EX-4.88 3 ex4_88.htm EXHIBIT 4.88 ex4_88.htm
EXHIBIT 4.88



DATED: May 25th, 2009


AMARIN CORPORATION, PLC
 
 
ESTER NEUROSCIENCES LTD.
 
 
MEDICA II MANAGEMENT L.P.
(AS THE SELLERS’ REPRESENTATIVE)
 
 
 
 

AMENDMENT AND WAIVER AGREEMENT



















Certain portions of this Exhibit have been omitted pursuant to a request for “Confidential Treatment” under Rule 24b-2 of the Securities and Exchange Commission.  Such portions have been redacted and bracketed in the request and appear as [*] in the text of this Exhibit.  The omitted confidential information has been filed with the Securities and Exchange Commission.


 
 

 


THIS AMENDMENT AND WAIVER AGREEMENT dated as of May 25th, 2009 (this “Agreement”)
 
AMONG:
 
(1)  
AMARIN CORPORATION, PLC, a public limited company incorporated under the laws of England and Wales (the “Buyer”);
 
(2)  
ESTER NEUROSCIENCES LTD., an Israeli company (the “Company”); and
        
(3)  
MEDICA II MANAGEMENT L.P., a Cayman Islands limited partnership, in its capacity as the Sellers’ Representative appointed pursuant to Section 13 of that certain Stock Purchase Agreement dated December 5, 2007 between Buyer, the Security Holders (each a “Seller” and collectively the “Sellers”) of the Company, the Company, and the Sellers' Representative.
 

 
RECITALS:
 
A.  
The Buyer, the Sellers, the Company and the Sellers' Representative entered into a Stock Purchase Agreement dated December 5, 2007, as subsequently amended by Amendment No. 1 (“Amendment No. 1”)  to Stock Purchase Agreement dated April 7, 2008 (together the “SPA”).
 
B.  
The Buyer is continuing various activities to conclude its auditing and reporting of the Phase IIa Clinical Study.
 
C.  
The Buyer announced in September 2008 that following a change in strategic direction, the Buyer would seek partnerships for its CNS pipeline, including Monarsen in MG.  At the date of this Agreement, the Buyer does not intend to conduct any new development work on Monarsen but intends to seek to enter into an agreement with a third party partner whereby such third party partner would conduct any such development work in the future.
 
D.  
The parties hereto acknowledge that it is necessary to agree a number of amendments to, and waivers under, the SPA to reflect the circumstances described in Recitals C and E and to facilitate the Buyer’s intention to seek a future partnership for Monarsen in MG.
 
E.  
The Buyer has agreed to make a settlement payment to the Sellers in the form of Buyer Ordinary Shares and to amend certain provisions of the SPA relating to the Escrow Fund in consideration of the Sellers’ Representative and each of the Sellers agreeing to the amendments and waivers referred to herein and to terminate and extinguish any obligations of the Buyer to pay the Milestone Ia Consideration to the Sellers pursuant to the SPA (all of the foregoing as set forth in detail under Section 2).
 
F. 
The parties hereto have also agreed certain terms which supplement the SPA and which are also set forth in this Agreement.
 

 
IN CONSIDERATION OF THE MUTUAL COVENANTS CONTAINED HEREIN, AND OTHER GOOD AND VALUABLE CONSIDERATION, THE RECEIPT AND ADEQUACY OF WHICH ARE HEREBY ACKNOWLEDGED, IT IS HEREBY AGREED AS FOLLOWS:
 

 
1
DEFINITIONS / REPRESENTATIONS AND WARRANTIES

1.1
Definitions:

All capitalized terms used in this Agreement, and not otherwise defined herein, shall have the meanings ascribed to them in the SPA.

 
 

 



“Accelerated Payment” has the meaning set forth in Section 3.4.3.

Accelerated Payment Allocation Schedule” means the schedule to be prepared by the Sellers’ Representative and submitted to the Buyer prior to the payment of any Accelerated Payment setting forth the allocation of the Accelerated Payment to the Sellers.

Actual Milestone II Consideration” has the meaning set forth in Section 3.4.2.

Additional Milestone II Consideration” has the meaning set forth in Section 3.3.3.

Effective Date” has the meaning set forth in Section 2.1.1.
 
MG Field” means the treatment of MG in humans.
 
MG Phase II Third Party Partner Consideration” means any Third Party Partner Consideration received by the Buyer in respect of the grant of any MG Sub-license up to the date preceding the completion of the MG Phase II Development Program.
 
MG Sub-license” means a sub-license granted to any Person (other than an Affiliate of Buyer) to any Company Business Intellectual Property in the MG Field.
 
Milestone Ib Shortfall Amount” has the meaning set forth in Section 3.3.3.
 
Proposed Partnership Agreement” has the meaning set forth in Section 3.1.3.
 
Reduced Milestone Ib Payment” has the meaning set forth in Section 3.3.3.
 
“Releasor” and “Releasee” have the meanings set forth in Section 4.
 
Repayable Amount” has the meaning set forth in Section 3.4.2.
 
Settlement Payment” has the meaning set forth in Section 2.1.
 
Shortfall Advance Payment(s)” has the meaning set forth in Section 3.4.2.
 
Shortfall Advance Payment Allocation Schedule” means the schedule to be prepared by the Sellers’ Representative and submitted to the Buyer prior to the payment of any Shortfall Advance Payment setting forth the allocation of the Shortfall Advance Payment to the Sellers.
 
SPA Future Waiver” has the meaning set forth in Section 2.1.4.
 
Termination Agreement” has the meaning set forth in Section 3.5.
 
Terminated Section 12 Provisions” has the meaning set forth in Section 2.2.
 
Third Party Partner” has the meaning set forth in Section 3.3.
 
Third Party Partner Consideration” means all milestone and license payments in cash that the Buyer is paid by the Third Party Partner under the Proposed Partnership Agreement and any Non-MG Sub-license Fees and any other consideration that the Buyer is paid as aforesaid that is not in the form of cash, the value of which shall be determined pursuant to Section 3.4.4.
 
211 Month Trigger Date”, “27 Month Trigger Date”, “30 Month Trigger Date” and “Ultimate Transfer Date” have the meanings set forth in Section 3.5.
 
“United States Dollar” and “US$” and “$” means the lawful currency of the United States of America.
 

 
 

 


 
1.2  
Representations and Warranties of Sellers’ Representative:

The Sellers’ Representative represents and warrants to the Buyer, as of the date hereof and as of the Effective Date, that:

 
1.2.1
the Sellers’ Representative continues to hold all the authorities and powers granted by the Sellers to the Sellers’ Representative under Section 13 of the SPA;

1.2.2  
the Sellers’ Representative has full authority and power to enter into this Agreement on behalf of each Seller and has all necessary authority and power to bind each Seller to each of the provisions of this Agreement;

1.2.3  
all necessary corporate, shareholder and other legal action has been taken by the Sellers’ Representative to authorize the execution, delivery and performance by it of this Agreement.  The Sellers’ Representative has duly executed and delivered this Agreement. This Agreement is the legal, valid and binding obligation of the Sellers’ Representative, enforceable against it in accordance with its respective terms, except as enforceability of such objections may be limited by bankruptcy, insolvency, reorganization, moratorium and other similar laws now or hereafter in effect relating to or limiting creditors’ rights generally and general principles of equity relating to the availability of specific performance and injunctive and other forms of equitable relief;

 
1.2.4
the Sellers’ Representative will execute this Agreement in its capacity as the Sellers’ Representative and, based on its authority as such, as agent and attorney-in-fact of each Seller (so appointed under Section 13 of the SPA); and

 
1.2.5
the Sellers’ Representative acknowledges that the Buyer is entering into this Agreement with each of the Sellers in reliance on the provisions of Section 13 of the SPA (including, without limitation, Section 13(g) of the SPA) and the representations and warranties of the Sellers’ Representative set forth in this Section 1.2.

1.3
Representations and Warranties of Buyer:

Buyer represents and warrants to the Sellers' Representative and to each Seller, as of the date hereof and as of the Effective Date, that:

 
1.3.1
Organization and Good Standing:  The Buyer has been duly incorporated and is validly existing as a public limited company under the laws of England and Wales and has all necessary corporate power and authority to perform all of its obligations under this Agreement.
 
 
 
1.3.2
Power and Authorization:  The Buyer has all requisite power and authority to execute and deliver this Agreement, to perform its obligations hereunder and to carry out the transactions contemplated hereby. All necessary corporate, shareholder and other legal action has been taken by the Buyer to authorize the execution, delivery and performance by it of this Agreement.  The Buyer has duly executed and delivered this Agreement. This Agreement is the legal, valid and binding obligation of the Buyer, enforceable against it in accordance with its respective terms, except as enforceability of such objections may be limited by bankruptcy, insolvency, reorganization, moratorium and other similar laws now or hereafter in effect relating to or limiting creditors’ rights generally and general principles of equity relating to the availability of specific performance and injunctive and other forms of equitable relief.

 
1.3.3
Buyer Ordinary Shares:  As of the Effective Date, subject to Section 2.1.1, upon issuance and delivery of the Buyer Ordinary Shares comprising the Settlement Payment: (a) such Buyer Ordinary Shares will have been duly authorized and validly issued and will be fully paid and non-assessable, will have been issued in compliance with all applicable English laws and the ADSs representing Amarin Shares will have been issued in compliance with all applicable U.S. securities laws, and will not have been issued in violation of any preemptive right, resale right, right of first refusal or similar right, (b) such delivery will convey to the Sellers good, valid and

 
 

 

marketable title to such Buyer Ordinary Shares, free and clear of any Encumbrances (other than applicable securities laws), and subject to Section 9.6 of the SPA, the Buyer will have complied with all applicable rules in connection with the issuance of freely tradeable Buyer Ordinary Shares on Nasdaq.

1.4
Representations and Warranties of each Seller:

Each Seller represents and warrants to the Buyer, severally, as of the date hereof and as of the Effective Date that:

 
1.4.1
Organization and Good Standing:  Such Seller is duly organized, validly existing and in good standing under the laws of its jurisdiction of incorporation, formation or organization, as applicable, and has (as applicable) all necessary corporate, partnership or limited liability company power and authority, as the case may be, to perform all of its obligations under this Agreement.

 
1.4.2
Power and Authorization:  Such Seller has all legal right, power, authority and legal capacity to execute and deliver this Agreement, to perform its obligations hereunder and to carry out the transactions contemplated hereby.

 
1.4.3
Status of Shareholder:  Such Seller is not a “U.S. Person” as defined by Rule 902 of Regulation S promulgated under the Securities Act, was not formed (if an entity) by a “U.S. Person” as defined by United States jurisdiction, and was not formed (if an entity) for the purpose of investing in securities not registered under the Securities Act.  Such Seller is not acquiring the Buyer Ordinary Shares for the benefit of a “U.S. Person” as defined by Rule 902 of Regulation S.  Such Seller is outside the United States.  Such Seller acknowledges, agrees and covenants that it will not engage in hedging transactions with regard to Buyer Ordinary Shares prior to the expiration of the distribution compliance period specified in Rule 903 of Regulation S promulgated under the Securities Act, unless in compliance with the Securities Act.  Absent another exemption from registration, such Seller will not resell Buyer Ordinary Shares to “U.S. Persons” or within the United States, unless pursuant to registration of such Buyer Ordinary Shares under the Securities Act.

 
1.4.4
Reliance Upon Seller’s Representations:  Such Seller understands that the issuance and sale thereto of Buyer Ordinary Shares will not be registered under the Securities Act on the ground that such issuance and sale will be exempt from registration under the Securities Act pursuant to Regulation S promulgated under the Securities Act and that Buyer’s reliance on such exemption is based on each Seller’s representations set forth herein.

 
1.4.5
Receipt of Information:  Such Seller has had an opportunity to ask questions and receive answers from Buyer regarding the terms and conditions of the issuance and sale of the Buyer Securities and the business, properties, prospects and financial condition of Buyer and to obtain any additional information requested, and has received and considered all information such Seller deems relevant to make an informed decision to purchase Buyer Securities.  Neither such inquiries nor any other investigation conducted by or on behalf of such Seller or its representatives or counsel shall modify, amend or affect such Seller’s right to rely the Buyer’s representations and warranties contained in this Agreement.

 
1.4.6
Restricted Securities:  Such Seller understands that the Buyer Ordinary Shares have not been registered under the Securities Act and such Seller will not sell, offer to sell, assign, pledge, hypothecate or otherwise transfer any of the Buyer Ordinary Shares during the 40 days following the Effective Date.  Such Seller agrees that Buyer may place stop transfer orders with Citibank N.A. (the “Transfer Agent”) (or any other transfer agent) with respect to the Buyer Ordinary Shares in order to implement the restrictions on transfer set forth in this Agreement.

 
1.4.7
Independent Investment:  Such Seller acknowledges that it is aware of its obligations as a beneficial owner of Buyer Ordinary Shares pursuant to Section 12(d) of the Exchange Act.


 
 

 


1.5
No other Representations and Warranties:

Each of the parties hereto acknowledges that it has not made any representation or warranty to any other party hereto, express or implied, as to the matters set forth in this Agreement, or any matter related thereto, except as specifically and explicitly set forth in this Agreement.


2
SETTLEMENT PAYMENT / RELEASE OF ESCROW FUND

2.1
The Buyer has agreed with the Sellers’ Representative and the Sellers to make a settlement payment (the “Settlement Payment”) to the Tax Trustee for the Sellers in the form of 1,315,789 Buyer Ordinary Shares in consideration of the agreement of the Sellers’ Representative and of each Seller to the amendment, termination and waiver of certain provisions of the SPA (as set forth in this Agreement) and subject to the following additional terms:

 
2.1.1
as soon as practicable following the date hereof, taking into account the then relevant issues arising under U.S. securities laws, but not later than 60 days hereafter, the Buyer shall issue to the Tax Trustee  (the date of such issuance, the "Effective Date") 1,315,789 Buyer Ordinary Shares that are freely tradeable on Nasdaq (pursuant to an effective Buyer registration statement, Regulation S or other applicable exemption from registration under the Securities Act) in discharge of the obligation to pay the Settlement Payment under Section 2.1;

 
2.1.2
for the avoidance of doubt, and as a consequence of the amendment to the SPA set forth in Section 2.2, no amount of the Settlement Payment will be paid by the Buyer to the Escrow Agent for deposit to the Escrow Fund;

 
2.1.3
all and any obligations of the Buyer to pay to the Sellers the Milestone Ia Consideration pursuant to Section 2.1(d) and Section 9.2 of the SPA shall be extinguished in full and, with effect from the Effective Date and at all times thereafter, the Buyer shall have no liability of any nature to any Seller under Section 2.1(d) and/or Section 9.2 of the SPA or otherwise in respect of the Milestone Ia Consideration; and

 
2.1.4
subject to Section 3.4.1 and Section 3.5.5, the Sellers’ Representative on behalf of each Seller (pursuant to Section 14.5 of the SPA), and each Seller, hereby fully waives all of its rights of any nature whatsoever, on a perpetual basis, to require or enforce performance by the Buyer of the requirements of Section 2.1(h), Section 2.1(e) and/or Section 2.1(f) of the SPA (“SPA Future Waiver”) and the Buyer shall have no liability of any nature to the Sellers following the Effective Date for breach of, or absence of performance of, any of the provisions of Section 2.1(h), Section 2.1(e) and/or Section 2.1(f) of the SPA.

2.2
The Buyer and the Sellers’ Representative agree that on the  expiry of the Escrow Period as such term has been originally defined in the SPA, i.e., on June 6, 2009, the parties shall execute and deliver the Final Instruction to Escrow Agent, in the form of Exhibit 2.2 hereto, informing the Escrow Agent that the parties irrevocably instruct the Escrow Agent to pay to the Sellers on such date all of the Remaining Escrow Fund in the manner set forth in the Escrow Agreement.

Further, the parties agree that, on the Effective Date, the following provisions of Section 12 of the SPA, Sections 12.1(i), 12.2(i)(a), 12.2(ii), 12.3(a) (other than with respect to Section 5.2, with respect to which Section 12.3(a) shall continue to apply in accordance with the terms of the SPA), 12.3(c), 12.6(f), 12.6(g) and 12.11 (the “Terminated Section 12 Provisions”), shall terminate and have no further force or effect, such that:

 
2.2.1
any and all of Buyer's rights and remedies for any Damages incurred as set forth in the Terminated Section 12 Provisions ("Covered Liabilities") shall terminate, and neither Buyer nor any Buyer Indemnified Party shall have any other claims, rights or remedies against any of the Sellers after the Effective Date, whether under the SPA or under any applicable law or otherwise, for such Covered Liabilities.

 
 

 



 
2.2.2
any and all of Sellers’ rights and remedies for any Damages incurred as set forth in the Terminated Section 12 Provisions ("Covered Liabilities") shall terminate, and none of the Sellers nor any Seller Indemnified Party shall have any other claims, rights or remedies against the Buyer after the Effective Date, whether under the SPA or under any applicable law or otherwise, for such Covered Liabilities.

For the avoidance of doubt, all the provisions of Section 12 other than the Terminated Section 12 Provisions shall be unchanged by this Agreement and shall continue in full force and effect in accordance with their terms, it being understood that all the provisions of Section 12, other than the Terminated Section 12 Provisions, shall continue in full force and effect solely with respect to the Sellers' obligations under Section 12.1(ii) of the SPA (which are subject to the waiver and release in Section 4 hereof), the Sellers' obligations under Section 12.2(i)(b) of the SPA, and Buyer's obligations under Sections 12.3(a) (only with respect to Section 5.2), 12.3(b) (which are subject to the waiver and release in Section 4 hereof) and 12.3(d) of the SPA, and that all such provisions shall be read subject to the amendments to such Section 12 as stated in this Section 2.2.


3
FUTURE DEVELOPMENT OF MONARSEN / INTENTION TO PARTNER MONARSEN

3.1
It is acknowledged by the Sellers’ Representative and each Seller that the intentions of the Buyer as at the date hereof and the Effective Date as regards any future development and/or commercialization activities in respect of Monarsen are as follows:

 
3.1.1
the Buyer is currently completing certain activities to finalise the Buyer’s auditing and reporting of the Phase IIa Clinical Study and, save the completion of such activities and the activities described in Section 3.1.3 below, the Buyer does not intend to conduct any additional development and/or commercialization activities on Monarsen, (including, without limitation, any MG Phase II Development Program, US Phase III Clinical Study or Phase III Clinical Study);

 
3.1.2
as a result of the Buyer’s cessation of all development activities on Monarsen as described in Section 3.1.1 above, and save in the circumstances outlined in Section 3.5.5 below where the Buyer would re-commence development activities on Monarsen in MG, Milestone Ib and Milestone II will not be achieved by the Buyer in the future and the potential for future payment to the Sellers of such milestones will be as set forth in Section 3.3;
 
 
3.1.3
as more fully described in Section 3.3, the Buyer intends to seek to enter into an agreement (the “Proposed Partnership Agreement”) with a third party partner whereby such third party partner would conduct future development and/or commercialization activities on Monarsen in MG PROVIDED HOWEVER that the parties hereto agree that the provisions of this first paragraph of Section 3.1.3 and the provisions of Section 3.3 are only expressions of the Buyer’s intentions and no such provision comprises or contains any legally binding obligation on the Buyer.
 
The parties hereto further agree that the foregoing proviso is without prejudice to the provisions of Section 3.5, which, for the avoidance of doubt, constitute legally binding obligations of the parties hereto.
 
3.2
Upon agreement with the Sellers’ Representative, the Sellers’ Representative will make available to  the Buyer a certain portion of the business time of  Prof. Eli Hazum as may be reasonably required by the Buyer to enable the Buyer to conclude the Buyer’s auditing and reporting of the Phase IIa Clinical Study and to make any reports to, or respond to any queries of, or in relation to any inspections or investigations of, any regulatory authority in Europe, the USA or any other jurisdiction in relation to the Phase IIa Clinical Study.
 
3.3
The Buyer intends to seek to negotiate with any potential third party partner which is an experienced company in the business of developing drugs (“Third Party Partner”) to include the following terms in the Proposed Partnership Agreement:
 

 
 

 


 
 
3.3.1
the Third Party Partner would have direct obligations to the Sellers, including diligence obligations as regards future development activities relating to Monarsen in MG identical to the Diligence Obligation set forth in Section 2.1(h) of the SPA, and including reporting and audit obligations (provided, however, that if the Third Party Partner is not a publicly traded company, then its reporting and audit obligations shall be broadened as required to provide Sellers' Representative reasonable comfort in such circumstances);
 
 
3.3.2
the Third Party Partner would have an obligation to pay to the Sellers a milestone payment of [********]2 in cash within 14 days after the Milestone Ib Date (the "First Payment Date") and would assume the obligations to the Sellers as regards Milestone II set forth in Section 2.1(f) of the SPA (other than Section 2.1(f)(iv) of the SPA, which is hereby terminated);
 
 
3.3.3
if in the negotiation of the matters described in Section 3.3.2, the Third Party Partner is not agreeable to pay to the Sellers a milestone payment of [********] in cash on the First Payment Date, and is only agreeable to pay a cash milestone that is less than [********] (“Reduced Milestone Ib Payment”) resulting in a shortfall amount (the “Milestone Ib Shortfall Amount”), without prejudice to the provisions of Section 3.4.2, the Buyer intends to seek to negotiate with the Third Party Partner an addition to the Milestone II Consideration whereby the Third Party Partner would assume the obligations to the Sellers as regards Milestone II set forth in Section 2.1(f) of the SPA (other than Section 2.1(f)(iv) of the SPA, which is hereby terminated) and agree to pay an additional cash payment to the Sellers within 14 days after the Milestone II Date, in addition to the Milestone II Consideration, equal to the Milestone Ib Shortfall Amount (“Additional Milestone II Consideration”); and
 
 
3.3.4
the Third Party Partner would have direct obligations to the Buyer, separate and distinct from the Third Party Partner’s obligations described in Section 3.3.1 above, including diligence obligations and payment obligations.
 
3.4
If the Buyer executes a Proposed Partnership Agreement, the following additional provisions shall apply as between the Buyer and the Sellers:

 
3.4.1
without prejudice to Section 2.1.4, all and any obligations of the Buyer to pay to the Sellers the Milestone Ib Consideration pursuant to Section 2.1(e) and Section 9.2 of the SPA; and/or the Milestone II Consideration pursuant to Section 2.1(f) of the SPA; and the provisions of Section 2.1(h), shall be terminated and extinguished in full and, with effect from the effective date of the Proposed Partnership Agreement and at all times thereafter, the Buyer shall have no liability of any nature to any Seller under Section 2.1(e) and Section 9.2 of the SPA in respect of the Milestone Ib Consideration, or under Section 2.1(f) of the SPA in respect of the Milestone II Consideration, or under any of the provisions of Section 2.1(h);

3.4.2  
in the event that, under the Proposed Partnership Agreement, the Third Party Partner does not agree to pay to the Sellers a milestone payment of [********] in cash on the First Payment Date, or to assume the obligations to the Sellers as regards Milestone II set forth in Section 2.1(f) of the SPA (other than Section 2.1(f)(iv) of the SPA, which is hereby terminated), then Buyer agrees to make advance payments (“Shortfall Advance Payment(s)”) to each Seller equal to its portion (as set forth on the Shortfall Advance Payment Allocation Schedule) in cash, of the following amounts:

 
(1)
the amount that reflects the difference between [********] and the aggregate amount actually paid to the Sellers by the Third Party Partner on the First Payment Date; and

 
(2)
the amount that reflects the difference between [********] (or [********], as may be applicable under Section 2.1(f)(ii) of the SPA) and the aggregate amount actually paid to the Sellers by the Third Party Partner on the Milestone II Date (or the other

 
 
  _________________________
 
 
CONFIDENTIAL INFORMATION OMITTED AND FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION. ASTERISKS [*] DENOTE SUCH OMISSIONS.
 

 
 

 

 
applicable payment date), as applicable, plus the Additional Milestone II Consideration (“Actual Milestone II Consideration”);

such Shortfall Advance Payments(s) to be paid by Buyer only from any Third Party Partner Consideration the Buyer actually receives from the Third Party Partner less any Accelerated Payments made to the Sellers under Section 3.4.3, and less any Non-MG Consideration made to the Sellers under Section 2.1(g) of the SPA PROVIDED HOWEVER that the Sellers’ Representative shall irrevocably instruct the Third Party Partner to pay to Buyer the amount (“Repayable Amount”) of any such Shortfall Advance Payments (or part thereof), out of the payment agreed to be made by the Third Party Partner to the Sellers of the Milestone II Consideration and any Additional Milestone II Consideration, only if and to the extent that the Milestone II Consideration and any Additional Milestone II Consideration is actually due to the Sellers.  The Repayable Amount shall be calculated as follows:

Reduced Milestone Ib Payment  + (plus) Shortfall Advance Payment(s)  + (plus)  Accelerated Payments   + (plus)  Non-MG Consideration  + (plus)  Actual Milestone II Consideration

– (less)

[********]3

– (less)

Milestone II Consideration

= (equals)  Repayable Amount;

 
3.4.3
in addition, the Buyer shall pay to each Seller a payment (the “Accelerated Payment”) equal to its portion (as set forth on the Accelerated Payment Allocation Schedule) in cash, of [**] of any MG Phase II Third Party Partner Consideration actually received from the Third Party Partner within 10 Business Days after such MG Phase II Third Party Partner Consideration has been actually received by the Buyer or its Affiliates;

 
3.4.4
if the Buyer is paid milestone or license payments by the Third Party Partner under the Proposed Partnership Agreement that are not in the form of cash, save in the case of Non-MG Sub-license Fees (which are governed by Section 2.1(g) of the SPA), the parties hereto will negotiate in good faith to agree terms as to how to value such payments under this Agreement.
 
3.5
Subject to the provisions of Sections 3.5.1 to 3.5.5, if the Buyer has not executed the Proposed Partnership Agreement on the date which is 21 months following the date hereof (the “21 Month Trigger Date”), within 30 days of the such date (the “Ultimate Transfer Date”), the Seller's Representative may, but is not bound to, request in writing that, in accordance with the termination agreement described in Sections 3.5.1 and 3.5.2, the Buyer shall transfer to the Sellers’ Representative (or such persons as directed by the Sellers’ Representative) all of its right, title and interest in the entire issued share capital of the Company:

 
3.5.1
prior to any transfer of the share capital of the Company by the Buyer to the Sellers’ Representative (or such persons as directed by the Sellers’ Representative), the parties hereto shall enter into a termination agreement (the “Termination Agreement”) , whereby the shares will be transferred by the Buyer to the Sellers’ Representative (or such persons as directed by the Sellers’ Representative), without consideration, subject to the representations and warranties of the Buyer set forth in Section 3.5.2 and otherwise on an “as is” basis; the SPA will be terminated in full and the parties hereto will agree mutual, full and perpetual waivers and releases under the SPA (pursuant to provisions in identical form to the waivers and releases set forth in Section 4); and, subject to Section 3.5.2, the Sellers’ Representative and each Seller

 
 
  _________________________
 
 
CONFIDENTIAL INFORMATION OMITTED AND FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION. ASTERISKS [*] DENOTE SUCH OMISSIONS.
 

 
 

 

 
will fully indemnify the Buyer in relation to any claims taken by any third party against the Buyer at any time following the Ultimate Transfer Date relating to any activities of the Company, past, present or future;

 
3.5.2
in addition, the Buyer shall confirm to the Sellers’ Representative and the Sellers in the Termination Agreement (and provide any documentation reasonably required by the Sellers’ Representative to support such confirmations) that as of the Ultimate Transfer Date, (a) the shares of the Company being transferred to the Sellers’ Representative or to another person on its behalf are free and clear of any Encumbrances; (b) the Company owns the patents listed in Exhibit 3.5.2 and has no other assets; (c) such patents are owned free and clear of any Encumbrances and (d) the Company owes no monies to any third party; and the Buyer shall also confirm to the Sellers’ Representative whether any claims or proceedings are pending or threatened against the Company on the Ultimate Transfer Date or whether the Buyer has any other liability to any third party of which the Buyer is actually aware;

 
3.5.3
notwithstanding the aforesaid, prior to the 21 Month Trigger Date, the Buyer shall be entitled  to notify  the Sellers’ Representative (such written notice to be accompanied by  supporting evidence), of its desire to extend the 21 Month Trigger Date to the date which is 6 months thereafter (the “27 Month Trigger Date”) which extension shall be approved by the Sellers’ Representative (such approval not to be unreasonably withheld or delayed) in circumstances where the Buyer can demonstrate to the Sellers' Representative’s satisfaction that it has made substantial progress towards the execution of the Proposed Partnership Agreement and that execution of such Proposed Partnership Agreement is reasonably likely within such 6-month period; if such extension is approved,  the Ultimate Transfer Date shall be similarly extended;

 
3.5.4
notwithstanding the aforesaid, prior to the 27 Month Trigger Date, the Buyer shall be entitled, to notify the Sellers’ Representative in writing (such written notice to be accompanied by supporting evidence) of its desire to extend the 27 Month Trigger Date to the date which is 3 months thereafter (the “30 Month Trigger Date”), which extension shall be approved by the Sellers’ Representative (such approval not to be unreasonably withheld or delayed) in circumstances where the Buyer can demonstrate to the Sellers' Representative’s satisfaction, that the execution of the Proposed Partnership Agreement is reasonably likely within such 3-month period; if such extension is approved, the Ultimate Transfer Date shall be similarly extended;

 
3.5.5
if prior to the 27 Month Trigger Date the Buyer notifies the Seller in writing that it has determined that it will re-commence development activities on Monarsen in MG, then, subject to the Sellers’ Representative consenting in writing to the Buyer re-commencing development activities on Monarsen in MG (such consent not to be unreasonably withheld or delayed), such development activities will re-commence and all of the provisions of this Clause 3.5, save this Section 3.5.5, and the SPA Future Waiver shall forthwith terminate, no transfer of the share capital as described above will occur thereafter, and with effect from the date of the afore-mentioned consent of the Sellers’ Representative, the Buyer shall be fully bound by, and liable for any breach of, the provisions of Sections 2.1(h), Section 2.1(e) and Section 2.1(f) of the SPA, without any change.  For the avoidance of doubt, the re-commencement of development activities by the Buyer under this Section 3.5.5 shall not in itself trigger any payment by the Buyer to the Sellers.

3.6
From the date hereof until the earlier of (i) the execution of the Proposed Partnership Agreement, or (ii) the execution of the Termination Agreement, or (iii) the notice of Buyer to the Sellers' Representative as set forth in Section 3.5.5, the Buyer shall report in writing to the Sellers’ Representative, on a six monthly basis, providing an update of the progress of its activities in that period in relation to the negotiation and execution of a Proposed Partnership Agreement. Such reports shall be provided to the Sellers’ Representative not later than the 15th day following June 30, 2009 and the end of each six month period thereafter. Further, a full and complete copy of any Proposed Partnership Agreement, if executed, shall be delivered to the Sellers’ Representative, together with a summary of the financial terms of any agreement entered into by the Buyer and the Third Party Partner contemporaneously with, or within 3 months prior to or following the date of  the Proposed Partnership Agreement.
 

 

 
 

 


 

4
WAIVER OF ACCRUED RIGHTS / MUTUAL RELEASES UNDER SPA

4.1
With effect from the Effective Date, each party to the SPA and each of its Affiliates (each a “Releasor”) hereby:

 
4.1.1
waives any accrued rights that Releasor may have accrued against the other parties to the SPA and each of its Affiliates, officers, directors, representative, agents and employees and the assigns and successors in interest of any of the foregoing entities (“Releasees”), whether known or unknown, foreseen or unforeseen, fixed or contingent, of any nature whatsoever from the beginning of time to the Effective Date under the SPA or otherwise; and

 
4.1.2
fully and finally releases and discharges the Releasees from any and all manner of actions, claims, promises, debts, sums of money, demands, obligations, in law or in equity, directly or indirectly, whether known or unknown, foreseen or unforeseen, fixed or contingent, of any nature whatsoever that Releasor may have by reason of any act, omission, matter, provision, cause or thing whatsoever from the beginning of time to the Effective Date under the SPA or otherwise.


5           MISCELLANEOUS

The parties hereto agree that the following provisions of the SPA (Sections 9.3, 9.7, 14.3, 14.4, 14.5, 14.6, 14.7, 14.8, 14.9, 14.10, 14.1, 14.12, 14.13, 14.14) shall apply to this Agreement in the same manner as they apply in the SPA.

All costs, expenses and Taxes incurred in connection with this Agreement, the Proposed Partnership Agreement and any related agreement or otherwise in connection herewith or therewith shall be paid by the party incurring such cost, expense or Tax.
 
For the avoidance of doubt, all shares, monies and other consideration due to the Sellers hereunder shall be issued or paid by the Buyer, when due, to the Tax Trustee in accordance with Section 13(h) of the SPA.


6
NO OTHER AMENDMENTS

Save as amended by Amendment No. 1 and this Agreement, the SPA shall remain in full force and effect without any change.


 
 

 



IN WITNESS WHEREOF the parties hereto have executed this Agreement.
 
 
SIGNED
 
 
By:  /s/ Thomas Lynch      
        for and on behalf of
       AMARIN CORPORATION, PLC
 
 
SIGNED
 
 
By:  /s/ Alan Cooke      
        for and on behalf of
        ESTER NEUROSCIENCES LTD.
 
 
SIGNED
 
 
By:  /s/ Ehud Geller      
        for and on behalf of
        MEDICA II MANAGEMENT L.P
        (AS THE SELLERS’ REPRESENTATIVE)




 
 

 

Exhibit 2.2

Final Instruction to Escrow Agent


 
Amarin Corporation plc
Medica II Management L.P., as Sellers’ Representative
 
Date: June 6, 2009
 

Brightman Almagor Freidman Trustees
1 Azrieli Center, Tel Aviv 67021
Israel

 
Dear Sirs:
 
Reference is hereby made to that certain Escrow Agreement made as of December 18, 2007, by and among yourselves (the “Escrow Agent”), Amarin Corporation plc (the “Buyer”), and Medica II Management L.P. (the “Sellers’ Representative”) (the "Escrow Agreement"; all capitalized terms used herein and not otherwise defined herein shall have the meanings ascribed to them in the Escrow Agreement).
 
This is to advise you that on the date hereof, the “Escrow Period” has been effectively terminated at the time this letter of instruction is issued to you, without any Indemnity Claims of Buyer or Buyer Indemnified Parties and, consequently, no Indemnity Claim Notice that has ever been given.

Accordingly, pursuant to Section 6.6 of the Escrow Agreement, the Buyer and the Sellers' Representative hereby irrevocably instruct you to pay to the Sellers all of the Remaining Escrow Fund in accordance with the Allocation Schedule that was provided to you by the Sellers' Representative prior to the date hereof, and hereby notify you of the termination of the Escrow Agreement and your release, after you properly affect the above payment to the Sellers, of any further duty, obligation or liability to the parties hereto.

The Sellers agree that pursuant to Section 7 of the Escrow Agreement, the Sellers shall pay all of the Escrow Agency’s fees and reasonable costs and expenses from the Remaining Escrow Fund and that the Buyer shall leave no liability whatsoever to you to pay any such fees and expenses.

We thank you for your service.

 
 
SIGNED
 
 
By:
for and on behalf of
AMARIN CORPORATION, PLC
 
 
 
SIGNED
 
 
By:
for and on behalf of
MEDICA II MANAGEMENT L.P
(AS THE SELLERS’ REPRESENTATIVE)

 
 

 



Exhibit 3.5.2

List of patents


Family:  1961
Title:   Genetically Engineered Human Cholinesterases


Inventors
Inventor ID
Inventor Name
Main
1390
Zakut Haim
 
1118
Soreq Hermona
v


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
1961-00
Priority
Abandoned
Israel
21/03/1989
89703
31/10/2001
Aug-01
02/03/2002
89703
   
1961-00
Priority
Abandoned
Israel
21/03/1989
89703
31/10/2001
Aug-01
02/03/2002
89703
   
1961-01
 
Abandoned
Canada
21/03/1990
2,012,720-1
   
20/09/1990
     
1961-02
 
Abandoned
US
20/03/1990
07/496,554
           
1961-03
 
Abandoned
Europe
20/03/1990
90105274
   
14/06/1995
388906
   
1961-04
 
Abandoned
France
20/03/1990
90105274
   
14/06/1995
388906
   
1961-05
 
Abandoned
Switzerland
20/03/1990
90105274
   
14/06/1995
388906
   
1961-06
 
Abandoned
Great Britain
20/03/1990
90105274.6
   
14/06/1995
388906
   
1961-07
 
Abandoned
Germany
20/03/1990
90105274.6
   
14/06/1995
69020019
   
1961-08
CIP
Granted
US
08/02/1993
08/111,314
   
21/01/1997
5,595,903
   







 
 

 



Family:  2042
Title:
Synthetic Antisense Deoxyoligonucleotide and Pharmaceutical Compositions Containing the Same

Inventors
Inventor ID
Inventor Name
Main
1513
Eckstein Fritz
 
1118
Soreq Hermona
v



 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2042-00
Priority
Granted
Israel
15/04/1992
101600
29/02/2000
JOURNAL 11/99
30/05/2000
101600
   
2042-01
PCT
Exhausted
PCT
15/04/1993
PCT/EP93/00911
28/10/1993
WO 93/21202
       
2042-02
NP
Abandoned
Japan
15/04/1993
517984/93
           
2042-03
NP
Granted
Europe
15/04/1993
93911467.4
   
05/04/1997
EP 0636137 B1
   
2042-04
NP
Abandoned
Australia
15/04/1993
40399/93
   
14/12/1995
665087
   
2042-05
NP
Abandoned
US
12/01/1994
08/318,826
   
04/06/1999
5,891,725
   
2042-06
NP
Granted
Canada
15/04/1993
2,118,235
   
15/7/2008
2118235
   
2042-07
CIP
Granted
US
05/02/1998
08/850,347
   
29/08/2000
6,110,742
   
2042-08
NP
Granted
France
15/04/1993
     
03/12/1997
636137
   
2042-09
NP
Granted
Great Britain
15/04/1993
93911467.4
02/01/1995
 
03/12/1997
636137
   
2042-10
NP
Granted
Germany
15/10/1994
93 911467.4
02/01/1995
 
03/12/1997
693 08 833.8-08
   

 
 

 
 

 



Family:  2098
Title:
Transgenic Animal Assay System for Anticholinesterases Substances

Inventors
Inventor ID
Inventor Name
Main
1777
Shani Moshe
 
1390
Zakut Haim
 
1118
Soreq Hermona
v

 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2098-00
Priority
Abandoned
US
28/02/1994
08/202,755
           
2098-01
CIP
Abandoned
US
09/01/1995
08/370,156
   
03/08/1999
5,932,780
   
2098-02
PCT
Exhausted
PCT
28/02/1995
PCT/US95/02806
31/08/1995
WO 95/23158
       
2098-03
NP
Abandoned
Europe
28/02/1995
95913580.7
           
2098-04
CIP
Granted
US
06/03/1997
08/814,095
   
15/02/2000
6,025,183
   



Family:  2151
Title:
A Method and Composition for Enabling Passage Through BBB

Inventors
Inventor ID
Inventor Name
Main
1882
Friedman Alon
 
1881
Kaufer Daniela
 
1118
Soreq Hermona
v


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2151-00
Priority
Expired
US
20/11/1996
60/031,194
           
2151-01
Priority2
Expired
US
12/12/1996
60/035,266
           
2151-02
PCT
Exhausted
PCT
20/11/1997
PCT/US97/21696
28/05/1998
WO 98/22132
       
2151-03
From Priority
Granted
US
20/11/1997
08/975,084
   
07/10/2001
6,258,780
   
2151-04
NP
Granted
Israel
20/11/1997
129990
24/01/2005
Pat Journal 11/2004
25/04/2005
129990
   
2151-05
NP
Abandoned
Australia
20/11/1997
53642/98
06/10/1998
 
04/12/2001
732043
   
2151-06
NP
Abandoned
Canada
20/11/1997
2,272,280
           
2151-07
NP
Abandoned
Europe
20/11/1997
97950711.8
           
2151-08
NP
Filed
Japan
20/11/1997
10-523989
           




 
 

 



Family:  2304
Title:
Synthetic Antisense Oligodeoxynucleotides and Pharmaceutical Compositions Containing them


Inventors
Inventor ID
Inventor Name
Main
1513
Eckstein Fritz
 
1882
Friedman Alon
 
1881
Kaufer Daniela
 
1118
Soreq Hermona
v


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2304-00
Priority
Expired
US
12/12/1996
60/035,266
           
2304-01
PCT
Exhausted
PCT
12/12/1997
PCT/US97/23598
18/06/1998
WO 98/26062
       
2304-02
CIP
Granted
US
12/12/1997
08/990,065
   
19/09/2000
6,121,046
   
2304-03
NP
Allowed
Israel
12/12/1997
130162
           
2304-04
NP
Granted
Australia
12/12/1997
53856/98
   
14/12/2000
727611
   
2304-05
NP
Examination
Canada
12/12/1997
2,274,985
           
2304-06
NP
Granted
Europe*
12/12/1997
97950993.2
15/09/1999
951536
24/1/2007
EP0951536
   
2304-07
NP
Filed
Japan
12/12/1997
10-527069
           
2304-08
CIP
Abandoned
US
 
09/572,630
           
(*) Validated in GB, FR, DE & CH





 
 

 


Family:  2325
Title:
Antisense and Non-Catalytic Properties


Inventors
Inventor ID
Inventor Name
Main
1118
Soreq Hermona
v

Licensee
 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2325-00
Priority
Expired
US
03/06/1997
60/040,203
           
2325-01
PCT
Exhausted
PCT
03/06/1998
PCT/US98/04503
09/11/1998
WO 98/39486
       
2325-02
NP
Abandoned
Australia
03/06/1998
64521/98
     
AB
   
2325-03
NP
Abandoned
Canada
03/06/1998
2,283,068
           
2325-04
NP
Granted
US
03/06/1998
09/380,532
   
11/05/2002
6,475,998
   
2325-05
NP
Abandoned
Europe
 
98910229.8
     
Abandoned
   



Family:  2356
Title:
Use of A Specific AChE Peptide (I4) As A Growth Factor

Inventors
Inventor ID
Inventor Name
Main
1969
Deutch Varda
 
1382
Eldor Amiram
 
1970
Grisaru Dan
 
1118
Soreq Hermona
v
     



 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2356-00
Priority
Granted
Israel
31/05/1999
130224
19/02/2004
Pat Journal 12/2003
20/05/2004
130224
   
2356-01
From Priority
Abandoned
Israel
09/02/1999
131707
           
2356-02
PCT
Exhausted
PCT
31/05/2000
PCT/IL00/00311
12/07/2000
WO 00/73427
       
2356-03
CIP
Granted
US
30/11/2001
09/998,042
20/02/2003
US-2003-0036632-A1
27/06/2006
7,067,486
   
2356-04
CIP of CIP
Published
US
04/11/2006
11/401,670
22/03/2007
US-2007-0065882-A1
       





 
 

 




Family:  2463
Title:
Novel Uses of Antibodies Against Ache and Peptides thereof

Inventors
Inventor ID
Inventor Name
Main
1882
Friedman Alon
 
1881
Kaufer Daniela
 
1118
Soreq Hermona
v






 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2463-00
Priority
Abandoned
Israel
31/05/1999
130225
           
2463-01
PCT
Exhausted
PCT
31/05/2000
PCT/IL00/00312
12/02/2000
WO 00/73343
       
2463-02
NP
Granted
US
31/05/2000
09/980,263
   
20/06/2006
7,063,948
   
2463-03
NP
Granted
Europe
31/05/2000
931517.7
20/03/2002
1187853
23/02/2005
1187853
   
2463-04
NP
Filed
Canada
31/05/2000
2,371,675
           
2463-05
NP
Allowed
Israel
31/05/2000
146850
           
2463-06
DIV
Published
US
02/10/2006
11/352,073
06/08/2006
US-2006-0121536-A1
       





 
 

 


Family:  2584
Title:
Antisense Oligonucleotide Against Human Ache and Uses thereof AS3 (EN101)

Inventors
Inventor ID
Inventor Name
Main
1118
Soreq Hermona
v


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2584-00
Priority
Filed
Israel
24/05/2001
143379
           
2584-01
PCT
Exhausted
PCT
24/05/2002
PCT/IL02/00411
01/09/2003
WO 03002739
       
2584-02
CIP of NP
Granted
US
27/03/2003
10/402,016
20/11/2003
US-2003-0216344-A1
07/11/2006
7,074,915
   
2584-03
NP
Examination
Europe
24/05/2002
2726406.8
25/02/2004
1390493
       
2584-04
NP
Filed
Canada
24/05/2002
2,458,806
           
2584-05
NP
Allowed
Australia
24/05/2002
20002256873
   
18/10/2007
20002256873
   
2584-06
NP
Filed
Japan
24/05/2002
2003-509100
           
2584-07
NP
Examination
India
24/05/2002
01497/KOLNP/2003
           
2584-08
NP
Examination
New Zealand
24/05/2002
529549
           
2584-09
DIV of CIP
Published
US
02/01/2006
11/346,145
08/10/2006
US-2006-0178333-A1
       





 
 

 


Family:  2806
Title:
Ache Antisense Deoxyoligonucleotide As Anti-Inflammatory Agent

Inventors
Inventor ID
Inventor Name
Main
3170
Yirmiya Raz
 
1118
Soreq Hermona
v


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2806-00
Priority
Filed
Israel
26/10/2003
158600
           
2806-01
PCT
Exhausted
PCT
26/10/2004
PCT/IL2004/000978
           
2806-02
CIP
Abandoned
US
26/10/2004
11/187,719
           
 
CON
Filed
US
18/4/2007
11/788,321
           
2806-03
NP
Published
Europe
23/10/2004
4791840.4
26/07/2006
1682072
       
2806-04
NP
Examination
Canada
26/10/2004
2,543,305
           
2806-05
NP
Filed
Japan
26/10/2004
2006-537550
           


Family:  2816
Title:
ARP As an Inducer of Granulocytopoiesis, Uses and Methods thereof (Hematopoietic Stem Cells)

Inventors
Inventor ID
Inventor Name
Main
1969
Deutch Varda
 
1970
Grisaru Dan
 
2637
Perry Chava
 
2638
Pick Marjorie
 
1118
Soreq Hermona
v


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
2816-00
Priority
Filed
Israel
02/12/2004
160376
       
Tel-Aviv Sourasky Medical Center
50
2816-01
PCT
Exhausted
PCT
02/10/2005
PCT/IL2005/000185
       
Tel-Aviv Sourasky Medical Center
50
2816-02
NP
Filed
US
02/10/2005
10/589,116
27/9/2007
2007/0224181A1
   
Tel-Aviv Sourasky Medical Center
50


 
 

 




Family:
Title:
ANTISENSE OLIGONUCLEOTIDES AGAINST ACETYLCHOLINESTERASE FOR TREATING INFLAMMATORY DISEASES


Inventors
Inventor ID
Inventor Name
Main
 
Eli Hazum
 


 
Application
Publication
Patent
Co-Applicant
Patent ID
Continuity
Status
Country
Date
Number
Date
Number
Date
Number
Name
%
 
Priority
Filed
US
04/10/2006
60/790,546
           
 
PCT
Exhausted
PCT
29/3/2007
PCT/IL2007/000413
18/10/2007
WO2007/116395
       
 
NP
Filed
US
10/08/2008
12/296,455
           
 
NP
Filed
Australia
29/3/2007
2007237059
           
 
NP
Filed
New Zealand
29/3/2007
571861
           
 
NP
Filed
Europe
29/3/2007
PCT/IL2007/000413
           
 
NP
Filed
Canada
29/3/2007
PCT/IL2007/000413
           
 
NP
Filed
Israel
29/3/2007
194431
           
 
NP
Filed
Japan
29/3/2007
PCT/IL2007/000413