-----BEGIN PRIVACY-ENHANCED MESSAGE----- Proc-Type: 2001,MIC-CLEAR Originator-Name: webmaster@www.sec.gov Originator-Key-Asymmetric: MFgwCgYEVQgBAQICAf8DSgAwRwJAW2sNKK9AVtBzYZmr6aGjlWyK3XmZv3dTINen TWSM7vrzLADbmYQaionwg5sDW3P6oaM5D3tdezXMm7z1T+B+twIDAQAB MIC-Info: RSA-MD5,RSA, KvljzQFIUDxkTFMB5g9prKzUwqEeWafUAark6//I11vwc99tFFFfid3gvW2cskE1 9+a20CTzpR9S/el8bbJ38w== 0000899681-98-000345.txt : 19980602 0000899681-98-000345.hdr.sgml : 19980602 ACCESSION NUMBER: 0000899681-98-000345 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 2 CONFORMED PERIOD OF REPORT: 19980514 ITEM INFORMATION: ITEM INFORMATION: FILED AS OF DATE: 19980601 SROS: NASD FILER: COMPANY DATA: COMPANY CONFORMED NAME: ALLIANCE PHARMACEUTICAL CORP CENTRAL INDEX KEY: 0000736994 STANDARD INDUSTRIAL CLASSIFICATION: IN VITRO & IN VIVO DIAGNOSTIC SUBSTANCES [2835] IRS NUMBER: 141644018 STATE OF INCORPORATION: NY FISCAL YEAR END: 0630 FILING VALUES: FORM TYPE: 8-K SEC ACT: SEC FILE NUMBER: 000-12950 FILM NUMBER: 98640466 BUSINESS ADDRESS: STREET 1: 3040 SCIENCE PARK RD CITY: SAN DIEGO STATE: CA ZIP: 92121 BUSINESS PHONE: 6195584300 MAIL ADDRESS: STREET 1: 3040 SCIENCE PARK ROAD CITY: SAN DIEGO STATE: CA ZIP: 92121 FORMER COMPANY: FORMER CONFORMED NAME: OTISVILLE BIOPHARM INC DATE OF NAME CHANGE: 19890310 FORMER COMPANY: FORMER CONFORMED NAME: OTISVILLE BIOTECH INC DATE OF NAME CHANGE: 19861216 8-K 1 SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 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) MAY 14, 1998 ALLIANCE PHARMACEUTICAL CORP. (Exact name of registrant as specified in its charter) - ------------------------------------------------------------------------------- New York 0-12900 14-1644018 - ------------------------------------------------------------------------------- (State or other jurisdiction of (Commission File Number) (IRS Employer ID incorporation) Number) - ------------------------------------------------------------------------------- 3040 SCIENCE PARK ROAD, SAN DIEGO, CA 92121 (Address of principal executive offices)(Zip Code) Registrant's Telephone Number, including area code: (619)-558-4300 - ------------------------------------------------------------------------------- (Former name or former address, if changed since last report) ITEM 5. OTHER EVENTS. On May 14, 1998, the Registrant and Ortho Biotech, Inc. and the R. W. Johnson Pharmaceutical Research Institute, both subsidiaries of Johnson & Johnson, entered into an agreement to restructure their collaboration with respect to the development of the Registrant's OXYGENT product. The agreement is being filed as an exhibit to this Current Report on form 8-K. OXYGENT is the Registrant's intravascular oxygen carrier to temporarily augment oxygen delivery in surgical and other patients at risk of acute tissue oxygen deficit. ITEM 7. FINANCIAL STATEMENTS, PRO FORMA FINANCIAL INFORMATION AND EXHIBITS. (a) Financial Statements of Business Acquired. - Not applicable. (b) Pro Forma Financial Information. - Not applicable. (c) Exhibits. 10.1 Copy of Agreement dated May 14, 1998 between the Registrant and Ortho Biotech, Inc. and the R. W. Johnson Pharmaceutical Research Institute, both subsidiaries of Johnson & Johnson, with respect to the restructuring of the relationship between the Registrant and such companies. 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 thereunto duly authorized. ALLIANCE PHARMACEUTICAL CORP. By: /s/ Theodore D. Roth Name: Theodore D. Roth Title:President Dated: June 1, 1998 EX-10.1 2 EXHIBIT 10.1 May 14, 1998 Ortho Biotech, Inc. The R. W. Johnson Pharmaceutical Research Institute, a division of Ortho Pharmaceutical Corporation U.S. Route 202 Raritan, New Jersey 08869 Ladies and Gentlemen: This will confirm our agreement with respect to restructuring the arrangement between your companies (respectively, "Ortho" and "PRI" and, collectively, the "Companies") as contemplated by the agreement dated August 16, 1994 (the "Agreement") between the Companies and our company ("Alliance"), as follows: 1. Terms defined in the Agreement have the same meaning when used in this letter. 2. Following the date of this letter, Alliance will be fully responsible, at its own expense, for the development of the Licensed Product, except that Alliance will be entitled to payment for expenses (the "Section 13.1 Expenses") incurred during the 90-day period following the date of this letter, in accordance with Sections 13.1 and 15.1(d) of the Agreement, and to payment for the expenses incurred prior to the date hereof as to which it is entitled to be paid pursuant to the Agreement. 3. The Companies will deliver to Alliance such marketing, pre-clinical and clinical data (including Know-How) as may be reasonably helpful to Alliance in continuing its development of the Licensed Product, and, during the next twelve months, each of the Companies will make its relevant personnel reasonably available to Alliance to discuss the Know-How and data. The Companies will also transfer to Alliance the IND for the Licensed Product. 4. Articles 2 through 6, 7.3, 8 through 14, 15.2, 16 and 26 of the Agreement inclusive shall terminate; provided, however, that, during the 90-day period after the date hereof, Alliance may continue to incur development expenses (as contemplated by the Agreement in the case of a termination thereof) up to a maximum of $3.5 million, which shall be reasonably documented and subject to audit in accordance with the Agreement, and which shall be deemed to be Section 13.1 Expenses. 5. Before entering into a development or marketing or license agreement for the "First Licensed Product" (as defined below), Alliance will give the Companies notice (the "Alliance Notice") containing its offer to the Companies to enter into a development or marketing or license agreement for the First Licensed Product which offer shall include exclusive rights in the First Licensed Product for all injectable indications in humans and for at least the United States, France, Germany, Italy and the United Kingdom. "First Licensed Product" means the Licensed Product now under development by Alliance or a Licensed Product containing the same perfluorocarbon components. The Alliance Notice will include the financial and other material terms which Alliance is prepared to accept, and, if requested by the Companies, Alliance will also make available to them clinical or other data reasonably necessary to permit the Companies to evaluate the technical and marketing potential of the First Licensed Product. If requested by either of the Companies before the expiration of a 60-day period (the "Initial Period") after receipt of the Alliance Notice, each of the parties will negotiate in good faith in order to reach an agreement (a "Definitive Agreement") with respect to the terms set forth in the Alliance Notice; provided, however, that, if not so requested, or if a Definitive Agreement shall not be executed before the expiration of a 120-day period (the "Second Period") following receipt of an Alliance Notice, Alliance may negotiate and execute a Definitive Agreement with one or more third parties; and provided, further, that (i) if the Companies shall pay to Alliance one million dollars (the "premium"), determined by the Companies as set forth below, before the expiration of the Initial Period (regardless of whether the Companies have requested that Alliance negotiate a Definitive Agreement with them), the Companies shall have a right of first refusal (on customary terms) with respect to a Definitive Agreement acceptable to Alliance and one or more third parties if the financial and other material terms thereof are less favorable to Alliance than the financial and other material terms which Alliance was prepared to accept as set forth in the Alliance Notice and (ii) Alliance shall have the right (the "Alliance Termination Right") to terminate such right of first refusal upon payment to the Companies of an amount equal to 200% of the premium. During the Initial Period and during the Second Period, in case either or both of the Companies request that Alliance negotiate a Definitive Agreement with them prior to the end of the Initial Period, Alliance will not enter into or continue negotiations for a Definitive Agreement with any third party. In the event of any dispute as to the value of the financial and other material terms included in the Alliance Notice, any of the parties may refer such dispute to any mutually acceptable third party, whose decision shall be final, conclusive and binding upon the parties hereto and whose fees and expenses shall be borne one-half by the Companies, on the one hand, and one-half by Alliance on the other. In the event that the parties cannot agree on a mutually acceptable third party, such third party shall be chosen by the American Arbitration Association in accordance with its rules then obtaining. Notwithstanding the foregoing: (i) any Definitive Agreement with one or both of the Companies shall provide for a credit against amounts due thereunder from either of them in an amount equal to the amount of the Section 13.1 Expenses; and (ii) Alliance will not deliver an Alliance Notice to the Companies prior to the expiration of nine months from the date hereof, and Alliance will not exercise the Alliance Termination Right prior to the expiration of three months after the last day of the Initial Period, unless, in either case, Alliance (a) shall have first received a bona fide offer to enter into a development and marketing agreement for the First Licensed Product which Alliance is prepared to accept, and (b) it shall deliver a copy of such bona fide offer to the Companies, together with the Alliance Notice, the terms of which shall be no more favorable to Alliance than those set forth in the bona fide offer, except to the extent necessary to conform to the requirements of the first sentence of this paragraph 5. 6. It is understood that (i) so long as the Companies shall have rights under paragraph 5, none of the parties hereto shall institute any action or proceeding against the others with respect to any matter arising under or relating to the Agreement that has accrued prior to the date hereof, and (ii) in the event of any Definitive Agreement, whether with one or both of the Companies or with a third party, or in the event that the Alliance Termination Right shall have been exercised, in accordance with paragraph 5, Alliance and the Companies will exchange mutual releases of all obligations and liabilities accruing on or before the date hereof arising under or relating to the Agreement. 7. Prior to provision of the Alliance Notice, Alliance will keep the Companies reasonably informed as to its Development progress, and, to that end, will have its appropriate personnel meet at least once every three months with representatives of the Companies to discuss such Development. If the foregoing is acceptable to you, please execute the duplicate of this letter in the place indicated and return it to us, at which point it will become a binding agreement between us. Very truly yours, ALLIANCE PHARMACEUTICAL CORP. By: /s/ Theodore D. Roth --------------------- ACCEPTED AND AGREED: ORTHO BIOTECH, INC. By: /s/ Jules Musing ------------------ R.W. JOHNSON PHARMACEUTICAL RESEARCH INSTITUTE, A DIVISION OF ORTHO PHARMACEUTICAL CORPORATION By: /s/ Robert Wills ---------------------- -----END PRIVACY-ENHANCED MESSAGE-----