Welcome to our dedicated page for Kamada news (Ticker: KMDA), a resource for investors and traders seeking the latest updates and insights on Kamada stock.
Kamada Ltd. (KMDA) is a leading biopharmaceutical company that specializes in plasma-derived protein therapeutics, targeting orphan indications. Utilizing its proprietary platform technology, Kamada excels in the extraction and purification of proteins from human plasma, producing highly-purified, liquid forms of alpha-1 antitrypsin (AAT) and other plasma-derived proteins. AAT is recognized for its immunomodulatory, anti-inflammatory, tissue-protective, and antimicrobial properties.
One of Kamada's flagship products is Glassia®, the first and only liquid, ready-to-use, intravenous plasma-derived AAT product approved by the U.S. Food and Drug Administration (FDA). Kamada markets Glassia in the U.S. through a strategic partnership with Baxter International. In addition to Glassia, Kamada offers a diverse product portfolio, including nine other pharmaceutical products distributed globally.
Kamada's robust late-stage product pipeline underscores its commitment to innovation in the specialty therapeutics market. The company operates through two primary segments: the Proprietary Products segment and the Distribution segment, with the majority of revenue derived from the Proprietary Products segment. Kamada's product categories encompass lung diseases, vaccines, hemophilia, immunoglobulins, critical care, and diagnostics.
Recently, Kamada announced a significant development in its strategic partnership with Kedrion Biopharma. The companies have executed a binding memorandum of understanding for an 8-year extension of the KEDRAB® US distribution agreement, starting January 2024. This agreement includes potential expansion of Kedrion's distribution of KEDRAB® beyond the U.S. and collaboration on expanding Kedrion products' distribution in Israel.
KEDRAB® is a Human Rabies Immune Globulin (HRIG) used for passive, transient post-exposure prophylaxis (PEP) of rabies infection, approved by the FDA in August 2017. The agreement signifies a significant milestone for Kamada, maximizing the future growth and value potential of this important product. Kamada continues to prioritize patient care and remains a pivotal player in the plasma-derived therapies sector.
Kamada (NASDAQ: KMDA) reported strong Q3 2024 financial results with revenues of $41.7 million, up 10% year-over-year, and nine-month revenues of $121.9 million, up 15%. Q3 Adjusted EBITDA reached $8.8 million, an 11% increase, while nine-month Adjusted EBITDA was $25.4 million, up 43%. The company raised its full-year Adjusted EBITDA guidance to $32-35 million and maintained revenue guidance of $158-162 million. Cash from operations reached $37.2 million in the first nine months, with $72.0 million available cash as of September 30. Kamada expanded operations with a new plasma collection center in Houston, TX.
Kamada (NASDAQ: KMDA) announced it will release its Q3 and nine-months financial results for the period ended September 30, 2024, before U.S. markets open on November 13, 2024. The company will host an investment community conference call at 8:30am Eastern Time on the same day. Shareholders can participate by dialing specific numbers for U.S., Israel, and International access. The call will also be available via webcast.
Kamada (NASDAQ: KMDA; TASE: KMDA.TA), a global biopharmaceutical company specializing in rare and serious conditions and plasma-derived products, announced its participation in the Stifel 2024 Healthcare Conference in New York. CEO Amir London will deliver a corporate overview on November 18, 2024, at 10:55 a.m. ET. The event will be held from November 18-19, 2024. Investors can arrange one-on-one meetings through Stifel representatives, and a live webcast will be available on Kamada's website with a 30-day replay option.
Kamada (NASDAQ: KMDA; TASE: KMDA.TA) has expanded its plasma collection operations by opening a new center in Houston, TX. The 12,000 square foot facility, operated by Kamada Plasma, is designed to support over 50 donor beds with an estimated annual collection capacity of 50,000 liters. It will collect both normal source plasma and specialty plasma, such as Anti-Rabies and Anti-D, and is expected to be one of the largest specialty plasma collection sites in the U.S.
The company plans to submit regulatory applications to the FDA and EMA in the first half of 2025 for approval of the Houston site. Kamada is also constructing a third plasma collection center in San Antonio, TX, set to open in the first half of 2025. Each center is projected to contribute annual revenues of $8 million to $10 million in sales of normal source plasma at full capacity.
Kamada reported strong financial results for Q2 and H1 2024. Revenues for Q2 2024 were $42.5 million, a 13% increase YoY, and $80.2 million for H1 2024, up 18% YoY. Q2 2024 adjusted EBITDA was $9.1 million, a 51% increase YoY, and $16.6 million for H1 2024, up 68% YoY. Net income for Q2 2024 was $4.4 million ($0.08 per share), and $6.8 million ($0.12 per share) for H1 2024. Kamada reiterated its full-year revenue guidance of $158-$162 million and adjusted EBITDA of $28-$32 million. Increased sales of KEDRAB and CYTOGAM in the US market were primary revenue drivers. Operating expenses rose due to higher S&M and R&D costs associated with marketing and the advanced Inhaled AAT clinical trial. Kamada generated $15.0 million of cash from operating activities in H1 2024 and held $56.5 million in cash and equivalents as of June 30, 2024. The company continues to explore new business opportunities and expects double-digit growth beyond 2024.
Kamada (NASDAQ: KMDA; TASE: KMDA.TA), a commercial stage global biopharmaceutical company specializing in rare and serious conditions and plasma-derived products, has announced its upcoming financial results release. The company will disclose its second quarter and first half 2024 financial results on August 14, 2024, before U.S. financial markets open.
Following the release, Kamada's management will host an investment community conference call at 8:30am Eastern Time on the same day. Shareholders and interested parties can participate via phone or webcast. The call will be archived on the company's website for 90 days.
Kamada reported strong first quarter 2024 financial results with a 23% increase in revenues and a 96% rise in profitability. The company's top-line growth was driven by U.S. sales of KEDRAB® and CYTOGAM®. Kamada increased its full-year revenue guidance to $158-162 million and adjusted EBITDA to $28-32 million. The company remains optimistic about its growth prospects beyond 2024.
Kamada will announce its first quarter 2024 financial results on May 8, 2024, before the U.S. financial markets open. The company, known for its rare condition treatments, will host an investment community conference call to discuss the results.
FAQ
What is the current stock price of Kamada (KMDA)?
What is the market cap of Kamada (KMDA)?
What does Kamada Ltd. specialize in?
What is Kamada's flagship product?
Who are Kamada's strategic partners?
What are the main product categories of Kamada?
What recent agreement has Kamada announced?
What is KEDRAB®?
How does Kamada derive its majority of revenue?
What are the key properties of alpha-1 antitrypsin (AAT)?
Which markets does Kamada distribute its pharmaceutical products?