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The
Food and Drug Administration has recently given a Texas
laboratory - which isolated acemannan in 1984 - permission
to begin human trials on HIV and AIDS patients using their
trademarked acemannan compound, reported the Fall 1994
issue of The Journal, a publication of the IASC.
Phase
I of the trials will begin in a few months and follow on
the heels of a Canadian government -sponsored Phase III
study, which used oral acemannan in their human trials,
conducted at the Texas Health Science Center in Houston.
They also conducted a "safety study" using
injectable acemannan, the publication reported.
"As
The Journal understands the action of acemannan, it is not
a 'cure' for AIDS," the publication said.
"Rather, it arrests the syndrome's progression,
enabling the patient to live out a more or less normal
life span, when used in conjunction with AZT."
The
Texas laboratory is not releasing details of its treatment
program.
Ian
Tizard of Texas A&M University at College Station, who
is on temporary assignment at the University of California
at San Francisco, reported in the August 21, 1991 issue of
Medical Tribune that acemannan, a compound of Aloe vera,
"helps AZT (the AIDS drug) block the human
immunodeficiency virus from spreading to other cells, and
may interfere with HIV replication."
Outrageous:
The FDA approved intravenous administration of Aloe (i.e.
acemannan) in a very successful study (circa 1993/1994);
yet, the FDA takes the public position that intravenous
administration of aloe is against the law --- What law?
More
outrageous: When two separate Freedom of Information
Requests were submitted to the FDA to obtain information
regarding the FDA's involvement in human studies of Aloe
(i.e. acemannan). The FDA replied:
"The
information is proprietary …"
"We have no information …"
WHAT
IS THE FDA COVERING-UP?
WHO IS THE FDA COVERING FOR?
The
Maryland Attorney General still refuses to allow T-UP,
Inc. to provide information to the public about
concentrated aloe's many potential benefits:
- In
spite of numerous successful studies, including FDA
approved Phase I Safety investigations
- In
spite of the fact that one company has submitted an
investigative new drug (IND) application to the FDA
for the testing of aloe (i.e. acemannan) in humans;
that IND has still not been approved six years after
being submitted.
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