SECURITIES AND EXCHANGE COMMISSION
Washington, D.C.
20549
Form 6-K
Report of Foreign Private Issuer
Pursuant to Rule 13a-16 or 15d-16
of the Securities Exchange Act of 1934
For the month of August,
2006
Commission File Number 000-31062
Oncolytics Biotech Inc.
(Translation of registrants name into
English)
Suite 210, 1167 Kensington Crescent NW
Calgary, Alberta, Canada T2N 1X7
(Address of principal executive offices)
Indicate by check mark whether the registrant files or will file annual reports
under cover Form 20-F or Form 40-F.
Indicate by check mark if the registrant is submitting the Form 6-K in paper as
permitted by Regulation S-T Rule 101(b)(1): o
Note: Regulation S-T Rule 101(b)(1) only permits the submission in paper of a
Form 6-K if submitted solely to provide an attached annual report to security
holders.
Indicate by check mark if the registrant is submitting the Form 6-K in paper as
permitted by Regulation S-T Rule 101(b)(7): o
Note: Regulation S-T Rule 101(b)(7) only permits the submission in paper of a
Form 6-K if submitted to furnish a report or other document that the registrant
foreign private issuer must furnish and make public under the laws of the
jurisdiction in which the registrant is incorporated, domiciled or legally
organized (the registrants home country), or under the rules of the home
country exchange on which the registrants securities are traded, as long as
the report or other document is not a press release, is not required to be and
has not been distributed to the registrants security holders, and, if
discussing a material event, has already been the subject of a Form 6-K
submission or other Commission filing on EDGAR.
Indicate by check mark whether by furnishing the information contained in this
Form, the registrant is also thereby furnishing the information to the
Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of
1934.
If Yes is marked, indicate below the file number assigned to the registrant
in connection with Rule 12g3-2(b): 82 -
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210, 1167 Kensington Crescent NW
Calgary, Alberta
Canada T2N 1X7 |
FOR IMMEDIATE RELEASE
Oncolytics Biotech Inc. Completes Patient Enrolment in
U.S. Phase I Systemic Administration Clinical Trial
CALGARY, AB, August 23, 2006 Oncolytics Biotech Inc. (Oncolytics) (TSX:ONC, NASDAQ:ONCY) is
pleased to announce that it has completed patient enrolment in its Phase I U.S. clinical trial
investigating the systemic delivery of REOLYSIN® to treat patients with advanced
cancers. A total of 18 patients were treated in the Phase I trial with REOLYSIN® at
escalating dosages of 1x108, 3x108, 1x109, 3x109,
1x1010 or 3x1010 TCID50. A maximum tolerated dose (MTD) was not
reached and the treatment appears to have been well tolerated by the patients.
The clinical trial is an open-label, dose-escalation Phase I study in which a single dose of
REOLYSIN® was administered intravenously to patients diagnosed with selected advanced or
metastatic solid tumours that are refractory (have not responded) to standard therapy or for which
no curative standard therapy exists. The primary objective of the study is to determine the MTD,
dose limiting toxicity and safety profile of REOLYSIN®. Secondary objectives include
the evaluation of viral replication, immune response to the virus and any evidence of anti-tumour
activity.
The principal investigator for the trial is Dr. Sanjay Goel, Assistant Professor and
Attending Physician in the Department of Medical Oncology, Montefiore Medical Center and Albert
Einstein College of Medicine, New York City.
About Oncolytics Biotech Inc.
Oncolytics is a Calgary-based biotechnology company focused on the development of oncolytic viruses
as potential cancer therapeutics. Oncolytics clinical program includes a variety of Phase I and
Phase I/II human trials using REOLYSIN®, its proprietary formulation of the human
reovirus, alone and in combination with radiation. For further information about Oncolytics,
please visit www.oncolyticsbiotech.com
This press release contains forward-looking statements, within the meaning of Section 21E of
the Securities Exchange Act of 1934, as amended. Forward-looking statements, including the
Companys expectations related to the Phase I U.S. systemic administration clinical trial, and the
Companys belief as to the potential of REOLYSIN® as a cancer therapeutic, involve known
and unknown risks and uncertainties, which could cause the Companys actual results to differ
materially from those in the forward-looking statements. Such risks and uncertainties include,
among others, the availability of funds and resources to pursue research and development projects,
the efficacy of REOLYSIN® as a cancer treatment, the success and timely completion of
clinical studies and trials, the Companys ability to successfully commercialize
REOLYSIN®, uncertainties related to the research and development of pharmaceuticals and
uncertainties related to the regulatory process. Investors should consult the Companys quarterly
and annual filings with the Canadian and U.S. securities commissions for additional information on
risks and uncertainties relating to the forward looking statements. Investors are cautioned against
placing undue reliance on forward-looking statements. The Company does not undertake to update
these forward-looking statements.
FOR FURTHER INFORMATION PLEASE CONTACT:
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Oncolytics Biotech Inc. |
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The Equicom Group |
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The Investor Relations Group |
Cathy Ward |
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Nick Hurst |
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Damian McIntosh |
210, 1167 Kensington Cr NW |
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20 Toronto Street |
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11 Stone Street, 3rd Floor |
Calgary, Alberta T2N 1X7 |
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Toronto, Ontario M5C 2B8 |
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New York, NY 10004 |
Tel: 403.670.7377 |
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Tel: 416.815.0700 ext. 226 |
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Tel: 212.825.3210 |
Fax: 403.283.0858 |
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Fax: 416.815.0080 |
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Fax: 212.825.3229 |
cathy.ward@oncolytics.ca |
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nhurst@equicomgroup.com |
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dmcintosh@investorrelationsgroup.com |
www.oncolyticsbiotech.com |
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