Kamada Reports Strong Second Quarter and First Half 2025 Financial Results with 11% Year-Over-Year 6-Month Top Line Growth and a 35% Increase in Profitability; Raises Full-Year Profitability Guidance

Rhea-AI Summary

Kamada (NASDAQ: KMDA) reported strong financial results for Q2 and H1 2025, with significant growth in both revenue and profitability. First half 2025 revenues reached $88.8 million, up 11% year-over-year, while Q2 revenues were $44.8 million, a 5% increase. The company's adjusted EBITDA for H1 2025 grew 35% to $22.5 million, representing a 25% margin.

Based on robust performance, Kamada raised its 2025 adjusted EBITDA guidance to $40-44 million and maintained revenue guidance of $178-182 million. The company received FDA approval for its Houston plasma collection center, with an estimated annual revenue potential of $8-10 million at full capacity. Additionally, Kamada continues to advance its Phase 3 InnovAATe clinical trial for inhaled Alpha-1 Antitrypsin therapy.

Positive

• First half 2025 revenues increased 11% to $88.8 million
• Adjusted EBITDA grew 35% to $22.5 million in H1 2025
• Net income increased 67% to $11.3 million in H1 2025
• FDA approval received for Houston plasma collection center
• Strong cash position of $66.0 million as of June 30, 2025
• Raised full-year adjusted EBITDA guidance to $40-44 million

Negative

• Gross margins decreased from 45% to 42% in Q2 2025
• Cash from operations declined from $14.0M to $8.0M in Q2 2025
• Cash balance reduced from $78.4M to $66.0M due to special dividend payment

Insights

Financial Analyst

Kamada shows robust 11% revenue growth and 35% EBITDA growth, raises guidance, demonstrating strong operational execution and profitable growth trajectory.

Kamada's Q2 and H1 2025 results demonstrate impressive financial momentum with $88.8 million in first-half revenues, up 11% year-over-year, and Q2 revenues of $44.8 million, a 5% increase. More notable is the company's profitability surge, with H1 adjusted EBITDA reaching $22.5 million - a substantial 35% increase, representing a 25% margin. The Q2 adjusted EBITDA of $10.9 million shows a 20% year-over-year improvement.

Management's confidence is evident in their upward revision of 2025 adjusted EBITDA guidance to $40-44 million from the previous $38-42 million, while maintaining revenue projections of $178-182 million. This suggests efficient operational expense management, as demonstrated by the $1.4 million reduction in quarterly operating expenses compared to Q2 2024.

The FDA approval of Kamada's Houston plasma collection center represents a significant operational milestone. With an estimated annual collection capacity of 50,000 liters and potential revenue contribution of $8-10 million at full capacity, this facility strengthens the company's vertical integration strategy and raw material self-sufficiency.

Kamada's strong cash position of $66 million (despite paying a $11.5 million special dividend) provides financial flexibility for the business development opportunities management has highlighted as a strategic focus. The net income increase to $7.4 million ($0.13 per diluted share) in Q2 2025 from $4.4 million ($0.08 per share) in Q2 2024 represents a 68% improvement in bottom-line performance.

The company's product portfolio diversification is paying dividends, with growth drivers including increased GLASSIA sales in non-U.S. markets, distribution segment growth, VARIZIG U.S. sales, and GLASSIA royalty income. While gross margins slightly contracted in Q2 to 42% from 45% due to product mix shifts, the six-month gross margin remained stable at 45%, indicating the company can maintain profitability while growing revenue.

The advancement of the InnovAATe Phase 3 clinical trial for inhaled Alpha-1 Antitrypsin therapy, with an interim futility analysis expected by year-end, represents a potential future growth catalyst if successful, though investors should monitor this development closely as clinical trials inherently carry risk.

• First Half 2025 Total Revenues were $88.8 Million, up 11% Year-over-Year; Revenues for 2025 Second Quarter were $44.8 Million, up 5% Year-over-Year

• First Half 2025 Adjusted EBITDA of $22.5 Million, up 35% Year-over-Year and Representing 25% Margin of Revenues; Second Quarter Adjusted EBITDA of $10.9 Million, up 20% Year-over-Year
• Robust First Half Results and Positive Outlook for Remainder of 2025 Support Increased Adjusted EBITDA Guidance to $40 Million-$44 Million, and Reiteration of Full-Year Revenue Guidance of $178 Million-$182 Million
• Announced FDA Approval of its Plasma Collection Center in Houston, Texas, which is Now Cleared to Commence Commercial Sales
• Company Continues to Focus on Securing Commercial-Stage Business Development Opportunities to Support Continued Long-Term Profitable Growth
• Conference Call and Live Webcast Today at 8:30am ET

REHOVOT, Israel and HOBOKEN, N.J., Aug. 13, 2025 (GLOBE NEWSWIRE) -- Kamada Ltd. (NASDAQ: KMDA; TASE: KMDA.TA), a global biopharmaceutical company with a portfolio of marketed products indicated for rare and serious conditions and a leader in the specialty plasma-derived field, today announced financial results for the three months and six months ended June 30, 2025.

“Results for the second quarter and first half of 2025 were strong, and we continue to generate significant profitable growth through the diversity of our commercial product portfolio and disciplined management of operational expenses,” said Amir London, Kamada’s Chief Executive Officer. “Total revenues for the first half of the year were $88.8 million, representing an 11% increase year-over-year, and adjusted EBITDA was $22.5 million, up 35% year-over-year, representing a 25% margin of revenues. Based on our strong performance in the first half of the year and positive outlook for the remainder of 2025, we are increasing our annual adjusted EBITDA guidance of between $40 million to $44 million and reiterating our full-year 2025 revenue guidance of between $178 million to $182 million."

“We continue to invest in our strategic growth pillars through continuous organic growth, as demonstrated by our financial results, while focusing on securing business development and M&A opportunities to expand our portfolio of marketed products, thereby supporting continued profitable growth. In addition, we continue to ramp up plasma collection at our three Texas-based plasma collection centers and were pleased to recently receive U.S. FDA approval of our state-of-the-art plasma collection center in Houston, TX, which is now cleared to commence commercial sales. As previously stated, the center has annual collection capacity of approximately 50,000 liters of plasma and an estimated annual revenue contribution of $8 million to $10 million at its full capacity. Moreover, we continue to advance our ongoing pivotal Phase 3 InnovAATe clinical trial for our inhaled Alpha-1 Antitrypsin therapy. Enrollment is progressing, and we remain on track to conduct an interim futility analysis by the end of the year,” concluded Mr. London.

Financial Highlights for the Three Months Ended June 30, 2025

• Total revenues were $44.8 million in the second quarter of 2025, up 5% compared to $42.5 million in the second quarter of 2024. The increase in revenues was driven by the diversity of the Company’s portfolio, primarily attributable to increased sales of GLASSIA® in ex-U.S. markets, increased sales in our Distribution segment, VARIZIG® U.S. sales, and GLASSIA royalty income.

• Gross profit and gross margins were $18.9 million and 42%, respectively, in the second quarter of 2025, compared to $19.0 million and 45%, respectively, in the second quarter of 2024.The decrease in both metrics is attributable to changes in product sales mix.
• Operating expenses, including R&D, S&M, G&A and other expenses, totaled $11.9 million in the second quarter of 2025, as compared to $13.3 million in the second quarter of 2024. The decrease is driven by disciplined management of operational expenses.
• Net income was $7.4million, or $0.13per diluted share, in the second quarter of 2025, as compared to $4.4 million, or $0.08 per diluted share, in the second quarter of 2024.
• Adjusted EBITDA, as detailed in the tables below, was $10.9 million in the second quarter of 2025, up 20% as compared with the $9.1 million achieved in the second quarter of 2024.
• Cash provided by operating activities was $8.0 million in the second quarter of 2025, as compared to cash provided by operating activities of $14.0 million in the second quarter of 2024.

Financial Highlights for the Six Months Ended June 30, 2025

• Total revenues for the first six months of 2025 were $88.8 million, an 11% increase from the $80.2 million generated in the first six months of 2024. The increase in revenues was driven by the diversity of the Company’s portfolio, primarily attributable to increased sales of GLASSIA in ex-U.S. markets, increased sales in our Distribution segment, VARIZIG U.S. sales and GLASSIA royalty income.
• Gross profit and gross margins for the first six months of 2025 were $39.7 million and 45%, respectively, compared to $35.7 million and 45%, respectively, in the first half of 2024. The increase in gross profit is in line with the increase in total revenues.
• Operating expenses, including R&D, S&M, G&A and other expenses, totaled $24.8 million in the first six months of 2025, as compared to $26.0 million in the first half of 2024. The decrease is driven by disciplined management of operational expenses.
• Net income for the first six months of 2025 was $11.3 million, or $0.19 per diluted share, up 67% as compared to net income of $6.8 million or $0.12 per diluted share, in the first six months of 2024.
• Adjusted EBITDA, as detailed in the tables below, was $22.5 million in the first six months of 2025, a 35% increase as compared to $16.6 million in the first six months of 2024.
• Cash provided by operating activities during the first six months of 2025 was approximately $7.5 million, as compared to $15.0 million during the first six months of 2024. The decrease is associated with an increase in working capital.

Balance Sheet Highlights
As of June 30, 2025, the Company had cash and cash equivalents of $66.0 million, as compared to $78.4 million as of December 31, 2024. The decrease in cash balance is associated with the payment of a special cash dividend in the total amount of $11.5 million.

Recent Corporate Highlights

• Announced that the U.S. Food and Drug Administration (FDA) has approved the supplement to the Company’s existing Biologics License Application (BLA) for its collection center in Houston, TX. The center is now cleared to commence commercial sales of normal source plasma. The 12,000 square foot Houston facility supports 50 donor beds, with a planned capacity of approximately 50,000 liters per year and is anticipated to be one of the largest sites for specialty plasma collection in the U.S.

• Kamada awarded the Israeli Outstanding Exporter Award for 2024. The award was granted by the Israeli Ministry of Economy and Industry for the Company’s growing export revenues. The award was presented to Mr. London by the President of the State of Israel, Mr. Isaac Herzog.

Fiscal 2025 Guidance
Kamada is increasing its adjusted EBITDA guidance from a range of $38 million to $42 million to a range of $40 million to $44 million and continues to expect to generate fiscal year 2025 total revenues in the range of $178 million to $182 million, representing double digit top- and bottom-line growth year-over-year.

Conference Call Details
Kamada's management will host an investment community conference call on Wednesday, August 13 at 8:30am Eastern Time to discuss these results and answer questions. Shareholders and other interested parties may participate in the call by dialing 1-877-413-7208 (from within the U.S.), 1-201-689-8555 (International), or 1-809-406-247 Investors (from Israel) using conference I.D. 13754604. The call will be webcast live on the internet at: https://viavid.webcasts.com/starthere.jsp?ei=1726126&tp_key=61b4d50ef5

Non-IFRS financial measures
We present EBITDA and adjusted EBITDA because we use these non-IFRS financial measures to assess our operational performance, for financial and operational decision-making, and as a means to evaluate period-to-period comparisons on a consistent basis. Management believes these non-IFRS financial measures are useful to investors because: (1) they allow for greater transparency with respect to key metrics used by management in its financial and operational decision-making and provide investors with a meaningful perspective on the current underlying performance of the Company’s core ongoing operations; and (2) they exclude the impact of certain items that are not directly attributable to our core operating performance and that may obscure trends in the core operating performance of the business. Non-IFRS financial measures have limitations as an analytical tool and should not be considered in isolation from, or as a substitute for, our IFRS results. We expect to continue reporting non-IFRS financial measures, adjusting for the items described below, and we expect to continue to incur expenses similar to certain of the non-cash, non-IFRS adjustments described below. Accordingly, unless otherwise stated, the exclusion of these and other similar items in the presentation of non-IFRS financial measures should not be construed as an inference that these items are unusual, infrequent or non-recurring. EBITDA and adjusted EBITDA are not recognized terms under IFRS and do not purport to be an alternative to IFRS terms as an indicator of operating performance or any other IFRS measure. Moreover, because not all companies use identical measures and calculations, the presentation of EBITDA and adjusted EBITDA may not be comparable to other similarly titled measures of other companies. EBITDA is defined as net income (loss), plus income tax expense, plus or minus financial income or expenses, net, plus or minus income or expense in respect of securities measured at fair value, net, plus or minus income or expenses in respect of currency exchange differences and derivatives instruments, net, plus depreciation and amortization expense, whereas adjusted EBITDA is the EBITDA plus non-cash share-based compensation expenses and certain other costs.

For the projected 2025 adjusted EBITDA information presented herein, the Company is unable to provide a reconciliation of this forward measure to the most comparable IFRS financial measure because the information for these measures is dependent on future events, many of which are outside of the Company’s control. Additionally, estimating such forward-looking measures and providing a meaningful reconciliation consistent with the Company’s accounting policies for future periods is meaningfully difficult and requires a level of precision that is unavailable for these future periods and cannot be accomplished without unreasonable effort. Forward-looking non-IFRS measures are estimated in a manner consistent with the relevant definitions and assumptions noted in the Company’s adjusted EBITDA for historical periods.

About Kamada
Kamada Ltd. (the “Company”) is a global biopharmaceutical company with a portfolio of marketed products indicated for rare and serious conditions and a leader in the specialty plasma-derived therapies field. The Company’s strategy is focused on driving profitable growth through four primary growth pillars: First, organic growth from its commercial activities, including continued investment in the commercialization and life cycle management of its proprietary products, which include six FDA-approved specialty plasma-derived products: KEDRAB®, CYTOGAM®, GLASSIA®, WINRHO SDF®, VARIZIG® and HEPAGAM B®, as well as KAMRAB®, KAMRHO (D)® and two types of equine-based anti-snake venom products, and the products in the distribution segment portfolio, mainly through the launch of several biosimilar products in Israel. Second: the Company aims to secure significant new business development, in-licensing, collaboration and/or merger and acquisition opportunities, which are anticipated to enhance the Company’s marketed products portfolio and leverage its financial strength and existing commercial infrastructure to drive long-term growth. Third: the Company is expanding its plasma collection operations to support revenue growth through the sale of normal source plasma to other plasma-derived manufacturers, and to support its increasing demand for hyper-immune plasma. The Company currently owns three operating plasma collection centers in the United States, in Beaumont Texas, Houston Texas, and San Antonio, Texas. Lastly, the Company is leveraging its manufacturing, research and development expertise to advance the development and commercialization of additional product candidates, targeting areas of significant unmet medical need, with the lead product candidate Inhaled AAT, for which the Company is continuing to progress the InnovAATe clinical trial, a randomized, double-blind, placebo-controlled, pivotal Phase 3 trial. FIMI Opportunity Funds, the leading private equity firm in Israel, is the Company’s controlling shareholder, beneficially owning approximately 38% 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) increasing its adjusted EBITDA guidance to a range of $40 million to $44 million and reiteration of 2025 full-year guidance of $178 million to $182 million, 2) double digit growth in fiscal year 2025, 3) continued investment in the Company's four strategic growth pillars, consisting of organic commercial growth, business development and M&A transactions, plasma collection operations, and advancement of the pivotal Phase 3 Inhaled AAT program, 4) continued progress of the InnovAATe clinical trial and conducting an interim futility analysis by the end of 2025, 5) continued focus on securing commercial-stage business development and M&A opportunities to expand the portfolio of marketed products to support continued long-term profitable growth, 6) plasma collection center in Houston, TX, supporting 50 donor beds, with planned capacity of approximately 50,000 liters per year and is anticipated to be one of the largest sites for specialty plasma collection in the U.S., and 7) expected annual revenues contribution from sales of normal source plasma collected in the Houston collection centers at $8 million to $10 million at full capacity. 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. 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 evolving nature of the conflicts in the Middle East and the impact of such conflicts in Israel, the Middle East and the rest of the world, the impact of these conflicts on market conditions and the general economic, industry and political conditions in Israel, the U.S. and globally, effect of tariffs on overall international trade and specifically on Kamada’s ability to continue maintaining expected sales and profit levels in light of such tariffs, the effect on establishment and timing of business initiatives, Kamada’s ability to leverage new business opportunities and integrate it with its existing product portfolio, unexpected results of clinical and development programs, regulatory delays, and other risks detailed in Kamada’s filings with the U.S. Securities and Exchange Commission (the “SEC”) including those discussed in its most recent Annual Report on Form 20-F and in any subsequent reports on Form 6-K, each of which is on file or furnished with the SEC and available at the SEC’s website at www.sec.gov. 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
IR@kamada.com

Brian Ritchie
LifeSci Advisors, LLC
212-915-2578
britchie@LifeSciAdvisors.com

---tables to follow---

CONDENSED CONSOLIDATED STATEMENTS OF FINANCIAL POSITION
	As of								As of
	June 30,								December 31,
	2025				2024				2024
	Unaudited
Assets
Current Assets
Cash and cash equivalents	$	65,985			$	56,547			$	78,435
Trade receivables, net		30,501				26,228				21,547
Other accounts  receivables		4,704				4,940				5,546
Inventories		82,079				78,713				78,819
Total Current Assets		183,269				166,428				184,347
Non-Current Assets
Property, plant and equipment, net		37,894				31,971				36,245
Right-of-use assets		9,250				7,552				9,617
Intangible assets, Goodwill and other long-term assets		99,640				106,517				103,226
Goodwill		30,313				30,313				30,313
Contract assets		7,807				8,257				8,019
Deferred taxes		-				-				488
Total Non-Current Assets		184,904				184,610				187,908
Total Assets	$	368,173			$	351,038			$	372,255
Liabilities
Current Liabilities
Current maturities of lease liabilities		1,866				1,494				1,631
Current maturities of other long term liabilities		9,850				12,610				10,181
Trade payables		25,077				19,532				27,735
Other accounts payables		8,804				7,233				9,671
Deferred revenues		177				27				171
Total Current Liabilities		45,774				40,896				49,389
Non-Current Liabilities
Lease liabilities		9,549				7,065				9,431
Contingent consideration		18,884				17,085				20,646
Other long-term liabilities		32,782				34,238				32,816
Deferred taxes		659				-				-
Employee benefit liabilities, net		571				602				509
Total Non-Current Liabilities		62,445				58,990				63,402
Shareholder’s Equity
Ordinary shares		15,077				15,023				15,028
Additional paid in capital  net		268,243				266,313				266,933
Capital reserve due to translation to presentation currency		(3,490	)			(3,490	)			(3,490	)
Capital reserve from hedges		456				(12	)			51
Capital reserve from share-based payments		5,226				6,444				6,316
Capital reserve from employee benefits		374				283				364
Accumulated deficit		(25,932	)			(33,409	)			(25,738	)
Total Shareholder’s Equity		259,954				251,152				259,464
Total Liabilities and Shareholder’s Equity	$	368,173			$	351,038			$	372,255

CONDENSED CONSOLIDATED STATEMENTS OF PROFIT OR LOSS AND OTHER COMPREHENSIVE INCOME
	Six months period ended								Three months period ended								Year ended
	June 30,								June 30,								December 31,
	2025				2024				2025				2024				2024
	Unaudited								Unaudited
Revenues from proprietary products	$	78,453			$	72,904			$	38,436			$	39,146			$	141,447
Revenues from distribution		10,319				7,304				6,318				3,326				19,506
Total revenues		88,772				80,208				44,754				42,472				160,953
Cost of revenues from proprietary products		40,580				38,338				20,842				20,718				73,708
Cost of revenues from distribution		8,514				6,168				4,983				2,803				17,278
Total cost of revenues		49,094				44,506				25,825				23,521				90,986
Gross profit		39,678				35,702				18,929				18,951				69,967
Research and development expenses		7,465				9,098				3,219				4,803				15,185
Selling and marketing expenses		9,068				9,361				4,558				4,730				18,428
General and administrative expenses		8,265				7,564				4,067				3,778				15,702
Other expenses		14				-				14				-				601
Operating income		14,866				9,679				7,071				5,640				20,051
Financial income		987				788				453				508				2,118
Income (expenses) in respect of currency exchange differences and derivatives instruments, net		(723	)			315				(974	)			191				(94	)
Financial expense in respect of contingent consideration and other long- term liabilities.		(2,380	)			(3,550	)			(605	)			(1,705	)			(8,081	)
Financial expenses		(384	)			(304	)			(192	)			(145	)			(660	)
Income before tax on income		12,366				6,928				5,753				4,489				13,334
Taxes on income		(1,026	)			(137	)			1,623				(63	)			1,128
Net Income	$	11,340			$	6,791			$	7,376			$	4,426			$	14,462
Other Comprehensive Income (loss) :
Amounts that will be or that have been reclassified to profit or loss when specific conditions are met
Gain (loss) on cash flow hedges		563				(95	)			677				(24	)			(30	)
Net amounts transferred to the statement of profit or loss for cash flow hedges		(158	)			(57	)			(104	)			-				(59	)
Items that will not be reclassified to profit or loss in subsequent periods:
Remeasurement gain (loss) from defined benefit plan		10				8				2				1				89
Total comprehensive income (loss)	$	11,755			$	6,647			$	7,951			$	4,403			$	14,462
Earnings per share attributable to equity holders of the Company:
Basic net earnings per share		0.20			$	0.12			$	0.13			$	0.08			$	0.25
Diluted net earnings per share		0.19			$	0.12			$	0.13			$	0.08			$	0.25

CONDENSED CONSOLIDATED INTERIM STATEMENTS OF CASH FLOWS
	Six months period Ended								Three months period Ended								Year Ended
	June, 30								June, 30								December 31,
	2025				2024				2025				2024				2024
	Unaudited
	U.S Dollars In thousands
Cash Flows from Operating Activities
Net income	$	11,340			$	6,791			$	7,376			$	4,426			$	14,462
Adjustments to reconcile net income to net cash provided by (used in) operating activities:
Adjustments to the profit or loss items:
Depreciation and impairment		7,357				6,466				3,746				3,229				13,808
Financial expenses net		2,500				2,751				1,318				1,151				6,717
Cost of share-based payment		270				476				95				235				874
Taxes on income		1,026				137				(1,623	)			63				(1,128	)
Loss (gain) from sale of property and equipment		(8	)			(1	)			-				(1	)			11
Change in employee benefit liabilities, net		74				(11	)			58				(7	)			52
		11,219				9,818				3,594				4,670				20,334
Changes in asset and liability items:
Increase in trade receivables, net		(8,670	)			(6,755	)			(2,113	)			(7,365	)			(1,977	)
Decrease in other accounts receivables		1,078				942				1,749				1,458				593
Decrease (increase) in inventories		(3,260	)			9,765				(3,721	)			5,634				9,659
Decrease in contract asset		212				239				118				127				476
Increase (decrease) in trade payables		(4,131	)			(5,092	)			(383	)			3,693				1,226
Increase (decrease) in other accounts payables		(883	)			(1,038	)			1,161				1,013				1,413
Increase (decrease) in deferred revenues		6				(121	)			(28	)			1				23
		(15,648	)			(2,060	)			(3,217	)			4,561				11,413
Cash received (paid) during the period for:
Interest paid		(384	)			(266	)			(208	)			(137	)			(594	)
Interest received		987				788				453				508				2,118
Taxes (paid) received		(6	)			(88	)			23				(65	)			(139	)
		597				434				268				306				1,385
Net cash provided by operating activities	$	7,508			$	14,983			$	8,021			$	13,963			$	47,594

CONDENSED CONSOLIDATED INTERIM STATEMENTS OF CASH FLOWS (continued)
	Six months period Ended								Three months period Ended								Year Ended
	June, 30								June, 30								December 31,
	2025				2024				2025				2024				2024
	Unaudited																Audited
	U.S Dollars In thousands
Cash Flows from Investing Activities
Purchase of property and equipment and intangible assets		(3,482	)			(5,692	)			(2,014	)			(3,010	)			(10,740	)
Proceeds from sale of property and equipment		8				1				-				1				1
Net cash used in investing activities		(3,474	)			(5,691	)			(2,014	)			(3,009	)			(10,739	)
Cash Flows from Financing Activities
Proceeds from exercise of share base payments		49				2				3				1				7
Repayment of lease liabilities		(418	)			(571	)			(404	)			(327	)			(1,251	)
Repayment of other long-term liabilities		(4,509	)			(7,848	)			(4,184	)			(2,352	)			(12,667	)
Dividends Paid		(11,534	)			-				(11,534	)			-				-
Net cash used in financing activities		(16,412	)			(8,417	)			(16,119	)			(2,678	)			(13,911	)
Exchange differences on balances of cash and cash equivalent		(72	)			31				(153	)			77				(150	)
Increase (decrease) in cash and cash equivalents		(12,450	)			906				(10,265	)			8,353				22,794
Cash and cash equivalents at the beginning of the period		78,435				55,641				76,250				48,194				55,641
Cash and cash equivalents at the end of the period	$	65,985			$	56,547			$	65,985			$	56,547			$	78,435
Significant non-cash transactions
Right-of-use asset recognized with corresponding lease liability	$	509			$	521			$	157			$	215			$	3,304
Purchase of property and equipment and Intangible assets	$	1,030			$	272			$	1,030			$	272			$	1,955

NON-IFRS MEASURES
	Six months period ended								Three months period ended								Year ended
	June 30,								June 30,								December 31,
	2025				2024				2025				2024				2024
	In thousands
Net income	$	11,340			$	6,791			$	7,376			$	4,426			$	14,462
Taxes on income		1,026				137				(1,623	)			63				(1,128	)
Financial expense (income), net		2,500				2,751				1,318				1,151				6,717
Depreciation and amortization expense		7,357				6,466				3,746				3,229				13,218
Non-cash share-based compensation expenses		270				476				95				235				867
Adjusted EBITDA	$	22,493			$	16,621			$	10,912			$	9,104			$	34,136

FAQ

What were Kamada's (KMDA) Q2 2025 earnings results?

Kamada reported Q2 2025 revenues of $44.8 million (up 5% YoY) and net income of $7.4 million ($0.13 per share), compared to $4.4 million in Q2 2024.

What is Kamada's revenue guidance for 2025?

Kamada maintains its 2025 revenue guidance of $178-182 million and raised adjusted EBITDA guidance to $40-44 million.

What is the expected revenue from Kamada's new Houston plasma collection center?

The Houston plasma collection center has an estimated annual revenue potential of $8-10 million at full capacity, with approximately 50,000 liters of annual plasma collection capacity.

How much cash does Kamada (KMDA) have as of Q2 2025?

Kamada reported $66.0 million in cash and cash equivalents as of June 30, 2025, down from $78.4 million at the end of 2024 due to a special dividend payment.

What was Kamada's profit margin in H1 2025?

Kamada achieved a gross margin of 45% and an adjusted EBITDA margin of 25% in the first half of 2025.