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Senetek Initiates Clinical Trials of Pyratine 6 for Acne Rosacea



    Senetek PLC (OTCBB: SNTKY), a life sciences product development
    company targeting the science of aging, has initiated clinical trials
    of its Pyratine 6 compound (PRK 124) for Acne Rosacea after evaluating
    positive results from a comparison of separate clinical trials of
    Pyratine 6 and Kinetin, Senetek's original anti-aging active
    ingredient.

    An independent comparative analysis evaluated the effectiveness of
    Senetek's second-generation patented cytokinin, Pyratine 6 (PRK 124)
    relative to its original anti-aging active ingredient, Kinetin. The
    analysis compared results of separate clinical studies conducted at
    the University of California, Irvine (Kinetin) and at the independent
    research laboratory RCTS, Inc. in Irving, Texas (Pyratine 6). The
    subjects in the Pyratine 6 clinical trial scored significantly higher
    on each measure than those in the Kinetin study throughout the 12
    weeks of evaluation. In some measures the comparison was particularly
    notable, such as fine wrinkles (22% improvement with Pyratine 6 vs. 2%
    improvement with Kinetin after eight weeks), skin roughness (86%
    improvement with Pyratine 6 vs. 35% improvement with Kinetin after
    eight weeks) and overall skin aging (24% vs. 3% after eight weeks).

    The Pyratine 6 study also featured additional evaluative
    methodologies not included in the Kinetin study, such as the NOVA
    Dermal Phase Meter for measuring the skin's moisture content, and
    expert evaluations of reductions in erythema (redness) and acne
    lesions. The NOVA apparatus measured increases in skin moisture
    content of 35% and 41% after eight and twelve weeks, respectively. The
    evaluations found 42% and 62% reductions in erythema after two and
    four weeks, respectively, and a 45% reduction in acne lesions after
    twelve weeks. Pyratine 6 was well tolerated by all subjects, producing
    no measurable skin irritation or signs of allergic contact dermatitis
    with twice-daily application over the 12 week study period.

    Frank Massino, Chief Executive Officer of Senetek commented, "The
    data collected through the comparative analysis of Pyratine 6 and
    Kinetin has given us significant reason to focus our efforts on taking
    the strategic steps necessary to launch Pyratine 6 commercially as an
    anti-aging compound as well as initiate clinical trials to prove that
    Pyratine 6 can also be used as an effective treatment for Acne
    Rosacea. Following our success with Kinetin, we are excited about the
    potential for Pyratine 6 as it presents yet another valuable
    opportunity for our Company."

    Enrollment has begun on the new Senetek sponsored Institutional
    Review Board (IRB)-approved pilot clinical study of Pyratine 6 for
    treatment of Rosacea, to be conducted at the University of California
    at Irvine. The comparative analysis results also have influenced one
    of the Company's prospective licensees, a major cosmetic company, to
    commence separate clinical trials of Pyratine 6 for Acne Rosacea and
    for skin whitening.

    Acne Rosacea is a common chronic dermatosis characterized by
    inflammatory lesions and persistent erythema (redness) conservatively
    estimated to afflict some 16 million people in the U.S. and 45 million
    people worldwide. Acne Rosacea is currently primarily treated with
    oral antibiotics such as tetracycline and erythromycin and topical
    antibiotics such as metronidazole, which involve long-term
    tolerability and other health concerns.

    About Senetek PLC

    Senetek is a life sciences-driven product development and
    licensing company with a portfolio of intellectual properties
    targeting the science of aging, including skincare and dermatological
    therapeutics, erectile dysfunction and nutrition. Senetek holds
    patents on the use of Kinetin and its analog Zeatin, naturally
    occurring cytokinins that have proven effective in improving the
    appearance of aging skin with virtually none of the side effects
    associated with acid-based active ingredients, which it has licensed
    to Valeant Pharmaceuticals International, and on a number of second
    generation cytokinins and other plant-derived compounds. Senetek's
    researchers at the University of Aarhus in Denmark also are
    collaborating with a broad range of academic and government-based
    research enterprises, including The Institute of Experimental Botany
    of the Czech Academy of Sciences, and with the Department of
    Dermatology, University of California at Irvine, to identify and
    evaluate additional new biologically active compounds for this high
    growth field. In addition, Senetek has entered into exclusive licenses
    for Europe and North America, respectively, for its patented
    combination drug treatment for erectile dysfunction, Invicorp(R), has
    an exclusive manufacturing distributorship for its proprietary
    diagnostic monoclonal antibodies, and recently sold, with retained
    rights of profit participation, its patented drug delivery system,
    Reliaject(R).

    Visit Senetek PLC's Web site at http://www.senetekplc.com.

    Safe Harbor Statement

    This news release contains statements that may be considered
    'forward-looking statements' within the meaning of the Private
    Securities Litigation Reform Act, including those that might imply
    commercial potential and successful evaluation and development of new
    compounds. Forward-looking statements by their nature involve
    substantial uncertainty, and actual results may differ materially from
    those that might be suggested by such statements. Important factors
    identified by the Company that it believes could result in such
    material differences are described in the Company's Annual Report on
    Form 10-K/A for the year 2005. However, the Company necessarily can
    give no assurance that it has identified or will identify all of the
    factors that may result in any particular forward-looking statement
    materially differing from actual results, and the Company assumes no
    obligation to correct or update any forward-looking statements which
    may prove to be inaccurate, whether as a result of new information,
    future events or otherwise.