Company's plans and strategy as outlined in this presentation apply to the date of their publication and may be changed at the decision of the Board of Directors or the Company's management, as may happen from time to time. The evaluations in this presentation were provided by the Company's management and are not necessarily the only evaluations available.
This presentation includes forecasts, estimates, indexes, and other information relating to future events and/or matters whose occurrence is uncertain and are not under the Company's control. Such details are regarded as forward-looking information, as defined in the Securities Law, 5728-1968. Such events may not happen, in whole or in part, or may happen in a manner substantially different from any forecast. This forward-looking information is based on subjective assessments and assumptions by the Company's management and is derived from facts and data regarding the Company's current business activities. These subjective assessments and assumptions are inherently uncertain, as they involve risks that result from the Company's activities and are not controlled by the Company, any of which, or a combination thereof, may negatively affect the outcomes of such Company activities. Furthermore, should any forecasts and assessments turn out to be true or should any events or developments occur that have an impact on the general environment, market conditions, or external elements that affect Company activities, these shall be regarded as events that can neither be assessed beforehand nor be controlled by the Company. This presentation includes scientific, statistical, and other data published by third parties, the contents of which have not been reviewed by the Company.
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This presentation may contain information that has been or will be presented differently in reports published by the Company for the general public. Such information may include data characterized and/or edited and/or segmented differently in the reports published by the company for the general public.

Company Established in 2000 Specializes in a variety of disciplines – R&D, manufacturing and marketing of cell imaging and analysis systems for cancer diagnostic testing

Global Distribution Agreements •Abbott Molecular •Sanmed Bio (China)

Company's systems regulatory approvals: •FDA - USA •NMPA - China •CE IVDR - Europe •Medical Device - Israel
• KFDA - Korea

Team of 25 employees Global R&D and Service Center in Rehovot, Israel

Over 650 systems installed around the world

Annual revenue from instrument sales and service contracts of approximately 30 million NIS per year Profitable with a positive cash flow
Fully owned US subsidiary engaging in marketing, sales, and rendering service to North American clients

BioView's instruments are sold to pathology, cytogenetics, and cytology laboratories

Business collaborations with industry leading liquid biopsy test manufacturers, which integrated the company instruments with their product offering

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To become a leading company developing, marketing, and selling liquid biopsy-based medical tests to improve the treatment and monitoring of cancer patients as well as minimize any discomfort and risks of existing tests

Advantages • Regulatory approvals in key markets
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Challenges • Recurring sales revenues generated through service contracts and upgrades

BioView systems help standardize analysis and reporting and facilitate the expansion of laboratory services. System performance is validated by clinical studies that served as the basis of the systems FDA and CE clearances. The system can accommodate multiple applications, including analysis and clinical reporting for:

Metaphase-based Blood cancer Bladder cancer Lung cancer Breast cancer cancer analysis






Duet-3 Scan of up to 50 samples in single run

Allegro Plus Accord Plus Scan of up to 8 samples in single run

Single slide scan

SoloWeb
Remote secured analysis and reporting via web browser


• Invasive procedure
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Single-click operation
Compact design



High sample capacity
High Throughput


Industry leader specializing in automated liquid biopsy imaging and analysis.
The company maintains extensive collaborations with companies that develop liquid biopsy-based tests and utilize BioView imaging systems as an integral part of their clinical assay.
Lung cancer Brain cancer Breast cancer Liver cancer Head and neck cancer Detection Monitoring Therapy selection Diagnostic services for pharmaceutical companies

Significant potential for expansion to both clinical and pharmacological markets
Leveraging BioView's knowledge and experience to respond to an existing unmet clinical need


Development of a liquid biopsy test includes; preparing and processing blood sample, detecting and characterizing of cancer cells - to obtain actionable clinical data for treatment of cancer patients









Development of a liquid biopsy test includes; preparing and processing blood sample, detecting and characterizing of cancer cells - to obtain actionable clinical data for treatment of cancer patients

Sell test services to pharmaceutical companies for drug research and development

Selling tests to hospitals and laboratories for clinical use


~900,000 ~50,000 ~206,000
New patients are diagnosed every year globally with a projected 30% increase in 10 years
New patients are diagnosed in the USA every year

Cancer patients in USA on average per year
Cost of patient-monitoring by PET-CT Cost of patient treatment. \$4,000 - \$6,000 ~\$10,000
15-30% of patients respond to treatment

Personalized care to raise the rate of patients responding to drugs and prevent patient suffering due to 1 ineffective treatment
Monitoring patients during treatment for 2therapeutic resistance
Monitoring and early detection of cancer spread to facilitate 3alteration of treatment
270,000 90,000 Patients per year Patients per year
450,000 Patients per year



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https://gco.iarc.fr/today/online-analysis-
pie?v=2020&mode=population&mode\_population=continents&population=900&populations=900&key=total&sex= 0&cancer=14_1_3_4_2&type=0&statistic=5&prevalence=0&population_group=0&ages_group%5B%5D=0&ages_gr oup%5B%5D=17&nb_items=7&group_cancer=1&include_nmsc=0&include_nmsc_other=1&half_pie=0&donut=0

https://gco.iarc.fr/today/online-analysis-
pie?v=2020&mode=population&mode\_population=continents&population=900&populations=900&key=total&sex= 0&cancer=14_1_3_4_2&type=2&statistic=5&prevalence=1&population_group=0&ages_group%5B%5D=0&ages_gr oup%5B%5D=17&nb_items=7&group_cancer=1&include_nmsc=0&include_nmsc_other=1&half_pie=0&donut=0

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| Monitoring and early detection of cancer spreading from the tumor and appropriate treatment adaptation (450,000) |
Personalized treatment adaptation intended to raise the rate of patients responding to drugs and preventing patient suffering due to unnecessary and ineffective treatment (270,000) |
Monitoring patients during treatment for the identification of therapeutic resistance (90,000) |
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|---|---|---|---|---|---|
| Testing cost \$ 600 | |||||
| Market share upon obtaining regulatory approval |
Two tests per year % market penetration, Year 1: 1% % market penetration, Year 2: 2.5% % market penetration, Year 3: 5% |
% market penetration, Year 1: 2% % market penetration, Year 2: 5% % market penetration, Year 3: 10% |
% market penetration, Year 1: 2% % market penetration, Year 2: 5% % market penetration, Year 3: 10% |
||
| Year 1 Revenue | \$ 5.4 million | \$ 3.2 million | \$ 1.1 million | ||
| Year 1 Total Revenue | \$ 9.7 million | ||||
| Year 2 Revenue | \$ 13.5 million | \$ 8.1 million | \$ 2.7 million | ||
| Year 2 Total Revenue | \$ 24.3 million | ||||
| Year 3 Revenue | \$ 27 million | \$ 16.2 million | \$ 5.4 million | ||
| Year 3 Total Revenue | \$ 48.6 million |

~200,000
new patients are diagnosed in the USA every year
36% of treated patients, the cancer will return Over 2 million
people are monitored per year for cancer recurrence
biopsy testing cost ~\$2,000
\$90,000-\$250,000
the cost of treatments per patient per year. With some treatments, up to 50% of patients do not respond


Total: 1,414,259
https://gco.iarc.fr/today/online-analysis-
pie?v=2020&mode=population&mode_population=countries&population=900& populations=900&key=total&sex=1&cancer=27&type=0&statistic=5&prevalence= 0&population\_group=0&ages\_group%5B%5D=0&ages\_group%5B%5D=17&nb\_it ems=7&group_cancer=1&include_nmsc=0&include_nmsc_other=1&half_pie=0& donut=0


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| Test purpose | Potential indemnification by insurance companies (USD) |
Number of patients per year |
Number of tests per patient per year |
Total market potential per year |
|---|---|---|---|---|
| Personalized treatment adaptation |
1500 | 512,000 | 1 | \$ 768 million |
| Post-treatment patient monitoring |
500 | 1,995,000 | 1 | \$ 997 million |


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