Immunotech Laboratories, Inc. Announces Successful Completion of Phase I & Phase II Field Trials of the Company’s Patented ...
2014年8月28日 - 10:00PM
ビジネスワイヤ(英語)
Immunotech Laboratories, Inc. (OTCMARKETS:IMMB) Immunotech
Laboratories, Inc. announced today that the Phase I and Phase II
field trials in Bulgaria of the Company’s HIV/AIDS and Hepatitis C
virus treatment (“ITV-1 Treatment”) have been successfully
completed. The clinical test are being conducted through Immunotech
Laboratories, BG (“IMMB-BG”) a 49% owned subsidiary of Immunotech
Laboratories. Since 2013, IMMB-BG hired and funded the Clinical
Research Organization (“CRO”) to conduct all preclinical and
monitoring Phase III clinical studies. The product for the
Bulgarian study was produced under GMP conditions by a U.S.
Contract Manufacturing Facility.
The toxicity testing of ITV-1 on animals has also been
successfully completed as well as a complete pharmacokinetics (PK)
analysis of how the treatment is distributed through the blood
system. The Company is making its application for the permit to
move to Phase III full scale clinical testing on patients. The
initial testing will begin upon receipt of the Phase III permit
which the Company expects to receive within 60 days of acceptance
of the application.
About Immunotech Laboratories, Inc.
Headquartered in Monrovia, CA, Immunotech Laboratories is a drug
development company committed to the commercialization of its
proprietary proteins for the treatment of debilitating infectious
diseases. The Company strives to become a leader in
immuno-therapeutic treatment and prevention of HIV/AIDS, Cancer and
other immuno related disorders.
For more information visit: http://www.immunotechlab.com
Safe Harbor Statement: This news release contains
forward-looking statements that involve risks and uncertainties
associated with financial projections, budgets, milestone
timelines, clinical development, regulatory approvals, and other
risks described by Immunotech Laboratories, Inc. from time to time
in its periodic reports filed with the SEC. IPF is not approved by
the US Food and Drug Administration or by any comparable regulatory
agencies elsewhere in the world. While Immunotech Laboratories
believes that the forward-looking statements and underlying
assumptions contained therein are reasonable, any of the
assumptions could be inaccurate, including, but not limited to, the
ability of Immunotech Laboratories to establish the efficacy of IPF
in the treatment of any disease or health condition, the
development of studies and strategies leading to commercialization
of IPF in the United States, the obtaining of funding required to
carry out the development plan, the completion of studies and tests
on time or at all, and the successful outcome of such studies or
tests. Therefore, there can be no assurance that the
forward-looking statements included in this release will prove to
be accurate. In light of the significant uncertainties inherent in
the forward-looking statements included herein, Immunotech
Laboratories or any other person that the objectives and plans of
Immunotech Laboratories will be achieved should not regard the
forward-looking statements as a representation.
Immunotech Laboratories, Inc.GIC813-213-8156Houston, Texas
Immunotech Laborator (CE) (USOTC:IMMB)
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Immunotech Laborator (CE) (USOTC:IMMB)
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から 4 2024 まで 4 2025
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