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Senesco Opens New Clinical Trial Site

Key Takeaway: Senesco Opens New Clinical Trial Site Alliance and is Treating the First West Coast Patient BRIDGEWATER, N.J. (October 23, 2013) - Senesco Technologies, Inc. ("Senesco" or the "Company") (OTC QB: SNTID) reported the treatment of the first patient at the Company's newly opened

Full Press Release Details

Senesco Opens New Clinical Trial Site
Alliance and is Treating the First West Coast Patient
BRIDGEWATER, N.J. (October 23, 2013)
- Senesco Technologies, Inc. ("Senesco" or the "Company") (OTC QB: SNTID) reported the treatment
of the first patient at the Company's newly opened clinical-trial site at Seattle Cancer Care Alliance (SCCA). This patient
is part of Senesco's Phase 1b/2a clinical study of its therapeutic drug candidate, SNS01-T, targeting B-cell cancers.
"We are excited to add SCCA as a
clinical site," stated Leslie J. Browne, Ph.D., President and Chief Executive Officer of Senesco. "It is our first
site on the west coast and we anticipate its urban location will help attract patients who meet our patient enrollment needs."
SCCA is a cancer treatment center that
unites physician scientists from Fred Hutchinson Cancer Research Center, UW Medicine and Seattle Children's. The organization
strives to provide outstanding care to cancer patients and to further improve survival rates. By bringing together the cancer-related
patient-care services of the three institutions, SCCA builds on existing strengths, allows easier interactions among the cancer
experts in each organization and provides improved access to resources.
"We are very pleased to have added
another patient to group 3 of the SNS01-T study," stated Alice S. Bexon, M.D., Vice President of Clinical Development. "At
the current dose level of 0.2 mg/kg, which is in the range where an effect was seen in preclinical cancer models, we are looking
for a stronger effect than was seen at lower doses in groups 1 and 2."
The study is an open-label, multiple-dose,
dose-escalation study, which is evaluating the safety and tolerability of SNS01-T when administered by intravenous infusion to
approximately 15 relapsed or refractory multiple myeloma, mantle cell (MCL) or diffuse large B-cell lymphoma (DLBCL) patients.
While the primary objective of this study is to evaluate safety and tolerability, the effect of SNS01-T on tumor response and time
to relapse or progression will be assessed using multiple well-established metrics including measurement of monoclonal protein
in multiple myeloma and CT imaging in MCL and DLBCL.
About Senesco Technologies,
Senesco Technologies is a clinical-stage
biotech company specializing in cancer therapeutics. Its proprietary gene regulation technology has demonstrated the ability to
eliminate cancerous cells and protect healthy cells from premature death. The Company is currently in a phase 1b/2a trial with
a product that treats B-cell cancers, which include multiple myeloma, chronic lymphocytic leukemia, and non-Hodgkin's B-cell
lymphomas. The technology was developed over the last 15 years through the discovery that the genetic pathway for cell growth control
is common to both plants and humans.
SNS01-T is a novel approach to cancer therapy
that is designed to selectively trigger apoptosis in B-cell cancers such as multiple myeloma, and, mantle cell and diffuse large
B-cell lymphomas. Senesco is the sponsor of the Phase 1b/2a study that is actively enrolling patients at Mayo Clinic in Rochester,
MN, the University of Arkansas for Medical Sciences in Little Rock, the Mary Babb Randolph Cancer Center in Morgantown, WV, the
John Theurer Cancer Center at Hackensack University Medical Center in Hackensack, NJ and the Seattle Cancer Care Alliance in Seattle,
Forward-Looking Statements
Certain 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 continue as a going concern; 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 current uncertainty in the patent landscape surrounding
small inhibitory RNA and the Company's ability to successfully defend its intellectual property or obtain the necessary licenses
at a cost acceptable to the Company, if at all; 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 quotation of the Company's common stock on an over-the-counter
securities market, 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.
RedChip Companies, Inc.
Tel: 1-800-RED-CHIP (733-2447), ext. 104
Joel Brooks Heather Branham
Chief Financial Officer 908-393-9393
info@senesco.com
Last updated: Oct 24, 2013