prospectussupplement2-424b3.htm
Prospectus
Supplement dated October 24,
2007
Filed
Pursuant to
Rule 424(b)(3)
File
No.
333-133975
File
No.
333-141209
DOR
BioPharma, Inc.
This
prospectus supplement supplements:
·
|
the
prospectus dated March 20, 2007, as supplemented by the prospectus
supplement dated August 17, 2007, relating to the offer and sale
by the
selling stockholders identified in the prospectus of up to 26,341,261
shares of our common stock; and
|
·
|
the
prospectus dated April 18, 2007, as supplemented by the prospectus
supplement dated August 17, 2007, relating to the offer and sale
by the
selling stockholders identified in the prospectus of up to 18,717,301
shares of our common stock.
|
Recent
Event
On
October 18, 2007, the U.S. Food and Drug Administration (“FDA”) issued to us a
not approvable letter for orBec® (oral
beclomethasone dipropionate). The FDA has requested data from additional
clinical trials to demonstrate the safety and efficacy of orBec®. Additionally,
the
FDA has requested information with respect to other sections of our new drug
application that was filed with the FDA on September 21, 2006.
This
prospectus supplement should be read in conjunction with, and may not be
utilized without, the relevant prospectus and prospectus supplement, which
are
to be delivered with this prospectus supplement. This prospectus supplement
is
qualified by reference to the relevant prospectus and prospectus supplement,
except to the extent that the information in this prospectus supplement updates
and supersedes the information contained in such prospectus, including any
supplements or amendments thereto.
Neither
the Securities and Exchange Commission nor any state securities commission
has
approved or disapproved of these securities or determined if this prospectus
is
truthful or complete. Any representation to the contrary is a criminal
offense.