UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): July 5, 2011
AVI BioPharma, Inc.
(Exact name of registrant as specified in its charter)
Oregon | 001-14895 | 93-0797222 | ||
(State or other jurisdiction of incorporation) |
(Commission File Number) |
(IRS Employer Identification No.) |
3450 Monte Villa Parkway, Suite 101
Bothell, WA 98021
(Address of principal executive offices, including zip code)
(425) 354-5038
(Registrants telephone number, including area code)
(Former name or former address, if changed since last report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
¨ | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
¨ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
¨ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
¨ | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 8.01 | Other Events. |
On July 5, 2011, Nationwide Childrens Hospital in Columbus, Ohio, the site of the Companys planned Phase 2 clinical trial of eteplirsen for the treatment of Duchenne muscular dystrophy (the Study), informed the Company that it had received verbal confirmation from its Institutional Review Board that the Study can be initiated. The final approved study protocol remained consistent with the originally submitted study design and included only minor revisions related to routine, non-invasive laboratory assessments.
As previously disclosed, the Company expects to initiate the Study in the third quarter of 2011 and anticipates Study results in the second quarter of 2012.
This Current Report on Form 8-K contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Forward-looking statements are identified by such words as believe, expect, anticipate and words of similar import and are based on current expectations that involve risks and uncertainties, such as the Companys plans, objectives, expectations and intentions. All statements other than historical or current facts are forward-looking statements, including, without limitation, statements about the Companys plans to initiate a Phase 2 clinical trial in eteplirsen in the third quarter of 2011 and the expected timing of clinical trial results. These forward-looking statements are subject to certain risks and uncertainties that could cause actual results to differ materially from those anticipated in the forward-looking statements. These statements, like all statements in this report, speak only as of their date.
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
AVI BioPharma, Inc. | ||||
By: | /s/ Christopher Garabedian | |||
Christopher Garabedian | ||||
President and Chief Executive Officer |
Date: July 6, 2011