Notes
to Consolidated Financial Statements
Note
1 – Basis of presentation
Galmed
Pharmaceuticals Ltd. (the “Company”) was incorporated in Israel on July 31, 2013 and commenced operations on February 2,
2014. The Company holds a wholly-owned subsidiary, Galmed International Ltd., which was incorporated in Malta. Galmed International Ltd.
previously held a wholly-owned subsidiary, Galmed Medical Research Ltd., which was incorporated in Israel, and had been an inactive company
since 2015 and was liquidated in February 2019.
The
Company also holds two additional wholly-owned subsidiaries, Galmed Research and Development Ltd and Galtopa Therapeutics Ltd., both
of which are incorporated in Israel.
The
Company is a clinical-stage biopharmaceutical company primarily focused on the development of Aramchol and Amilo-5MER. The Company has
an operating history limited to pre-clinical and clinical drug development. Historically, the Company has focused almost exclusively
on developing its product candidate, Aramchol for the treatment of liver diseases. In May 2022, the Company announced its plan to expand
into new anti-fibrotic indications to maximize the potential of Aramchol while at the same time discontinuing the open label part of
its ARMOR Study having reached its objectives. Simultaneously, the Company initiated a cost reduction plan and is continuing to evaluate
its strategic options alternatives and its structuring to best optimize its resources to enhance shareholder value and achieve its goals.
As a result of the cost reduction plan, the Company discontinued any non-essential research and development activities and reduced its
headcount by approximately 60% leaving a core team of management and research and development personnel. The Company expects to continue
reducing head count in order to further reduce costs. Following the discontinuation of the open label part of the ARMOR Study, the Company
does not currently expect to initiate the second part of the ARMOR Study. The Company is currently exploring the feasibility of developing
Aramchol for other indications outside of liver disease and anti-fibrotic indications and the Company continues to collaborate with the
Hebrew University in the development of Amilo-5MER, however the Company has no current plans to initiate a clinical trial for Aramchol
or Amilo-5MER.
The
Company funded its research and development programs and operations to date primarily through proceeds from private placements and public
offerings. The Company currently has no products approved for marketing and has not generated any revenue from product sales to date.
As of September 30, 2022, the Company had cash and cash equivalents of $4.1 million, restricted cash of $0.1 million, and marketable
debt securities of $15.1 million.
The
Company has incurred operating losses in each year since inception. The Company’s loss attributable to holders of its ordinary
shares for the nine months period ended September 30, 2022 was approximately $15.2 million. As of September 30, 2022, the Company had
an accumulated deficit of $183.4 million. Substantially all of its operating losses resulted from costs incurred in connection with the
Company’s development program and from general and administrative costs associated with its operations.
The
Company will need to raise substantial, additional capital to fund its operations and to develop Aramchol for, and beyond its current
development stage and any future commercialization, as well as any additional indications.
Based
on the Company’s current operating plan, the Company’s management currently estimates that its cash position will support
its current operations as currently conducted for more than 12 months from the date of issuance of these financial statements.
These
unaudited interim consolidated financial statements have been prepared as of September 30, 2022 and for the three and nine months period
then ended. Accordingly, certain information and footnote disclosures normally included in annual financial statements prepared in accordance
with U.S. GAAP have been omitted. These unaudited interim consolidated financial statements should be read in conjunction with the audited
financial statements and the accompanying notes of the Company for the year ended December 31, 2021 that are included in the Company’s
Annual Report on Form 20-F, filed with the Securities and Exchange Commission on May 2, 2022 (the “Annual Report”). The results
of operations presented are not necessarily indicative of the results to be expected for the year ending December 31, 2021.
GALMED
PHARMACEUTICALS LTD.
Notes
to Consolidated Financial Statements
Note
2 – Summary of significant accounting policies
The
significant accounting policies that have been applied in the preparation of the unaudited consolidated interim financial statements
are identical to those that were applied in preparation of the Company’s interim most recent annual financial statements in connection
with its Annual Report on Form 20-F.
In
May 2021, the FASB issued Update 2021-04, Earnings Per Share (Topic 260), Debt—Modifications and Extinguishments (Subtopic 470-50),
Compensation—Stock Compensation (Topic 718), and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic
815-40): Issuer’s Accounting for Certain Modifications or Exchanges of Freestanding Equity-Classified Written Call Options (a consensus
of the FASB Emerging Issues Task Force). The amendments in this Update affect all entities that issue freestanding written call options
that are classified in equity. Specifically, the amendments affect those entities when a freestanding equity-classified written call
option is modified or exchanged and remains equity classified after the modification or exchange. The amendments that relate to the recognition
and measurement of EPS for certain modifications or exchanges of freestanding equity-classified written call options affect entities
that present EPS in accordance with the guidance in Topic 260, Earnings Per Share. The effect of implementing this ASU is immaterial.
Note
3 – Stockholders’ Equity
| 1. | In
February 2022, the Company granted options to purchase 40,000 ordinary shares of the Company
to one of its officers. The options are exercisable at $1.61 per share, have a 10-year term
and vest over a period of four years. |
| | |
| 2. | During
July 2022, the Company sold an additional 114,982 ordinary shares under its ATM program for
total net proceeds of approximately $0.1 million |
Management’s
Discussion and Analysis of Financial Condition and Results of Operations
All
references to “we,” “us,” “our,” “the Company” and “our Company”, in this
Form 6-K are to Galmed Pharmaceuticals Ltd. And its subsidiaries, unless the context otherwise requires. All references to “shares”
or “ordinary shares” are to our ordinary shares, NIS 0.01 nominal par value per share. All references to “Israel”
are to the State of Israel. “U.S. GAAP” means the generally accepted accounting principles of the United States. Unless otherwise
stated, all of our financial information presented in this Form 6-K has been prepared in accordance with U.S. GAAP. Any discrepancies
in any table between totals and sums of the amounts and percentages listed are due to rounding. Unless otherwise indicated, or the context
otherwise requires, references in this Form 6-K to financial and operational data for a particular year refer to the fiscal year of our
company ended December 31 of that year.
Our
reporting currency and financial currency is the U.S. dollar. In this Form 6-K, “NIS” means New Israeli Shekel, and “$,”
“US$” and “U.S. dollars” mean United States dollars.
Cautionary
Note Regarding Forward-Looking Statements
This
Form 6-K contains forward-looking statements about our expectations, beliefs or intentions regarding, among other things, our product
development efforts, business, financial condition, results of operations, strategies or prospects. In addition, from time to time, we
or our representatives have made or may make forward-looking statements, orally or in writing. Forward-looking statements can be identified
by the use of forward-looking words such as “believe,” “expect,” “intend,” “plan,” “may,”
“should,” “anticipate,” “could,” “might,” “seek,” “target,” “will,”
“project,” “forecast,” “continue” or their negatives or variations of these words or other comparable
words or by the fact that these statements do not relate strictly to historical matters. These forward-looking statements may be included
in, among other things, various filings made by us with the SEC, press releases or oral statements made by or with the approval of one
of our authorized executive officers. Forward-looking statements relate to anticipated or expected events, activities, trends or results
as of the date they are made. Because forward-looking statements relate to matters that have not yet occurred, these statements are inherently
subject to risks and uncertainties that could cause our actual results to differ materially from any future results expressed or implied
by the forward-looking statements. Many factors could cause our actual activities or results to differ materially from the activities
and results anticipated in forward-looking statements, including, but not limited to, the factors summarized below:
| ● | the
timing and cost of our any pre-clinical or clinical trial, for our product candidates; |
| | |
| ● | completion
and receiving favorable results of any pre-clinical or clinical trial; |
| ● | the
impact of the COVID-19 pandemic on our operations; |
| | |
| ● | regulatory
action with respect to Aramchol or any other product candidate by the U.S. Food and Drug
Administration, or the FDA, or the European Medicines Authority, or EMA, including but not
limited to acceptance of an application for marketing authorization, review and approval
of such application, and, if approved, the scope of the approved indication and labeling; |
| | |
| ● | the
commercial launch and future sales of Aramchol and any future product candidates; |
| | |
| ● | our
ability to comply with all applicable post-market regulatory requirements for Aramchol or
any other product candidate in the countries in which we seek to market the product; |
| | |
| ● | our
ability to achieve favorable pricing for Aramchol or any other product candidate; |
| | |
| ● | our
expectations regarding the commercial market for non-alcoholic steato-hepatitis, or NASH,
in patients or any other targeted indication; |
| | |
| ● | third-party
payor reimbursement for Aramchol or any other product candidate; |
| | |
| ● | our
estimates regarding anticipated capital requirements and our needs for additional financing; |
| | |
| ● | market
adoption of Aramchol or any other product candidate by physicians and patients; |
| | |
| ● | the
timing, cost or other aspects of the commercial launch of Aramchol or any other product candidate; |
| | |
| ● | our
ability to obtain and maintain adequate protection of our intellectual property; |
| | |
| ● | the
possibility that we may face third-party claims of intellectual property infringement; |
| | |
| ● | our
ability to manufacture our product candidates in commercial quantities, at an adequate quality
or at an acceptable cost; |
| ● | our
ability to establish adequate sales, marketing and distribution channels; |
| | |
| ● | intense
competition in our industry, with competitors having substantially greater financial, technological,
research and development, regulatory and clinical, manufacturing, marketing and sales, distribution
and personnel resources than we do; |
| | |
| ● | the
development and approval of the use of Aramchol or any other product candidate for additional
indications or in combination therapy; |
| | |
| ● | our
ability to maintain the listing of our ordinary share on The Nasdaq Capital Market; |
| | |
| ● | our
expectations regarding licensing, acquisitions and strategic operations. |
We
believe these forward-looking statements are reasonable; however, these statements are only current predictions and are subject to known
and unknown risks, uncertainties and other factors that may cause our or our industry’s actual results, levels of activity, performance
or achievements to be materially different from those anticipated by the forward-looking statements. We discuss many of these risks in
our Annual Report on Form 20-F for the year ended December 31, 2021 filed with the SEC on May 2, 2022 in greater detail under the heading
“Risk Factors” and elsewhere in the Annual Report and in our Report on Form 6-K filed with the SEC on August 4, 2022 and
this Form 6-K. Given these uncertainties, you should not rely upon forward-looking statements as predictions of future events.
All
forward-looking statements attributable to us or persons acting on our behalf speak only as of the date hereof and are expressly qualified
in their entirety by the cautionary statements included in this report. We undertake no obligations to update or revise forward-looking
statements to reflect events or circumstances that arise after the date made or to reflect the occurrence of unanticipated events. In
evaluating forward-looking statements, you should consider these risks and uncertainties.
Overview
We
are a biopharmaceutical company focused on the development of Aramchol. Historically, we have focused almost exclusively on developing
Aramchol for the treatment of liver disease. We are also collaborating with the Hebrew University in the development of Amilo-5MER, a
5 amino acid synthetic peptide.
In
May 2022, we announced our plan to expand into new anti-fibrotic indications to maximize the potential of Aramchol while at the same
time discontinuing the open label part of its ARMOR Study having reached its objectives. Simultaneously, we initiated a cost reduction
plan and are continuing to evaluate our strategic alternatives and our structuring to best optimize our resources to enhance shareholder
value and achieve its goals. As a result of the cost reduction plan, we discontinued any non-essential research and development activities
and reduced our headcount by approximately 60% leaving a core team of management and research and development personnel. We expect to
continue reducing head count in order to further reduce costs. Following the discontinuation of our open label part of the ARMOR Study,
we do not currently expect to initiate the second part of the ARMOR Study.
We
are currently exploring the feasibility of developing Aramchol for other indications outside of liver disease and anti-fibrotic indications
and we continue to collaborate with the Hebrew University in the development of Amilo-5MER, however
we have no current plans to initiate a clinical trial for Aramchol or Amilo-5MER and are continuing to evaluate our strategic alternatives
and our structuring. We have not stated a definitive timeline for completion of the evaluation process and there can be no assurance
that the evaluation process will result in our pursuing any strategic alternative, or that a strategic alternative, if any, would be
completed successfully or at all. There can be no assurance that the review will result in any transaction or other strategic change
or outcome. We do not intend to comment further until we determine that further disclosure is appropriate or necessary.
Financial
Overview
To
date, we have funded our operations primarily through proceeds from private placements and public offerings. At September 30, 2022, we
had current assets of $20.5 million, which includes cash and cash equivalents of $4.1 million, marketable debt securities of $15.2 million,
other receivables of $1.1 million and restricted cash of $0.1 million. This compares with current assets of $36.1 million at December
31, 2021, which includes cash and cash equivalents of $2.9 million, marketable debt securities of $31.9 million, other receivables if
$1.1 million and restricted cash of $0.1 million. Although we provide no assurance, we believe that such existing funds will be sufficient
to continue our business and operations as currently conducted for more than 12 months from the date of issuance of this Form 6-K. However,
we will continue to incur operating losses, which may be substantial over the next several years, and we expect that we will need to
obtain additional funds to further develop our research and development programs.
Costs
and Operating Expenses
Our
current costs and operating expenses consist of two components: (i) research and development expenses; and (ii) general and administrative
expenses.
Research
and Development Expenses
Our
research and development expenses consist primarily of outsourced development expenses, salaries and related personnel expenses and fees
paid to external service providers, patent-related legal fees, costs of pre-clinical studies and clinical trials and drug and laboratory
supplies. We account for all research and development expenses as they are incurred. Increases or decreases in research and development
expenditures are primarily attributable to the number and/or duration of the pre-clinical and clinical studies that we conduct.
We
expect that a substantial amount of our research and development expense in the future will be incurred in support of our current and
anticipated pre-clinical and clinical development projects. Due to our current research and development activities, the inherently unpredictable
nature of pre-clinical and clinical development studies, and unpredictability of our evaluation of strategic alternatives, we are unable
to estimate with any certainty the costs we will incur in the continued development of Aramchol and Amilo-5MER. Clinical development timelines, the probability of success and development costs can differ materially from expectations. Nevertheless, we expect
to decrease our research and development expenses in the short term as a result of the discontinuation of the open label part of the
ARMOR Study, implementation of our cost reduction plan, and our evaluation of strategic alternatives.
The
lengthy process of completing initial trials and seeking regulatory approval for Aramchol requires the expenditure of substantial resources.
Any failure or delay in completing clinical trials, or in obtaining regulatory approvals, could cause a delay in generating product revenue
and cause our research and development expenses to increase and, in turn, have a material adverse effect on our operations. Because of
the factors set forth above, we are not able to estimate with any certainty when we would recognize any net cash inflows from our projects.
General
and Administrative Expenses
General
and administrative expenses consist primarily of compensation for employees in executive and operational roles, including finance/accounting,
legal and other operating positions in connection with our activities. Our other significant general and administrative expenses include
non-cash stock-based compensation costs and facilities costs (including the rental expense for our offices in Tel Aviv, Israel), professional
fees for outside accounting and legal services, travel costs, investors relations, insurance premiums and depreciation.
Our
general and administrative expenses may decrease further as a result of our cost reduction plan although this may be offset by increases
in professional and advisory fees as we evaluate our strategic alternatives.
Financial
Income, Net
Our
financial income, net consists mainly of interest income from marketable debt securities and foreign currency gains. Our financial expense
consists of fees associated with banking activities and losses from realization of marketable debt securities.
Results
of Operations
The
table below provides our results of operations for the three and nine months ended September 30, 2022 as compared to the three and nine
months ended September 30, 2021.
| |
Three months ended
September 30, | | |
Nine months ended
September 30, | |
| |
2022 | | |
2021 | | |
2022 | | |
2021 | |
| |
(unaudited) | | |
(unaudited) | | |
(unaudited) | | |
(unaudited) | |
| |
(In thousands, except per share data) | |
Research and development expenses | |
| 4,241 | | |
| 6,541 | | |
| 11,617 | | |
| 20,957 | |
General and administrative expenses | |
| 1,139 | | |
| 1,304 | | |
| 3,585 | | |
| 4,432 | |
Total operating expenses | |
| 5,380 | | |
| 7,845 | | |
| 15,202 | | |
| 25,389 | |
Financial expense (income), net | |
| (30 | ) | |
| (131 | ) | |
| 25 | | |
| (374 | ) |
Net loss | |
| 5,350 | | |
| 7,714 | | |
| 15,227 | | |
| 25,015 | |
Other comprehensive loss (income): | |
| (106 | ) | |
| 183 | | |
| 705 | | |
| 347 | |
Comprehensive loss | |
| 5,244 | | |
| 7,897 | | |
| 15,932 | | |
| 25,362 | |
Basic and diluted net loss per share | |
$ | 0.21 | | |
$ | 0.31 | | |
$ | 0.61 | | |
$ | 1.02 | |
Research
and Development Expenses
Our
research and development expenses amounted to approximately $4.2 million and approximately $11.6 million during the three and nine months
ended September 30, 2022, respectively, representing a decrease of approximately $2.3 million, or 35%, and approximately $9.4 million,
or 45%, respectively, compared to approximately $6.5 million and approximately $21.0 million, respectively, for the comparable period
in 2021.
The
decrease during the three months ended September 30, 2022 primarily resulted from a decrease in clinical trial expenses in connection
with our the discontinuation of our open label part of the ARMOR Study of approximately $1.3 million. The decrease during the
nine months ended September 30, 2022 primarily resulted from a decrease in clinical trial expenses of approximately $5.2 million as well
a decrease in drug development expenses in of approximately $1.8 million, both in connection with the discontinuation of our open label
part of the ARMOR Study.
General
and Administrative Expenses
Our
general and administrative expenses amounted to approximately $1.1 million and approximately $3.6 million during the three and nine months
ended September 30, 2022, respectively, representing a decrease of approximately $0.2 million, or 15%, and approximately $0.8 million,
or 18%, respectively, to approximately $1.3 million and approximately $4.4 million, respectively, for the comparable period in 2021.
The
decrease in general and administrative expenses for the three months ended September 30, 2022 resulted primarily from a decrease in non-cash
stock-based compensation expenses of approximately $0.3 million. The decrease in general and administrative expenses for the nine months
ended September 30, 2022 resulted primarily from a decrease in salaries and benefits expenses of approximately $0.5 million.
Operating
Loss
As
a result of the foregoing, for the three and nine months ended September 30, 2022, our operating loss was approximately $5.4 million
and approximately $15.2 million, respectively, representing a decrease of $2.4 million, or 31%, and a decrease of $10.2 million, or 40%,
respectively, as compared to approximately $7.8 million and approximately $25.4 million, respectively, for the comparable period in 2021.
Financial
expense (income), Net
Our
financial income, net amounted to approximately $0.03 million and financial expense of approximately $0.02 million during the three and
nine months ended September 30, 2022, respectively, representing a decrease of approximately $0.1 million, or 77%, and approximately
$0.4 million, or 107%, respectively, compared to financial income, net of $0.1 million and $0.4 million, respectively, for the comparable
period in 2021.
The
decrease during the three and nine months ended September 30, 2022 primarily relates to a decrease in the interest income from short-term
deposits and marketable debt securities and from loss of realization of marketable debt securities.
Net
Loss
As
a result of the foregoing, for the three and nine months ended September 30, 2022, our net loss was approximately $5.3 million and approximately
$15.2 million, respectively, representing a decrease of $2.4 million, or 31%, and a decrease of $9.8 million, or 39%, respectively, as
compared to approximately $7.7 million and approximately $25.0 million, respectively, for the comparable period in 2021.
Liquidity
and Capital Resources
To
date, we have funded our operations primarily through proceeds from private placements and public offerings and we have incurred substantial
losses since our inception. As of September 30, 2022, we had an accumulated deficit of approximately $183.4 million and positive working
capital (current assets less current liabilities) of approximately $15.4 million. We expect that operating losses will continue for the
foreseeable future.
As
of September 30, 2022, we had cash and cash equivalents of approximately $4.1 million, restricted cash of approximately $0.1 million,
and marketable debt securities of approximately $15.2 million invested in accordance with our investment policy, totaling approximately
$19.3 million, as compared to approximately $2.9 million, $0.1 million and $31.9 million as of December 31, 2021, respectively, totaling
approximately $34.9 million. The decrease is mainly attributable to the $14.5 million negative cash flow from operating activities during
the nine months ended September 30, 2022.
We
had negative cash flow from operating activities of approximately $14.5 million for the nine months ended September 30, 2022, as compared
to negative cash flow from operating activities of approximately $25.9 million for the nine months ended September 30, 2021. The negative
cash flow from operating activities for the nine months ended September 30, 2022 is mainly attributable to our net loss of approximately
$15.2 million.
We
had positive cash flow from investing activities of approximately $15.6 million for the nine months ended September 30, 2022, as compared
to a positive cash flow from investing activities of approximately $5.1 million for the nine months ended September 30, 2021. The positive
cash flow from investing activities for the nine months ended September 30, 2022 was primarily due to the sale of available for sale
securities.
We
had positive cash flow from financing activities of approximately $0.1 million for the nine months ended September 30, 2022, as compared
to a positive cash flow from financing activities of approximately $17.4 million for the nine months ended September 30, 2021. The positive
cash flow from financing activities for the nine months ended September 30, 2022 was due to net proceeds from selling of 114,982 shares
under our ATM offering.
On
March 26, 2021, we entered into a Sales Agreement with Cantor Fitzgerald & Co. and Canaccord Genuity LLC, as sales agents, pursuant
to which we may offer and sell ordinary shares “at the market” (“ATM offering”) having an aggregate offering
price of up to $50.0 million from time to time through the sales agents subject to the limits of General Instruction I.B.5 to Form F-3,
also known as the baby shelf rule.
Although
we provide no assurance, we believe that our existing funds will be sufficient to continue our business and operations as currently conducted
for more than 12 months from the date of issuance of this Report on Form 6-K. However, additional funding will be necessary to fund our
ARMOR Study, our Amilo-5MER program and ongoing research and development work, to advance our product candidates through regulatory approval
and into commercialization, if approved and the evaluation of our strategic alternatives. We may obtain additional funding through debt
or equity financings, governmental grants or through entering into collaborations, strategic alliances or license agreements to increase
the funds available to support our operating and capital needs. Although we have been successful in raising capital in the past, there
is no assurance that we will be successful in obtaining additional financing on terms acceptable to us. Specifically, the general downturn
in global financial markets has limited our ability to access capital, which is negatively affecting our liquidity. If funds are not
available, we may be required to further delay, reduce the scope of or eliminate research or development plans for, or commercialization
efforts with respect to Aramchol, Amilo-5MER and/or our other pre-clinical and clinical programs. This may raise substantial doubts about
our ability to continue as a going concern.
The
extent of our future capital requirements will depend on many other factors, including:
| ● | the
progress and costs of our pre-clinical studies and other research and development activities; |
| | |
| ● | the
impact of the COVID-19 pandemic on our operations; |
| | |
| ● | the
scope, prioritization and number of our research and development programs; |
| | |
| ● | the
amount of revenues and contributions we receive under future licensing, development and commercialization
arrangements with respect to Aramchol or any other product candidtate; |
| | |
| ● | the
costs of the development and expansion of our operational infrastructure; |
| | |
| ● | the
costs and timing of obtaining regulatory approval for Aramchol, Amilo-5MER or any other product
candidate; |
| | |
| ● | the
ability of us, or our collaborators, to achieve development milestones, marketing approval
and other events or developments under our potential future licensing agreements; |
| ● | the
costs of filing, prosecuting, enforcing and defending patent claims and other intellectual
property rights; |
| | |
| ● | the
costs and timing of securing manufacturing arrangements for clinical or commercial production; |
| | |
| ● | the
costs of contracting with third parties to provide sales and marketing capabilities for us; |
| | |
| ● | the
costs of acquiring or undertaking development and commercialization efforts for any future
products, product candidates or platforms; |
| | |
| ● | the
magnitude of our general and administrative expenses; |
| | |
| ● | any
cost that we may incur under future in- and out-licensing arrangements relating to Aramchol,
Amilo-5MER or any other product candidate; |
| | |
| ● | market
conditions; |
| | |
| ● | our
ability to maintain the listing of our orindary share on The Nasdaq Capital Market; and |
| | |
| ● | our
ability to identify, evaluate and complete any strategic alternative that yields value for
our shareholders. |
Trend
Information
We
are a development stage company, and it is not possible for us to predict with any degree of accuracy the outcome of our research, development
or commercialization efforts. As such, it is not possible for us to predict with any degree of accuracy any significant trends, uncertainties,
demands, commitments or events that are reasonably likely to have a material effect on our net loss, liquidity or capital resources,
or that would cause financial information to not necessarily be indicative of future operating results or financial condition. However,
to the extent possible, certain trends, uncertainties, demands, commitments and events are in this “Management’s Discussion
and Analysis of Financial Condition and Results of Operations”.
Controls
and Procedures
As
a “foreign private issuer”, we are only required to conduct the evaluations required by Rules 13a-15(b) and 13a-15(d) of
the Exchange Act as of the end of each fiscal year and therefore have elected not to provide disclosure regarding such evaluations at
this time.