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This document provides consent information for participants in a phase 1b clinical trial testing the combination of bemcentinib and standard chemotherapy for patients with metastatic pancreatic cancer. It outlines the study objectives, procedures, risks, and participant rights.
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How to fill out phase 1b research consent
How to fill out phase 1b research consent
01
Read the entire consent form thoroughly.
02
Understand the purpose of the phase 1b research study.
03
Review the potential risks and benefits outlined in the document.
04
Complete any required personal information sections.
05
Initial any sections that require acknowledgment of understanding.
06
Sign and date the consent form where indicated.
07
Ask the research team any questions you may have before submitting the form.
Who needs phase 1b research consent?
01
Patients considering participation in a phase 1b clinical trial.
02
Investigators conducting the research study.
03
Institutional review boards (IRBs) overseeing the study.
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What is phase 1b research consent?
Phase 1b research consent is a formal agreement obtained from participants in clinical trials, specifically in Phase 1b studies, that outlines the nature, purpose, and potential risks of the research.
Who is required to file phase 1b research consent?
Researchers and institutions conducting Phase 1b clinical trials are required to file phase 1b research consent.
How to fill out phase 1b research consent?
To fill out phase 1b research consent, follow the guidelines provided by the Institutional Review Board (IRB), ensuring all participant information, study details, risks, and benefits are clearly outlined and understandable.
What is the purpose of phase 1b research consent?
The purpose of phase 1b research consent is to ensure that participants are fully informed about the study, understand their rights, and voluntarily agree to participate.
What information must be reported on phase 1b research consent?
Phase 1b research consent must report information such as the study’s purpose, procedures, potential risks and benefits, confidentiality provisions, and the right to withdraw.
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