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Combining SNS01-T with Bortezomib Significantly Increases Its Effectiveness in Model of Multiple Myeloma BRIDGEWATER, N.J. (September 10 th , 2012) - Senesco Technologies, Inc. ("Senesco" or the "Company") (NYSE MKT: SNT

Key Takeaway: SNS01-T with Bortezomib Significantly Increases Its in Model of Multiple Myeloma N.J. (September 10th, 2012) - Senesco Technologies, Inc. ("Senesco" or the "Company") (NYSE MKT: SNT) announced today that the combination of bortezomib (the active component of VELCADE marketed

Full Press Release Details

SNS01-T with Bortezomib Significantly Increases Its
in Model of Multiple Myeloma
N.J. (September 10th, 2012) - Senesco Technologies, Inc. ("Senesco" or the "Company")
(NYSE MKT: SNT) announced today that the combination of bortezomib (the active component of VELCADE
marketed by Millennium, The Takeda Oncology Company) and SNS01-T, the subject of Senesco's
on-going multiple myeloma clinical study, performs significantly better than either treatment alone in mouse xenograft models.
"We are very pleased to have shown that SNS01-T enhances
the ability of bortezomib to inhibit tumor growth in the mouse model and could be a way to lower the dose and reduce the severity
of treatment-related side effects of bortezomib ," said Leslie J. Browne, Ph.D., President and CEO of Senesco. Dr. Browne
added, "Since treatment increasingly involves combination therapy, it is important that SNS01-T works well when added to
current multiple myeloma drugs."
Mice implanted in the flank with
human myeloma RPMI 8226 cells were treated with SNS01-T (0.375 mg/Kg IV), one of two different
dose levels of bortezomib (0.2, 0.5 mg/Kg IP) alone or in combination with SNS01-T (0.375 mg/Kg IV). SNS01-T and bortezomib were
administered twice weekly for 6 weeks. The study used an inactive nanoparticle as the control. SNS01-T monotherapy achieved 59%
tumor growth inhibition, which exceeded that of bortezomib alone at either the 0.2 mg/kg dose (22% inhibition) or at 0.5 mg/kg
(39 % inhibition). However, the combination of SNS01-T with 0.5 mg/kg of bortezomib resulted in 89 % tumor inhibition which was
significantly more effective than either SNS01-T or bortezomib alone.
recently reported that the combination of SNS01-T with lenalidomide (the active component of REVLIMID
marketed by Celgene Corporation, also a leading treatment for multiple myeloma), strongly inhibited human multiple
myeloma tumor growth during 6 weeks of treatment in mice and resulted in no regrowth of tumors after an additional 8 weeks without
myeloma is an incurable cancer of plasma cells, a type of white blood cell derived from B-lymphocytes, normally responsible for
the production of antibodies, in which abnormal cells accumulate in the bone marrow leading to bone lesions and interfering with
the production of normal blood cells. Senesco was previously granted orphan drug status for SNS01-T, the Company's lead drug
candidate for treatment of multiple myeloma.
Senesco Technologies, Inc.
a leader in eIF5A technology, is running a clinical study in multiple myeloma with its lead therapeutic candidate SNS01-T, which
targets B-cell cancers by selectively inducing apoptosis by modulating eukaryotic, translation, initiation Factor 5A (eIF5A), which
is believed to be an important regulator of cell growth and cell death. Accelerating apoptosis may have applications in treating
cancer, while delaying apoptosis may have applications in treating certain inflammatory and ischemic diseases. Senesco has already
partnered with leading-edge companies engaged in agricultural biotechnology and is entitled to earn research and development milestones
and royalties if its gene-regulating platform technology is incorporated into its partners' products.
statements included in this press release are forward-looking statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Actual results could differ materially from such statements expressed or implied herein as a result of a variety
of factors, including, but not limited to: the Company's ability to recruit patients for its clinical trial; the ability
of the Company to consummate additional financings; the development of the Company's gene technology; the approval of the
Company's patent applications; the successful implementation of the Company's research and development programs and
collaborations; the success of the Company's license agreements; the acceptance by the market of the Company's products;
the timing and success of the Company's preliminary studies, preclinical research and clinical trials; competition and the
timing of projects and trends in future operating performance, the Company's ability to comply with the continued listing
standards of the NYSE Amex, as well as other factors expressed from time to time in the Company's periodic filings with the
Securities and Exchange Commission (the "SEC"). As a result, this press release should be read in conjunction with the
Company's periodic filings with the SEC. The forward-looking statements contained herein are made only as of the date of
this press release, and the Company undertakes no obligation to publicly update such forward-looking statements to reflect subsequent
events or circumstances.
Senesco Technologies, Inc.
Leslie J. Browne, Ph.D.
Last updated: Sep 10, 2012