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Proc-Type: 2001,MIC-CLEAR
Originator-Name: webmaster@www.sec.gov
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<SEC-DOCUMENT>0000898430-96-000126.txt : 19960117
<SEC-HEADER>0000898430-96-000126.hdr.sgml : 19960117
ACCESSION NUMBER:		0000898430-96-000126
CONFORMED SUBMISSION TYPE:	424B3
PUBLIC DOCUMENT COUNT:		1
FILED AS OF DATE:		19960116
SROS:			NASD

FILER:

	COMPANY DATA:	
		COMPANY CONFORMED NAME:			OXIS INTERNATIONAL INC
		CENTRAL INDEX KEY:			0000109657
		STANDARD INDUSTRIAL CLASSIFICATION:	PHARMACEUTICAL PREPARATIONS [2834]
		IRS NUMBER:				941620407
		STATE OF INCORPORATION:			DE
		FISCAL YEAR END:			1231

	FILING VALUES:
		FORM TYPE:		424B3
		SEC ACT:		1933 Act
		SEC FILE NUMBER:	033-61087
		FILM NUMBER:		96503677

	BUSINESS ADDRESS:	
		STREET 1:		6040 N CUTTER CIRCLE STE 317
		CITY:			PORTLAND
		STATE:			OR
		ZIP:			97217
		BUSINESS PHONE:		5032833911

	MAIL ADDRESS:	
		STREET 1:		6040 N CUTTER CIRCLE STE 317
		CITY:			PORTLAND
		STATE:			OR
		ZIP:			97217

	FORMER COMPANY:	
		FORMER CONFORMED NAME:	DDI PHARMACEUTICALS INC
		DATE OF NAME CHANGE:	19920703

	FORMER COMPANY:	
		FORMER CONFORMED NAME:	DIAGNOSTIC DATA INC /DE/
		DATE OF NAME CHANGE:	19850312
</SEC-HEADER>
<DOCUMENT>
<TYPE>424B3
<SEQUENCE>1
<DESCRIPTION>424B(3) AND (C)
<TEXT>

<PAGE>
 
                                        Filed pursuant to Rule 424(b)(3) and (c)
                                        promulgated under the Securities Act of
                                        1933, as amended.
                                        File No. 33-61087


                           OXIS INTERNATIONAL, INC.

                               SUPPLEMENT NO. 1
                            DATED JANUARY 15, 1996
                    TO PROSPECTUS DATED SEPTEMBER 13, 1995



SUMMARY

     This is Supplement No.1 (the "Supplement") to the Prospectus dated
September 13, 1995 (the "Prospectus") for OXIS International, Inc., a Delaware
corporation (the "Company").  This Supplement forms a part of, and must be
accompanied or preceded by, the Prospectus.  All cross-references used herein
are to the Prospectus, and capitalized terms used herein have the same
definitions as set forth in the Prospectus.

     The primary purposes of this Supplement are to :

     (a) Update the discussion contained in the Prospectus  concerning trials by
a major customer of the Company of a drug based upon the Company's product,
bovine superoxide dismutase; and

     (b) Update information regarding the status and effect of certain interim
financing being undertaken by the Company.

EACH POTENTIAL INVESTOR SHOULD THOROUGHLY REVIEW THE PROSPECTUS AND THIS
SUPPLEMENT PRIOR TO SUBSCRIBING FOR INTERESTS IN THE COMPANY.
<PAGE>
 
DRUG TRIAL OF DISMUTEC

     Sanofi Winthrop, Inc. ("Sanofi"), a major customer of the Company,
announced in October 1995 that a second Phase III trial of its drug DISMUTEC(tm)
(a chemically-modified form of the Company's bovine superoxide dismutase) for
treatment of patients with closed head injury failed to show a statistically
significant improvement between the treatment and control groups. As a result,
bovine superoxide dismutase sales to Sanofi (35% of the Company's 1994 revenues)
are not expected to continue.


PRIVATE PLACEMENT OF COMPANY SECURITIES

     In two closings on December 1, 1995 and December 20, 1995, the Company
concluded a round of financing by sales of 8% convertible subordinated
debentures due December 31, 1997, with warrants, entirely to overseas investors
through a placement agent.  The debentures are initially convertible into an
aggregate of 1,004,000 shares of Company Common Stock, and the warrants may be
initially exercised for an aggregate of twenty percent of such number of shares,
i.e., 200,800 shares of Common Stock. The securities sold (including the
underlying Common Stock) are not registered under the Securities Act of 1933, as
amended (the "Securities Act"), and may not be re-offered or re-sold absent
registration under the Securities Act or available exemptions from such
registration requirements.  The offering of debentures and warrants raised an
aggregate of $1,255,000 for the Company, prior to commissions and expenses.
Following such offering, it is anticipated that further financing will be needed
before the end of the first quarter of 1996 to allow the Company to continue its
planned research and development programs and marketing of additional products.
The unavailability of such financing could cause the Company to cease or curtail
its operations, and/or delay or prevent the development and marketing of the
Company's potential therapeutic products.

                                       2
</TEXT>
</DOCUMENT>
</SEC-DOCUMENT>
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