6-K

Galmed Pharmaceuticals Ltd. (GLMD)

6-K 2022-05-02 For: 2022-05-02
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Added on April 06, 2026

UNITEDSTATES

SECURITIESAND EXCHANGE COMMISSION

Washington,D.C. 20549

FORM6-K

Report of Foreign Private Issuer Pursuant to Rule 13a-16 or 15d-16

Under the Securities Exchange Act of 1934

For the Month of May 2022

001-36345

(Commission File Number)

GALMEDPHARMACEUTICALS LTD.

(Exact name of Registrant as specified in its charter)

16Tiomkin St.

TelAviv 6578317, Israel

(Address of principal executive offices)

Indicate by check mark whether the registrant files or will file annual reports under cover

Form 20-F or Form 40-F.

Form 20-F ☒ Form 40-F ☐

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by

Regulation S-T Rule 101(b)(1): ____

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by

Regulation S-T Rule 101(b)(7): ____

Attached hereto and incorporated herein by reference is a press release, dated May 2, 2022, and entitled “Galmed Pharmaceuticals Provides Business Update and Reports Fourth Quarter and Year End 2021 Financial Results”.


EXHIBITINDEX

Exhibit No. Description
99.1 Press Release, dated May 2, 2022

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

Galmed Pharmaceuticals Ltd.
Date:<br> May 2, 2022 By: /s/ Allen Baharaff
Allen<br> Baharaff
President<br> and Chief Executive Officer

Exhibit99.1

GalmedPharmaceuticals Provides Business Update and Reports Fourth Quarter and Year End 2021 Financial

Results- Conference Call and Webcast Today at 8:30 a.m. ET / 5:30 a.m. PT -

TEL AVIV, Israel, May. 2, 2022 /PRNewswire/ — Galmed Pharmaceuticals Ltd. (Nasdaq: GLMD) (“Galmed” or the “Company”), a clinical-stage biopharmaceutical company focused on the development of the liver targeted SCD1 modulator Aramchol™, an oral therapy for the treatment of nonalcoholic steatohepatitis, or NASH and fibrosis, provides today updated information on the Company’s scientific and clinical development programs and reports financial results for the three and twelve months ended December 31, 2021.

RecentClinical & Scientific Developments

Announced<br> positive interim results from Open-Label part of the ARMOR study showing that treatment with Aramchol 300mg BID resulted in a high<br> rate of fibrosis improvement using three separate biopsy reading methodologies (NASH CRN, Ranked paired reading and a Quantitative<br> Digital Pathology image analysis and artificial intelligence (AI) method), with a larger treatment effect with longer duration of<br> therapy.
Results<br> of post baseline biopsies performed either at 24 weeks or at 48 weeks from 46 subjects with NASH and F1-3 that received Aramchol<br> showed greater histological improvement at week 48 in both paired and AI evaluations (65% and 100% respectively) compared to NASH<br> CRN scoring (40%).

FinancialSummary – Full Year 2021 vs. Full Year 2020; 4Q21 vs. 4Q20:

For<br> the three and twelve months ended December 31, 2021, the Company recorded a net loss of $7.5 million and $32.5 million or $0.30 and<br> $1.32 per share, respectively, compared with a net loss of $10.3 million and $28.8 million, or $0.48 and $1.35 per share, for the<br> three and twelve months ended December 31, 2020.
Research<br> and development expenses were $27.2 million for the twelve months ended December 31, 2021, compared with $26.1 million for the twelve<br> months ended December 31, 2020. The increase for the twelve months resulted primarily from an increase in clinical trial expenses<br> in connection with the Company’s ongoing ARMOR study, partially offset by a decrease in expenses related to CMC and formulation<br> expenses.
For<br> the three months ended December 31, 2021, research and development expenses totaled $6.3 million, which compares with $9.0 million<br> for the same period in 2020. The decrease for the three months resulted primarily from a decrease in clinical trial expenses and<br> a decrease in expenses related to CMC and formulation expenses.
The<br> Company incurred general and administrative expenses of $5.7 million for the twelve months ended December 31, 2021, compared with<br> $4.1 million for the twelve months ended December 31, 2020.The increase for the twelve months primarily resulted from an increase<br> in salaries and benefits expenses, and as well from an increase in the cost of the Company’s D&O insurance policy premium.
For<br> the three months ended December 31, 2021, general and administrative expenses totalled $1.2 million, which compares with $1.3<br> million for the same period in 2020.
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Financial<br> income, net amounted to $0.4 million for the twelve months ended December 31, 2021, compared with $1.4 million for the twelve months<br> ended December 31, 2020. For the three months ended December 31, 2021, financial income, net totalled $0.04 million, which<br> compares with $0.07 million for the same period in 2020.
Cash<br> and cash equivalents, restricted cash, short-term deposits, and marketable debt securities totaled $34.9 million as of December 31,<br> 2021, compared with $51.0 million as of December 31, 2020.

More detailed information can be found in the Company’s Annual Report on Form 20-F, a copy of which has been filed with the Securities and Exchange Commission and posted on the Company’s website at www.galmedpharma.com. You may request a copy of the Company’s Form 20-F, at no cost to you, by writing to the Chief Financial Officer of the Company at 16 Tiomkin Street, Tel Aviv, Israel, 6578317 or by calling +972-3-693-8448.

ConferenceCall & Webcast:

May2, 2022, 8:30 AM ET


Toll Free: 1-877-425-9470

Toll/International: 1-201-389-0878

Israel Toll Free: 1 809 406 247

Conference ID: 13727793

Webcast: https://viavid.webcasts.com/starthere.jsp?ei=1535647&tp_key=893b75d833


ReplayDial-In Numbers


Toll Free: 1-844-512-2921

Toll/International: 1-412-317-6671

Replay Pin Number: 13727793

Replay Start: Monday May 2, 2022, 11:30 AM ET

Replay Expiry: Monday May 16, 2022, 11:59 PM ET


GalmedPharmaceuticals Ltd.

Galmed Pharmaceuticals Ltd. is a clinical stage drug development biopharmaceutical company for liver, metabolic and inflammatory diseases. Our lead compound, Aramchol™, a backbone drug candidate for the treatment of NASH and fibrosis is currently in a Phase 3 registrational study. We are also collaborating with the Hebrew University in the development of Amilo-5MER, a 5 amino acid synthetic peptide.

Forward-LookingStatements:

This press release may include forward-looking statements. Forward-looking statements may include, but are not limited to, statements relating to Galmed’s objectives, plans and strategies, as well as statements, other than historical facts, that address activities, events or developments that Galmed intends, expects, projects, believes or anticipates will or may occur in the future. These statements are often characterized by terminology such as “believes,” “hopes,” “may,” “anticipates,” “should,” “intends,” “plans,” “will,” “expects,” “estimates,” “projects,” “positioned,” “strategy” and similar expressions and are based on assumptions and assessments made in light of management’s experience and perception of historical trends, current conditions, expected future developments and other factors believed to be appropriate. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statements. Many factors could cause Galmed’s actual activities or results to differ materially from the activities and results anticipated in forward-looking statements, including, but not limited to, the following: the timing and cost of Galmed’s pivotal Phase 3 ARMOR trial, or the ARMOR Study or any other pre-clinical or clinical trials; completion and receiving favorable results of the ARMOR Study for Aramchol or any other pre-clinical or clinical trial; the impact of the COVID-19 pandemic; regulatory action with respect to Aramchol or any other product candidate by the FDA or the EMA; the commercial launch and future sales of Aramchol or any other future products or product candidates; Galmed’s ability to comply with all applicable post-market regulatory requirements for Aramchol or any other product candidate in the countries in which it seeks to market the product; Galmed’s ability to achieve favorable pricing for Aramchol or any other product candidate; Galmed’s expectations regarding the commercial market for NASH patients or any other indication; third-party payor reimbursement for Aramchol or any other product candidate; Galmed’s estimates regarding anticipated capital requirements and Galmed’s 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; the development and approval of the use of Aramchol or any other product candidate for additional indications or in combination therapy; and Galmed’s expectations regarding licensing, acquisitions and strategic operations. More detailed information about the risks and uncertainties affecting Galmed is contained under the heading “Risk Factors” included in Galmed’s most recent Annual Report on Form 20-F filed with the SEC on May 2, 2022, and in other filings that Galmed has made and may make with the SEC in the future. The forward-looking statements contained in this press release are made as of the date of this press release and reflect Galmed’s current views with respect to future events, and Galmed does not undertake and specifically disclaims any obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

GALMEDPHARMACEUTICALS LTD.

ConsolidatedBalance Sheets (Audited)

U.S.Dollars in thousands, except share data and per share data

As of December 31,
2021 2020
Assets
Current assets
Cash and cash equivalents $ 2,884 $ 6,947
Restricted cash 114 113
Short-term deposits - 3,807
Marketable debt securities 31,931 40,132
Other accounts receivable 1,125 812
Total current assets 36,054 51,811
Operating lease right-of-use assets 406 394
Property and equipment, net 145 176
Total non-current assets 551 570
Total assets $ 36,605 $ 52,381
Liabilities and stockholders’ equity
Current liabilities
Trade payables $ 4,871 $ 7,046
Other accounts payable 1,008 966
Total current liabilities 5,879 8,012
Non-current liabilities
Operating lease liabilities, net of current portion $ 229 $ 216
Total non-current liabilities 229 216
Stockholders’ equity
Ordinary shares, par value NIS 0.01 per share; Authorized 50,000,000 shares; Issued and outstanding: 25,088,414 shares as of December 31, 2021; 21,325,975 shares as of December 31, 2020 70 58
Additional paid-in capital 198,772 179,530
Accumulated other comprehensive income (loss) (171 ) 272
Accumulated deficit (168,174 ) (135,707 )
Total stockholders’ equity 30,497 44,153
Total liabilities and stockholders’ equity $ 36,605 $ 52,381

GALMEDPHARMACEUTICALS LTD.

ConsolidatedStatements of Operations (Audited)

U.S.Dollars in thousands, except share data and per share data

Year ended December 31,
2021 2020 2019
Research and development expenses 27,220 26,082 18,180
General and administrative expenses 5,661 4,128 4,196
Total operating loss 32,881 30,210 22,376
Financial income, net (414 ) (1,439 ) (1,915 )
Net loss $ 32,467 $ 28,771 $ 20,461
Basic and diluted net loss per share $ 1.32 $ 1.35 $ 0.97
Weighted-average number of shares outstanding used in computing basic and diluted net loss per share 24,597,638 21,280,787 21,114,399

GALMEDPHARMACEUTICALS LTD.

ConsolidatedStatements of Cash Flows (Audited)

U.S.Dollars in thousands

Year ended December 31,
2021 2020 2019
Cash flow from operating activities
Net loss for the year $ (32,467 ) $ (28,771 ) $ (20,461 )
Adjustments required to reconcile net loss to net cash used in operating activities:
Depreciation and amortization 42 39 35
Amortization of discount (premium) on marketable debt securities 121 90 (105 )
Gain on sale of marketable debt securities (37 ) (527 ) (9 )
Finance expenses 6 31 3
Interest income from short-term deposits 7 (285 ) (63 )
Stock-based compensation expense 1,886 2,066 2,231
Changes in operating assets and liabilities:
Decrease (increase) in other accounts receivable (313 ) 15 (609 )
Increase (decrease) in trade payables (2,175 ) 1,047 4,185
Increase (decrease) in other accounts payable 38 8 (144 )
Net cash used in operating activities (32,892 ) (26,287 ) (14,937 )
Cash flow from investing activities
Purchase of property and equipment (11 ) (44 ) (12 )
Increase in restricted deposit (1 ) - -
Investment in securities, available for sale (13,569 ) (55,034 ) (72,600 )
Proceeds from sale of securities, available for sale 21,243 47,198 101,098
Proceeds from (investment in) short-term deposits, net 3,800 24,416 (21,808 )
Net cash provided by investing activities 11,462 16,536 6,678
Cash flow from financing activities
Issuance of ordinary shares in at-the-market offering, net of issuance costs 8,147 - -
Issuance of ordinary shares, net of issuance costs ^(**)^ 9,221 707 -
Proceeds from exercise of options (*) 61 143
Net cash provided by financing activities 17,368 768 143
Decrease in cash, cash equivalents and restricted cash (4,062 ) (8,983 ) (8,116 )
Cash and cash equivalents and restricted cash at the beginning of the year 7,060 16,043 24,159
Cash, cash equivalents and restricted cash at the end of the year $ 2,998 $ 7,060 $ 16,043
Supplemental disclosure of cash flow information:
Cash received from interest $ 562 $ 1,192 $ 1,953
Non-cash transactions:
Recognition of right-of-use asset and lease liabilities from adoption of ASU 2016-02, net $ - $ - $ 653
Right-of-use assets obtained in exchange for new operating lease liabilities, net $ 199 $ 35 $ -
(*) Represents<br> amount less than $1
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Contact: Guy Nehemya, Chief Operating Officer, Galmed Pharmaceuticals Ltd., investor.relations@galmedpharma.com, +972-3-693-8448