Kamada and Kedrion Biopharma Announce Publication of Results from the Registration Study of KEDRAB® (Rabies Immune Globulin [Human]) in Human Vaccines & Immunotherapeutics Medical Journal
Kamada Ltd. - Ordinary Shares (KMDA)
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Source: GlobeNewswire
The Successful Study was Basis for U.S. Food & Drug Administration Approval of KEDRAB® in 2017 Post-Marketing U.S. Pediatric Study Data Expected in 2H ‘2020 Abstract will be Presented at the Upcoming 2019 Rabies In The Americas (RITA) Conference REHOVOT, Israel and FORT LEE, N.J., Oct. 29, 2019 (GLOBE NEWSWIRE) -- Kamada Ltd. (NASDAQ: KMDA; TASE: KMDA) and Kedrion Biopharma two leading plasma-derived protein therapeutics companies, announced today that the results of their registration study for KEDRAB® [Rabies Immune Globulin (Human)] were published in Human Vaccines & Immunotherapeutics, a peer-reviewed medical journal covering research into vaccines and immunotherapeutics in humans. The full article titled is “Safety and efficacy results of simulated post-exposure prophylaxis with human immune globulin (HRIG; KEDRAB) co-administered with active vaccine in healthy subjects: a comparative phase 2/3 trial," The 2017 U.S. Food and Drug Administration (FDA) approval of KEDRAB for
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- Kamada Reports Continued Profitable Growth with Strong Third Quarter and Nine Month 2024 Financial Results; Raises Full-Year Profitability GuidanceGlobeNewswire
- Kamada to Announce Third Quarter and Nine-Months Ended September 30, 2024 Financial Results and Host Conference Call on November 13, 2024GlobeNewswire
- Kamada to Present at the Stifel 2024 Healthcare ConferenceGlobeNewswire
KMDA
Earnings
- 11/13/24 - In-Line
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Analyst Actions
- 11/14/24 - HC Wainwright
KMDA
Sec Filings
- 12/11/24 - Form 6-K
- 11/14/24 - Form SC
- 11/13/24 - Form 6-K
- KMDA's page on the SEC website