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Kamada Ltd.

Foreign Filer Report May 18, 2020

6874_rns_2020-05-18_981f63af-e9eb-4361-8eb6-faea16098ef9.pdf

Foreign Filer Report

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Pursuant to Rule 13a-16 or 15d-16 of the Securities Exchange Act of 1934

For the Month of May 2020

Commission File Number 001-35948

Kamada Ltd. (Translation of registrant's name into English)

UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549

FORM 6-K

Report of Foreign Private Issuer

2 Holzman Street Science Park, P.O. Box 4081 Rehovot 7670402 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): ____

Indicate by check mark whether the registrant by furnishing the information contained in this Form is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934.

Yes ☐ No ☒

If "Yes" is marked, indicate below the file number assigned to the registrant in connection with Rule 12g3-2(b): 82-____

This Form 6-K is being incorporated by reference into the Registrant's Form S-8 Registration Statements, File Nos. 333-192720, 333-207933, 333-215983, 333-222891 and 333-233267, and the Registrant's Form F-3 Registration Statement, as amended, File No. 333-214816.

The following exhibit is attached:

99.1 Press Release: Kamada Reports First Quarter 2020 Financial Results and Highlights Recent Corporate Progress 99.2 Kamada Ltd.'s Consolidated Financial Statements as of March 31, 2020 (Unaudited)

SIGNATURE

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 hereunto duly authorized.

Date: May 18, 2020 KAMADA LTD.

By: /s/ Orna Naveh

Orna Naveh General Counsel and Corporate Secretary

EXHIBIT NO. DESCRIPTION

99.1 Press Release: Kamada Reports First Quarter 2020 Financial Results and Highlights Recent Corporate Progress
99.2 Kamada Ltd.'s Consolidated Financial Statements as of March 31, 2020 (Unaudited)

Kamada Reports First Quarter 2020 Financial Results and Highlights Recent Corporate Progress

  • Total Revenues were \$33.3 Million, an Increase of 24% Year-over-Year
  • Net Income was \$5.2 Million, an Increase of 6% Year-over-Year
  • Company Reports Continued Progress of its Development Program of a Plasma-Derived Hyperimmune IgG Therapy for COVID-19; Product Availability for Clinical and Compassionate Use Treatment for COVID-19 patients in Israel is Expected by End of the Second Quarter of 2020
  • Company's Manufacturing Plant Continues to Operate Without Significant Disruption During Ongoing Coronavirus (COVID-19) Outbreak
  • Kamada Reiterates Full-Year 2020 Total Revenue Guidance of \$132 Million to \$137 Million

REHOVOT, Israel – May 18, 2020 — Kamada Ltd. (NASDAQ: KMDA; TASE: KMDA.TA), a plasma-derived biopharmaceutical company, today announced financial results for the three months ended March 31, 2020.

"As the ongoing COVID-19 global pandemic continues to create substantial complications in daily life and business operations, we are focused on the safety and well-being of our employees, who continue to find innovative solutions to support our patients and partners," said Amir London, Kamada's Chief Executive Officer. "These efforts contributed to our strong performance in the first quarter of the year. Total revenues were \$33.3 million, an increase of 24 percent year-over-year. These results were driven by similar year-over year increase in sales of both our Proprietary and Distributed products. Based on our strong performance in the first quarter and our current outlook for the remainder of the year, we are reiterating our guidance of total revenues of between \$132 million and \$137 million for full-year 2020."

"To date, our manufacturing plant remains operational with no effect on business continuity, even amidst the emergency regulations enforced in Israel in recent months due to the COVID-19 pandemic. Moreover, based on the most recent interactions with our U.S. distribution partners regarding finished product inventory levels available for distribution in the U.S and our planned supply for the remainder of the year, we do not anticipate meaningful supply shortages in the foreseeable future in the U.S. market for GLASSIA® or KEDRAB®. In addition, based on currently available inventory levels and planned supply of our Distributed products in Israel, we do not anticipate significant supply shortages in the foreseeable future. Going forward, although certain COVID-19 pandemic-related dynamics may affect market demand and production conditions, we intend to maintain our current manufacturing and supply plans, and increased inventory levels of raw materials through our suppliers and service providers in order to appropriately manage any potential supply disruptions and secure continued manufacturing," continued Mr. London.

"As previously reported, during the first quarter, we were able to quickly focus our efforts on the development and manufacturing of a plasmaderived hyperimmune IgG product for COVID-19, which leverages our proprietary IgG platform technology, as a potential treatment for COVID-19 patients. We are pleased to report today that we have secured adequate quantities of COVID-19 convalescent plasma in Israel. This has enabled us to initiate manufacturing of the product, which is expected to be available by the end of the second quarter for compassionate use treatment in Israel, based on Israeli Ministry of Health (IMOH) regulations. Concurrently, we have ongoing discussions with the IMOH with regard to the potential initiation of related clinical trials. In addition, we were excited to recently announce our global collaboration with Kedrion Biopharma, which will allow us to more rapidly develop our plasma-derived hyperimmune IgG product for COVID-19 and broaden our international reach," concluded Mr. London.

Financial Highlights for the Three Months Ended March 31, 2020

  • Total revenues were \$33.3 million in the first quarter of 2020, a 24% increase from the \$26.8 million recorded in the first quarter of 2019
  • Revenues from the Proprietary Products segment in the first quarter of 2020 were \$25.3 million, a 24% increase from the \$20.4 million reported in the first quarter of 2019
  • Revenues from the Distribution segment were \$8.0 million in the first quarter of 2020, a 24% increase from the \$6.4 million recorded in the first quarter of 2019
  • Gross profit was \$11.5 million in the first quarter of 2020, a 2% increase from the \$11.2 million reported in the first quarter of 2019; overall gross profitability differences are affected by changes in product sales mix between the quarters
  • Operating expenses, including R&D, Sales & Marketing, G&A, and Other expenses, totaled \$6.6 million in the first quarter of 2020, as compared to \$6.0 million in the first quarter of 2019. This increase was primarily driven by increased R&D expenses specifically related to the initiation of the Company's pivotal Phase 3 InnovAATe clinical trial, which is designed to evaluate the Company's proprietary inhaled Alpha-1 Antitrypsin therapy for treatment of Alpha-1 Antitrypsin Deficiency
  • Net income was \$5.2 million, or \$0.12 per share, in the first quarter of 2020, as compared to net income of \$4.9 million, or \$0.12 per share, in the first quarter of 2019
  • Adjusted EBITDA, as detailed in the tables below, was \$6.3 million in the first quarter of 2020, as compared to \$6.7 million in the first quarter of 2019
  • Cash used in operating activities was \$1.9 million in the first quarter of 2020, as compared to cash provided by operating activities of \$6.1 million in the first quarter of 2019. This change in operating activity cash flow is specifically related to timing of payments to suppliers on account of inventories which are expected to be sold later this year

Balance Sheet Highlights

As of March 31, 2020, the Company had cash, cash equivalents, and short-term investments of \$96.4 million, as compared to \$73.9 million at December 31, 2019. This includes the net proceeds generated from the \$25 million private placement transaction with the FIMI Opportunity Fund closed in February 2020.

Recent Corporate Highlights

  • Plasma-derived hyperimmune IgG product for COVID-19
    • o Announced a collaboration with Kedrion Biopharma for the development, manufacturing and distribution of a plasma-derived hyperimmune IgG product for COVID-19
    • o Initiated manufacturing of the product based on collected convalescent plasma in Israel; product is expected to be available for clinical and compassionate use treatment in Israel by the end of the second quarter
  • Inhaled AAT product
    • o Enrolment in the pivotal Phase 3 InnovAATe clinical trial, which continued through February 2020, was temporarily halted due to the impact of COVID-19 pandemic on healthcare systems. Patients already recruited to the study continued treatment as planned. The Company anticipates resuming enrollment into the study in the third quarter of 2020, pending appropriate conditions at clinical trial sites.
    • o InnovAATe clinical trial is designed to evaluate the Company's proprietary inhaled Alpha-1 Antitrypsin therapy for treatment of Alpha-1 Antitrypsin Deficiency
    • o Obtained U.S. Food and Drug Administration (FDA) acceptance for the protocol design of a 30 patients sub-study, designed to evaluate the effect of Kamada's Inhaled AAT on pharmacokinetics of IV-AAT and collect safety and immunogenicity data, including the effect of antidrug antibodies (ADA) on AAT levels in plasma. Initiation of this sub-study has been delayed due to COVID-19 pandemic effect

Conference Call

Kamada management will host an investment community conference call on Monday, May 18, at 8:30am Eastern Time to discuss these results and answer questions. Shareholders and other interested parties may participate in the conference call by dialing 877-407-0792 (from within the U.S.), 1809 406 247 (from Israel), or 201-689-8263 (International) and entering the conference identification number: 13699990. The call will also be webcast live on the Internet on the Company's website at www.kamada.com.

About Kamada

Kamada Ltd. ("the Company") is a commercial stage plasma-derived biopharmaceutical company focused on orphan indications, with an existing marketed product portfolio and a late-stage product pipeline. The Company uses its proprietary platform technology and know-how for the extraction and purification of proteins from human plasma to produce Alpha-1 Antitrypsin (AAT) in a highly-purified, liquid form, as well as other plasmaderived immune globulins. The Company's flagship product is GLASSIA®, the first liquid, ready-to-use, intravenous plasma-derived AAT product approved by the U.S. FDA. The Company markets GLASSIA in the U.S. through a strategic partnership with Takeda Pharmaceuticals Company Limited and in other countries through local distributors. The Company's second leading product is KamRab®, a rabies immune globulin (Human) for post-exposure prophylaxis against rabies infection. KamRab is FDA approved and is being marketed in the U.S. under the brand name KEDRAB® through a strategic partnership with Kedrion S.p.A. In addition to Glassia and KEDRAB, the Company has a product line of four other plasma-derived pharmaceutical products administered by injection or infusion, that are marketed through distributors in more than 15 countries, including Israel, Russia, Brazil, India and other countries in Latin America and Asia. The Company has late-stage products in development, including an inhaled formulation of AAT for the treatment of AAT deficiency. In addition, the Company's intravenous AAT is in development for other indications, such as GvHD and prevention of lung transplant rejection. The Company leverages its expertise and presence in the plasma-derived protein therapeutics market by distributing more than 20 complementary products in Israel that are manufactured by third parties. FIMI Opportunity Fund, the leading private equity investor in Israel, is the Company's lead shareholder, beneficially owning approximately 21% of the outstanding ordinary shares.

Cautionary Note Regarding Forward-Looking Statements

This release includes forward-looking statements within the meaning of Section 21E of the U.S. Securities Exchange Act of 1934, as amended, and the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that are not historical facts, including statements regarding 1) the total revenues to be in the range of \$132 million to \$137 million for fiscal 2020; 2) not anticipating meaningful supply shortages in the foreseeable future in the U.S. market for GLASSIA® or KEDRAB®; 3) not anticipating significant supply shortages in the foreseeable future for Kamada's Distributed products in Israel; 4) anticipating maintaining current manufacturing and supply plans; 5) increasing inventory levels of raw materials through suppliers and service providers in order to appropriately manage any potential supply disruptions and secure continued manufacturing; 6) anticipating availability for clinical and compassionate-use treatment in Israel of a plasmaderived hyperimmune IgG product for COVID-19, from COVID-19 convalescent plasma, by the end of the second quarter of 2020; 7) anticipating that the global collaboration with Kedrion Biopharma will allow Kamada to speed up the development of the plasma-derived hyperimmune IgG product for COVID-19 and broaden the product's international reach; and 8) anticipating that Phase 3 InnovAATe clinical trial will resume enrollment in the third quarter of 2020. Forward-looking statements are based on Kamada's current knowledge and its present beliefs and expectations regarding possible future events and are subject to risks, uncertainties and assumptions. Actual results and the timing of events could differ materially from those anticipated in these forward-looking statements as a result of several factors including, but not limited to, the continued evolvement of the COVID-19 pandemic, its effect and duration, availability of sufficient raw materials required to maintain manufacturing plans, the effects of the COVID-19 pandemic and related government mandates on the availability of adequate levels of work-force required to maintain manufacturing plans, disruption to the supply chain due to COVID-19 pandemic, continuation of inbound and outbound international delivery routes, continued demand for Kamada's products, including GLASSIA and KEDRAB, in the U.S. market and its distributed products in Israel, ability to obtain regulatory approval for clinical trials of the plasma-derived hyperimmune IgG product for COVID-19, unexpected results of clinical studies and on-going compassionate-use treatments, ability to find doctors and medical facilities to collaborate on compassionate-use treatments, Kamada's ability to manage operating expenses, additional competition in the markets that Kamada competes, regulatory delays, prevailing market conditions and the impact of general economic, industry or political conditions in the U.S., Israel or otherwise. The forward-looking statements made herein speak only as of the date of this announcement and Kamada undertakes no obligation to update publicly such forward-looking statements to reflect subsequent events or circumstances, except as otherwise required by law.

CONTACTS:

Chaime Orlev Chief Financial Officer [email protected]

Bob Yedid LifeSci Advisors, LLC 646-597-6989 [email protected]

Consolidated Balance Sheets

As of March 31, As of
December 31,
2019
2020
2019
Unaudited
Audited
U.S Dollars in thousands
Assets
Current Assets
Cash and cash equivalents \$ 49,288 \$ 22,037 \$ 42,662
Short-term investments 47,124 33,800 31,245
Trade receivables, net 26,266 23,210 23,210
Other accounts receivables 1,736 3,442 3,272
Inventories 41,787 31,708 43,173
Total Current Assets 166,201 114,197 143,562
Non-Current Assets
Property, plant and equipment, net 24,379 24,642 24,550
Right-of-use assets 3,800 4,187 4,022
Other long term assets 1,053 174 352
Deferred expenses 421 - -
Deferred taxes 939 1,895 1,311
Total Non-Current Assets 30,592 30,898 30,235
Total Assets \$ 196,793 \$ 145,095 \$ 173,797
Liabilities
Current Liabilities
Current maturities of bank loans \$ 465 \$ 470 \$ 489
Current maturities of lease liabilities 928 961 1,020
Trade payables 18,440 15,255 24,830
Other accounts payables 4,875 4,424 5,811
Deferred revenues 649 461 589
Total Current Liabilities 25,357 21,571 32,739
Non-Current Liabilities
Bank loans 138 591 257
Lease liabilities 3,663 4,036 3,981
Deferred revenues 569 605 232
Employee benefit liabilities, net 1,251 823 1,269
Total Non-Current Liabilities 5,621 6,055 5,739
Shareholder's Equity
Ordinary shares 11,647 10,412 10,425
Additional paid in capital net 204,702 179,352 180,819
Capital reserve due to translation to presentation currency (3,490) (3,490) (3,490)
Capital reserve from hedges 264 11 8
Capital reserve from financial assets measured at fair value through other comprehensive
income
- 118 145
Capital reserve from share-based payments 8,903 9,463 8,844
Capital reserve from employee benefits (356) 4 (359)
Accumulated deficit (55,855) (78,401) (61,073)
Total Shareholder's Equity 165,815 117,469 135,319
Total Liabilities And Shareholder's Equity \$ 196,793 \$ 145,095 \$ 173,797
Three months period ended
March 31,
Year ended
December 31,
2020
2019
2019
Unaudited Audited
U.S Dollars in thousands
Revenues from proprietary products \$ 25,317 \$ 20,381 \$ 97,696
Revenues from distribution 7,973 6,416 29,491
Total revenues 33,290 26,797 127,187
Cost of revenues from proprietary products 14,947 10,490 52,425
Cost of revenues from distribution 6,892 5,123 25,025
Total cost of revenues 21,839 15,613 77,450
Gross profit 11,451 11,184 49,737
Research and development expenses 3,347 2,766 13,059
Selling and marketing expenses 940 1,092 4,370
General and administrative expenses 2,312 2,094 9,194
Other expense 2 23 330
Operating income 4,850 5,209 22,784
Financial income 317 280 1,146
Income (expense) in respect of securities measured at fair value, net 102 (52) (5)
Income (expense) in respect of currency exchange differences and derivatives instruments, net 432 (313) (651)
Financial expense (77) (71) (293)
Income before tax on income 5,624 5,053 22,981
Taxes on income 406 130 730
Net Income \$ 5,218 \$ 4,923 \$ 22,251
Other Comprehensive Income (loss) :
Amounts that will be or that have been reclassified to profit or loss when specific conditions
are met
Gain (loss) from securities measured at fair value through other comprehensive income (188) 108 143
Gain on cash flow hedges 241 74 92
Net amounts transferred to the statement of profit or loss for cash flow hedges 34 (2) (23)
Items that will not be reclassified to profit or loss in subsequent periods:
Remeasurement gain (loss) from defined benefit plan - - (388)
Tax effect 27 (28) (11)
Total comprehensive income \$ 5,332 \$ 5,075 \$ 22,064
Earnings per share attributable to equity holders of the Company:
Basic income per share \$ 0.12 \$ 0.12 \$ 0.55
Diluted income per share \$ 0.12 \$ 0.12 \$ 0.55

Consolidated Statements of Cash Flows

Three months period Ended
March 31,
Year Ended
December 31,
2020
2019
Unaudited
2019
Audited
U.S Dollars in thousands
Net income \$ 5,218 \$ 4,923 \$ 22,251
Adjustments to reconcile net income to net cash provided by operating activities:
Adjustments to the profit or loss items:
Depreciation and impairment 1,192 1,127 4,519
Financial expenses (income), net (774) 156 (197)
Cost of share-based payment 258 315 1,163
Taxes on income 406 130 730
Loss (gain) from sale of property and equipment - (6) (2)
Change in employee benefit liabilities, net (18) 36 94
1,064 1,758 6,307
Changes in asset and liability items:
Decrease (increase) in trade receivables, net (3,016) 4,727 5,117
Decrease (increase) in other accounts receivables 1,513 131 (214)
Decrease (increase) in inventories 1,386 (2,392) (13,857)
Decrease (increase) in deferred expenses (421) (246) 399
Increase (decrease) in trade payables (7,216) (2,368) 6,259
Increase (decrease) in other accounts payables (1,180) (510) 863
Increase (decrease) in deferred revenues 397 (63) (283)
(8,537) (721) (1,716)
Cash received (paid) during the year for:
Interest paid (55) (63) (243)
Interest received 451 172 1,106
Taxes paid (61) (8) (134)
335 101 729
Net cash provided by (used in) operating activities \$ (1,920) \$ 6,061 \$ 27,571

Consolidated Statements of Cash Flows

Three months period Ended
March 31,
2020
2019
2019
Unaudited
U.S Dollars in thousands
Cash Flows from Investing Activities
Investment in short term investments, net \$
(15,646) \$
(1,058) \$
1,727
Purchase of property and equipment and intangible assets (896) (304) (2,300)
Proceeds from sale of property and equipment - 6 9
Net cash used in investing activities (16,542) (1,356) (564)
Cash Flows from Financing Activities
Proceeds from exercise of share base payments 5 3 16
Repayment of lease liabilities (278) (263) (1,070)
Repayment of long-term loans (123) (115) (476)
Proceeds from issuance of ordinary shares, net 24,894 - -
Net cash provided by (used in) financing activities 24,498 (375) (1,530)
Exchange differences on balances of cash and cash equivalent 590 (386) (908)
Increase in cash and cash equivalents 6,626 3,944 24,569
Cash and cash equivalents at the beginning of the year 42,662 18,093 18,093
Cash and cash equivalents at the end of the year \$
49,288
\$
22,037 \$
42,662
Significant non-cash transactions
Purchase of property and equipment through capital lease \$
58
\$
4,431 \$
5,035
Purchase of property and equipment \$
579
\$
235 \$
992

Adjusted EBITDA

Three months period Ended
March 31,
Year ended
December 31,
2020 2019 2019
U.S. Dollars in thousands
Net income (loss) \$ 5,218 \$ 4,923 \$ 22,251
Taxes on income 406 130 730
Financial income, net (774) 156 (197)
Depreciation and amortization expense 1,192 1,127 4,519
Cost of share - based payments 258 315 1,163
Adjusted EBITDA \$ 6,300 \$ 6,651 \$ 28,466

Adjusted Net Income

Three months period Ended
March 31,
Year ended
December 31,
2020
2019
2019
U.S. Dollars in thousands
Net income (loss) \$
5,218
\$ 4,923 \$ 22,251
Cost of share - based payments 258 315 1,163
Adjusted net income \$
5,476
\$ 5,238 \$ 23,414

KAMADA LTD.

CONSOLIDATED FINANCIAL STATEMENTS

AS OF MARCH 31, 2020

TABLE OF CONTENTS

Page
Consolidated Balance Sheets 2
Consolidated Statements of Comprehensive Income 3
Consolidated Statements of Changes in Equity 4-6
Consolidated Statements of Cash Flows 7-8
Notes to the Consolidated Financial Statements 9-15
- - - - - - - - - - -

CONSOLIDATED BALANCE SHEETS

As of
March 31,
As of
December 31,
2020 2019 2019
Unaudited Audited
Assets U.S Dollars in thousands
Current Assets
Cash and cash equivalents \$ 49,288 \$ 22,037 \$
42,662
Short-term investments 47,124 33,800 31,245
Trade receivables, net 26,266 23,210 23,210
Other accounts receivables 1,736 3,442 3,272
Inventories 41,787 31,708 43,173
Total Current Assets 166,201 114,197 143,562
Non-Current Assets
Property, plant and equipment, net 24,379 24,642 24,550
Right-of-use assets 3,800 4,187 4,022
Other long term assets 1,053 174 352
Deferred expenses 421 - -
Deferred taxes 939 1,895 1,311
Total Non-Current Assets
30,592 30,898 30,235
Total Assets \$ 196,793 \$ 145,095 \$
173,797
Liabilities
Current Liabilities
Current maturities of bank loans \$ 465 \$ 470 \$
489
Current maturities of lease liabilities 928 961 1,020
Trade payables 18,440 15,255 24,830
Other accounts payables 4,875 4,424 5,811
Deferred revenues 649 461 589
Total Current Liabilities 25,357 21,571 32,739
Non-Current Liabilities
Bank loans 138 591 257
Lease liabilities 3,663 4,036 3,981
Deferred revenues 569 605 232
Employee benefit liabilities, net 1,251 823 1,269
Total Non-Current Liabilities 5,621 6,055 5,739
Shareholder's Equity
Ordinary shares 11,647 10,412 10,425
Additional paid in capital net 204,702 179,352 180,819
Capital reserve due to translation to presentation currency (3,490) (3,490) (3,490)
Capital reserve from hedges 264 11 8
Capital reserve from financial assets measured at fair value through other comprehensive
income
- 118 145
Capital reserve from share-based payments 8,903 9,463 8,844
Capital reserve from employee benefits (356) 4 (359)
Accumulated deficit (55,855) (78,401) (61,073)
Total Shareholder's Equity 165,815 117,469 135,319
Total Liabilities And Shareholder's Equity \$ 196,793 \$ 145,095 \$
173,797

The accompanying Notes are an integral part of the Consolidated Financial Statements.

Consolidated Statements of Comprehensive Income

Three months period ended
March 31,
Year ended
December 31,
2020 2019 2019
Unaudited Audited
U.S Dollars in thousands
Revenues from proprietary products \$
25,317
\$ 20,381 \$ 97,696
Revenues from distribution 7,973 6,416 29,491
Total revenues 33,290 26,797 127,187
Cost of revenues from proprietary products 14,947 10,490 52,425
Cost of revenues from distribution 6,892 5,123 25,025
Total cost of revenues 21,839 15,613 77,450
Gross profit 11,451 11,184 49,737
Research and development expenses 3,347 2,766 13,059
Selling and marketing expenses 940 1,092 4,370
General and administrative expenses 2,312 2,094 9,194
Other expense 2 23 330
Operating income 4,850 5,209 22,784
Financial income 317 280 1,146
Income (expense) in respect of securities measured at fair value, net *
Income (expense) in respect of currency exchange differences and derivatives instruments,
102 (52) (5)
net 432 (313) (651)
Financial expense (77) (71) (293)
Income before tax on income 5,624 5,053 22,981
Taxes on income 406 130 730
Net Income \$
5,218
\$ 4,923 \$ 22,251
Other Comprehensive Income (loss) :
Amounts that will be or that have been reclassified to profit or loss when specific
conditions are met
Gain (loss) from securities measured at fair value through other comprehensive income (188) 108 143
Gain on cash flow hedges 241 74 92
Net amounts transferred to the statement of profit or loss for cash flow hedges 34 (2) (23)
Items that will not be reclassified to profit or loss in subsequent periods:
Remeasurement gain (loss) from defined benefit plan - - (388)
Tax effect 27 (28) (11)
Total comprehensive income \$
5,332
\$ 5,075 \$ 22,064
Earnings per share attributable to equity holders of the Company:
Basic income per share \$
0.12
\$ 0.12 \$ 0.55
Diluted income per share \$
0.12
\$ 0.12 \$ 0.55

* Refer to note 5c for additional information.

The accompanying Notes are an integral part of the Consolidated Financial Statements.

CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY

Share
capital
Additional
paid in
capital
Capital
reserve from
securities
measured at
fair value
through other
comprehensive
income
Capital
reserve
due to
translation
to
presentation
currency
Capital
reserve
from
hedges
Unaudited
Capital
reserve
from
share
based
payments
Capital
reserve
from
employee
benefits
Accumulated
deficit
Total
equity
In thousands
Balance as of January 1,
2020 (audited)
\$ 10,425 \$
180,819
\$
145
\$ (3,490) \$ 8 \$
8,844
\$
(359) \$
(61,073) \$135,319
Net income - - - - - - -
5,218
5,218
Other comprehensive
income (loss)
- - (188) - 275 - - -
87
Tax effect - - 43 - (19) - 3 -
27
Total comprehensive
income (loss)
- - (145) - 256 - 3
5,218
5,332
Issuance of ordinary shares
Exercise and forfeiture of
share-based payment into
shares
1,217
5
23,684
199
-
-
-
-
-
-
-
(199)
-
-
-
24,901
-
5
Cost of share-based
payment
- - - - - 258 - -
258
Balance as of March 31,
2020
\$ 11,647 \$
204,702
\$ -
\$
(3,490) \$ 264 \$
8,903
(356) \$
\$
(55,855) \$165,815

The accompanying Notes are an integral part of the Consolidated Financial Statements.

CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY

Share
capital
Additional
paid in
capital
Capital
reserve from
securities
measured at
fair value
through other
comprehensive
income
Capital
reserve
due to
translation
to
presentation
currency
Capital
reserve
from
hedges
Unaudited
Capital
reserve
from
sharebased
payments
Capital
reserve
from
employee
benefits
Accumulated
deficit
Total
equity
U.S Dollars in thousands
Balance as of January 1,
2019 (audited)
Cumulative effect of
initially application of
IFRS 16
\$ 10,409 \$
-
179,147 \$
-
34 \$
-
(3,490) \$
-
(57) \$
-
9,353 \$
-
- 4 \$
(300)
(83,024) \$112,376
(300)
Balance as at January 1,
2019 (after initially
application of IFRS 16)
Net income
10,409
-
179,147
-
34
-
(3,490)
-
(57)
-
9,353
-
4
-
(83,324)
4,923
112,076
4,923
Other comprehensive
income
Tax effect
-
-
-
-
108
(24)
-
-
72
(4)
-
-
-
-
-
-
180
(28)
Total comprehensive
income (loss)
- - 84 - 68 - - 4,923 5,075
Exercise and forfeiture of
share-based payment
into shares
3 205 - - - (205) - - 3
Cost of share-based
payment
- - - - - 315 - - 315
Balance as of March 31,
2019
\$ 10,412 \$ 179,352 \$ 118 \$ (3,490) \$ 11 \$ 9,463 \$ 4 \$ (78,401) \$117,469

The accompanying Notes are an integral part of the Consolidated Financial Statements.

CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY

Share
capital
Additional
paid in
capital
Capital
reserve from
securities
measured at
fair value
through other
comprehensive
income
Capital
reserve
due to
translation
to
presentation
currency
Capital
reserve
from
hedges
Audited
Capital
reserve
from
sharebased
payments
Capital
reserve
from
employee
benefits
Accumulated
deficit
Total
equity
U.S Dollars in thousands
Balance as of January 1,
2019 (audited)
Cumulative effect of
initially application
\$ 10,409 \$ 179,147 \$ 34 \$ (3,490) \$ (57) \$ 9,353 \$ 4 \$ (83,024) \$112,376
ofIFRS 16
Balance as at January 1,
2019 (after initially
application of IFRS 16)
-
10,409
-
179,147
-
34
-
(3,490)
-
(57)
0
9,353
0
4
(300)
(83,324)
(300)
112,076
Net income
Other comprehensive
income
Tax effect
-
-
-
-
-
-
-
143
(32)
-
-
-
-
69
(4)
-
-
-
-
(388)
25
22,251
-
-
22,251
(176)
(11)
Total comprehensive
income
Exercise and forfeiture of
- - 111 - 65 - (363) 22,251 22,064
share-based payment into
shares
Cost of share-based
16 1,672 - - - (1,672) - - 16
payment
Balance as of December
31, 2019
-
\$ 10,425 \$
-
180,819 \$
-
145 \$
-
(3,490) \$
-
8 \$
1,163
8,844 \$
-
(359) \$
- 1,163
(61,073) \$135,319

The accompanying Notes are an integral part of the Consolidated Financial Statements.

CONSOLIDATED STATEMENTS OF CASH FLOWS

Three months period Ended
March 31,
2020
Year Ended
December 31,
2019 2019
Unaudited Audited
U.S Dollars
in
thousands
U.S Dollars
in
thousands
Net income \$ 5,218 \$ 4,923 \$ 22,251
Adjustments to reconcile net income to net cash provided by operating activities:
Adjustments to the profit or loss items:
Depreciation and impairment 1,192 1,127 4,519
Financial expenses (income), net (774) 156 (197)
Cost of share-based payment 258 315 1,163
Taxes on income 406 130 730
Loss (gain) from sale of property and equipment - (6) (2)
Change in employee benefit liabilities, net (18) 36 94
1,064 1,758 6,307
Changes in asset and liability items:
Decrease (increase) in trade receivables, net (3,016) 4,727 5,117
Decrease (increase) in other accounts receivables 1,513 131 (214)
Decrease (increase) in inventories 1,386 (2,392) (13,857)
Decrease (increase) in deferred expenses (421) (246) 399
Increase (decrease) in trade payables (7,216) (2,368) 6,259
Increase (decrease) in other accounts payables (1,180) (510) 863
Increase (decrease) in deferred revenues 397 (63) (283)
(8,537) (721) (1,716)
Cash received (paid) during the year for:
Interest paid (55) (63) (243)
Interest received 451 172 1,106
Taxes paid (61) (8) (134)
335 101 729
Net cash provided by (used in) operating activities \$ (1,920) \$ 6,061 \$ 27,571

The accompanying Notes are an integral part of the Consolidated Financial Statements.

CONSOLIDATED STATEMENTS OF CASH FLOWS

Three months period Ended
March 31,
2020
2019
Unaudited
Year Ended
December 31,
2019
Audited
U.S Dollars
in
thousands
Cash Flows from Investing Activities thousands
Investment in short term investments, net \$ (15,646) \$ (1,058) \$ 1,727
Purchase of property and equipment and intangible assets (896) (304) (2,300)
Proceeds from sale of property and equipment - 6 9
Net cash used in investing activities (16,542) (1,356) (564)
Cash Flows from Financing Activities
Proceeds from exercise of share base payments 5 3 16
Repayment of lease liabilities (278) (263) (1,070)
Repayment of long-term loans (123) (115) (476)
Proceeds from issuance of ordinary shares, net 24,894 - -
Net cash provided by (used in) financing activities 24,498 (375) (1,530)
Exchange differences on balances of cash and cash equivalent 590 (386) (908)
Increase in cash and cash equivalents 6,626 3,944 24,569
Cash and cash equivalents at the beginning of the year 42,662 18,093 18,093
Cash and cash equivalents at the end of the year \$ 49,288 \$ 22,037 \$ 42,662
Significant non-cash transactions
Purchase of property and equipment through capital lease \$ 58 \$ 4,431 \$ 5,035
Purchase of property and equipment \$ 579 \$ 235 \$ 992

The accompanying Notes are an integral part of the Consolidated Financial Statements.

Note 1:- General

Kamada Ltd. ("the Company") is a plasma-derived biopharmaceutical company focused on orphan indications, with an existing marketed product portfolio and a late-stage product pipeline. The Company uses its proprietary platform technology and know-how for the extraction and purification of proteins from human plasma to produce Alpha-1 Antitrypsin (AAT) in a highly-purified, liquid form, as well as other plasma-derived immune globulins. The Company's flagship product is Glassia® ("Glassia"), the first liquid, ready-to-use, intravenous plasma-derived AAT product approved by the U.S. FDA. The Company markets Glassia in the U.S. through a strategic partnership with Takeda Pharmaceuticals Company Limited ("Takeda") and in other countries through local distributors. The Company's second leading product is KamRab®, a rabies immune globulin (Human) for post-exposure prophylaxis against rabies infection. KamRab is FDA approved and is being marketed in the U.S. under the brand name KedRab® ("KedRab") through a strategic partnership with Kedrion S.p.A. In addition to Glassia and KedRab, the Company has a product line of four other plasma-derived pharmaceutical products administered by injection or infusion, that are marketed through distributors in more than 15 countries, including Israel, Russia, Brazil, India and other countries in Latin America and Asia. The Company has late-stage products in development, including an inhaled formulation of AAT for the treatment of AAT deficiency. In addition, the Company's intravenous AAT is in development for other indications, such as GvHD and prevention of lung transplant rejection. The Company leverages its expertise and presence in the plasma-derived protein therapeutics market by distributing more than 20 complementary products in Israel that are manufactured by third parties.

Pursuant to the agreement with Takeda (as detailed on Note 17 of the Company's annual financial statements as of December 31, 2019) the Company will continue to produce Glassia for Takeda through 2021. Takeda is planning to complete the technology transfer of Glassia, and pending FDA approval, will initiate its own production of Glassia for the U.S. market in 2021. Accordingly, following the transition of manufacturing to Takeda, the Company will terminate the manufacturing and sale of Glassia to Takeda resulting in a significant reduction in revenues. Pursuant to the agreement, upon initiation of sales of Glassia manufactured by Takeda, Takeda will pay royalties to the Company at a rate of 12% on net sales through August 2025, and at a rate of 6% thereafter until 2040, with a minimum of \$5 million annually, for each of the years from 2022 to 2040.

These Financial Statements have been prepared in a condensed format as of March 31, 2020 and for the three months then ended ("interim consolidated financial statements").

These financial statements should be read in conjunction with the Company's annual financial statements as of December 31, 2019 and for the year then ended and the accompanying notes ("annual consolidated financial statements").

Note 2:- Significant Accounting Policies

a. Basis of preparation of the interim consolidated financial statements:

The interim consolidated financial statements have been prepared in accordance with generally accepted accounting principles for the preparation of financial statements for interim periods, as prescribed in IAS 34, "Interim Financial Reporting".

b. Implementation of new accounting standards

The accounting policy applied in the preparation of the interim consolidated financial statements is consistent with that applied in the preparation of the annual consolidated financial statements, except for the following:

Amendments to IFRS 9, IFRS 7 and IAS 39

In September 2019, the IASB published an amendment to IFRS 9, "Financial Instruments", IFRS 7, "Financial Instruments: Disclosures" and IAS 39," Financial Instruments: Recognition and Measurement" ("the Amendment").

In view of global regulatory changes, numerous countries have considered introducing a reform in the benchmark Interbank Offered Rates ("IBORs") (LIBOR, the London Interbank Offered Rate, being one of the most common examples) and switching to a risk-free interest rate alternative ("RFR") which extensively rely on data of specific transactions. The IBOR reform leads to uncertainty regarding the dates and amounts to be attributed to future cash flows relating to both hedging instruments and hedged items that rely on existing IBORs.

According to the existing accounting guidance of IFRS 9 and IAS 39, entities that have entered into the above hedges are facing uncertainty as a result of the IBOR reform which is likely to affect their ability to continue meeting the effective hedging requirements underlying existing transactions as well as the hedging requirements of future transactions. In order to resolve this uncertainty, the IASB issued the Amendment to offer transitional reliefs for entities that apply IBOR-based hedge accounting. The Amendment represents phase one in the reform that will include additional amendments in the future.

The Amendment also permits certain reliefs in applying the hedge accounting effectiveness tests during the period of transition from IBORs to RFRs. These reliefs assume that the benchmark interest underlying the hedge will not change as a result of the expected interest reform. The reliefs will be effective indefinitely, until the occurrence of one of the events specified in the Amendment. The Amendment also requires entities to provide specific disclosures of the application of any reliefs.

Note 2:- Significant Accounting Policies (cont.)

The Amendment was applied retrospectively for annual periods beginning on or after January 1, 2020.

The Company estimates that the adoption of the Amendment will have no effect on its financial statements since it does not currently enter into substantial IBOR-based hedges.

Note 3:- Significant events in the reporting period

a. Effects of the COVID-19 Outbreak:

Following the global COVID-19 outbreak, there has been a decrease in economic activity worldwide, including Israel. The spread of the COVID-19 pandemic led, inter alia, to a disruption in the global supply chain, a decrease in global transportation, restrictions on travel and work that were announced by the State of Israel and other countries worldwide as well as a decrease in the value of financial assets and commodities across all markets in Israel and the world.

To date the Company's manufacturing plant remains operational with no effect on business continuity.

The Company intends to maintain its current manufacturing and supply plans and increased its inventory levels of raw materials through our suppliers and service providers in order to appropriately manage any potential supply disruptions and secure continued manufacturing. In addition, the Company is actively engaging its freight carriers to ensure inbound and outbound international delivery routes remain operational and identify alternative routes, if needed.

The Company is complying with the State of Israel mandates and recommendations with respect to its work-force management and currently maintains the work-force levels required to support its ongoing commercial operations. The Company has taken a number of precautionary health and safety measures to safeguard its employees and continues to monitor and assess orders issued by the State of Israel and other applicable governments to ensure compliance with evolving COVID-19 guidelines.

Note 3:- Significant events in the reporting period (cont.)

While the impact of the COVID-19 pandemic on the Company's financial results for the first quarter of 2020 was not material, and the Company expects meeting its annual sales guidance, a number of COVID-19 pandemic-related dynamics may still affect market demand for the Company's products, availability of raw materials and potential effects on the Company's employees all of which may have an effect on the Company's future financial position and results of operations.

  • b. On February 10, 2020, the Company closed a private placement with FIMI Opportunity Fund 6, L.P. and FIMI Israel Opportunity Fund 6, Limited Partnership (the "FIMI Funds"), a then 12.99% stockholder of the Company. Pursuant to the private placement the Company issued 4,166,667 ordinary shares at a price of \$6.00 per share, for an aggregate net proceeds of \$24,894 thousands. Upon closing of the private placement, the FIMI Funds ownership represented approximately 21% of the Company's outstanding shares. Concurrently, the Company entered into a registration rights agreement with the FIMI Funds, pursuant to which the FIMI Funds are entitled to customary demand registration rights (effective six months following the closing of the transaction) and piggyback registration rights with respect to all shares held by FIMI Funds. Mr. Ishay Davidi, Ms. Lilach Asher Topilsky and Mr. Amiram Boehm, members of our board of directors, are executives of the FIMI Funds.
  • c. On March 25, 2020, the Company's shareholders approved the grant of options to purchase 90,000 Ordinary Shares of the Company at an exercise price of NIS 21.34 per share and 30,000 Restricted Shares ("RS") to the Company's Chief Executive Officer. The fair value of the options and of the RSs was \$166 thousands and \$167 thousands, respectively, estimated based on the binomial option valuation model.

In addition, on such date, the Company's shareholders approved the grant of options to purchase 212,000 Ordinary Shares of the Company at an exercise price of NIS 23.67 per share to members of the Company's Board of Directors. The fair value of the options calculated on the date of grant was estimated at \$356 thousands using the binomial option valuation model.

Note 4:- Operating Segments

a. General:

The company has two operating segments, as follows:

Proprietary Products - Medicine development, manufacture and sale of plasma-derived therapeutics products.

Distribution - Distribution in Israel of drugs manufactured by third parties, majority of which are produced from plasma or its derivatives products.

b. Reporting on operating segments:

Three months period ended
March 31, 2020
Proprietary
Products
Distribution
Total
U.S Dollars in thousands
Unaudited
Revenues \$
25,317
\$ 7,973 \$ 33,290
Gross profit \$
10,370
\$ 1,081 \$ 11,451
Unallocated operational expenses (6,601)
Finance income (expense), net 774
Income before taxes on income \$ 5,624

Note 4:- Operating Segments (cont.)

b. Reporting on operating segments (continued):

Three months period ended
March 31, 2019
Proprietary
Products
Distribution Total
U.S Dollars in thousands
Unaudited
Revenues \$
20,381
\$ 6,416 \$ 26,797
Gross profit \$
9,891
\$ 1,293 \$ 11,184
Unallocated operational expenses (5,975)
Finance income (expense), net (156)
Income before taxes on income \$ 5,053
Year ended December 31, 2019
Proprietary
Products
Distribution Total
U.S Dollars in thousands
Audited
Revenues \$ 97,696 \$ 29,491 \$
127,187
Gross profit \$ 45,271 \$ 4,466 \$ 49,737
Unallocated operational expenses
Finance income (expense), net
(26,953) 197
Income before taxes on income \$ 22,981

Note 4:- Operating Segments (cont.)

c. Reporting on operating segments by geographic region:

Three months period ended March 31, 2020
Proprietary
Products
Distribution Total
U.S Dollars in thousands
Unaudited
Geographical markets
U.S.A. \$
22,721
\$ - \$ 22,721
Israel 589 7,973 8,562
Europe 553 - 553
Latin America 858 - 858
Asia 113 113
Others 483 - 483
\$
25,317
\$ 7,973 \$ 33,290

Three months period ended March 31, 2019

Proprietary
Products Distribution Total
U.S Dollars in thousands
Unaudited
Geographical markets
U.S.A. \$
18,062
\$ - \$ 18,062
Israel 547 6,416 6,963
Europe 873 - 873
Latin America 239 - 239
Asia 660 - 660
Others - - -
\$
20,381
\$ 6,416 \$ 26,797
Year ended December 31, 2019
Proprietary
Products Distribution Total
U.S Dollars in thousands
Audited
Geographical markets
U.S.A. \$
84,572
\$ - \$ 84,572
Israel 2,468 29,491 31,959
Europe 4,701 - 4,701
Latin America 3,792 - 3,792
Asia 2,067 - 2,067
Others 96 - 96
\$
97,696
\$ 29,491 \$ 127,187

Note 5:- Financial Instruments

a. Classification of financial instruments by fair value hierarchy

Financial assets (liabilities) measured at fair value

March 31, 2020 Level 1 Level 2
U.S Dollars in thousands
Derivatives instruments - (245)
\$ - \$ (245)
March 31, 2019
Debt securities (corporate and government) measured at fair value through other comprehensive income \$ 1,661 \$ 8,849
Derivatives instruments - 19
\$ 1,661 \$ 8,868
December 31, 2019
Debt securities (corporate and government) measured at fair value through other comprehensive income \$ 4,289 \$ 8,543
Derivatives instruments - 15
\$ 4,289 \$ 8,558

b. During the three months ended March 31, 2020 there were no transfers from Level 1 to Level 2, and to or from Level 3 due to the fair value measurement of any financial instrument.

c. During the three months ended March 31, 2020, the Company divested all of its investments in debt securities (corporate and government) and realized the fair value of such debt securities through other comprehensive income. As a result, the Company recognized \$102 thousands in Consolidated Statements of Comprehensive Income.


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