Form 8-K

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

 

 

 

FORM 8-K

 

CURRENT REPORT

 

Pursuant to Section 13 or 15(d) of

the Securities Act of 1934

 

 

 

 

Date of Report (Date of earliest event reported):     

  October 7, 2004

 

 

 

XCYTE THERAPIES, INC.
(Exact name of registrant as specified in its charter)

 

 

Delaware   0-50626   91-1707622

(State or other jurisdiction of

incorporation or organization)

 

Commission

File Number

 

(I.R.S. Employer

Identification Number)

 

 

1124 Columbia Street, Suite 130

Seattle, Washington 98104

(Address of principal executive offices and zip code)

 

 

(Registrant’s telephone number, including area code)       (206) 262-6200

 

 

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:

 

¨ 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 1.01 Entry into a Material Definitive Agreement.

 

On October 7, 2004, the Company entered into Amendment No. 5 to its Services Agreement with Lonza Biologics PLC (“Lonza”) dated June 6, 2000. Under the terms of the amendment, Lonza will provide certain process analyses and other services related to the manufacturing of antibodies used in the Company’s Xcellerate Technology.

 

On October 7, 2004, the Company entered into Amendment No. 7 to its Services Agreement with Lonza dated June 6, 2000. Under the terms of the amendment, Lonza will provide certain process analyses and other services related to the manufacturing of antibodies used in the Company’s Xcellerate Technology.

 

Item 9.01 Financial Statements and Exhibits.

 

  (c) Exhibits.

 

See Index to Exhibits attached hereto.

 

2


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.

 

XCYTE THERAPIES, INC.
By:  

/s/ Joanna S. Black


   

Joanna S. Black

Duly Authorized Officer of Registrant

General Counsel, Vice President and
Secretary

 

Date: October 7, 2004

 

3


INDEX TO EXHIBITS

 

Exhibit Number

 

Description of Document


10.1†  

Amendment No. 7 dated October 7, 2004 to the Services Agreement dated June 6, 2000 between Xcyte Therapies, Inc. and Lonza Biologics PLC.

10.2†  

Amendment No. 5 dated October 7, 2004 to the Services Agreement dated June 6, 2000 between Xcyte Therapies, Inc. and Lonza Biologics PLC.


Certain information in these exhibits has been omitted and filed separately with the Securities and Exchange Commission pursuant to a confidential treatment request under 17 C.F.R. Sections 200.80(b)(4), 200.83 and 230.406.

 

4

Amendment No. 7 dated October 7, 2004

Exhibit 10.1

 

Confidential treatment has been requested for portions of this exhibit. The copy filed herewith omits the information subject to the confidentiality request. Omissions are designated as [**]. A complete version of this exhibit has been filed separately with the Securities and Exchange Commission.

 

AMENDMENT NO. 7

 

TO THE

 

SERVICES AGREEMENT

 

between

 

LONZA BIOLOGICS PLC

 

and

 

XCYTE THERAPIES INC

 

RELATING TO [**]

 

Page 1 of 11


THIS AMENDMENT is made the 7th day of October 2004.

 

BETWEEN

 

1. Lonza Biologics plc of 228 Bath Road, Slough, SL1 4DX, Berkshire, England (“LB”) and

 

2. Xcyte Therapies Inc of 1124 Columbia Street, Suite 130, Seattle, Washington 98104, USA (“Customer”).

 

WHEREAS

 

A. The parties have entered into an Agreement dated 6th June 2000 relating to the supply of Services (as therein defined), and

 

B. The parties now wish to amend the terms of the Agreement

 

THEREFORE it is hereby agreed by and between the parties that the Agreement shall be amended as follows: -

 

1. Stage 22, 23, 24 shall be added to Schedule 2 as follows:

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 2 of 11


Notes:

 

  1. The provision of Services herein may be based on the need to sample and or analyse additional GMP manufacturing batches of [**] or manufacturing batches of [**] specifically operated as [**].

 

  2. The provision of additional Services as requested by the Customer or as recommended by LB in order to generate information for a regulatory submission or license application for the Customer’s product [**], may be dependant upon samples or analysis from additional GMP manufacturing batches of [**], or manufacturing batches of [**] specifically operated as [**].

 

  3. The provision of validation Services regarding the Customer product [**] does not constitute agreement to manufacture the product [**].

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 3 of 11


SCHEDULE 2

 

CONTENTS

 

1   Supply of Customer Materials and Customer Know How
2   Activities to be undertaken by LB
22   Stage 22 – Process [**] Analysis
23   Stage 23 – Process [**] Analysis
24   Stage 24 – Stability [**] Analysis

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 4 of 11


1 Supply of Customer Materials and Customer Know How

 

Prior to commencement of the Services at LB or, if appropriate, prior to the commencement of the relevant Stage of the Services, Customer shall supply LB with the following:

 

  (i) Information relating to the operation of Customer analytical tests as agreed between the Customer and LB

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 5 of 11


2 Activities to be undertaken by LB

 

22   Stage 22 – Process [**] Analysis
    22.1   Objectives
        22.1.1   To perform a [**] based on generic LB data and existing product specific data applicable to the [**] process for the evaluation of [**].
    22.2   Activities
        Substage 22A – [**]
        22.2.1   Identify key process parameters that could potentially impact on product quality and [**] during the [**] process steps.
        22.2.2   Determine the applicability of existing Product-specific data and generic LB data.
        22.2.3   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
            A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
        22.2.4   Assess with the Customer the requirement for further Product-specific information to be generated.
        Note:   If a validation study is required for some or all steps in the [**] process then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
        Substage 22B – [**]
        22.2.5   Identify key process parameters that could potentially impact on product quality and [**] during the [**] process steps.
        22.2.6   Determine the applicability of existing Product-specific data and generic LB data.
        22.2.7   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 6 of 11


            A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**] .
        22.2.8   Assess with the Customer the requirement for further Product-specific information to be generated.
        Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
        Note:   Additional product specific data may need to be generated from additional [**] which are sampled specifically for the purpose of generating samples for additional [**]. Data may need to be generated from the operation of a [**].
            A full set of [**] studies for [**] may take an estimated [**] to complete.
    22.3   Timeline
        The stage, including the review of generic and specific data will be completed with the issue of the report of activities and it is estimated that this report will be issued [**] from the commencement of the Stage.
23   Stage 23 – Process [**] Analysis
    23.1   Objectives
        23.1.1   To perform a [**] based on generic LB data and existing product specific data applicable to the [**] process for the evaluation of [**].
    23.2   Activities
        Substage 23A – [**]
        23.2.1   Carry out a technical review of generic data available to support the [**].
        23.2.2  

Draw up a [**] table of available data and additional data required to be generated by analysis of [**].

 

        23.2.3   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
            A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
        23.2.4   Assess with the Customer the requirement for further Product-specific information to be generated. Identify what [**] from previous batches are available. In addition identify sample points at selected points in the [**].

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 7 of 11


        Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
        Substage 23B – [**]
        23.2.5   Carry out a technical review of generic data available to support the [**].
        23.2.6   Draw up a [**] of available data and additional data required to be generated by analysis of [**].
        23.2.7   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
            A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
        23.2.8   Assess with the Customer the requirement for further Product-specific information to be generated. Identify what [**] from previous batches are available. In addition identify sample points at selected points in the [**].
        Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
        Note:   Additional product specific data may need to be generated from [**] which are sampled specifically for the purpose of generating samples for additional [**].
            A full set of [**] studies for [**] may take an estimated [**] to complete.
    23.3   Timescale
        The stage, including the review of generic and specific data will be completed with the issue of the report of activities and it is estimated that this report will be issued [**] from the commencement of the Stage.
24   Stage 24 – Stability [**] Analysis
    24.1   Objective
        24.1.1   To perform a [**] based on generic LB data and existing product specific data applicable to the [**] process for the evaluation of the [**] from the [**] process.
    24.2   Activities
        24.2.1   Carry out a technical review of generic data available to support the [**]. Draw up a [**] table of available data and additional data required to be generated by analysis of [**].

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 8 of 11


    24.2.2   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
        A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
    24.2.3   Assess with the Customer the requirement for further Product-specific information to be generated. Identify what [**] from previous batches are available. In addition identify sample points at selected points in the [**] of future [**] batches.
    Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
    Note:   Additional product specific data may need to be generated from additional [**] which are sampled specifically for the purpose of generating samples for additional [**].
        A full study to determine the [**] may take an estimated [**] to complete.
24.3   Timescale
    The stage, including the review of generic and specific data will be completed with the issue of the report of activities and it is estimated that this report will be issued [**] from the commencement of the Stage.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 9 of 11


SCHEDULE 3

 

Price and Terms of Payment

 

2. Price

 

In consideration for LB carrying out the Services as detailed in Schedule 2 the Customer shall pay LB as follows:

 

Stage


     

Price1

(UK £ Sterling)


Stage 22   Process[**] Analysis   Substage 17A – [**]
        Substage 17B – [**]
Stage 23   Process[**] Analysis   Substage 18A – [**]
        Substage 18B – [**]
Stage 24   Stability [**] Analysis   [**]

 

Notes:

 

  (1) As described in Clause 4 – “Delivery, Transportation of Product and Customer tests”] of the Terms and Conditions, additional costs and expenses incurred by LB in arranging insurance and transportation in order to ship samples, Product, and Cell Line shall be charged to the Customer in addition to the price.

 

3.   Payment
    Payment by the Customer of the Price for each Stage shall be made against LB’s invoices as follows:
    2.1   For Stage 22A
        [**] upon commencement of Stage 22A
        [**] upon completion of Stage 22A
    2.2   For Stage 22B
        [**] upon commencement of Stage 22B
        [**] upon completion of Stage 22B
    2.2   For Stage 23A
        [**] upon commencement of Stage 23A
        [**] upon completion of Stage 23A
    2.2   For Stage 23B
        [**] upon commencement of Stage 23B
        [**] upon completion of Stage 23B
    2.3   For Stage 24
        [**] upon completion of Stage 24.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 10 of 11


4. Save as herein provided all other terms and conditions of the Agreement shall remain in full force and effect.

 

IN WITNESS WHEROF the parties have caused this Amendment to be executed by their representatives thereunto duly authorised as of the day and year first written.

 

Signed by   /s/ Ronald J. Berenson
for and on behalf of Xcyte Therapies Inc.    
Signed by   /s/ Judith Symes
for and on behalf of Lonza Biologics plc.    

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 11 of 11

Amendment No. 5 dated October 7, 2004

Exhibit 10.2

 

Confidential treatment has been requested for portions of this exhibit. The copy filed herewith omits the information subject to the confidentiality request. Omissions are designated as [**]. A complete version of this exhibit has been filed separately with the Securities and Exchange Commission.

 

AMENDMENT NO. 5

 

TO THE

 

SERVICES AGREEMENT

 

between

 

LONZA BIOLOGICS PLC

 

and

 

XCYTE THERAPIES INC

 

RELATING TO [**]

 

Page 1 of 11


THIS AMENDMENT is made the 7th day of October 2004.

 

BETWEEN

 

1. Lonza Biologics plc of 228 Bath Road, Slough, SL1 4DX, Berkshire, England (“LB”) and

 

2. Xcyte Therapies Inc of 1124 Columbia Street, Suite 130, Seattle, Washington 98104, USA (“Customer”).

 

WHEREAS

 

A. The parties have entered into an Agreement dated 6th June 2000 relating to the supply of Services (as therein defined), and

 

B. The parties now wish to amend the terms of the Agreement

 

THEREFORE it is hereby agreed by and between the parties that the Agreement shall be amended as follows: -

 

1. Stage 17, 18, 19 shall be added to Schedule 2 as follows:

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 2 of 11


Notes:

 

  1. The provision of Services herein may be based on the need to sample and or analyse additional GMP manufacturing batches of [**] or manufacturing batches of [**] specifically operated as [**].

 

  2. The provision of additional Services as requested by the Customer or as recommended by LB in order to generate information for a regulatory submission or license application for the Customer’s product [**], may be dependant upon samples or analysis from additional GMP manufacturing batches of [**], or manufacturing batches of [**] specifically operated as [**].

 

  3. The provision of validation Services regarding the Customer product [**] does not constitute agreement to manufacture the product [**].

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 3 of 11


SCHEDULE 2

 

CONTENTS

 

1 Supply of Customer Materials and Customer Know How

 

2 Activities to be undertaken by LB

 

  17 Stage 17 – Process [**] Analysis

 

  18 Stage 18 – Process [**] Analysis

 

  19 Stage 19 – Stability [**] Analysis

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 4 of 11


1 Supply of Customer Materials and Customer Know How

 

Prior to commencement of the Services at LB or, if appropriate, prior to the commencement of the relevant Stage of the Services, Customer shall supply LB with the following:

 

  (i) Information relating to the operation of Customer analytical tests as agreed between the Customer and LB

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 5 of 11


2   Activities to be undertaken by LB
    17   Stage 17 – Process [**] Analysis
        17.1   Objectives
            17.1.1   To perform a [**] based on generic LB data and existing product specific data applicable to the [**] process for the evaluation of [**].
        17.2   Activities
            Substage 17A – [**]
            17.2.1   Identify key process parameters that could potentially impact on product quality and [**] during the [**] process steps.
            17.2.2   Determine the applicability of existing Product-specific data and generic LB data.
            17.2.3   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
                A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
            17.2.4   Assess with the Customer the requirement for further Product-specific information to be generated.
            Note:   If a validation study is required for some or all steps in the [**] process then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
            Substage 17B – [**]
            17.2.5   Identify key process parameters that could potentially impact on product quality and [**] during the [**] process steps.
            17.2.6   Determine the applicability of existing Product-specific data and generic LB data.
            17.2.7   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 6 of 11


                A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
            17.2.8   Assess with the Customer the requirement for further Product-specific information to be generated.
            Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
            Note:   Additional product specific data may need to be generated from additional [**] which are sampled specifically for the purpose of generating samples for additional [**]. Data may need to be generated from the operation of a [**].
                A full set of [**] studies for [**] may take an estimated [**] to complete.
        17.3   Timeline
            The stage, including the review of generic and specific data will be completed with the issue of the report of activities and it is estimated that this report will be issued [**] from the commencement of the Stage.
    18   Stage 18 – Process [**] Analysis
        18.1   Objectives
            18.1.1   To perform a [**] based on generic LB data and existing product specific data applicable to the [**] process for the evaluation of [**].
        18.2   Activities
            Substage 18A – [**]
            18.2.1   Carry out a technical review of generic data available to support the [**].
            18.2.2   Draw up a [**] table of available data and additional data required to be generated by analysis of [**].
            18.2.3   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
                A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 7 of 11


            18.2.4   Assess with the Customer the requirement for further Product-specific information to be generated. Identify what [**] from previous batches are available. In addition identify sample points at selected points in the [**].
            Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
            Substage 18B – [**]
            18.2.5   Carry out a technical review of generic data available to support the [**].
            18.2.6   Draw up a [**] of available data and additional data required to be generated by analysis of [**].
            18.2.7   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
                A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
            18.2.8   Assess with the Customer the requirement for further Product-specific information to be generated. Identify what [**] from previous batches are available. In addition identify sample points at selected points in the [**].
            Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
            Note:   Additional product specific data may need to be generated from [**] which are sampled specifically for the purpose of generating samples for additional [**].
                A full set of [**] studies for[**] may take an estimated [**] to complete.
        18.3   Timescale
            The stage, including the review of generic and specific data will be completed with the issue of the report of activities and it is estimated that this report will be issued [**] from the commencement of the Stage.
    19   Stage 19 – Stability [**] Analysis
        19.1   Objective
            19.1.1   To perform a [**] based on generic LB data and existing product specific data applicable to the [**] process for the evaluation of the [**] from the [**] process.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 8 of 11


        19.2   Activities
            19.2.1   Carry out a technical review of generic data available to support the [**]. Draw up a [**] table of available data and additional data required to be generated by analysis of [**].
            19.2.2   A draft of the final report will be prepared by LB and sent to the Customer for review. Upon receipt of written comments from the Customer, LB will revise the report and send a final draft to the Customer. Upon receipt of written comments on the final draft the parties shall agree any modifications required and LB will issue a final report of activities to the Customer.
                A timetable will be set for review of the reports, it is estimated that the initial review by the Customer and revision by LB will each take approximately [**] and the final review and revision will each take approximately [**].
            19.2.3   Assess with the Customer the requirement for further Product-specific information to be generated. Identify what [**] from previous batches are available. In addition identify sample points at selected points in the [**] of future [**] batches.
            Note:   If a validation study is required for some or all steps in the [**] then this will be designed in consultation with the Customer and covered by Amendment to the Agreement.
            Note:   Additional product specific data may need to be generated from additional [**] which are sampled specifically for the purpose of generating samples for additional [**].
                A full study to determine the [**] may take an estimated [**] to complete.
        19.3   Timescale
            The stage, including the review of generic and specific data will be completed with the issue of the report of activities and it is estimated that this report will be issued [**] from the commencement of the Stage.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

Page 9 of 11


SCHEDULE 3

 

Price and Terms of Payment

 

2. Price

 

In consideration for LB carrying out the Services as detailed in Schedule 2 the Customer shall pay LB as follows:

 

Stage


       

Price1

(UK £ Sterling)


Stage 17    Process [**] Analysis   

Substage 17A – [**]

 

Substage 17B – [**]

Stage 18    Process[**] Analysis   

Substage 18A – [**]

 

Substage 18B – [**]

Stage 19    Stability[**] Analysis    [**]

 

Notes:

 

  (1) As described in Clause 4 – “Delivery, Transportation of Product and Customer tests” of the Terms and Conditions, additional costs and expenses incurred by LB in arranging insurance and transportation in order to ship samples, Product, and Cell Line shall be charged to the Customer in addition to the price.

 

3. Payment

 

Payment by the Customer of the Price for each Stage shall be made against LB’s invoices as follows:

 

2.1   For Stage 17A
    [**] upon commencement of Stage 17A
    [**] upon completion of Stage 17A
2.2   For Stage 17B
    [**] upon commencement of Stage 17B
    [**] upon completion of Stage 17B
2.2   For Stage 18A
    [**] upon commencement of Stage 18A
    [**] upon completion of Stage 18A
2.2   For Stage 18B
    [**] upon commencement of Stage 18B
    [**] upon completion of Stage 18B
2.3   For Stage 19
    [**] upon completion of Stage 19.

 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

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4. Save as herein provided all other terms and conditions of the Agreement shall remain in full force and effect.

 

IN WITNESS WHEREOF the parties have caused this Amendment to be executed by their representatives thereunto duly authorised as of the day and year first written.

 

Signed by

for and on behalf of Xcyte Therapies Inc.

 

/s/ Ronald J. Berenson


Signed by

for and on behalf of Lonza Biologics plc.

 

/s/ Judith Symes


 

[**] Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions.

 

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