NOTES
TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
For
the Three Months Ended March 31, 2023 and 2022
(Unaudited)
NOTE
1 – DESCRIPTION OF BUSINESS
a.
General
Orgenesis
Inc. is a global biotech company working to unlock the potential of Cell and Gene Therapies (“CGTs”) in an affordable and
accessible format. CGTs can be centered on autologous (using the patient’s own cells) or allogenic (using master banked donor cells)
and are part of a class of medicines referred to as advanced therapy medicinal products, or ATMPs. The Company is mostly focused on autologous
therapies that can be manufactured under processes and systems that are developed for each therapy using a closed and automated approach
that is validated for compliant production near the patient for treatment of the patient at the point of care, or POCare. This approach
has the potential to overcome the limitations of traditional commercial manufacturing methods that do not translate well to commercial
production of advanced therapies due to their cost prohibitive nature and complex logistics to deliver such treatments to patients (ultimately
limiting the number of patients that can have access to, or can afford, these therapies).
To
achieve these goals, the Company has developed a collaborative worldwide network of research institutes and hospitals who are engaged
in the POCare model, or the Company’s POCare Network, and a pipeline of licensed POCare advanced therapies that can be processed
and produced under such closed and automated processes and systems, or POCare Therapies. The Company is developing its pipeline of advanced
therapies and with the goal of entering into out-licensing agreements for them. The Company’s cellular therapies, though defined
as drug products, conceptually differ from other drug modalities in that they are based on reprogramming of cells sourced from the patient
or from a donor. In most cases, they are individually produced per patient in a highly sterile and controlled environment, and their
efficacy is optimized when administered a short time following production as fresh product.
To
advance the execution of the Company’s goal of bringing such therapies to market, the Company has designed and built the Company’s
POCare Platform - a scalable infrastructure of technology and services that ensures a central quality system, replicability and standardization
of infrastructure and equipment, and centralized monitoring and data management. The platform is constructed on POCare Centers that serve
as hubs that implement locally the Company’s POCare quality system, Good Manufacturing Practices, training procedures, quality
control testing, incoming supply of materials and oversee the actual production in the Orgenesis Mobile Processing Units & Labs,
or OMPULs.
POCare
Services
The
Company’s subsidiary Morgenesis LLC (“Morgenesis”) is responsible for most of the Company’s POCare services platform.
The POCare Services platform is utilized by parties such as biotech companies and hospitals for the supply of their products. Morgenesis
services include adapting the process to the platform and supplying the products, or POCare Services. These are services for third party
companies and for CGT’s that are not necessarily based on the Company’s POCare Therapies. POCare services that the Company
and its affiliated entities perform include:
● |
Process
development of therapies, process adaptation, and optimization inside the OMPULs, or “OMPULization”; |
● |
Adaptation
of automation and closed systems to serviced therapies; |
● |
Incorporation
of the serviced therapies compliant with GMP in the OMPULs that the Company designs and built; |
● |
Tech
transfers and training of local teams for the serviced therapies at the POCare Centers; |
● |
Processing
and supply of the therapies and required supplies under GMP conditions within the Company’s POCare Network, including required
quality control testing; and |
● |
Contract
Research Organization services for clinical trials. |
The
POCare Services are performed in decentralized hubs that provide harmonized and standardized services to customers, or POCare Centers.
The Company is working to expand the number and scope of the Company’s POCare Centers with the intention of providing an efficient
and scalable pathway for CGT therapies to reach patients rapidly at lowered costs. Our POCare Services are designed to allow rapid capacity
expansion while integrating new technologies to bring together patients, doctors and industry partners with a goal of achieving standardized,
regulated clinical development and production of therapies.
POCare
Services Operations via Subsidiaries
The
Company currently conducts its core business operations itself and through its subsidiary Morgenesis (of which the Company currently
owns 76.9%) and the following Morgenesis’ subsidiaries which are all wholly owned except as otherwise stated below (collectively,
the “Subsidiaries”).
● | Orgenesis
Maryland LLC, which is the center of POCare Services activity in North America and is currently
focused on setting up and providing POCare Services and cell-processing services to the POCare
Network. |
● | Tissue
Genesis International LLC, a Texas company currently focused on development of the Company’s
technologies and therapies. |
● | Orgenesis
Services SRL, which is currently focused on expanding the Company’s POCare Network
in Belgium. |
● | Orgenesis
Germany GmbH, which is currently focused on providing CRO services to the POCare Network. |
● | Orgenesis
Korea Co. Ltd., which is a provider of cell-processing and pre-clinical services in Korea.
The Company owns 94.12% of the Korean Subsidiary. |
● | Orgenesis
Biotech Israel Ltd., which is a provider of process development and cell-processing services
in Israel. |
● | Orgenesis
Australia PTY LTD, which was transferred to Morgenesis in January 2023 and is currently focused
on the development of the Company’s POC Network in Australia. |
● | Theracell
Laboratories private company, a Greek company currently focused on expanding the Company’s
POCare Network. |
● | ORGS
POC CA Inc, incorporated in 2023, which is currently focussed on expanding the Company’s
POCare Network in California. |
POCare
Therapies
The
Company’s POCare Network is an alternative to the traditional pathway of drug development. The Company collaborates with academic
institutions and entities that have been spun out from such institutions. The Company is in close contact with researchers who are experts
in the field of the drug and also partners with leading hospitals and research institutes. Based on such collaborations, the Company
enters into in-licensing agreements with relevant institutions for promising therapies with the aim of adapting them to a point-of-care
setting through regional or strategic biological partnerships. It then is able to out-license its own therapeutic developments, as well
as those therapies developed from in-licensing agreements, to out-licensing partners at preferred geographical regions.
This
approach lowers overall development costs through minimizing pre-clinical development costs incurred by the Company, and through receiving
of the additional funding from grants and/or payments by regional partners.
The
Company’s therapies development subsidiaries are:
● | Koligo
Therapeutics, Inc., a Kentucky corporation, which is a regenerative medicine company, specializing
in developing personalized cell therapies. It is currently focused on commercializing its
metabolic pipeline via the POCare Network throughout the United States and in international
markets. |
| |
● | Orgenesis
CA, Inc. a Delaware corporation, which is currently focused on development of technologies
and therapies in California. |
● | Orgenesis
Belgium SRL which is currently focused on product development. Since its incorporation, the
subsidiary been awarded grants in excess of 18 million Euro from the Walloon region for several
projects (DGO6 grants). |
| |
● | Orgenesis
Switzerland Sarl, which is currently focused on providing group management services. |
| |
● | MIDA
Biotech BV, which is currently focused on research and development activities, was granted
a 4 million Euro grant under the European Innovation Council Pathfinder Challenge Program
which supports cutting-edge science and technology. The grant is for technologies enabling
the production of autologous induced pluripotent stem cells (iPSCs) using microfluidic technologies
and artificial intelligence (AI). |
| |
● | Orgenesis
Italy SRL which is currently focused on R&D activities. |
| |
● | Orgenesis
Ltd., an Israeli subsidiary which is focused on R&D and a provider of R&D management
services for out licenced products. Israel as a hub for biotech research and pioneers in
this field. |
| |
● | Orgenesis
Austria GmbH which is focused on R&D. |
Through
March 31, 2023, the Company had an accumulated deficit of $125 million. For the three months ended March 31, 2023 the Company incurred negative cashflows from operating activities
of $7.2 million. The Company’s activities have been funded primarily by generating revenue,
offerings of the Company’s securities and convertible loans. There is no assurance that the Company’s business will generate
sustainable positive cash flows to fund its business operations.
If
there are further increases in operating costs for facilities expansion, research and development, commercial and clinical activity or
decreases in revenues from customers, the Company will need to use mitigating actions such as to seek additional financing or postpone
expenses that are not based on firm commitments. In addition, in order to fund the Company’s operations until such time that the
Company can generate sustainable positive cash flows, the Company may need to raise additional funds.
Current
and projected cash resources and commitments, as well as the other factors mentioned above, raise a substantial doubt about the Company’s
ability to continue as a going concern to meet the Company’s current operations for the next 12 months. Management plans include
raising additional capital to fund the Company’s operations and to repay the Company’s outstanding loans when they become
due, as well as exploring additional avenues to increase revenue and reduce capital expenditures. If the Company is unable to raise sufficient
additional capital or meet revenue targets, it may have to curtail certain activities.
The
estimation and execution uncertainty regarding the Company’s future cash flows and management’s judgments and assumptions
in estimating these cash flows is a significant estimate. Those assumptions include reasonableness of the forecasted revenue, operating
expenses, and uses and sources of cash.
NOTE
2 – BASIS OF PRESENTATION
The
accompanying unaudited condensed consolidated financial statements have been prepared on the same basis as the annual consolidated financial
statements. In the opinion of management, the financial statements reflect all normal and recurring adjustments necessary to fairly state
the financial position and results of operations of the Company. The information included in this Quarterly Report on Form 10-Q should
be read in conjunction with the consolidated financial statements and accompanying notes included in the Company’s Annual Report
on Form 10-K for the year ended December 31, 2022, as filed with the Securities and Exchange Commission (“SEC”) on March
22, 2023. The year-end balance sheet data was derived from the audited consolidated financial statements as of December 31, 2022, but
not all disclosures required by generally accepted accounting principles in the United States (“U.S. GAAP”) are included
in this Quarterly Report on Form 10-Q.
b. | Significant
accounting policies |
The
accounting policies adopted are consistent with those of the previous financial year except as described below:
Use
of Estimates in the Preparation of Financial Statements
The
preparation of our consolidated financial statements in conformity with U.S. GAAP requires us to make estimates, judgments and assumptions
that may affect the reported amounts of assets, liabilities, equity, revenues and expenses and related disclosure of contingent assets
and liabilities. On an ongoing basis, we evaluate our estimates, judgments, and methodologies. We base our estimates on historical experience
and on various other assumptions that we believe are reasonable, the results of which form the basis for making judgments about the carrying
values of assets, liabilities and equity, the amount of revenues and expenses and determining whether an acquisition is a business combination
or a purchase of asset. Actual results could differ from those estimates.
Recently
adopted accounting pronouncements
In
June 2016, the FASB issued ASU 2016-13 “Financial Instruments—Credit Losses—Measurement of Credit Losses on Financial
Instruments.” This guidance replaces the current incurred loss impairment methodology with a methodology that reflects expected
credit losses and requires consideration of a broader range of reasonable and supportable information to inform credit loss estimates.
The guidance will be effective for Smaller Reporting Companies (SRCs, as defined by the SEC) for the fiscal year beginning on January
1, 2023, including interim periods within that year. The adoption of this guidance did not have a material impact on the Company’s consolidated financial statements.
In
October 2021, the FASB issued ASU 2021-08 “Business Combinations (Topic 805), Accounting for Contract Assets and Contract Liabilities
from Contracts with Customers”, which requires contract assets and contract liabilities acquired in a business combination to be
recognized and measured by the acquirer on the acquisition date in accordance with ASC 606, Revenue from Contracts with Customers. The
guidance will result in the acquirer recognizing contract assets and contract liabilities at the same amounts recorded by the acquiree.
The guidance should be applied prospectively to acquisitions occurring on or after the effective date. The guidance is effective for
fiscal years beginning after December 15, 2022, including interim periods within those fiscal years. Early adoption is permitted, including
in interim periods, for any financial statements that have not yet been issued. The adoption of this guidance did not have a material
impact on the Company’s consolidated financial statements.
Reclassifications
Certain
reclassifications have been made to the prior year’s financial statements to conform to the current year presentation. These reclassifications
had no net effect on previously reported results of operations.
NOTE
3 – SEGMENT INFORMATION
In
connection with the investment by an affiliate of Metalmark Capital Partners (“Metalmark”) in the Company in November
2022 (“the Metalmark Investment”), the Company separated its operations into two operating segments: operations of
Morgenesis (the “Morgenesis” segment) and therapies related activities (the “Therapies” segment). Prior to
that, the Company conducted all its operations as one segment. The Morgenesis operations segment includes mainly POCare Services,
while the therapies related segment includes the Company’s therapeutic development operations.
Because
the Company conducted all its operations as one segment prior to the Metalmark Investment, the above changes were reflected through retroactive
revision of prior period segment information based on the subsidiaries that were transferred to Morgenesis. Certain activities of these
subsidiaries have changed after they were transferred to Morgenesis operations segment.
The
Company’s Chief Executive Officer (“CEO”), who is the chief operating decision maker (“CODM”), reviews
financial information prepared on a consolidated basis, accompanied by disaggregated information about revenues and contributed profit
by the two identified reportable segments to make decisions about resources to be allocated to the segments and assess their performance.
The
Company does not review assets by segment. Therefore, the measure of assets has not been disclosed for each segment.
Segment
data for the three months ended March 31, 2023 is as follows:
SCHEDULE
OF SEGMENT REPORTING
| |
Morgenesis | | |
Therapies | | |
Eliminations | | |
Consolidated | |
| |
(in
thousands) | |
Revenues | |
$ | 6,914 | | |
$ | 130 | | |
$ | - | | |
$ | 7,044 | |
Revenues from related
party | |
| - | | |
| - | | |
| - | | |
| - | |
Total revenues | |
| | | |
| | | |
| | | |
| | |
Cost of revenues* | |
| (2,308 | ) | |
| (178 | ) | |
| - | | |
| (2,486 | ) |
Gross profit | |
| 4,606 | | |
| (48 | ) | |
| - | | |
| 4,558 | |
Cost of development
services and research and development expenses* | |
| (2,081 | ) | |
| (1,076 | ) | |
| - | | |
| (3,157 | ) |
Operating expenses* | |
| (1,714 | ) | |
| (2,314 | ) | |
| - | | |
| (4,028 | ) |
Other income, net | |
| 2 | | |
| - | | |
| - | | |
| 2 | |
Depreciation and amortization | |
| (385 | ) | |
| (193 | ) | |
| - | | |
| (578 | ) |
Loss from extinguishment in connection with
convertible loan | |
| - | | |
| (283 | ) | |
| - | | |
| (283 | ) |
Financial Expenses, net | |
| (266 | ) | |
| (378 | ) | |
| - | | |
| (644 | ) |
Share in net income
of associated companies | |
| - | | |
| (2 | ) | |
| - | | |
| (2 | ) |
* | | Excluding Depreciation,
amortization expenses |
Segment
data for the three months ended March 31, 2022 is as follows:
| |
Morgenesis | | |
Therapies | | |
Eliminations | | |
Consolidated | |
| |
(in
thousands) | |
Revenues | |
$ | 6,343 | | |
| 1,942 | | |
$ | (1,708 | ) | |
$ | 6,577 | |
Revenues from related
party | |
| 635 | | |
| - | | |
| - | | |
| 635 | |
Total revenues | |
| 6,978 | | |
| 1,942 | | |
| (1,708 | ) | |
| 7,212 | |
Cost of revenues* | |
| (350 | ) | |
| (289 | ) | |
| - | | |
| (639 | ) |
Gross profit | |
| 6,628 | | |
| 1,653 | | |
| (1,708 | ) | |
| 6,573 | |
Cost of development
services and research and development expenses* | |
| (3,476 | ) | |
| (4,445 | ) | |
| 1,428 | | |
| (6,493 | ) |
Operating expenses* | |
| (709 | ) | |
| (2,413 | ) | |
| 280 | | |
| (2,842 | ) |
Depreciation and amortization | |
| (190 | ) | |
| (284 | ) | |
| - | | |
| (474 | ) |
Financial Expenses, net | |
| (551 | ) | |
| 338 | | |
| - | | |
| (213 | ) |
Share in net income
of associated companies | |
| 1 | | |
| (548 | ) | |
| - | | |
| (547 | ) |
* | | Excluding Depreciation,
amortization expenses |
NOTE
4 – EQUITY
On
February 23, 2023, the Company entered into a securities purchase agreement (the “Purchase Agreement”) with certain institutional
and accredited investors (the “Purchaser”) relating to the issuance and sale of 1,947,368 shares (the “Shares”)
of common stock, par value $0.0001 per share (the “Common Stock”), and warrants to purchase up to 973,684 shares of Common
Stock (the “Warrants”) at a purchase price of $1.90 per share of Common Stock and accompanying Warrants in a registered direct
offering (the “Offering”). The Offering closed on February 27, 2023 (the “Closing Date”).
The
Warrants have an exercise price of $1.90 per share, are exercisable immediately and will expire five years following the date of issuance.
The Warrants have an alternate cashless exercise option (beginning on or after the earlier of (a) the thirty-day anniversary of the date
of the Purchase Agreement and (b) the date on which the aggregate composite trading volume of Common Stock following the public announcement
of the pricing terms exceeds 13,600,000 shares), to receive an aggregate number of shares equal to the product of (x) the aggregate number
of shares of Common Stock that would be issuable upon a cash exercise and (y) 1.0. The aggregate gross proceeds to the Company from the
Offering was $3.7 million, before deducting placement agent cash fees equal to 7.0% of the gross proceeds received and other expenses
from the Offering payable by the Company. The Company intends to use the net proceeds from the Offering for working capital and general
corporate purposes, including the Company’s therapy related activities.
As
of May 10, 2023, 845,378
warrants were exercised.
NOTE
5 – CONVERTIBLE LOANS
New
convertible loans
On
January 10, 2023 (the “Effective Date”), the Company entered into the following agreements: (i) a convertible loan agreement
(the “NewTech Convertible Loan Agreement”) with NewTech Investment Holdings, LLC (the “NewTech Lender”), pursuant
to which the NewTech Lender loaned the Company $4,000,000 (the “NewTech Loan Amount”), and (ii) a convertible loan agreement
(the “Malik Convertible Loan Agreement”, together with the NewTech Convertible Loan Agreement, the “Convertible Loan
Agreements”) with Ariel Malik (the “Malik Lender”, together with the NewTech Lender, the “Lenders”), pursuant
to which the Malik Lender loaned the Company $1,000,000 (the “Malik Loan Amount”, together with the NewTech Loan Amount,
the “Loan Amount”).
The
terms of the NewTech Convertible Loan Agreement and the Malik Loan Agreement are identical. Interest is calculated at 8% per annum (based
on a 365-day year); provided, that if an Event of Default (as defined in the Convertible Loan Agreements) has occurred and is continuing,
the Outstanding Amount (as defined herein) will be calculated at 15.0% per annum. The Loan Amount and all accrued but unpaid interest
thereon (collectively, the “Outstanding Amount”) shall either (i) be repaid in cash or (ii) convert to shares of common stock,
par value $0.0001 per share (“Common Stock”), of the Company on the third anniversary of the Effective Date (the “Maturity
Date”). The Maturity Date may be extended by the Lender upon the written consent of the Lender. The Outstanding Amount may be prepaid
by the Company in whole or in part at any time with the prior approval of the Lender.
At
any time prior to or on the Maturity Date, any Lender may provide the Company with written notice to convert all or part of the Outstanding
Amount into shares of our Common Stock equal to the quotient obtained by dividing (x) the Outstanding Amount by (y) a price equal to
$2.464 per share (subject to adjustment for certain capital events, such as stock splits) (the “Conversion Price”).
The
Convertible Loan Agreements contain customary affirmative and negative covenants, including a minimum share reserve, transactions with
affiliates, and restrictions on the incurrence of additional debt. Each Lender’s obligation to fund its respective Loan Amount
is subject to customary closing conditions and deliverables.
Under
the terms of the Convertible Loan Agreements, the Company will use the proceeds from the Loan Amount to (i) redeem the loan amount from
the previously disclosed Convertible Loan Agreement, dated as of May 19, 2022 between Orgenesis and Ricky Steven Neumann, as amended
by the previously disclosed certain Convertible Loan Extension Agreement, dated as of October 23, 2022, by and between Orgenesis and
Ricky Steven Neumann, and (ii) for general corporate purposes. Pursuant to the terms, the Company repaid said loan upon receipt of the
Loan Amount. The use of proceeds from any Additional Loan Amount (as defined in the Convertible Loan Agreements) will be to redeem existing
indebtedness; provided, that $3,000,000 of the Additional Loan Amount may be used for general corporate purposes.
In
connection with such loan, the Company agreed to issue the NewTech Lender warrants representing the right to purchase 405,844 shares
of Common Stock, at an exercise price of $2.50 per share and the Malik Lender warrants representing the right to purchase 101,461 shares
of Common Stock, at an exercise price of $2.50 per share. Such Warrants will be exercisable at any time beginning six months and one
day after closing and ending 36 months after the closing date.
Koligo
convertible loan
On
March 27, 2023, the Company’s subsidiary Koligo Therapeutics Inc. (“Borrower”), entered into a convertible loan agreement
(the “Convertible Loan Agreement”) with Yehuda Nir (the “Lender,” and together with the Borrower, the “Parties”),
pursuant to which the Lender agreed to loan the Borrower up to $5,000,000 (the “Loan Amount”). Interest is calculated at
8% per annum (based on a 365-day year) and is payable, along with the principal, on or before January 1, 2024 (the “Maturity Date”).
The Maturity Date may be extended by the Lender in the Lender’s sole and absolute discretion and any such extension(s) shall be
in writing signed by the Parties. The Loan Amount may be prepaid by the Borrower in whole or in part at any time with the prior written
approval of the Lender.
If
prior to December 31, 2023, the Borrower issues equity securities (“Equity Securities”) in a transaction or series of related
transactions resulting in aggregate gross proceeds to the Borrower of at least $5,000,000 (excluding conversion of the Loan Amount) (a
“Qualified Financing”), then the outstanding principal amount of the Loan Amount, and any and all accrued but unpaid interest
thereon (collectively, the “Outstanding Amount”), will automatically convert into such Equity Securities issued pursuant
to the Qualified Financing at a price per share equal to fifty percent (50%) of the price per share paid for each share of the Equity
Securities purchased for cash by the investors in the Qualified Financing (the “Mandatory Conversion”). The per share price
for the Mandatory Conversion shall be calculated on a fully diluted basis (including equity underlying all outstanding options, warrants,
and other convertible securities, but excluding the Equity Securities issuable upon the Mandatory Conversion).
The
Parties agreed that the Lender shall have the option to assign $1,500,000 of the Loan Amount due to the Lender under that certain convertible
loan agreement between the Lender and the Company dated April 21, 2022, as amended, (collectively the “Original Loan”), to
the Borrower (the “Loan Assignment”). The terms of the Loan Assignment will be the same as under the Original Loan, including
a maturity date of January 31, 2026 and an annual interest rate of 10%. The Loan Assignment will be subject to the Mandatory Conversion
as described above. As of the date of the issue of these financial statements, said assignment did not occur.
Under
the terms of the Convertible Loan Agreement, the Borrower agreed to use the Loan Amount to fund working capital and ongoing operations
and for no other purposes unless the Lender agrees in writing. As of March 31, 2023, Koligo received $485 thousand under the Convertible
Loan Agreement.
Extension
of existing loan agreements
On
January 12, 2023, the Company entered into (i) a Convertible Credit Line and Unsecured Convertible Note Extension #2 Agreement with Yosef
Dotan (the “Dotan Extension Agreement”), (ii) a Convertible Credit Line Extension Agreement with Aharon Lukach (the “Lukach
Extension Agreement”) and (iii) a Convertible Loans and Unsecured Convertible Notes Extension #2 Agreement with Yehuda Nir (the
“Nir Extension Agreement”), each which extended the maturity date of the convertible loans under their respective loan agreements
(as described below) to January 31, 2026. The aggregate principal amount of loans extended was $12 million and the interest rate on the
extended loans varied between 2% and 10%. In consideration for the extensions, (i) the interest rate on such principal amount of such
loans was increased to 10% per annum commencing on February 1, 2023 (except for the Nir Convertible Loan Agreement dated as of April
12, 2022, which already had a 10% per annum interest rate), (ii) the conversion price of the loans was reduced from $7.00 to $2.50 (except
for the Nir Convertible Loan Agreement dated as of April 12, 2022, which already had a $2.50 conversion price), (iii) the exercise price
of the warrants issuable upon conversion of the 2% Notes and the Nir Convertible Loan Agreement dated as of May 17, 2019 was reduced
to $2.50 per share and the term of such warrants was extended to January 31, 2026.
The
Dotan Extension Agreement related to a Convertible Credit Line Agreement dated as of October 3, 2019, as amended, of which $750,000
principal amount plus interest is outstanding, and 2%
Notes purchased from the Company on November 3, 2018, of which $250,000
principal amount plus interest is outstanding. Based on its analysis, the Company concluded that the change in terms referred to
Convertible Credit Line Agreement and the 2%
Notes should be accounted for as a modification and an extinguishment respectively.
The
Lukach Extension Agreement related to a Convertible Credit Line Agreement dated as of October 3, 2019, as amended, of which $750,000
principal amount plus interest is outstanding. Based on its analysis, the Company concluded that the change in terms referred to above
should be accounted for as a modification.
The
Nir Extension Agreement related to 2%
Notes purchased from the Company on November 3, 2018, as amended, of which $500,000
principal amount plus interest is outstanding,
a Convertible Loan Agreement dated as of May 17, 2019, of which $5,000,000
principal amount plus interest is outstanding,
and a Convertible Loan Agreement dated as of April 12, 2022, as amended, of which $5,000,000
principal amount plus interest is outstanding.
Based on its analysis, the Company concluded that the change in terms referred to the 2% Notes and Convertible Loan Agreement should
be accounted for as an extinguishment and a modification respectively.
NOTE
6 – LOSS PER SHARE
The
following table sets forth the calculation of basic and diluted loss per share for the period indicated:
SCHEDULE
OF BASIC AND DILUTED LOSS PER SHARE
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
Three Months Ended | |
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
(in thousands, except per share data) | |
Basic and diluted: | |
| | | |
| | |
Net loss attributable to Orgenesis Inc. | |
$ | 4,189 | | |
$ | 4,009 | |
Weighted average number of common shares outstanding | |
| 26,246,924 | | |
| 24,600,954 | |
Net loss per share | |
$ | 0.16 | | |
$ | 0.16 | |
For
the three months ended March 31, 2023 and March 31, 2022, all outstanding convertible notes, options and warrants have been excluded
from the calculation of the diluted net loss per share since their effect was anti-dilutive. Diluted loss per share does not include
8,390,035 shares underlying outstanding options and warrants and 6,987,879 shares upon conversion of convertible loans for the three
months ended March 31, 2023, because the effect of their inclusion in the computation would be antidilutive. Diluted loss per share does
not include 6,382,782 shares underlying outstanding options and warrants and 1,539,356 shares upon conversion of convertible loans for
the three months ended March 31, 2022, because the effect of their inclusion in the computation would be antidilutive.
NOTE
7 – REVENUES
Disaggregation
of Revenue
The
following table disaggregates the Company’s revenues by major revenue streams.
SCHEDULE
OF DISAGGREGATION OF REVENUE
| |
Three Months Ended | |
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
(in thousands) | |
Revenue stream: | |
| | | |
| | |
POCare development services | |
$ | - | | |
$ | 6,324 | |
Cell process development services and hospital services | |
| 2,308 | | |
| 888 | |
POCare cell processing | |
| 4,736 | | |
| - | |
Total | |
$ | 7,044 | | |
$ | 7,212 | |
A
breakdown of the revenues per customer constituted at least 10% of revenues is as follows:
SCHEDULE
OF BREAKDOWN OF REVENUES PER CUSTOMER
| |
Three Months Ended | |
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
(in thousands) | |
Revenue earned: | |
| | | |
| | |
Customer A (United States) | |
$ | 3,605 | | |
$ | 1,226 | |
Customer B (Greece) | |
$ | 2,022 | | |
$ | 661 | |
Customer C (United States) | |
$ | 750 | | |
$ | - | |
Customer D (Korea) | |
$ | - | | |
$ | 2,683 | |
Customer E (United Arab Emirates) | |
$ | - | | |
$ | 1,067 | |
Contract
Assets and Liabilities
Contract
assets are mainly comprised of trade receivables net of allowance for doubtful debts, which includes amounts billed and currently due
from customers.
The
activity for trade receivables is comprised of:
SCHEDULE
OF ACTIVITY FOR CONTRACT LIABILITIES
| |
Three Months Ended | |
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
(in thousands) | |
Balance as of beginning of period | |
$ | 36,183 | | |
$ | 15,245 | |
Elimination of acquisition receivables | |
| - | | |
| (1,337 | ) |
Additions | |
| 7,057 | | |
| 7,249 | |
Collections | |
| (5,454 | ) | |
| (4,042 | ) |
Exchange rate differences | |
| (47 | ) | |
| (40 | ) |
Balance as of end of period | |
$ | 37,739 | | |
$ | 17,075 | |
*
The activity of the related party included in the trade receivables activity above is comprised of:
| |
Three Months Ended | |
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
(in thousands) | |
Balance as of beginning of period | |
$ | - | | |
$ | 1,972 | |
Additions | |
| - | | |
| 635 | |
Collections | |
| - | | |
| (1,069 | ) |
Balance as of end of period | |
$ | - | | |
$ | 1,538 | |
The
activity for contract liabilities is comprised of:
SCHEDULE
OF ACTIVITY FOR CONTRACT LIABILITIES
| |
Three Months Ended | |
| |
March 31, 2023 | | |
March 31, 2022 | |
| |
(in thousands) | |
Balance as of beginning of period | |
$ | 70 | | |
$ | 59 | |
Additions | |
| 36 | | |
| 11 | |
Balance as of end of period | |
$ | 106 | | |
$ | 70 | |
NOTE
8 – OTHER SIGNIFICANT TRANSACTIONS DURING THE PERIOD
During
the three months ended March 31, 2023, the Company entered into updated joint venture (JV) agreements (JVAs) with Theracell Advanced
Biotechnology SA, Broaden Bioscience and Technology Corp, Image Securities FZC, Cure Therapeutics, and Med Centre for Gene and Cell Therapy
FZ-LLC and assigned certain rights and obligations under its JVAs to Texas Advanced Therapies LLC, a Delaware Limited Liability company
(“Texas AT”) not related to the Company. Texas AT will receive the Company’s option to require the incorporation of
the JV Entity, Company’s share in the JV Entity if and when the latter are incorporated, an option to invest additional funding
in the JV Entity, and board and veto rights on certain critical decisions in the JV Entity. The Company has retained the call option
to acquire the JV partner’s share in the JVE, to receive a royalty and a right to conclude the Manufacturing and Service Agreement
with the JV entity. Pursuant to the JVAs, the Company will no longer be entitled to the additional share of fifteen percent of the JVE’s
GAAP profit after tax granted as per the previous version of the JVAs. The Company also has no further obligation to provide any additional
funding to the JV entities. As of March 31, 2023, no JV entities were incorporated as per the JVAs.
NOTE
9 – LEGAL PROCEEDINGS
On
January 18, 2022, a complaint (the “Complaint”) was filed in the Tel Aviv District Court (the “Court”) against
us and the Israeli subsidiary, Prof. Sarah Ferber, Vered Caplan and Dr. Efrat Asa Kunik (collectively, the “defendants”)
by plaintiffs the State of Israel, as the owner of Chaim Sheba Medical Center at Tel HaShomer (“Sheba”), and Tel Hashomer
Medical Research, Infrastructure and Services Ltd. (collectively, the “plaintiffs”). In the Complaint, the plaintiffs are
seeking that the Court issue a declaratory remedy whereby the defendants are required to pay royalties to the plaintiffs at the rate
of 7% of the sales and 24% of any and all revenues in consideration for sublicenses related to any product, service or process that contain
know-how and technology of Sheba and any and all know-how and technology either developed or supervised by Prof. Ferber in the field
of cell therapy, including in the category of the point-of-care platform and any and all services and products in relation to the defendants’
CDMO activity. In addition, the plaintiffs seek that the defendants provide financial statements and pay NIS 10 million to the plaintiffs
due to the royalty provisions of the license agreement, dated February 2, 2012, between the Israeli subsidiary and Tel Hashomer Medical
Research, Infrastructure and Services Ltd. (the “License Agreement”). The Complaint alleges that the Company and the Israeli
subsidiary used know-how and technology of Sheba and know-how and technology either developed or supervised by Prof. Ferber while employed
by Sheba in the field of cell therapy, including in the category of the point-of-care platform and the services and products in relation
to the defendants’ CDMO activity and are entitled to the payment of certain royalties pursuant to the terms of the License Agreement.
The defendants have filed their statements of defense responding to this Complaint. The Company believes that the allegations in this
Complaint are without merit and intend to vigorously defend itself against the claims. Since a material loss is not considered probable,
no provision was made in the financial statements.
NOTE
10 – SUBSEQUENT EVENTS
On
May 5, 2023, the Company, Morgenesis and MM OS Holdings, L.P. (“MM”), an affiliate of Metalmark, entered into Amendment No.
1 (the “Amendment”) to the Unit Purchase Agreement dated November 4, 2022 (the “UPA”). Pursuant to the Amendment,
MM agreed to pay $5,000,000 in cash in exchange for 500,000 Class A Preferred Units of Morgenesis to support the continued expansion
of Orgenesis’ POCare Services business (the “Subsequent Investment”). The investment amount of the First
Future Investment (as defined in the UPA) will be reduced by the amount of the Subsequent Investment.