The following IIS study types may be considered for support:

• Prospective clinical or preclinical studies involving Taiho products
• Non-interventional research, such as epidemiology or outcomes studies, where the focus is on scientific understanding of the disease
• In vitro and in vivo studies

We do not provide support for the following:

• Proposals that are not aligned with our current areas of interest
• Studies that have already started or are completed
• Proposals that are conditioned upon past or future prescriptions or purchases of Taiho products
• Requests that create a conflict of interest for Taiho

To begin the process of submitting a proposal for initial evaluation, the submitter will be required to create and access a Taiho Oncology portal account and then complete a submission form and attach required documents. A complete and detailed submission will facilitate management and evaluation of your proposal.

1. Complete submission form
2. Attach required documents:
   • Study Proposal
   • Principal Sponsor-Investigator's Curriculum Vitae
   • Budget
3. Submit proposal
4. Taiho Oncology will send an email notification acknowledging receipt of submission.
5. Incomplete submissions that do not include required documents will not be processed until all requested information is received and will be returned to the submitter.
6. Upon receipt of a complete application and review by the internal review committee, Taiho Oncology will notify the submitter of the proposal review decision.

If approved, the full protocol must be submitted within 90 days of the study proposal approval notification.

Funding will be provided for approved protocols upon contract execution.

We will consider reasonable requests for funding in support of an IIS. All full proposal submissions must include an itemized budget with costs based on fair market value (FMV) evaluations to ensure that the amount of support is appropriate. Requestors may use their own template or the Taiho template that is provided here. Line item allocations should be specified for each aspect of the study, such as study start-up fees (e.g., IRB submission), study visits (e.g., physical exam, vital signs, pregnancy test), and publication costs (e.g., medical writer).

For study-specific items, or equipment that may be required, please provide a rental estimate from a vendor of choice. Please note that we do not provide support for the following:

• Salary and/or benefit payments for Investigators or study staff
• Education/training activities
• Costs that are deemed in excess of fair market value
• Capital equipment purchases (associated rental fees will be considered)
• Construction funds to build new facilities

Follow instructions provided on the HOW TO APPLY tab, or you may access the user guide for additional guidance.
Click on CREATE ACCOUNT in the top menu, or download the user guide for additional information.

• Use the "Forgot Password?" link to reset your password.
• If you do not receive the password reset email in your inbox, please check your Junk or Spam folder.

You may view the status of your submission via the MY SUBMISSIONS tab after you've logged into your account.

By submitting materials for review, you agree that the information is not confidential, nor proprietary, and may be referred to a number of different persons at Taiho to determine the level of interest in supporting your request.

Publications or other presentation of data derived from the IIS must be marked with an acknowledgement that the study was conducted with financial and/or in-kind support from Taiho, as a collaborator.