Skip to main content
Home
User account menu
  • IRBManager
  • CTSU
Main navigation
  • Home
  • About
    • Our Mission
    • Our History
    • Who’s Involved
    • About the Boards
      • Adult CIRB - Late Phase Emphasis Members
      • Adult CIRB - Early Phase
      • Pediatric CIRB
      • Cancer Prevention and Control CIRB
    • CIRB SOPs
    • List of Institutions
    • Studies
  • For New Users
    • Overview of the Study Review Process
    • Frequently Asked Questions about Navigating IRBManager
    • When To Use NCI CIRB, IRBManager, and CTSU Websites
  • For Institutions
    • IRBManager Basics
    • Overview of the Study Review Process
    • Becoming A Signatory Institution
    • Navigating The CIRB For NCI Division of Cancer Prevention (DCP) Consortia Sites And Cancer Prevention Clinical Trial Network (CP-CTNET) Organizations
    • Create and Update the Signatory Institution Worksheet
      • Completing The Annual Signatory Institution Worksheet
      • Establishing Your Signatory Institution
      • Short Form Q & A
    • Creating and Updating the Annual Principal Investigator Worksheet
      • Establishing a Principal Investigator
    • How to Open a Study
      • Opening a Study
    • Change the PI on a Study
      • Changing the PI on a Study
    • Submit a Study Closure
    • Report A Potential Unanticipated Problem Or A Serious Or Continuing Noncompliance
    • Request an Assent Waiver
      • Completing The Assent Waiver Worksheet
    • Notify the CIRB about the participation of an incarcerated participant
      • Completing The Notification of Incarcerated Participant Worksheet
      • Institution Q & A
      • Boilerplate Language Q & A
      • Finding Information Q & A
      • Guidelines For Permitted Boilerplate Language Additions
      • Individual Roles Within The CIRB
      • Institutions' Roles With The CIRB
      • Managing Your CTEP Registration
      • Oversight Q & A
      • Updating Your CIRB Institution Roster using RUMS
      • Updating Your CIRB Person Roster using RUMS
      • Viewing Your CIRB Roster
  • For Networks
    • Overview of the Study Review Process
    • CIRB Document Posting
    • Submitting Studies
      • Completing The Translation Application
      • Completing The Unanticipated Problem And/Or Serious or Continuing Noncompliance Submission Application
      • Completing The Waiver Of Consent Application
      • Determining Waiver Of Consent Requirements
      • End User Licensing Agreement (Eula) Consent Form Language Q & A
      • Review of Translated Consent Forms, PROs, and Other Patient-Facing Documents
      • Submitting Recruitment/participant Materials For Review
    • CIRB Meeting Schedules
  • For Board Members
    • Become A Board Member
    • Overview of the Study Review Process
    • Resources
      • Helpful URLs
      • IRBManager Training for Board Members
    • CIRB Meeting Schedules
  • Contact Us

Breadcrumb

  1. Home
  2. Completed

Completed

NRG-BR005

  • Read more about NRG-BR005

MDA2014-04-01

  • Read more about MDA2014-04-01

MDA2014-04-02

  • Read more about MDA2014-04-02

NWU2014-04-01

  • Read more about NWU2014-04-01

UAZ2015-05-02

  • Read more about UAZ2015-05-02

10050

  • Read more about 10050

NRG-GY011

  • Read more about NRG-GY011

10058

  • Read more about 10058

10017

  • Read more about 10017

MAY2016-07-01

  • Read more about MAY2016-07-01

Pagination

  • Previous page ‹‹
  • Page 27
  • Next page ››
Subscribe to Completed
Close

The NCI Central Institutional Review Board

401 N. Washington Street, Ste. 700
Rockville, MD 20850

The Central Institutional Review Board for the National Cancer of Institute is fully accredited by the Association for the Accreditation of Human Research Protection Program, Inc.