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 global biopharmaceutical company focused on specialty plasma-derived therapies and other biopharmaceutical products for rare and serious conditions. Its news flow reflects activity across commercial operations, clinical programs, plasma collection, and corporate strategy.
On this page, readers can follow Kamada news related to its proprietary products such as KEDRAB®, CYTOGAM®, GLASSIA®, WINRHO SDF®, VARIZIG® and HEPAGAM B®, as well as KAMRAB®, KAMRHO (D)® and equine-based anti-snake venom products. Company announcements frequently discuss revenue trends, adjusted EBITDA, and guidance, highlighting the contribution of its Proprietary Products and Distribution segments, including biosimilar launches in Israel and supply agreements in markets such as Canada.
News items also cover clinical and post-marketing research, including updates on the InnovAATe Phase 3 trial of Inhaled AAT for Alpha-1 Antitrypsin Deficiency and its subsequent discontinuation following an interim futility analysis, as well as the SHIELD study evaluating CYTOGAM in high-risk kidney transplant recipients. Regulatory and operational milestones, such as FDA approval of the Houston, Texas plasma collection center and expansion of plasma collection capacity across Kamada’s three Texas sites, are recurring topics.
Investors and followers of KMDA stock can use this feed to track quarterly and annual financial results, guidance updates, tender awards like the Canadian Blood Services supply extension, and participation in healthcare and investor conferences. Regularly reviewing this page provides a consolidated view of Kamada’s commercial progress, R&D developments, and strategic initiatives as reported in its press releases and related filings.
Kamada Ltd. (NASDAQ: KMDA) announced changes in its Board of Directors. Lilach Asher Topilsky, currently a Director and Senior Partner at FIMI Opportunity Funds, has been appointed Chairman, succeeding Leon Recanati, who remains a Director. Additionally, Ari Shamiss, a veteran hospital executive, has joined the Board. The leadership transition comes as Kamada boasts two FDA-approved products and a promising clinical pipeline, including an immunoglobulin product for COVID-19 under development. FIMI, the largest shareholder, recently made a significant investment in Kamada.
Kamada Ltd. (NASDAQ: KMDA) reported a 6% decrease in Q2 revenues, generating $33.1 million, compared to $35.3 million in 2019. However, H1 2020 revenues rose 7% to $66.4 million. Net income for Q2 was $3.5 million ($0.08/share), down from $6.1 million in Q2 2019. The company is developing a plasma-derived IgG product for COVID-19, with initial batches completed and a clinical trial underway. Cash position stands strong at $104.7 million. The full-year revenue guidance is maintained at $132 million to $137 million.