HST Global, Inc. Encouraged by FDA Approval of Dendreon’s Provenge
30 4월 2010 - 9:45PM
Business Wire
HST Global, Inc., (OTCBB:HSTC) today was encouraged by news of
the FDA approval of Dendreon Corp’s (NASDAQ: DNDN) Provenge drug
for prostate cancer. Provenge is aimed at certain men with advanced
prostate cancer and uses a man’s own immune system to fight the
disease.
Dr. Mitchell Gold, CEO and President of Dendreon stated "The FDA
approval of Provenge is a testament to the courage of the patients
and researchers who participated in our studies and is the
culmination of nearly 15 years of research and development by our
dedicated employees."
Ron Howell, President and CEO stated “We congratulate Dendreon
Corp on receiving the approval from the FDA, as this is a testament
to the perseverance and dedication of their entire corporate team.
We are encouraged by the FDA’s action in approving Provenge. HST is
committed to the acquisition and development of Health and Wellness
Centers offering proven alternative and immunotherapy drug
candidates that have shown high efficacy in the treatment of
various cancers.”
About HST Global, Inc.
HST Global, Inc. is an Integrated Biotechnology Health and
Wellness company that is developing and or acquiring a network of
Wellness Centers worldwide that are primarily focused on the
immunotherapy and alternative treatment of late stage cancer. In
addition, the company intends to acquire innovative products for
the treatment of late stage cancer. In this regard, the company
primarily focuses on immunotherapy and alternative product
candidates that are undergoing or have already completed
significant clinical testing for the treatment of late stage
cancer.
HST Global, Inc. wishes to inform readers that forward-looking
statements in this release are made pursuant to the "safe harbor"
provisions of the Private Securities Litigation Reform Act of 1995.
Readers are cautioned that such forward looking statements involve
risks and uncertainties including, without limitation, unforeseen
changes in the course of research and development activities and in
clinical trials by others; possible acquisitions of other
technologies, assets or businesses; possible actions by customers,
suppliers, competitors, regulatory authorities; and other risks
detailed from time to time in the Company's periodic reports filed
with the Securities and Exchange Commission.
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