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CRC Basic 2.0 Budgeting for Industry-Sponsored Clinical Trials

CRC Basic 2.0 Budgeting for Industry-Sponsored Clinical Trials. Julie Calahan, CCRP Clinical Trials Budget Analyst Health System Contracts Office. Clinical Trials Contracts Office. Annie Wong – Health System Contracts Director Signatory and Director of Clinical Trials unit.

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CRC Basic 2.0 Budgeting for Industry-Sponsored Clinical Trials

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  1. CRC Basic 2.0Budgeting for Industry-Sponsored Clinical Trials Julie Calahan, CCRP Clinical Trials Budget Analyst Health System Contracts Office

  2. Clinical Trials Contracts Office Annie Wong – Health System Contracts Director Signatory and Director of Clinical Trials unit Erick Jenkins – Clinical Trials Officer Supervises Clinical Trials unit, negotiates new and complex clinical trial agreements and assists in negotiation of UCOP master agreements, liaison with UC Office of the President and CTSC Andrew Jones – Clinical Trials Analyst Negotiates agreements under master clinical trial agreements and some new agreements Lorie Dilts – Clinical Trials Analyst Negotiates amendments and confidentiality agreements, office and database management Julie Calahan – Clinical Trials Budget Analyst Assists departments with budget development and negotiation, develop clinical trial budgeting policy

  3. Objectives • Roles of coverage analysis and internal budget • Components of a clinical trial budget • Budget template and examples • Budget negotiation tips and tactics • Resources and questions

  4. What is a clinical trial? • (for the purposes of application of 26% indirect rate*) • The controlled, clinical testing in human subjects of investigational new drugs, devices, treatments, or diagnostics, to assess their safety, efficacy, benefits, costs, adverse reactions and/or outcomes. • *This rate applies to the Total Direct Cost, and no budgeted item is excluded from the application of indirect. This rate applies regardless of whether a Clinical Trial is based on sponsor -initiated, or an investigator-initiated protocol.

  5. Industry Sponsored Clinical Trial Approval Process Receive Sponsor Packet (Protocol, CTA & Budget) PI Interest Send Sponsor Packet to Clinical Trial Budget Analyst and Research Abstractor • Research Team Drafts Internal Budget (UBT) • 1)Gather information from • Research Team Members (CRC, PI) • Quantim • Investigational Drug Services • Other Depts (CCRC, Radiology, Pathology) • 2) Use Research Query Tool for current research prices • 3) Complete Coverage Analysis Negotiate Budget & Payment Terms w/Sponsor (External Budget) Assistance provided by Research Abstractor and Budget Analyst • Research Team determine feasibility: • Scientific Merit • Financial Soundness • Pt Accrual Clinical Trial Contract Packet Forwarded to Dean’s Office for Signature No Send packet to Chair for Approval & Signature Tabled Yes • CT Contracts Office • Negotiates Contract Language • Signs Off on Final Budget

  6. The role of Coverage Analysis (CA) and internal budget (UBT)

  7. Coverage Analysis Works To Create Accurate Budget

  8. How can I use Coverage Analysis? • Use to create an accurate budget • Provides a list of study events in a Billing Grid • Early analysis will: • Identify all procedures • Identify CPT codes for research costs • Identify policies limiting insurance coverage • CTSC Coder provides assistance • Obtain research costs by CPT code • Cost Query Tool • Accurate costs=accurate budget • Accurate budgeting useful for feasibility, negotiations with sponsors, patient billing, invoicing

  9. Use the BG to prepare internal budget • Look up clinical trial costs by CPT code in Cost Query Tool • Base External budget on internal budget • Negotiate with sponsors • Billing, CTA, Consent Form match

  10. Medicare National Clinical Trial Policy • Coverage Analysis is a UC requirement for all studies with patient care services billed through UCDMC • At UC Davis we can determine when a clinical trial meets national policy guidelines by performing a Coverage Analysis • NCD explicitly defines coverage of clinical trial services

  11. What does sponsor pay for?What does 3rd party (Ins co) pay for? Sponsor Insurance/Medicare/Pt Acct needed to clinically manage pt care Insurance/Medicare/Pt Acct services pt receives if not in CT but part of protocol – SOC

  12. Billing Grid continued… • Tool to create an accurate budget • Identify the study events • Lists study events in the form of a CPT code • Research Costs can be found by CPT code • Lists who will be billed (sponsor or insurance billing) • Tool to reconcile billing statements

  13. Components of a clinical trial budget

  14. Start-up Costs Start Up Close Out Invoicables Per Patient Tasks Categories of tasks Complete Feasibility Questionnaire from Sponsor Review protocol & study flow Review by Scientific Review Committee (Cancer Ctr) Preparation and return of Sponsor/Site documents Pre-Study Site Selection visit, prepare for & attend Prepare, distribute, collect and copy financial disclosures Obtain and copy CV's Preparatory Research CMS determination Protocol-related tasks Budget-related tasks IRB Docs Training Pharmacy communication Communications w/Sponsor FEES Advertisement Office supplies Pharmacy start-up, inventory Translation of Informed Consent

  15. Close Out Costs Start Up Close Out Invoicables Per Patient Tasks Closeout Report Complete Queries Box up Study Records Transport Study Records for storage Closeout Visit, Prepare for & Attend Regulatory close with IRB Close out study account w/Extramural (incl.payroll transfer) Close out invoicing Producing addtl information after study close out

  16. Invoicable Costs Start Up Close Out Invoicables Per Patient Categories of Tasks Adverse events x 8 Monitoring Visits x2 Screen Failure x4 Annual Report x1 IRB Docs x1 Admin/Correspondence x1 Mods to Reg Documents Regulatory Binder, Maintain IRB, Communicate Modifications, incl 1572 Contracts, Communicate Modifications Invoicables may or may not happen Each category multiplied by the number of occurrences Must include to come up with the total budget

  17. Per Patient Costs Start Up Close Out Invoicables Per Patient

  18. Unified Budget Template (UBT)

  19. Internal Budget (UBT) Summary Shows anticipated revenue residuals/loss assuming full enrollment of patients completing entire study

  20. Factors impacting budgets • Composition of research personnel • The type, phase, and complexity of the protocols involved • Screen failure rates • The actual time it takes to perform the work • Given the organization of clinical trial research services within the research unit • Anticipated complications • Sample processing and/or shipping logistics • Patient treatment logistics and scheduling challenges • Data management in busy studies • Time limits on patient accrual reporting and data query resolution

  21. Start-up CostsIf you don’t ask for it, you won’t get itStart-up fees should always be non-refundable

  22. Close-Out and Other Invoicables

  23. Per Patient Costs – Study Procedures/Labs

  24. Per Patient Costs - Other

  25. Per Patient Costs - Study Activities

  26. Per Patient Costs Salary Calculator -linked to all costs throughout the budget

  27. Completed UBT

  28. Budget Negotiations

  29. Budget negotiations…… • Sponsor’s initial budget is STARTING POINT for negotiations (perform a thorough analysis of the specific protocol) • Keep in mind ……all sponsors and CROs have a business plan to make money • Communicate resources available to conduct trial • Expertise • Facilities • Access to large patient population • Remain neutral…establish that you represent the University and are negotiating the budget on behalf of the study team • A break-even point and bottom line should be determined

  30. Budget negotiations (con’t)….. • Keep the PI in your corner • Keep him/her informed • Ready to intervene • Ready to remind sponsor of the benefits of having UCD as a site • Keep momentum going if negotiations are moving quickly • Don’t let aggressive CROs push you around • Remain calm and exercise some patience • Reach out to resources within the UCD research community for advice

  31. Budget negotiations (con’t)….. • Payment Terms • REVIEW, REVIEW, REVIEW!!! • Advance vs. start-up • Interim Payments • Payment Withholding • Final Payment • Screen Failures

  32. Resources

  33. Resources • Clinical Trials Website • UCD Clinical Research Guidebook • Process Maps

  34. Research Costs - UCDHS Query Tool B6 FIN to provide cost data for clinical trial billing codes

  35. CPT Codes - Quantim

  36. Questions ??

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