EXHIBIT 99.1

News Release

February 11, 2015

Kamada Reports 2014 Fourth Quarter and Full Year Financial Results

Posts Record Revenue for the Fourth Quarter and Generates Net Profit

Conference call begins today at 8:30 a.m. Eastern time

NESS ZIONA, Israel (February 11, 2015) – Kamada Ltd. (NASDAQ and TASE: KMDA), a plasma-derived protein therapeutics company focused on orphan indications, announces financial results for the three and 12 months ended December 31, 2014.

Financial highlights of the 2014 fourth quarter include:

· Record total revenues of $25.8 million compared with $24.4 million for the fourth quarter of 2013 and $17.1 million for the third quarter of 2014;

· Gross profit of $8.0 million compared with $8.9 million in the year-ago fourth quarter and $4.4 million for the third quarter of 2014; and

· Adjusted net income of $2.4 million compared with $2.0 in the year-ago fourth quarter and adjusted net loss of $1.9 in the third quarter of 2014.

Clinical highlights of the 2014 fourth quarter and recent weeks include:

· Reported additional positive data from the Company’s ongoing open-label Phase 1/2 clinical trial extension study with its intravenous Alpha1-Proteinase Inhibitor–Human (AAT) to treat recently diagnosed type 1 diabetes (T1D) pediatric patients;

· Reported encouraging discussions with the European co-rapporteurs regarding a European filing for the Company’s inhaled AAT to treat alpha-1 antitrypsin deficiency (AATD);

· Reported that interim data from a Phase 1/2 clinical study of the Company’s proprietary AAT for the treatment of graft-versus-host-disease (GvHD) conducted by the Fred Hutchinson Cancer Research Center were highlighted in a poster presentation at the 56th American Society of Hematology Annual Meeting; and

· Granted orphan drug designation by the U.S. Food and Drug Administration (FDA) for the Company’s intravenous AAT to treat GvHD.

Management Commentary

“We are very pleased with our progress in the fourth quarter of 2014.  Record quarterly revenues underscore our ability to execute to plan and grow our core business, while generating significant cash flow supports our robust clinical development program,” stated David Tsur, co-founder and Chief Executive Officer of Kamada.

“Our strong partnership with Baxter, including the committed orders for the coming years and the consistent increase in the number of patients treated by Glassia, up 25% in 2014, gives us good visibility into the growing number of patients treated with Glassia worldwide, which weexpect will double within the next four to five years.  This growth is expected to provide the platform from which we can achieve our mid-term revenue goal of $100 million in 2017, including approximately 75% growth in the Proprietary Products Segment.

“Our clinical development programs continue to generate favorable data from studies with our intravenous AAT to treat newly diagnosed type 1 diabetes and to treat GvHD, both orphan indications with significant unmet medical need.”

“In addition, we expect to report data from our anti-rabies immunoglobulinU.S. Phase 2/3 clinical trial for the post-exposure prophylactic treatment of rabies by mid-year, and subject to positive data, to file a Biologics License Application (BLA) with the FDA in the second half of 2015.   We have a strategic partnership for the clinical development, sales and marketing of this product in the U.S. with Kedrion Biopharma.  With favorable data and a high-quality product, we look forward to Kedrion’s commercialization activities in an exciting market opportunity.”

“We remain very encouraged by the constructive dialogue we’ve had with the European co-rapporteurs regarding our plans to file for approval with the European Medicines Agency (EMA) for our inhaled AAT as a treatment for AATD.  They agreed that the application fulfills the requirements relating to unmet medical need and benefit to public health, and that it may meet the scope of Conditional Approval if the company convincingly proves the positive benefit-risk balance of the product by the time of Marketing Authorization Application (MAA) filing.  The co-rapporteurs have requested the addition of supplemental data analyses that may address the benefit-risk balance and support the already available safety and efficacy data.  We are in the process of conducting the additional analyses and plan to file the MAA with the EMA in this year’s fourth quarter.  In addition, we expect to present the complete data set from the Phase 2/3 clinical study in advance of the upcoming American Thoracic Society Annual Meeting in May 2015,” concluded Mr. Tsur.

Fourth Quarter Financial Results

Total revenues for the fourth quarter of 2014 of $25.8 million compare with $24.4 million for the fourth quarter of 2013.  Revenue from the Proprietary Products Segment was $20.0 million compared with $9.1 million in the third quarter of this year and $18.6 million in the year-ago quarter, with the changes being primarily due to ordering patterns of Glassia from Baxter.  Revenue from the Distributed Product Segment remained steady at $5.8 million during the fourth quarter of both 2014 and 2013.

Research and development (R&D) expenses in the fourth quarter of 2014 of $3.4 million decreased from $3.6 million in the fourth quarter of 2013 and from $4.2 million in the third quarter of 2014, due to changes in activity in support of various clinical studies including three key clinical trials, the closing and analysis of the European Phase 2/3 study of inhaled AAT, as well as a decrease in the fourth quarter of facility costs allocated to R&D use compared with prior quarters.

Selling, general and administrative (SG&A) expenses in the fourth quarter of 2014 of $2.4 million decreased from $2.9 million in the fourth quarter of 2013, largely due to a decrease in expenses for doubtful debt.

Gross profit for the fourth quarter of 2014 was $8.0 million compared with $8.9 million in the fourth quarter of 2013 and $4.4 million in the third quarter of 2014.  The decline versus the prior year was a result of lower revenue and product mix within the Distributed Product Segment, as well as excess capacity in the Proprietary Products Segment during the year leading to lower profitability in the short term and one time sales efforts in certain markets.

Gross margin declined to 31% from 36% in the fourth quarter of 2013 and increased from 26% in the third quarter of 2014.

For the fourth quarter of 2014, the Company reported operating income of $2.2 million compared with operating income of $2.4 million for the fourth quarter of 2013 and an operating loss of $2.5 million in the third quarter of 2014.  Net income for the fourth quarter of 2014 was $1.7 million or $0.05 per diluted share, compared with net income of $1.6 million or $0.04 per diluted share for the same period in 2013 and a net loss of $2.9 million or $0.09 per share in the third quarter of 2014.  Adjusted net income for the fourth quarter of 2014 was $2.4 million compared with adjusted net income of $2.0 million for the same period in 2013 and an adjusted net loss of $1.9 million in the third quarter of 2014.

Adjusted EBITDA for the fourth quarter of 2014 was $3.6 million compared with $3.5 million for the fourth quarter of 2013 and negative $0.8 million in the third quarter of 2014.

2014 Financial Results

Total revenues for 2014 were $71.9 million, compared with $70.6 million for 2013.  Revenue in the Proprietary Products Segment was $45.2 million for the year, compared with $50.7 million for 2013, which included a $4.5 million milestone payment. 2014 revenue in the Distributed Product Segment increased 34% to $26.7 million from $20.0 million in 2013. 

Gross profit for 2014 decreased to $15.6 million from $26.4 million in 2013, with gross margin declining to 22% from 37%.  Excluding the $3.0 million inventory write-off in the second quarter of 2014 and the $4.5 million milestone payment in the second quarter of 2013, gross profit for 2014 decreased to $18.6 million from $21.9 million in the prior year.

Operating loss for 2014 of $10.9 million compares with operating income of $3.7 million for 2013.  Net loss for the 2014 year was $12.6 million or $0.35 per share, compared with net income of $0.5 million or $0.01 per diluted share for the prior year. 

Adjusted EBITDA for 2014 was negative $4.4 million, compared with positive $9.4 million for 2013.

Balance Sheet Highlights

As of December 31, 2014, Kamada had cash, cash equivalents and short-term investments of $51.9 million, compared with $74.2 million as of December 31, 2013. During 2014, the Company used $9.9 million in cash to fund operations, $3.1 million for capital expenditures and $7.7 million for repayment of convertible debt.

Conference Call

Kamada management will host an investment community conference call today at 8:30 a.m. Eastern time to discuss these results and answer questions.  Shareholders and other interested parties may participate in the conference call by dialing 888-803-5993 (from within the U.S.), 706-634-5454 (from outside the U.S.) or 1-809-457-877 (toll-free from Israel) and entering the conference identification number: 72411145.

A replay of the call will be accessible beginning two hours after its completion through February 17, 2015 by dialing 855-859-2056 (from within the U.S.) or 404-537-3406 (from outside the U.S.) and entering the conference identification number: 72411145. The call will also be archived for 90 days at www.streetevents.com and www.kamada.com.

About Kamada

Kamada Ltd. is focused on plasma-derived protein therapeutics for orphan indications, and has a commercial product portfolio and a robust 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 proteins.   AAT is a protein derived from human plasma with known and newly-discovered therapeutic roles given its immunomodulatory, anti-inflammatory, tissue-protective and antimicrobial properties. The Company’s flagship product is Glassia®, the first and only liquid, ready-to-use, intravenous plasma-derived AAT product approved by the U.S. Food and Drug Administration. Kamada markets Glassia in the U.S. through a strategic partnership with Baxter International.  In addition to Glassia, Kamada has a product line of nine other injectable pharmaceutical products that are marketed through distributors in more than 15 countries, including Israel, Russia, Brazil, India and other countries in Latin America, Eastern Europe and Asia.  Kamada has five late-stage plasma-derived protein products in development, including an inhaled formulation of AAT for the treatment of AAT deficiency that completed pivotal Phase 2/3 clinical trials in Europe and entered Phase 2 clinical trials in the U.S.   Kamada also leverages its expertise and presence in the plasma-derived protein therapeutics market by distributing 10 complementary products in Israel that are manufactured by third parties.

Cautionary Note Regarding Forward-Looking Statements

This release includes forward-looking statements within the meaning of Section 27A of the U.S. Securities Act of 1933, as amended, 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, such as statements regarding assumptions and results related to financial results forecast, commercial results, timing and results of clinical trials and EMA and U.S. FDA authorizations.  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, unexpected results of clinical trials, delays or denial in the U.S. FDA or the EMA approval process, additional competition in the AATD market or further regulatory delays.  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:

Gil Efron CFO     ir@kamada.com	Anne Marie Fields LHA 212-838-3777
	afields@lhai.com

Tables to Follow

Consolidated Balance Sheets

	As of December 31,
	2014			2013
	In thousands
Current Assets
Cash and cash equivalents	$	14,546		$	59,110
Short-term investments		37,350			15,067
Trade receivables		17,993			17,882
Other accounts  receivables		2,359			3,694
Inventories		25,423			21,933
		97,671			117,686
Non-Current Assets
Long-term inventories					85
Property, plant and equipment, net		21,769			21,443
Long term assets		179			165
		21,948			21,693
		119,619			139,379
Current Liabilities
Short term credit and Current maturities of convertible debentures		7,492			8,718
Trade payables		16,530			14,093
Other accounts payables		4,045			4,313
Deferred revenues		2,821			5,454
		30,888			32,578
Non-Current Liabilities
Convertible debentures		-			7,498
Employee benefit liabilities, net		722			827
Deferred revenues		7,015			8,506
		7,737			16,831
Shareholder's Equity
Kamada Ltd.'s shareholders' equity:
Ordinary shares of NIS 1 par value: Authorized - 60,000,000 ordinary shares; Issued and outstanding    – 35,988,563 and 35,959,939 shares at December 31, 2014 and    2013, respectively		9,208			9,201
Additional paid in capital		158,417			157,100
Conversion option in convertible debentures		1,147			2,218
Capital reserve due to translation to presentation currency		(3,490	)		(3,490	)
Capital reserve from hedges		(116	)		156
Available for sale reserve		10			(27	)
Capital reserve from share-based payments		8,783			5,189
Capital reserve from employee benefits		(81	)		(129	)
Accumulated deficit		(92,884	)		(80,248	)
		80,994			89,970
	$	119,619		$	139,379

Consolidated Statements of Comprehensive Income

	For the year ended December 31,						For the 3 months ended December 31,
	2014			2013			2014			2013
	In thousands
Revenues from proprietary products	$	45,249		$	50,658		$	19,964		$	18,635
Revenues from distribution		26,676			19,965			5,827			5,797
Total revenues		71,925			70,623			25,791			24,432
Cost of revenues from proprietary products		32,900			27,104			12,455			10,587
Cost of revenues from distribution		23,406			17,112			5,288			4,979
Total cost of revenues		56,306			44,216			17,743			15,566
Gross profit		15,619			26,407			8,048			8,866
Research and development expenses		16,030			12,745			3,417			3,578
Selling and marketing expenses		2,898			2,100			857			546
General and administrative expenses		7,593			7,862			1,582			2,344
Operating income (loss)		(10,902	)		3,700			2,192			2,398
Financial income		1,611			289			572			44
Expense in respect of currency exchange and translation differences and derivatives instruments, net		(199	)		(369	)		(293	)		(203	)
Financial expense		(3,094	)		(3,153	)		(744	)		(679	)
Income before  taxes on income		(12,583	)		467			1,727			1,560
Taxes on income		52			24			(18	)		9
Net Income (loss)		(12,636	)		443			1,745			1,551
Other Comprehensive Income:
Net gain on available for sale		37			(27	)		(32	)		(27	)
Actuarial net gain of defined benefit		48			12			48
Net gain on cash flow hedge		(272	)		(73	)		(61	)
Total comprehensive income ( loss)	$	(12,823	)	$	355		$	1,700		$	1,524
Income  per share attributable to equity holders of the Company:
Basic income (loss) per share	$	(0.35	)	$	0.01		$	0.05		$	0.04
Diluted income (loss) per share	$	(0.35	)	$	0.01		$	0.05		$	0.04
Weighted-average number of ordinary shares used to compute income (loss) per share attributable to equity holders:
Basic		35,971,335			32,714,631			35,984,299			35,863,463
Diluted		35,971,335			33,674,337			37,324,697			36,179,510

Adjusted EBITDA

	For the year ended December 31					Three months ended December 31
	2014			2013		2014			2013
	Thousands of US dollar
Net income (loss)	$	(12,636	)	$	443	$	1,745		$	1,551
Income tax expense (income)		52			24		(18	)		9
Financial expense, net		1,483			2,864		172			630
Depreciation and amortization expense		2,788			3,001		747			734
Share-based compensation charges		3,751			1,327		676			412
Expense in respect of translation differences and derivatives instruments, net		199			369		293			203
One time management compensation					1,386
Adjusted EBITDA	$	(4,363	)	$	9,414	$	3,615		$	3,539

Adjusted net income (loss)

	For the year ended December 31					Three months ended December 31
	2014			2013		2014		2013
	Thousands of US dollar
Net income (loss)	$	(12,636	)	$	443	$	1,745	$	1,551
Share-based compensation charges		3,751			1,327		676		412
One time management compensation					1,386
Adjusted net income (loss)	$	(8,885	)	$	3,156	$	2,421	$	1,963

Consolidated Statements of Cash Flows

	For the year ended December 31,						For the 3 months ended December 31,
	2014			2013			2014			2013
	In thousands
Cash Flows from Operating Activities
Net Income (loss)	$	(12,636	)	$	443		$	1,745		$	1,551
Adjustments to reconcile net loss to net cash provided by operating activities:
Adjustments to the profit or loss items:
Depreciation and amortization		2,788			3,001			747			734
Financial expenses, net		1,682			3,233			465			833
Cost of share-based payment		3,751			1,327			676			412
Income tax expense		52			24			(18	)		9
Loss from sale of property and equipment		(2	)		73			(2	)
Change in employee benefit liabilities, net		(57	)		121			(120	)		(27	)
		8,214			7,779			1,748			1,961
Changes in asset and liability items:
Increase in trade receivables		(1,347	)		(3,445	)		(3,524	)		(462	)
Decrease (Increase)  in other accounts receivables		(50	)		(911	)		(345	)		164
Decrease (increase)  in inventories		(3,490	)		(1,182	)		126			511
Decrease (increase)  in deferred expenses		1,209			(1,231	)		(17	)		(1,387	)
Increase in trade payables		3,261			1,579			2,151			4,868
Increase (decrease)   in other accounts payables		(344	)		731			342			85
Increase (decrease) in deferred revenues		(4,125	)		(6,270	)		(1,653	)		(3,132	)
		(4,886	)		(10,729	)		(2,920	)		647
Cash paid during the year for:
Interest paid		(1,210	)		(1,968	)		(247	)		(395	)
Interest received		758			663			373			252
Taxes paid		(158	)		(42	)		-			(4	)
		(610	)		(1,347	)		126			(147	)
Net cash  provided by (used in)operating activities	$	(9,918	)	$	(3,854	)	$	699		$	4,012

Consolidated Statements of Cash Flows

	For the Year ended December 31,						For the 3 months ended December 31,
	2014			2013			2014			2013
	In thousands
Cash Flows from Investing Activities
Short-term investments	$	(23,746	)	$	1,732		$	2,878		$	(10,427	)
Purchase of property and equipment and intangible assets		(3,076	)		(5,643	)		(720	)		(1,218	)
Restricted cash, net											(3	)
Proceeds from sale of property and equipment		3			8			3			8
Net cash  provided by (used in)investing activities		(26,819	)		(3,903	)		2,161			(11,640	)
Proceeds from exercise of warrants and options		88			562			23			17
Proceeds from issuance of ordinary shares, net					52,953						(146	)
Short term credit from bank and others, net					(12	)					(6	)
Repayment of convertible debentures		(7,728	)		(4,295	)		(7,728	)		(4,295	)
Net cash provided by (used in) financing activities		(7,640	)		49,208			(7,705	)		(4,430	)
Exch Exchange differences on balances of cash and cash equivalent		(187	)		793			1,320			(64	)
Increase (Decrease) in cash and cash equivalents		(44,564	)		42,244			(3,525	)		(12,122	)
Cash and cash equivalents at the beginning of the year/period		59,110			16,866			18,071			71,232
Cash and cash equivalents at the end of the year /period	$	14,546		$	59,110		$	14,546		$	59,110
Significant non-cash transactions
Purchase of Property, Plant and equipment and intangible assets on credit	$	-		$	-		$	-		$	-
Issuance expenses accrued in other accounts payable	$	-		$	151		$	-		$	(84	)
Exercise of warrants presented as liability	$	-		$	23		$	-		$	-
Exercise of convertible debentures into shares	$	7		$	6,507		$	-		$	6,472