




Healthcare Industry News: alpha-1
News Release - April 2, 2008
Kamada Announces That It Had Successfully Met the Primary Endpoint in Its US Phase III Clinical Trial with Intravenous AAT
NESS ZIONA, Israel--(HSMN NewsFeed)--Kamada (TASE:KMDA), a biopharmaceutical company developing, producing and marketing a line of specialty, life-saving therapeutics, announced today that it has successfully met the primary endpoint in the Phase III US clinical trials with its intravenous alpha-1 Antitrypsin (AAT). The product is used to treat hereditary AAT deficiency which leads to Congenital Emphysema.Tsur added that "The role of the alpha-1 Foundation, the US patient organization dedicated to advance the case of the AAT deficient patients, as well as the dedication of the clinicians who conducted the trial with a high level of efficiency, cannot be underestimated in reaching this milestone. The trial was truly a collaborative effort with significant contributions from all parties involved."
"On behalf of the alpha-1 Foundation we would like to congratulate Kamada for this outstanding achievement," said John W. Walsh, President and Chief Executive Officer of the alpha-1 Foundation, and added: "The alpha-1 Foundation estimates that more than 100,000 potential patients in the U.S. alone suffer from Congenital Emphysema (otherwise known as “Genetic COPD” or “alpha-1”), a disease caused by an inherited deficiency of AAT, with less than 10 percent currently diagnosed and many of them not treated. In light of Kamada's recent progress and the potential of its AAT product, many US alpha-1 patients eagerly anticipate the product launch."
About Kamada
Kamada manufactures a line of highly-safe specific immunoglobulins and other plasma-derived therapeutics, using sophisticated chromatographic purification technology. Licensed and marketed in more than 15 countries, several of these specialty biopharmaceuticals hold registered and pending patents and are in advanced clinical trials.
Source: Kamada
Issuer of this News Release is solely responsible for its
content.
Please address inquiries directly to the issuing company.