Project Contract for Protocol 0303

Exhibit 10.3

*** Text omitted and filed separately

Confidential Treatment Requested

under 17 C.F.R. §§200.80(b)(4) and 240.24b-2

Project Contract for Protocol 0303

This Project Contract is entered into between Neurobiological Technologies, Inc. (“NTI”) and ICON Clinical Research, L.P., (“ICON”) as of the 1st day of May 2004 (the “Effective Date”) pursuant to the Master Services Agreement between the parties dated as of the 1st day of December 2003 (the “Master Agreement”). Except as modified by this Project Contract, the terms and conditions of the Master Agreement are incorporated herein by reference and shall govern the performance of the parties’ duties under this Project Contract. Capitalized terms used herein and not otherwise defined are used as defined in the Master Agreement.

1. Protocol. The study to be performed is entitled “A Phase III Randomized, Double-Blind, Dexamethasone-Sparing Study Comparing Human Corticotropin-Releasing Factor (hCRF) to Placebo for Control of Symptoms Associated with Peritumoral Brain Edema in Patients with Malignant Brain Tumor who Require Chronic Administration of High-Dose Dexamethasone, Protocol Number NTI 0303,” the original version of such Protocol is dated August 18, 2003 and was amended January 14, 2004 (the “Study”), and such Protocol is incorporated herein by reference, as may be amended from time to time.

2. ICON Proposal. The services to be performed by ICON for the Study (“Services”) are set forth in the assumptions attached as Exhibit A and incorporated herein by reference.

3. Costs and Payment Schedule. In consideration for ICON’s Services under this Project Contract, NTI agrees to pay ICON in accordance with the budget set forth in the attached Exhibit B and incorporated herein by reference. The total amount payable by NTI to ICON in respect of professional fees, exclusive of pass-through expenses, under this Project Contract for direct labor costs shall in no way exceed [***] without prior written consent of both parties. Pass-through expenses under this Project Contract are estimated to be [***].

4. Transfer of Obligations. Pursuant to 21 CFR §312.52, NTI hereby transfers to ICON and ICON hereby assumes all the obligations of NTI as sponsor of the Study as set forth in Exhibit C attached and incorporated herein by reference and included on Form FDA 1571, Section 13. NTI shall retain the right to assume any of the duties delegated to ICON at any time, and the Services and Exhibit B shall be adjusted accordingly.

5. Key Personnel. Key Personnel under this Project Contract are named in the attached Exhibit D.

6. Term. This Project Contract shall begin as of the Effective Date and shall be completed by December 31, 2006 when all of the Services are fully performed in accordance with this Project Contract, unless terminated earlier pursuant to the Master Agreement.

7. Licenses. By accepting ICON deliverables, NTI accepts responsibility for obtaining all required licenses to view, use and process such data, other than such licenses as it is necessary to have to view, use and process such data, and which ICON can provide at no or negligible cost to ICON because the licensed property is proprietary or sublicenseable by ICON, which licenses ICON hereby grants.

*Confidential Treatment Requested

8. Notices. Unless otherwise directed in writing by the receiving party, day-to-day correspondence relating to this Project Contract shall be delivered in accordance with the Master Agreement and addressed as follows:

If to NTI:		Neurobiological Technologies, Inc. Attn: Xxxxxxx XxXxxxxxxx Clinical Project Manager 0000 Xxxxx Xxxxx, Xxxxx 000 Xxxxxxxx, XX 00000 Phone: 000-000-0000 Fax: 000-000-0000 Email: xxxxxxxx@xxxx.xxx
If to ICON:		ICON Clinical Research, L. P. Xxxxx Xxxxx Contract Analyst — Business Development 000 Xxxxxx Xxxx Xxxxx Xxxxx, XX 00000 Phone: 000-000-0000 Fax: 000-000-0000 Email: xxxxxx@xxxxxx.xxx
With a copy to:		ICON Clinical Research, L. P. Xxxxxxx Xxxxxxx Director, Business Development 000 Xxxx Xxxxxxx Xxxxx, Xxxxx 000 Xxxxxxx Xxxx, XX 00000 Phone: (650) ..000-0000 Fax: (000) 000-0000 Email: xxxxxxxx@xxxxxx.xxx
9.      Invoices and Payments. All ICON invoices should be forwarded to NTI as follows:
		Attn: Xxxxxxx XxXxxxxxxx Clinical Project Manager 0000 Xxxxx Xxxxx, Xxxxx 000 Xxxxxxxx, XX 00000 Phone: 000-000-0000 Fax: 000-000-0000 Email: xxxxxxxx@xxxx.xxx

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All payments should be forwarded to ICON pursuant to Section 4.6 of the Master Agreement as follows. Payments shall be in the form of a check drawn on a U.S. bank, payable to ICON Clinical Research, L. P. and mailed to:

ICON Clinical Research, L. P.

Attn.: Xxxxx Xxxxxx, Vice President of Finance

X.X. Xxx 00-0000

Xxxxxxxxxxxx, XX 00000-0000

Tax I.D. Number: 00-0000000

10. Exhibits. The Exhibits attached hereto form an integral part of this Project Contract and are hereby incorporated by reference.

11. Entire Agreement. With respect to the Services performed under this Project Contract, this Project Contract, including the attached Exhibits, and the Master Agreement contain the entire agreement of the parties. Any modifications to this Project Contract must be in writing and signed by the parties.

IN WITNESS WHEREOF, the parties hereto have executed this Project Contract as of the dates stated below.

ICON Clinical Research, L.P.						Neurobiological Technologies, Inc.
By:		/s/ Xxxxxxx X. Xxxxxxx				By:		/s/ Xxxx Xxxx
Xxxxxxx X. Xxxxxxx, Ph.D.						Printed Name: Xxxx Xxxx
Vice President, Business Development						Title:		Senior VP, CMO
Date:		12/6/04				Date:		12/8/04

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Exhibit A

Assumptions

General Study Assumptions

• NTI supplied the protocol for this study.

• Protocol review and CRF design services are assumed to have been covered under a separate contractual arrangement with NTI, and thus no costs have been included for these services in this proposal.

• [***]

• An interim analysis has been planned for this study.

• ICON assumes that NTI will write the final integrated clinical and statistical report for this study, and that ICON biostatistics will review this report and provide comments to NTI.

Translations

• Any translations of the protocol, case report form (CRF), informed consent form (ICF), or other documents required for this study will be the responsibility of NTI.

Standard Operating Procedures (SOPs)

• Unless otherwise noted in these assumptions, ICON SOPs will be followed for this project.

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*Confidential Treatment Requested

Sites/Patients

		NTI 0303
Number of Sites		[***]
Number of Randomized Patients		200
Number of Completed Patients		200

Timelines

Milestone		Target Date
[***]		[***]
[***]		[***]
[***]		[***]
[***]		[***]
[***]		[***]
[***]		[***]
[***]*		[***]
[***]		[***]
Total ICON Involvement		32 Months

* Assumes the statistical analysis plan will be finalized and approved at least 4 months prior to the delivery o£ any tables, listings and graphs

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*Confidential Treatment Requested

Study Specifications

Project Task		NTI		ICON
Write Protocol (Covered under a previous consulting agreement.)		[***]		[***]
Design CRF (Covered under a previous consulting agreement)		[***]		[***]
Conduct Site Qualification Visits		[***]		[***]
Select Investigators		[***]		[***]
Negotiate Investigator Agreements		[***]		[***]
Administer Investigator Payments		[***]		[***]
Collect Site Regulatory Documents		[***]		[***]
Provide Randomization Schedule		[***]		[***]
Study Drug Storage and Shipment to Sites		[***]		[***]
Participate in Investigators’ Meeting		[***]		[***]
Conduct Site Initiation Visits		[***]		[***]
Conduct Interim Monitoring Visits		[***]		[***]
Conduct In-House Site Management		[***]		[***]
Provide Medical Monitoring		[***]		[***]
Process SEAs With Regulatory Authorities		[***]		[***]
Conduct Site Audits		[***]		[***]
Conduct Site Closeout Visits		[***]		[***]
Conduct Data Management Activities		[***]		[***]
Prepare Statistical Analysis Plan (SAP)		[***]		[***]
Provide Tables, Listings, and Graphs		[***]		[***]
Prepare Final Clinical Study Report		[***]		[***]

* These services were covered under a previous consulting agreement.

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*Confidential Treatment Requested

Data Management Assumptions

• This study will be processed using DataFax, version 3.5 or higher. DataFax is an electronic, image-based data processing system that does not require handling of hard copies of CRF pages. The master copy of CRF pages for patients enrolled by an investigator is stored at the study site. ICON will work with faxed images of the investigators’ CRF pages throughout the study. For costing purposes, it was assumed that the study site will fax all study CRF pages into DataFax. Electronic images of CRF pages will be delivered to NTI at the end of the study.

• ICON will assign a clinical data reviewer (CDR) to provide data review and CRF page sign-off within DataFax.

• Costs for CRF development and production have not been included in this proposal, as ICON assumes that they were included in a previous consulting agreement. For costing purposes, ICON presumes that a final, approved set of CRF templates will be available as a result of this previous agreement.

• ICON assumes that NTI will prepare a mockup of the CRF binders that will be sent to an outside printer for production and shipment. ICON will review the mockup and provide comments.

• ICON assumes that there will be a maximum of 26 unique CRF templates and up to [***] CRF pages/patient that will be completed by the investigational sites and entered into the study database.

• ICON estimates that a maximum of [***] CRF pages will be processed. This total consists of an average of [***] pages for each of 200 patients, or [***] original CRFs, along with the assumption that up to 35% of the CRF pages, or [***], will generate queries that will require additional data processing.

• The study nurse/coordinator at each study site will complete the CRF pages for all patient visits.

• Per NTI, up to [***] sites may be used for this study.

• As part of a separate consulting agreement, ICON has developed limited case report form completion instructions for use by the investigational sites. The instructions include directions for faxing CRF pages to ICON.

• ICON will conduct logic checks on CRF data up to 15 times during the clinical portion of the study.

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*Confidential Treatment Requested

• Following resolution of all queries at the end of the study, the database will be audited. ICON proposes a data audit scheme whereby the study database will be inspected by independent sampling of up to 50% of the CRF templates (i.e., 13 CRF templates, total). Supplemental audit/correction efforts will be undertaken should discrepancies in excess of those allowed by audit specifications be detected.

• The database will not be audited prior to the interim analysis.

• CRF templates will be selected for audit based upon the following criteria: (a) file contains safety data (e.g., adverse event, laboratory, study termination, serious adverse event, or death information); (b) file contains efficacy or other important outcome data; (c) file contains data that have been identified as potentially problematic (e.g., the site had problems filling out the form, or the form had fields that may have had a higher than usual rate of data entry errors). NTI will approve the selection of files to be subjected to audit.

• Approximately one week prior to anticipated data lock for each part of the study, ICON will randomly select records from each data file. The number of data records per data file that will be selected is shown below.

Number of Records Per Data File		Sample Size		Acceptance Number		Rejection Number
15		[***]		[***]		[***]
16-20		[***]		[***]		[***]
21-25		[***]		[***]		[***]
26-35		[***]		[***]		[***]
36-50		[***]		[***]		[***]
51-70		[***]		[***]		[***]
71-110		[***]		[***]		[***]
110-140		[***]		[***]		[***]
141-215		[***]		[***]		[***]
216-850		[***]		[***]		[***]
>850		[***]		[***]		[***]

• A data specialist will audit each data file by comparing the randomly selected data records to the raw data (CRF images from DataFax).

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*Confidential Treatment Requested

• The results of the audit for each data file will fall into one of three categories: (a) the number of defective records is less than or equal to the acceptance number, and the data file is accepted; (b) the number of defective records is greater than the rejection number due to a systematic error that, when corrected, renders the data file acceptable (i.e., the number of defective records is less than or equal to the acceptance number); or (c) the number of defective records is greater than the rejection number, and the data file is rejected.

• ICON will resolve the errors uncovered by the audit and make the necessary corrections to each data file. For data files that were rejected, ICON will randomly select records from the corrected data files and perform a second audit. For any data file that is rejected during the second audit, ICON will conduct a 100% quality control review. ICON will report the audit results to NTI.

• Data files for the study will be considered “locked” after all selected data files have passed audit inspection and corrections identified during the audit have been made.

• ICON assumes that it will provide up to 24 DataFax reports to NTI for this study. These reports will include information on visits completed and CRFs faxed, by site and patient number.

• ICON assumes that the study sites will complete serious adverse event forms for each SAE and fax them directly to the designated Medical Monitor. The designated Medical Monitor will review the completed forms, resolve any outstanding questions, and prepare any documentation necessary for the FDA.

• ICON assumes that it will receive up to ten (10) SAES during this study, and costs for data management services have been revised accordingly.

• NTI will be responsible for periodically reconciling the clinical study database with the SAE data on file at NTI.

• ICON assumes that one (1) data listing will be produced for use by NTI in reconciling the clinical database to the SAE data on file at NTI. Up to 12 critical fields will be included on the listing. This listing will be provided to NTI up to eight (8) times. This listing will be produced solely for the purpose of SAE reconciliation and does not correspond to any of the listings that will be generated by the ICON biostatistical and programming departments as part of the interim or final reports.

• One (1) additional data listing for Medical History will be provided. This will be used in conjunction with the AE listing to track steroid-related AEs. This listing will be sent to NTI up to eight (8) times.

• ICON assumes that there could be up to an average of 24 adverse events and 24 concomitant medications per patient that will require electronic encoding during this study.

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• ICON assumes that a central laboratory will be used for this study. Laboratory results will be transferred electronically to ICON up to six (6) times during the study. For costing purposes, ICON has assumed that laboratory data files will be sent to ICON as SAS datasets in transport format and that the datasets will contain the corrected, cumulative results available at the time of transfer.

• ICON will transfer a project archive to NTI following final approval of the clinical study report (CSR) for this study. This archive will include the following: SAS datasets containing the raw data, annotated case report forms, and PDF files containing patient CRF images (100 DPI). All SAS datasets supplied to NTI will be in SAS transport format.

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Biostatistics/SAS^® Programming Assumptions

• An interactive voice randomization system (IVRS) will be used to assign patients to treatment groups. A biased coin randomization scheme will be used. Under a separate consulting agreement, ICON Biostatistics has prepared specifications for the procedure so that the IVRS group can implement the procedure accurately.

• The IVRS group will periodically provide a spreadsheet to an unblinded ICON statistician assigned to the study. The spreadsheet will be used to QA the process (i.e., cross-check patient treatment group assignment balance by stratum). For costing purposes, ICON has assumed QA will occur following randomization of every 20 new patients.

• For the interim analysis, ICON assumes that there will be up to five (5) tables, one (1) figure, and six (6) listings. In addition, sample size calculations will be undertaken as part of the interim analysis.

• Interim tables, figures, and listings will be programmed using unaudited data from when 50% of the target patient enrollment has been reached.

• For the final analysis, ICON assumes that there will be up to 37 tables (26 unique and 11 replicate); five (5) figures (four (4) unique and one (1) replicate); and 33 listings.

• Replicate data displays (tables, listings, graphs) are those that are either an exact repeat of previously programmed displays rerun with a different patient subset, or essentially identical to displays previously programmed but containing different analysis variables.

• ICON will prepare the Statistical Analysis Plan (SAP) for the final report. For costing purposes, ICON has assumed that the SAP will include the following:

• Definition of variables to be analyzed, including the algorithm that will be used to compute all derived variables.

• Analysis procedures that will be employed, including mathematical models and SAS procedures where applicable.

• Naming conventions, abbreviations, and labels for groups and variables.

• Analysis conventions for missing data and early terminations.

• Mockup tables, figures, and listings (for unique tables, figures, and listings only).

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• The draft SAP will be prepared following final approval of the protocol for study NTI 0303. NTI will review the draft plan and provide one consolidated set of comments to ICON. Based on this input from NTI, ICON will make any requested modifications to the plan and submit it to NTI for review and approval. One additional iteration of the SAP has been budgeted, if necessary. Additional iterations will be at time and cost.

• Programming of tables, listings, and graphs will commence after approval of the final SAP by NTI. Up to ten (10) analysis datasets will be developed prior to the analysis. The analysis datasets will include analysis variables, demographic variables, and any other variables deemed necessary for the production of tables, data listings, or graphs. All variables will have labels attached to them and a separate format library will be created for variables that require formats. The analysis datasets should be the starting point for tables, listings, and graphs.

• ICON assumes that it will not be responsible for providing tables and listings for input to the annual report to the IND for hCRF during the course of the study. If NTI needs such tables and listings, they will be prepared under a separate consulting agreement.

• After database lock, ICON will provide draft tables, figures and data listings to NTI for review and approval. ICON assumes that NTI will return one set of consolidated, written comments to ICON. Based on these comments, ICON will finalize the tables, figures and data listings.

• ICON Biostatistics will prepare a statistical package for NTI to assist in its preparation of the final integrated clinical study report (CSR). The statistical package will include tables, figures, data listings, and descriptions of the study design, variables measured, and statistical methods of analysis.

• ICON Biostatistics will review the CSR, and will provide comments upon it.

• ICON Biostatistics will transfer a biostatistics archive to NTI following the final approval of the CSR. The archive will include hard copy and electronic copies of the final SAP, and the derived SAS datasets used for the final CSR. All SAS datasets supplied to NTI will be in transport format.

• ICON assumes that there will up to three (3) investigator meetings for this study and for study 0302, combined. Costs for biostatistical attendance at the December 2003 meeting were included under a different NTI study number, while costs for the attendance time at the July 2004 and December 2004 meetings will be charged to this study. Per previous arrangements with NTI, NTI will not be invoiced for travel time.

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IVRS Study Assumptions

IVRS Timelines

Major Milestones		Target Date
Project Award Date		[***]
Final, signed IVRS specifications/User Requirements		[***]
System “Go Live” Date		[***]
First Patient Randomized		[***]
Last Patient Randomized		[***]
Last Patient Treated		[***]
System completion - final data transfer		[***]
Study close-out (IVRS)		[***]

Study Information

		PROTOCOL
Duration of IVRS Involvement		29 months
Enrollment Period		[***]
Treatment period		4 months
Number of NA Sites		[***]
Number of W. Europe Sites		0
Number of ROW Sites		0
Number of Randomized Patients		200
Countries Involved		US
Languages Required		English, Spanish

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*Confidential Treatment Requested

System Development

• Each IVR system is developed within the parameters defined in the protocol and as specified by the study team. The following are involved in system set-up:

• Initial set-up meeting

• Script development

• System programming

• System testing and validation

• Computer and telephone configuration

• Import/data entry of site information

• Documentation

• Demonstration/Sample system

Reporting

• Confirmations will be faxed and/or emailed to the site immediately following a successful call to the IVRS. These one-page reports will re-state the information entered into the IVRS as well as list the assigned patient treatment.

• Real-time summary reports are available through a secure Internet connection. (Demonstration reports may be found at xxxx://xxxxxxxx.xxxxxx.xxx using [***]). These reports will list patient enrollment/randomizations per site and are available to access 24 hours/day. The sponsor will define who receives access to the Internet reports.

• Weekly data transfer reports are also available upon request.

System Maintenance

• We will maintain the IVRS for the duration of the study.

• Full backups of all data are performed nightly.

• 24-hour sponsor/site support is available throughout the life of the study.

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*Confidential Treatment Requested

Documentation

• We retain all documentation related to this study in compliance with relevant guidelines and regulations. All records are available for the sponsor or FDA auditors, and are maintained for a period of 15 years. Upon study completion, we will provide the sponsor with both a hard copy and electronic version of the IVRS database.

Project Management

• An IVRS project manager will be assigned to the study for the life of the project. He or she is responsible for managing system set-up, providing service to the study team and maintaining budgets and timelines.

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IVRS Services Requested

Interactive Voice Response System (IVRS)

Site capabilities		•      Randomization •      Subject Re-supply (2 calls) •      Subject discontinuation/completion •      Confirm receipt of drug shipment
Patient Capabilities		•      [***]
Sponsor capabilities		•      Site activation
Reporting
Site Level		•      Fax or email confirmation. A confirmation fax and/or email is sent after each successful call to the system •      Real-time site-specific summary reports available via the Internet
Sponsor Level		•      Up to five Real-time summary reports available via the Internet •      Weekly data transfer via one specified format (Can be transmitted as frequently as necessary)

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*Confidential Treatment Requested

Grant Administration Assumptions

Grant Payment Timelines

Milestone		0303
ICON Grant Payments Begins		[***]
Last Patient In		[***]
Last Patient Out		[***]
ICON Involvement Ends		[***]
Total ICON Involvement for Grant Payments		28 Months

Sites/Patients

		0303
Number of Sites (Administration of Payments)		[***]
Number of Patients		200

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*Confidential Treatment Requested

Grant Administration Assumptions

ICOTrack/ICONomics

• Costs include ICOTrack set-up, monthly maintenance, and ICON standard reports

• ICONomics, ICON’s grants management system, will be used to generate payments for investigators

• ICON assumes that NTI will provide clean data to ICON to be loaded into the ICOTrack system for subsequent use in site payments via ICONomics

Grant Administration

• ICON will administer payments due to investigators on a monthly basis

• NTI will be responsible for grant negotiations and any revisions to grant payments

• Any courier expenses will be passed through to NTI

• Pass-through Investigator fees have not been estimated

• Upon execution of the Work Order for these studies, ICON would request an initial payment equal to 15% of the total budget for investigator payments. ICON will draw down upon these funds to pay Investigator Grants and will provide NTI with monthly invoices accounting for such payments on an “as-paid” basis, without any added overhead, management fee or profit factor. NTI will not be responsible to pay any additional amounts for Investigator Grant payments until the initial payment reaches $10,000 or less, whereupon ICON will invoice NTI for an amount to replenish the funds to again equal 15% of the total budget for Investigator Grant Payments. If at any time funds are insufficient to cover Investigator Grant payments, ICON will delay payments to Investigators pending receipt of additional funds from NTI. At the end of the Projects, any excess funds held by ICON shall be returned to NTI

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Project Team Structure

Project Manager

ICON proposes Xxxxxx Xxxxx as the Project Manager for these studies. She will be allocated 5% (total) to the 0302 & 0303 studies and will be based in the North Wales, PA office. Project responsibilities include the following:

• Serve as NTI’s primary point of contact during the conduct of this program

• Perform all duties to ensure the success of sponsor programs as outlined in the clinical service agreement

• Manage budget reports and provide NTI with verbal and written updates

• Participate in teleconferences and on-site meetings as necessary with NTI to report on progress and promptly resolve issues

• Participate in training of ICONomics with NTI as necessary

• Oversee and coordinate the entry of status updates

• Authorize grants to investigators

Investigator Grants Manager

• Oversight of grants administration staff

Investigator Payments Administrator

• Process payments to investigators

• Provide historical payment info as requested

• Serve as a liaison to Accounts Payable

Investigator Payments Assistant

• Support Investigator Payments administrator

• Load ICONomics system with study specific information

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ICONomics - A Grants Management System

ICONomics Set-Up

Completing the detailed screens found in ICONomics Set-Up is the first step in setting up the payment process for a study in ICONomics. The system stores all the study-specific details of the payment schedules, types of payments that will be made for a given study, and standard defaults for all payment information. It also stores all investigator specific information for a study. This information includes items such as: the investigator name and address, payee and tax ID number for the investigator, the required currency for the site, any percentage breakouts of payments for a site to multiple payees, and the specifically negotiated payment details for the various elements of the study that the investigator will be performing.

Once the initial set-up is completed by the Information Systems staff, the payment amount details for the investigator, patient, and visit level payments, if applicable, are entered. Basic investigator site and demographic information is imported from the study’s ICOTrack database. This data cannot be edited on ICONomics Set-Up screens. Using the study’s investigator list, additional data entry is performed in two steps. First, the standard default information for schedules and all payments are entered. Once that is complete, the specific investigator level detail based on negotiated contracts is then entered. Only those authorized to work with this level of payment detail will have edit access to these data entry screens. Once the fields are entered and proofed, they are locked. Any changes to the fields are then recorded in a full audit trail.

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ICONomics Tracking

After the ICONomics Set-Up activities are completed, the information is then used to generate and track payments made throughout the course of the study. Based on the details of the study provided on the set-up questionnaire completed by the project manager, various payment triggers and details are established. Once this is done, a request for payment based on the items that need to be paid is then made. The designated member of the clinical team would then review the requested payments and approve or disapprove them as needed. Once approval has been received, the payment details for each site are generated. The payment details are then given to the Finance Department where the information is then uploaded into the ICON Financial System. Checks are then produced for the identified payees for the amounts specified from ICONomics. The ICON Financial System then produces a data file with check numbers, dates, and site information that is then downloaded into ICONomics to update all the line items that were paid, noting the check number and date on which they were paid Once this is done, a detailed report is generated that will accompany the check to the payee. Copies of these reports and checks are then also filed appropriately in the Finance Department.

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Exhibit B

Cost and Payment Schedule

Cost Estimates

Estimates of ICON professional fees and pass-through costs for this study are presented in the following table. These projected costs are reflective of the study assumptions presented in the next section. Should the study assumptions change, or upon finalization and ICON review of the protocol and CRF, the estimates provided herein may require modification.

ICON incorporates an annual increase into its staff charge out rates to account for salary increases, cost of living increases, benefits, and competition for staff within the industry. Therefore, ICON has blended staff charge out rates across the lifetime of the study. The blending of rates has been ‘weighted’ and is in direct correlation to the timelines presented herein. If the timelines require modification this will impact the rates accordingly.

Estimated costs representing the total proposed budget for this project are presented in the table below.

Project Cost Category		Total Cost
Data Management (DataFax)		[***]
Biostatistics/SAS® Programming		[***]
IVRS		[***]
Grant Administration		[***]
Subtotal Total Direct Fees		[***]
Estimated Pass-Through Costs (CRF Binders)		[***]
Total Study Budget		[***]

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*Confidential Treatment Requested

Data Management (DataFax) Costs

Data Management (Data Fax)
Activity		Total Cost
Project Initiation		[***]
DataFax Setup		[***]
Data Management		[***]
CRF Review		[***]
Quality Control		[***]
Processing Lab Data		[***]
Archiving		[***]
Meetings		[***]
DataFax Lite		[***]
Data Management Total		[***]

Biostatistics Costs

Biostatistics
Activity		Total Cost
Analysis Plan		[***]
Interim Analysis		[***]
Interim Report		[***]
Final Analysis		[***]
Final Report		[***]
Archiving		[***]
Meetings		[***]
Biostatistics Total		[***]

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*Confidential Treatment Requested

Grant Administration Costs

Investigator Grant Management
Activity		Unit		Number of Units		Price per Unit		Total Cost
Project Manager*		Month		28		$[***]		$[***]
Grant Administration**		Site / Month		728		$[***]		$[***]
ICOTrack / ICONomics Set-up		Set-up		1		$[***]		$[***]
ICOTrack / ICONomics Maintenance		Month		26		$[***]		$[***]
Grant Administration Total								$[***]
Less 6% Repeat Customer Discount								($[***])
Grant Administration Grand Total								$[***]

* Project Management is based on a total 7.8 hours per month

** Grant Administration costs are based on active site months plus 1 additional month, multiplied by the number of sites and the hourly rate of $60

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*Confidential Treatment Requested

IVRS Costs

IVRS		Total Cost
System Development
Initial Set-Up Meeting
Script Development
System Programming
Computer and Telephone Configuration
Import/data entry of site information
Documentation
Reporting set-up
Demonstration/Sample system
Generate Randomization List		$[***]
Prompt Recording
English: $[***]		$[***]
Additional languages: $[***] per language plus pass through cost estimated at $[***] per language 1 Language @ $[***]		$[***]
Monthly Service Fee
Month 1 @ $[***]
Month 2 @ $[***]
Month 3 @ $[***]
Month 4 @ $[***]
Months 5-29 @ $[***] per month
System Maintenance
24-hour support service
Project Management
Reporting
Telephone/fax costs		$[***]
Telecom Costs		$[***]
Investigator’s Meeting		$[***]
Preparation/Attendance/presentation at 1 meeting(s)
IVRS Total		$[***]

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*Confidential Treatment Requested

Pass-Through Costs

• Travel costs for meetings, overnight delivery, teleconference bridge costs, etc., have not been included in this estimate, but will be treated as pass-through expenses.

• ICON will arrange for 200 CRF binders to be produced and shipped by an outside vendor.

• Courier expenses for Grant Administration will be passed through.

• Pass-through Investigator fees have not been estimated.

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Payment Schedule

Data Management (Data Fax) and Biostatistics, Payment Schedule

Milestone		Payment		Total Cost
Execution of Project Contract (October 2004)		$[***]		$[***]
Monthly Payments (November 2004 - December 2006)		$[***]/ month for 25 months		$[***]
Total Cost				$[***]

Grant Administration Payment Schedule

The ICOTrack/ICONomics set-up fee is payable upon signature of final agreement. Project Manager, Grant Administration and ICOTrack / ICONomics Maintenance will be invoiced monthly for actual units incurred based on the costs outlined in the Grant Administration Cost Estimate section.

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*Confidential Treatment Requested

IVRS Payment Schedule

50% of system development fee is payable upon signature of final agreement. The remainder is payable when the system becomes operational. If enrollment is delayed, 25% of the monthly fee will be assessed for telephone and system maintenance. If applicable, travel expenses for set-up meeting will be pass-through.

The monthly fee will be assessed until IVRS is no longer required. A minimum number of months will be billed (66% of total number of months proposed) if all patients complete early. The monthly fee includes all telephone and fax charges. No additional pass-through costs will be assessed.

The cost for Investigator Meetings’ does not include pass-through expenses such as airfare, meals, etc. Additionally, the estimated cost includes 4 hours preparation, 8 hours of travel and a one-day meeting. Each additional day = $1000.00

Drug management costs are based upon a trigger level resupply scheme.

Randomization is dynamic and stratified. Randomization scheme to be provided by NTI.

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Exhibit C

Transfer of Obligations

Neurobiological Technologies, Inc., as sponsor of the Project Contract, hereby transfers responsibilities for the obligations set forth in Exhibit A and ICON Clinical Research, L. P. hereby assumes such obligations, in accordance with 21 C.F.R. section 312.52.

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Exhibit D

Key Personnel

ICON Clinical Research Personnel l. Xxxxx Xxxxxx

1. Xxxxx Xxxxxx

Senior Biostatistician

ICON Clinical Research, L. P.

000 Xxxx Xxxxxxx Xxxx

Xxxxxxx Xxxx, XX 00000

Phone: 000-000-0000

Fax: 000-000-0000

Email: xxxxxxx@xxxxxx.xxx

2. Xxxxx Xxxxx

Senior Database Administrator

ICON Clinical Research, L. P.

000 Xxxx Xxxxxxx Xxxx

Xxxxxxx Xxxx, XX 00000

Phone: 000-000-0000

Fax: 000-000-0000

Email: xxxxxx@xxxxxx.xxx

Neurobiological Technologies, Inc. Personnel

3. Xxxxxxx XxXxxxxxxx

Clinical Project Manager

Neurobiological Technologies, Inc.

0000 Xxxxx Xxxxx, Xxxxx 000

Xxxxxxxx, XX 00000

Phone: 000-000-0000

Fax: 000-000-0000

Email: xxxxxxxx@xxxx.xxx

30