|
Investor Relations: Philippe
Niemetz
PAN Consultants, Ltd. Tel:
800-477-7570
Tel: 212-344-6464 Fax:
212-618-1276
e-mail:p.niemetz@panconsultants.com |
Joseph M. Cummins, DVM, PhD Amarillo
Biosciences, Inc.
Tel: 806-376-1741 x 13 Fax:
806-376-9301
e-mail:jcummins@amarbio.com |
Amarillo Biosciences Appoints Kimball Miller, MD as Medical Director
Amarillo, Texas January 16, 2008 — Amarillo
Biosciences, Inc. (OTCBB: AMAR) today announced that it had appointed
Kimball Miller, MD its Medical Director. Dr. Miller will assist
the Company with all its human clinical trials; including the human influenza
studies that will be conducted in Australia and the USA .
Kimball Austin Miller, MD, MSHA is an academic, medical clinician, health
care administrator, management consultant and primary care provider with
more than 20 years’ experience in clinical practices ranging from
small adolescent groups to the Mayo Clinic. Dr. Miller has served
in academic faculty positions in several medical and business schools,
as a medical director of clinical sections in large multispecialty practices,
as an administrator of a physician-hospital organization, as well as
the chief medical officer of a multistate provider sponsored HMO.
“Dr. Kimball Miller will aid Amarillo Biosciences in its
human clinical trials and consult with us as to the best possible means
to insure that our studies are conducted in the most efficient manner
possible,” said Dr. Joseph M. Cummins, President and CEO, ABI. “With
Dr. Miller’s contribution, we expect to accelerate the process
of obtaining FDA approval for our low-dose oral interferon.”
About Amarillo Biosciences, Inc.
Amarillo Biosciences, Inc. is
a U.S. biotechnology firm operating in global partnership with the Hayashibara
Group, which also holds 12% of Amarillo Biosciences’ shares and has provided over $18 million
in loans, grants and equity investments. The company's primary focus
is extensive and ongoing R&D into the use of low-dose, orally administered
interferon as a treatment for a variety of conditions, including Sjogren's
syndrome, Behcet’s disease, and opportunistic infections in patients
who are HIV positive. In its 23-year history, the company has invested
nearly $38 million to establish oral interferon as a therapeutic agent.
The majority of those funds were invested in clinical trials in an effort
to achieve FDA approval for interferon. Additional information is available
at http://www.amarbio.com/.
Except for the historical information contained herein, the matters
discussed in this news release are forward-looking statements that involve
risks and uncertainties, including uncertainties related to product development,
uncertainties related to the need for regulatory and other government
approvals, dependence on proprietary technology, uncertainty of market
acceptance of oral interferon or the Company’s other product candidates
and other risks detailed from time to time in the Company’s filings
with the Securities and Exchange Commission. In particular, see “Item
1. Description of Business” of the Company’s Form 10-KSB
for the year ended December 31, 2006. --END--