SEC Form 424B5 filed by Chemomab Therapeutics Ltd.
Registration Statement No. 333- 275002
(To Prospectus dated November 3, 2023)

LifeSci Capital
|
|
Page
|
S-1 |
|
S-2 | |
S-5 | |
S-8 | |
S-9 | |
S-12 | |
S-13 | |
S-14 | |
S-15 |
|
S-25 | |
S-26 | |
S-27 | |
S-28 | |
S-29 | |
S-31 | |
S-32 |
|
Page
|
|
|
3
|
|
4
|
|
6
|
|
8
|
|
9
|
|
10
|
|
11
|
|
12
|
|
19
|
|
27
|
|
34
|
|
35
|
|
36
|
|
37
|
|
38
|
|
39
|
|
40
|
|
41
|
•
|
we have incurred significant losses since inception and anticipate that we will continue to incur increasing levels of operating losses over the next several years and for the foreseeable
future. We are unable to predict the extent of any future losses or when we will become profitable, if at all. Even if we become profitable, we may not be able to sustain or increase our profitability on a quarterly or annual basis;
|
|
|
•
|
we have a limited operating history and funding, which may make it difficult to evaluate our prospects and likelihood of success;
|
|
|
•
|
our business is highly dependent on the success of our lead product candidate, nebokitug, and any other product candidates that we advance into clinical studies. All of our programs will
require significant additional clinical development;
|
|
|
•
|
our central objective is to design and develop targeted treatments for inflammation and fibrosis with an initial focus on the antagonism of CCL24 signaling, which is known to regulate
fibrotic and inflammatory processes. While we have conducted extensive preclinical studies and four successful clinical trials in patients, our approach in the area of fibrotic diseases is novel and unproven and may not result in marketable
products;
|
•
|
the successful completion of clinical studies is a prerequisite to submitting a marketing application to the FDA and similar marketing applications to comparable foreign regulatory
authorities, for each product candidate and, consequently, the ultimate approval and commercial marketing of any product candidates. We may experience negative or inconclusive results, which may result in us deciding, or regulators requiring
us, to conduct additional clinical studies or trials or abandon some or all of our product development programs, which could have a material adverse effect on our business;
|
|
|
•
|
we may encounter difficulties enrolling patients in our clinical studies, including any public health emergencies and related clinical development activities could be delayed or otherwise
adversely affected;
|
|
|
•
|
our ongoing and future clinical studies may reveal significant adverse events or immunogenicity-related responses and may result in a safety profile that could delay or prevent regulatory
approval or market acceptance of our product candidate;
|
|
|
•
|
the regulatory approval processes of the FDA and comparable foreign authorities are lengthy, time consuming and inherently unpredictable, and if we are ultimately unable to obtain regulatory
approval for nebokitug or any other product candidates, our business will be substantially harmed;
|
•
|
if we do not achieve our projected development and commercialization goals in the timeframes we announce and expect, the commercialization of our product candidates may be delayed and our
business will be harmed;
|
|
|
•
|
we face substantial competition, which may result in others discovering, developing or commercializing products before or more successfully than us;
|
|
|
•
|
we have been granted Orphan Drug Designation for nebokitug in connection with three indications and may seek Orphan Drug Designation for other indications or product candidates, and we may be
unable to maintain the benefits associated with Orphan Drug Designation, including the potential for market exclusivity, and may not receive Orphan Drug Designation for other indications or for our other product candidates;
|
|
|
•
|
we expect to experience significant growth in the number of our employees over time and the scope of our operations, particularly in the areas of product candidate development, regulatory
affairs and sales and marketing. We will therefore need to expand our organization, and we may experience difficulties in managing this growth, which could disrupt our operations;
|
|
|
•
|
if we are unable to protect our patents or other proprietary rights, or if we infringe the patents or other proprietary rights of others, our competitiveness and business prospects may be
materially damaged. In addition, changes in patent laws or patent jurisprudence could diminish the value of patents in general, thereby impairing our ability to protect our product candidates;
|
|
|
•
|
risks related to our operations in Israel could materially adversely impact our business, financial condition and results of operations;
|
|
|
•
|
our principal executive offices are located in Israel and US and certain of our product candidates may be manufactured at third-party facilities located in Europe. In addition, our business
strategy includes potentially expanding internationally if any of our product candidates receives regulatory approval. A variety of risks associated with operating internationally could materially adversely affect our business;
|
|
|
•
|
holders of ADSs are not treated as holders of our ordinary shares;
|
•
|
holders of ADSs may not have the same voting rights as the holders of our ordinary shares and may not receive voting materials in time to be able to exercise their right to vote;
|
|
|
•
|
holders of ADSs may be subject to limitations on the transfer of their ADSs and the withdrawal of the underlying ordinary shares;
|
•
|
we are entitled to amend the deposit agreement and to change the rights of ADS holders under the terms of such agreement, or to terminate the deposit agreement, without the prior consent of
the ADS holders;
|
|
|
•
|
ADSs holders may not be entitled to a jury trial with respect to claims arising under the deposit agreement, which could result in less favorable outcomes to the plaintiff(s) in any such
action;
|
|
|
•
|
obtaining and maintaining our patent protection depends on compliance with various procedural, document submission, fee payment and other requirements imposed by governmental patent agencies,
and our patent protection could be reduced or eliminated for non-compliance with these requirements;
|
|
|
•
|
obtaining and maintaining regulatory approval of our product candidates in one jurisdiction does not mean that we will be successful in obtaining regulatory approval of our product candidates
in other jurisdictions;
|
|
|
•
|
even if we obtain regulatory approval for nebokitug or any product candidate, we will still face extensive and ongoing regulatory requirements and obligations and any product candidates, if
approved, may face future development and regulatory difficulties;
|
|
|
•
|
disruptions at the FDA and other government agencies caused by funding shortages or global health concerns could hinder our ability to hire, retain or deploy key leadership and other
personnel, or otherwise prevent new or modified products from being developed, approved or commercialized in a timely manner or at all, which could negatively impact our business;
|
|
|
•
|
if we do not achieve our projected development and commercialization goals in the timeframes we announce and expect, the commercialization of our product candidates may be delayed and our
business will be harmed;
|
|
|
•
|
even if nebokitug or any other product candidate we develop receives marketing approval, it may fail to achieve market acceptance by physicians, patients, third-party payors or others in the
medical community necessary for commercial success;
|
|
|
•
|
we rely completely on third-party suppliers to manufacture our clinical drug supplies for our product candidates, and we intend to rely on third parties to produce preclinical, clinical, and
commercial supplies of any future product candidates;
|
|
|
•
|
if we are unable to establish sales, marketing and distribution capabilities either on our own or in collaboration with third parties, we may not be successful in commercializing nebokitug,
if approved;
|
|
|
•
|
a variety of risks associated with operating internationally could materially adversely affect our business;
|
|
|
•
|
conditions in Israel, including the ongoing hostilities by Hamas and other terrorist organizations from the Gaza Strip and Israel’s war against them, may affect our operations;
|
|
|
•
|
because a certain portion of our expenses are incurred in currencies other than the U.S. Dollar, our results of operations may be harmed by currency fluctuations and inflation;
|
•
|
we received Israeli government grants for certain of their research and development activities as detailed below. The terms of those grants require us to satisfy specified conditions in order
to transfer outside of Israel the manufacture of products based on know-how funded by the Israel Innovation Authority or to transfer outside of Israel the know-how itself. If we fail to comply with the requirements of Israeli law in this
regard, we may be required to pay penalties, and it may impair our ability to sell our technology outside of Israel;
|
|
|
•
|
we will need to raise additional capital to fund our operations, which may be unavailable to us on acceptable terms or at all, or may cause dilution or place significant restrictions on our
ability to operate our business;
|
|
|
•
|
the trading price of the ADSs has been highly volatile, and is expected to continue to be volatile;
|
|
|
•
|
we have not paid dividends in the past and do not expect to pay dividends in the future, and, as a result, any return on investment may be limited to the value of the ADSs; and
|
|
|
•
|
if we fail to continue to meet all applicable Nasdaq requirements, Nasdaq may delist the ADSs, which could have an adverse impact on the liquidity and market price of the ADSs.
|
Securities we are offering
|
ADSs having an aggregate offering price of up to $7,258,687
|
|
ADSs to be outstanding immediately after this offering
|
Up to 25,461,629 ADSs, assuming sales of $7,258,687 ADSs in this offering at an offering price of $1.10 per ADS, the sale price of ADSs on the Nasdaq Capital Market on July 23, 2025. The actual number
of ADSs issued will vary depending on the sales price under this offering.
|
|
Plan of Distribution
|
An “at the market offering” made from time to time through our Agent. See “Plan of Distribution.”
|
|
Use of Proceeds
|
We intend to use the net proceeds for continued clinical development of our product candidates, research activities, and for other general corporate purposes. See “Use of Proceeds” on
page S-14 of this prospectus supplement.
|
|
Risk Factors
|
This investment involves a high degree of risk. See “Risk Factors” beginning on page S-9 of this prospectus supplement and in the documents incorporated by reference herein (including
under “Risk Factors” in our most recent Annual Report on Form 20-F) for a discussion of the risks you should carefully consider before deciding to invest in our securities.
|
|
Nasdaq Capital Market symbol
|
ADSs representing our ordinary shares are listed for trading on the Nasdaq Capital Market under the symbol “CMMB.”
|
|
Depositary
|
The Bank of New York Mellon
|
If we are classified as a passive foreign investment company (“PFIC”) for
U.S. federal income tax purposes, U.S. investors in our ADSs may be subject to adverse U.S. federal income tax consequences.
|
Assumed offering price per ADS
|
$
|
1.10
|
||||||
Net tangible book value per ADS as of March 31, 2025
|
$
|
0.55
|
||||||
Increase in net tangible book value per ADS attributable to new investors
|
$
|
0.13
|
||||||
As adjusted net tangible book value per ADS after this offering
|
$
|
0.68
|
||||||
Dilution per ADS to new investors in this offering
|
$
|
0.42
|
• 1,637,180 ADSs issuable upon the exercise of outstanding options to purchase ADSs, as of July 24, 2025, at a weighted average exercise price of $2.84 per ADS;
|
|
• 510,297 ADSs issuable upon the exercise of outstanding RSUs;
|
• an aggregate of 255,459 ADSs reserved for future issuance under our Share Incentive Plans, as of July 24, 2025, as well as any automatic increases in the number of ADSs reserved for future issuance
under the 2017 Equity-Based Incentive Plan and 2015 Incentive Plan ; and
|
|
• 261,929 ADSs issuable upon the exercise of outstanding warrants to purchase ADSs at a weighted average exercise price of $17.35 per ADS, which warrants are expected to remain outstanding at the
consummation of this offering.
|
|
•
|
on an actual basis; and
|
|
•
|
on an as adjusted basis to give effect to the sale of 6,598,806 ADSs in this offering, at an assumed public offering price of $1.10 per ADS, and
after deducting the estimated underwriting discounts and commissions and estimated offering expenses payable by us.
|
|
As of March 31, 2025
|
|||||||
|
(unaudited)
|
|||||||
|
Actual
|
As Adjusted
|
||||||
|
||||||||
Cash and cash equivalents and short-term bank deposits
|
$
|
10,703,000
|
$
|
17,631,940
|
||||
Shareholders’ equity
|
||||||||
Ordinary Shares, no par value - Authorized: 4,650,000,000 ordinary shares as of March 31, 2025
|
||||||||
Issued and outstanding: 377,256,460 ordinary shares issued and outstanding actual; ; 509,232,580 ordinary shares issued and outstanding as adjusted
|
||||||||
Additional paid-in capital
|
116,339,000
|
123,267,940
|
||||||
Accumulated deficit
|
( 105,946,000
|
)
|
( 105,946,000
|
)
|
||||
Total shareholders’ equity
|
$
|
10,393,000
|
$
|
17,321,940
|
||||
Total liabilities and shareholders’ equity
|
$
|
12,819,000
|
$
|
19,747,940
|
|
•
|
1,637,180 ADSs issuable upon the exercise of outstanding options to purchase ADSs, as of July 24, 2025, at a weighted average exercise price of $2.84 per ADS;
|
•
|
510,297 ADSs issuable upon the exercise of outstanding RSUs;
|
|
|
|
|
|
•
|
an aggregate of 255,459 ADSs reserved for future issuance under our Share Incentive Plans, as of July 24, 2025, as well as any automatic increases in the number of ADSs reserved for future issuance under the 2017
Equity-Based Incentive Plan and 2015 Incentive Plan; and
|
|
|
|
|
•
|
261,929 ADSs issuable upon the exercise of outstanding warrants to purchase ADSs at a weighted average exercise price of $17.35 per ADS, which warrants are expected to remain outstanding at
the consummation of this offering.
|
• |
banks, financial institutions or insurance companies;
|
• |
real estate investment trusts or regulated investment companies;
|
• |
dealers or brokers;
|
• |
traders that elect to mark to market;
|
• |
tax-exempt entities or governmental organizations;
|
• |
“individual retirement accounts” and other tax-deferred accounts;
|
• |
certain former citizens or long-term residents of the United States;
|
• |
persons who acquired our ADSs pursuant to the exercise of any employee share option or otherwise as compensation for the performance of services;
|
• |
persons holding our ADSs as part of a “hedging,” “integrated” or “conversion” transaction or as a position in a “straddle” for U.S. federal income tax purposes;
|
• |
persons that have a functional currency other than the U.S. dollar;
|
• |
partnerships or other pass-through entities and persons holding our ADSs through partnerships or other pass-through entities; or
|
• |
persons that own directly, indirectly or through attribution 10% or more of the total voting power or value of all of our outstanding shares.
|
• |
an individual who is a citizen or resident of the United States;
|
• |
a corporation (or other entity treated as a corporation for U.S. federal income tax purposes) created or organized in or under the laws of the United States or any state thereof, including
the District of Columbia;
|
• |
an estate the income of which is subject to U.S. federal income taxation regardless of its source; or
|
• |
a trust if such trust has validly elected to be treated as a United States person for U.S. federal income tax purposes or if (1) a court within the United States is able to exercise primary
supervision over its administration and (2) one or more United States persons have the authority to control all of the substantial decisions of such trust.
|
●
|
The research and expenditures are approved by the relevant Israeli government ministry, determined by the field of research;
|
●
|
the research and development is for the promotion of the company; and
|
●
|
the research and development is carried out by or on behalf of the company seeking such tax deduction, or that the expenditure is made by a person that carries out the research and does not
own an enterprise which is engaged in the field of research, or that such expenditure constitutes participation in research carried out by another person, in both cases, subject to the fulfillment of certain criteria set forth in Israeli tax
law.
|
Depositary and Transfer agent’s fees
|
$
|
66,582
|
||
Printing and engraving expenses
|
$
|
1,000
|
||
Legal fees and expenses
|
$
|
45,000
|
||
Total
|
$
|
112,582
|
●
|
the judgment was rendered by a court which was, according to the laws of the state of the court, competent to render the judgment;
|
●
|
the obligation imposed by the judgment is enforceable according to the rules relating to the enforceability of judgments in Israel and the substance of the judgment is not contrary to public
policy; and
|
●
|
the judgment is executory in the state in which it was given.
|
●
|
the judgment was given in a state whose laws do not provide for the enforcement of judgments of Israeli courts (subject to exceptional cases);
|
●
|
the enforcement of the judgment is likely to prejudice the sovereignty or security of the State of Israel;
|
●
|
the judgment was obtained by fraud;
|
●
|
the opportunity given to the defendant to bring its arguments and evidence before the court was not reasonable in the opinion of the Israeli court;
|
●
|
the judgment was rendered by a court not competent to render it according to the laws of private international law as they apply in Israel;
|
●
|
the judgment is contradictory to another judgment that was given in the same matter between the same parties and that is still valid; or
|
●
|
at the time the action was brought in the foreign court, a lawsuit in the same matter and between the same parties was pending before a court or tribunal in Israel.
|
|
●
|
our Annual Report on Form 20-F (File No. 001- 38807) for the fiscal year ended December
31, 2024, filed with the SEC on April 4, 2025;
|
|
●
|
our Reports on Form 6-K filed with the SEC on February 19, 2025, March 3, 2025, March 20, 2025, March 27, 2025, April 15, 2025, May 15, 2025, May 27, 2025, and July 1, 2025, (other than the portions of those reports deemed to be furnished and not filed); and
|
|
●
|
the description of share capital, which is set forth in Exhibit 2.1 of our Annual Report, and
as may be further updated or amended in any amendment or report filed for such purpose.
|
Kiryat Atidim, Building 7A Tel Aviv
Tel: +972 77 3310156
Attention: Chief Executive Officer

|
Page
|
|
|
3
|
|
|
|
4
|
|
|
|
6
|
|
|
|
8
|
|
|
|
9
|
|
|
|
10
|
|
|
|
11
|
|
|
|
12
|
|
|
|
19
|
|
|
|
27
|
|
|
|
34
|
|
|
|
35
|
|
|
|
36
|
|
|
|
37
|
|
|
|
38
|
|
|
|
39
|
|
|
|
40
|
|
|
|
41
|
• |
we have incurred significant losses since inception and anticipate that we will continue to incur increasing levels of operating losses over the next several years and for the foreseeable future;
|
• |
we are unable to predict the extent of any future losses or when we will become profitable, if at all;
|
• |
even if we become profitable, we may not be able to sustain or increase our profitability on a quarterly or annual basis;
|
• |
we have a limited operating history and funding, which may make it difficult to evaluate our prospects and likelihood of success;
|
• |
our business is highly dependent on the success of our lead product candidate, CM-101, and any other product candidates that we advance into clinical studies;
|
• |
all of our programs will require significant additional clinical development;
|
• |
our central objective is to design and develop targeted treatments for inflammation and fibrosis with an initial focus on the antagonism of CCL24 signaling, which is known to regulate fibrotic and inflammatory processes;
|
• |
while several studies are currently underway, our approach in the area of fibrotic diseases is novel and unproven and may not result in marketable products;
|
• |
the successful completion of clinical studies is a prerequisite to submitting a marketing application to the FDA and similar marketing applications to comparable foreign regulatory authorities, for each product candidate and,
consequently, the ultimate approval and commercial marketing of any product candidates;
|
• |
we may experience negative or inconclusive results, which may result in us deciding, or regulators requiring us, to conduct additional clinical studies or trials or abandon some or all of its product development programs, which could
have a material adverse effect on our business;
|
• |
we may encounter difficulties enrolling patients in our clinical studies, including due to the continuing effects of the COVID-19 pandemic, or other public health emergencies and related clinical development activities could be delayed
or otherwise adversely affected;
|
• |
our ongoing and future clinical studies may reveal significant adverse events or immunogenicity-related responses and may result in a safety profile that could delay or prevent regulatory approval or market acceptance of our product
candidate;
|
• |
the regulatory approval processes of the FDA and comparable foreign authorities are lengthy, time consuming and inherently unpredictable, and if we are ultimately unable to obtain regulatory approval for CM-101 or any other product
candidates, our business will be substantially harmed;
|
• |
if we do not achieve our projected development and commercialization goals in the timeframes we announce and expect, the commercialization of our product candidates may be delayed and our business will be harmed;
|
• |
we face substantial competition, which may result in others discovering, developing or commercializing products before or more successfully than us;
|
• |
we have been granted Orphan Drug Designation for CM-101 in connection with three indications and may seek Orphan Drug Designation for other indications or product candidates, and we may be unable to maintain the benefits associated
with Orphan Drug Designation, including the potential for market exclusivity, and may not receive Orphan Drug Designation for other indications or for its other product candidates;
|
• |
we expect to experience significant growth in the number of our employees over time and the scope of our operations, particularly in the areas of product candidate development, regulatory affairs and sales and marketing;
|
• |
we will therefore need to expand our organization, and we may experience difficulties in managing this growth, which could disrupt our operations;
|
• |
if we are unable to protect our patents or other proprietary rights, or if we infringe the patents or other proprietary rights of others, our competitiveness and business prospects may be materially damaged;
|
• |
changes in patent laws or patent jurisprudence could diminish the value of patents in general, thereby impairing our ability to protect our product candidates;
|
• |
risks related to our operations in Israel could materially adversely impact our business, financial condition and results of operations;
|
• |
our principal executive offices are located in Israel and certain of our product candidates may be manufactured at third-party facilities located in Europe. In addition, our business strategy includes potentially expanding
internationally if any of its product candidates receives regulatory approval;
|
• |
holders of ADSs may not have the same voting rights as the holders of our ordinary shares and may not receive voting materials in time to be able to exercise their right to vote;
|
• |
holders of ADSs may be subject to limitations on the transfer of their ADSs and the withdrawal of the underlying ordinary shares;
|
• |
we are entitled to amend the deposit agreement and to change the rights of ADS holders under the terms of such agreement, or to terminate the deposit agreement, without the prior consent of the ADS holders;
|
• |
ADSs holders may not be entitled to a jury trial with respect to claims arising under the deposit agreement, which could result in less favorable outcomes to the plaintiff(s) in any such action; and
|
• |
we presently anticipate that we will be classified as a passive foreign investment company, which could result in adverse U.S. federal income tax consequences to U.S. Holders of our ordinary shares.
|
•
|
FAST scores were improved in a higher proportion of CM-101-treated patients than in placebo patients.
|
•
|
CM-101-treated patients with higher FAST scores demonstrated greater improvements in key fibro-inflammatory biomarkers than patients with lower FAST scores or placebo patients.
|
|
•
|
amendments to our amended and restated articles of association;
|
|
•
|
appointment, terms of service or and termination of service of our auditors;
|
|
•
|
appointment of directors, including external directors (if applicable);
|
|
•
|
approval of certain related party transactions;
|
|
•
|
increases or reductions of our authorized share capital;
|
|
•
|
a merger; and
|
|
•
|
the exercise of our board of directors’ powers by a general meeting, if our board of directors is unable to exercise its powers and the exercise of any of its powers is required for our proper management.
|
Persons depositing or withdrawing ordinary shares or
ADS holders must pay |
|
|
For
|
$5.00 (or less) per 100 ADSs (or portion of 100 ADSs)
|
|
|
Issuance of ADSs, including issuances resulting from a distribution of ordinary shares or rights or other property Cancellation of ADSs for the purpose of withdrawal, including if the deposit agreement
terminates
|
|
|
|
|
$.05 (or less) per ADS
|
|
|
Any cash distribution to ADS holders
|
|
|
|
|
A fee equivalent to the fee that would be payable if securities distributed to you had been ordinary shares and the ordinary shares had been deposited for issuance of ADSs
|
|
|
Distribution of securities distributed to holders of deposited securities (including rights) that are distributed by the depositary to ADS holders
|
|
|
|
|
$.05 (or less) per ADS per calendar year
|
|
|
Depositary services
|
Persons depositing or withdrawing ordinary shares or
ADS holders must pay |
|
|
For
|
Registration or transfer fees
|
|
|
Transfer and registration of ordinary shares on our share register to or from the name of the depositary or its agent when you deposit or withdraw ordinary shares
|
|
|
|
|
Expenses of the depositary
|
|
|
Cable, telex and facsimile transmissions (when expressly provided in the deposit agreement)
Converting foreign currency to U.S. dollars
|
|
|
|
|
Taxes and other governmental charges the depositary or the custodian has to pay on any ADSs or ordinary shares underlying ADSs, such as stock transfer taxes, stamp duty or withholding taxes
|
|
|
As necessary
|
|
|
|
|
Any charges incurred by the depositary or its agents for servicing the deposited securities
|
|
|
As necessary
|
|
●
|
the title and ranking of the debt securities (including the terms of any subordination provisions);
|
|
●
|
the price or prices (expressed as a percentage of the principal amount) at which we will sell the debt securities;
|
|
●
|
any limit on the aggregate principal amount of the debt securities;
|
|
●
|
the date or dates on which the principal of the securities of the series is payable;
|
|
●
|
the rate or rates (which may be fixed or variable) per annum or the method used to determine the rate or rates (including any commodity, commodity index, stock exchange index or financial index) at which the
debt securities will bear interest, the date or dates from which interest will accrue, the date or dates on which interest will commence and be payable and any regular record date for the interest payable on any interest payment date;
|
|
●
|
the place or places where principal of, and interest, if any, on the debt securities will be payable (and the method of such payment), where the securities of such series may be surrendered for registration
of transfer or exchange, and where notices and demands to us in respect of the debt securities may be delivered;
|
|
●
|
the period or periods within which, the price or prices at which and the terms and conditions upon which we may redeem the debt securities;
|
|
●
|
any obligation we have to redeem or purchase the debt securities pursuant to any sinking fund or analogous provisions or at the option of a holder of debt securities and the period or periods within which,
the price or prices at which and in the terms and conditions upon which securities of the series shall be redeemed or purchased, in whole or in part, pursuant to such obligation;
|
|
●
|
the dates on which and the price or prices at which we will repurchase debt securities at the option of the holders of debt securities and other detailed terms and provisions of these repurchase obligations;
|
|
●
|
the denominations in which the debt securities will be issued, if other than denominations of $1,000 and any integral multiple thereof;
|
|
●
|
whether the debt securities will be issued in the form of certificated debt securities or global debt securities;
|
|
●
|
the portion of principal amount of the debt securities payable upon declaration of acceleration of the maturity date, if other than the principal amount;
|
|
●
|
the currency of denomination of the debt securities, which may be United States Dollars or any foreign currency, and if such currency of denomination is a composite currency, the agency or organization, if
any, responsible for overseeing such composite currency;
|
|
●
|
the designation of the currency, currencies or currency units in which payment of principal of, premium and interest on the debt securities will be made;
|
|
●
|
if payments of principal of, premium or interest on the debt securities will be made in one or more currencies or currency units other than that or those in which the debt securities are denominated, the
manner in which the exchange rate with respect to these payments will be determined;
|
|
●
|
the manner in which the amounts of payment of principal of, premium, if any, or interest on the debt securities will be determined, if these amounts may be determined by reference to an index based on a
currency or currencies or by reference to a commodity, commodity index, stock exchange index or financial index;
|
|
●
|
any provisions relating to any security provided for the debt securities;
|
|
●
|
any addition to, deletion of or change in the Events of Default described in this prospectus or in the indenture with respect to the debt securities and any change in the acceleration provisions described in
this prospectus or in the indenture with respect to the debt securities;
|
●
|
any addition to, deletion of or change in the covenants described in this prospectus or in the indenture with respect to the debt securities;
|
|
●
|
any depositaries, interest rate calculation agents, exchange rate calculation agents or other agents with respect to the debt securities;
|
|
●
|
the provisions, if any, relating to conversion or exchange of any debt securities of such series, including if applicable, the conversion or exchange price and period, provisions as to whether conversion or
exchange will be mandatory, the events requiring an adjustment of the conversion or exchange price and provisions affecting conversion or exchange;
|
|
●
|
any other terms of the debt securities, which may supplement, modify or delete any provision of the indenture as it applies to that series, including any terms that may be required under applicable law or
regulations or advisable in connection with the marketing of the securities; and
|
|
●
|
whether any of our direct or indirect subsidiaries will guarantee the debt securities of that series, including the terms of subordination, if any, of such guarantees. (Section 2.2)
|
●
|
we are the surviving entity or the successor person (if other than Chemomab ) is a corporation, partnership, trust or other entity organized and validly existing under the laws of any U.S. domestic
jurisdiction or the State of Israel and expressly assumes our obligations on the debt securities and under the indenture; and
|
●
|
immediately after giving effect to the transaction, no Default or Event of Default, shall have occurred and be continuing.
|
|
●
|
default in the payment of any interest upon any debt security of that series when it becomes due and payable, and continuance of such default for a period of 30 days (unless the entire amount of the payment
is deposited by us with the trustee or with a paying agent prior to the expiration of the 30-day period);
|
|
●
|
default in the payment of principal of any security of that series at its maturity;
|
|
●
|
default in the performance or breach of any other covenant or warranty by us in the indenture (other than a covenant or warranty that has been included in the indenture solely for the benefit of a series of
debt securities other than that series), which default continues uncured for a period of 60 days after we receive written notice from the trustee or Chemomab and the trustee receive written notice from the holders of not less than 25% in
principal amount of the outstanding debt securities of that series as provided in the indenture;
|
|
●
|
certain voluntary or involuntary events of bankruptcy, insolvency or reorganization of Chemomab; and
|
|
●
|
any other Event of Default provided with respect to debt securities of that series that is described in the applicable prospectus supplement. (Section 6.1)
|
|
●
|
that holder has previously given to the trustee written notice of a continuing Event of Default with respect to debt securities of that series; and
|
|
●
|
the holders of not less than 25% in principal amount of the outstanding debt securities of that series have made written request, and offered indemnity or security satisfactory to the trustee, to the trustee
to institute the proceeding as trustee, and the trustee has not received from the holders of not less than a majority in principal amount of the outstanding debt securities of that series a direction inconsistent with that request and has
failed to institute the proceeding within 60 days. (Section 6.7)
|
|
●
|
to cure any ambiguity, defect or inconsistency;
|
|
●
|
to comply with covenants in the indenture described above under the heading “Consolidation, Merger and Sale of Assets”;
|
|
●
|
to provide for uncertificated securities in addition to or in place of certificated securities;
|
|
●
|
to add guarantees with respect to debt securities of any series or secure debt securities of any series;
|
|
●
|
to surrender any of our rights or powers under the indenture;
|
|
●
|
to add covenants or events of default for the benefit of the holders of debt securities of any series;
|
|
●
|
to comply with the applicable procedures of the applicable depositary;
|
|
●
|
to make any change that does not adversely affect the rights of any holder of debt securities;
|
|
●
|
to provide for the issuance of and establish the form and terms and conditions of debt securities of any series as permitted by the indenture;
|
|
●
|
to effect the appointment of a successor trustee with respect to the debt securities of any series and to add to or change any of the provisions of the indenture to provide for or facilitate administration by
more than one trustee; or
|
|
●
|
to comply with requirements of the SEC in order to effect or maintain the qualification of the indenture under the Trust Indenture Act. (Section 9.1)
|
|
●
|
reduce the amount of debt securities whose holders must consent to an amendment, supplement or waiver;
|
|
●
|
reduce the rate of or extend the time for payment of interest (including default interest) on any debt security;
|
|
●
|
reduce the principal of or premium on or change the fixed maturity of any debt security or reduce the amount of, or postpone the date fixed for, the payment of any sinking fund or analogous obligation with
respect to any series of debt securities;
|
|
●
|
reduce the principal amount of discount securities payable upon acceleration of maturity;
|
|
●
|
waive a default in the payment of the principal of, premium or interest on any debt security (except a rescission of acceleration of the debt securities of any series by the holders of at least a majority in
aggregate principal amount of the then outstanding debt securities of that series and a waiver of the payment default that resulted from such acceleration);
|
|
●
|
make the principal of or premium or interest on any debt security payable in currency other than that stated in the debt security;
|
|
●
|
make any change to certain provisions of the indenture relating to, among other things, the right of holders of debt securities to receive payment of the principal of, premium and
interest on those debt securities and to institute suit for the enforcement of any such payment and to waivers or amendments; or
|
|
●
|
waive a redemption payment with respect to any debt security. (Section 9.3)
|
|
●
|
we may omit to comply with the covenant described under the heading “Consolidation, Merger and Sale of Assets” and certain other covenants set forth in the indenture, as well as any additional covenants which
may be set forth in the applicable prospectus supplement; and
|
|
●
|
any omission to comply with those covenants will not constitute a Default or an Event of Default with respect to the debt securities of that series (“covenant defeasance”).
|
|
●
|
depositing with the trustee money and/or U.S. government obligations or, in the case of debt securities denominated in a single currency other than U.S. Dollars, government obligations of the government that
issued or caused to be issued such currency, that, through the payment of interest and principal in accordance with their terms, will provide money in an amount sufficient in the opinion of a nationally recognized firm of independent
public accountants or investment bank to pay and discharge each installment of principal of, premium and interest on and any mandatory sinking fund payments in respect of the debt securities of that series on the stated maturity of those
payments in accordance with the terms of the indenture and those debt securities; and
|
|
●
|
delivering to the trustee an opinion of counsel to the effect that the holders of the debt securities of that series will not recognize income, gain or loss for United States federal income tax purposes as a
result of the deposit and related covenant defeasance and will be subject to United States federal income tax on the same amounts and in the same manner and at the same times as would have been the case if the deposit and related covenant
defeasance had not occurred. (Section 8.4)
|
|
●
|
the title of the warrants;
|
|
●
|
the aggregate number of the warrants;
|
|
●
|
the number of securities purchasable upon exercise of the warrants;
|
|
●
|
the designation and terms of the securities, if any, with which the warrants are issued, and the number of the warrants issued with each such offered security;
|
|
●
|
the date, if any, on and after which the warrants and the related securities will be separately transferable;
|
|
●
|
the price at which, and form of consideration for which, each security purchasable upon exercise of the warrants may be purchased;
|
|
●
|
the date on which the right to exercise the warrants will commence and the date on which the right will expire;
|
|
●
|
if applicable, the date on and after which such warrants and the related securities will be separately transferable;
|
|
●
|
information with respect to book-entry procedures, if any;
|
|
●
|
if applicable, a discussion of the material Israeli and U.S. income tax considerations applicable to the issuance or exercise of such warrants;
|
|
●
|
the anti-dilution and adjustment of share capital provisions of the warrants, if any;
|
|
●
|
the minimum or maximum amount of the warrants which may be exercised at any one time;
|
|
●
|
any circumstances that will cause the warrants to be deemed to be automatically exercised; and
|
|
●
|
any other material terms of the warrants.
|
|
●
|
the terms of the units and of the ordinary shares, rights and/or warrants comprising the units, including whether and under what circumstances the securities comprising the units may be traded separately;
|
|
|
|
|
●
|
a description of the terms of any unit agreement governing the units or any arrangement with an agent that may act on our behalf in connection with the unit offering;
|
|
|
|
|
●
|
a description of the provisions for the payment, settlement, transfer or exchange of the units; and
|
|
|
|
|
●
|
any material provisions of the governing unit agreement that differ from those described above.
|
|
●
|
through underwriters or dealers;
|
|
|
|
|
●
|
directly to a limited number of purchasers or to a single purchaser;
|
|
|
|
|
●
|
through agents; or
|
|
|
|
|
●
|
through any other method permitted by applicable law and described in the applicable prospectus supplement.
|
|
●
|
block transactions and transactions on the Nasdaq Capital Market or any other organized market where the securities may be traded;
|
|
|
|
|
●
|
purchases by a broker-dealer as principal and resale by the broker-dealer for its own account pursuant to a prospectus supplement;
|
|
|
|
|
●
|
ordinary brokerage transactions and transactions in which a broker-dealer solicits purchasers;
|
|
|
|
|
●
|
sales “at the market” into an existing trading market; or
|
|
|
|
|
●
|
sales in other ways not involving market makers or established trading markets, including direct sales to purchasers.
|
|
●
|
the name or names of any underwriters, dealers or agents;
|
|
|
|
|
●
|
the method of distribution;
|
|
|
|
|
●
|
the public offering price or purchase price and the proceeds to us from that sale;
|
|
|
|
|
●
|
the expenses of the offering;
|
|
|
|
|
●
|
any discounts or commissions to be allowed or paid to the underwriters, dealers or agents;
|
|
|
|
|
●
|
all other items constituting underwriting compensation and the discounts and commissions to be allowed or paid to dealers, if any; and
|
|
|
|
|
●
|
any other information regarding the distribution of the securities that we believe to be material.
|
●
|
the judgment is obtained after due process before a court of competent jurisdiction, according to the laws of the state in which the judgment is given and the rules of private international law prevailing in
Israel;
|
●
|
the prevailing law of the foreign state in which the judgment is rendered allows for the enforcement of judgments of Israeli courts;
|
●
|
adequate service of process has been effected and the defendant has had a reasonable opportunity to be heard and to present his or her evidence;
|
●
|
the judgment is not contrary to public policy of Israel, and the enforcement of the civil liabilities set forth in the judgment is not likely to impair the security or sovereignty of Israel;
|
●
|
the judgment was not obtained by fraud and does not conflict with any other valid judgment in the same matter between the same parties;
|
●
|
an action between the same parties in the same matter was not pending in any Israeli court at the time at which the lawsuit was instituted in the foreign court; and
|
●
|
the judgment is enforceable according to the laws of Israel and according to the law of the foreign state in which the relief was granted.
|
SEC registration fee
|
|
$
|
9,621
|
|
FINRA filing fee
|
|
|
3,140
|
|
Depositary and Transfer agent’s fees
|
|
|
*
|
|
Printing and engraving expenses
|
|
|
*
|
|
Legal fees and expenses
|
|
|
*
|
|
Accounting fees and expenses
|
|
|
*
|
|
Miscellaneous
|
|
|
*
|
|
|
|
|
|
|
Total
|
|
$
|
*
|
|
|
*
|
Estimated fees and expenses are not presently known. If required, to be provided by a prospectus supplement or as an exhibit to a Report on Form 6-K that is incorporated by reference into this prospectus.
|
●
|
the Company’s Annual Reports on Form 10-K for the years ended December 31, 2022 and December 31, 2021 filed with the SEC on March 20, 2023 (the “2022 Annual Report”) and March 30, 2022, respectively;
|
|
●
|
the Company’s Current Reports on Form 8-K filed with the SEC on January 3, 2023, January 11, 2023, February
21, 2023, February 21, 2023, May 11, 2023, June
5, 2023, June 16, 2023, and Reports on Form 6-K furnished with the SEC on July 3, 2023, August
8, 2023 and August 14, 2023; and
|
●
|
the description of our share capital, which is set forth in Exhibit 4.1 of the 2022 Annual Report, and as may be further updated or amended in any amendment or report filed for such purpose, including Exhibit 4.1 to our 2022 Annual Report on Form 10-K for the year ended December 31, 2022.
|

PROSPECTUS SUPPLEMENT