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Phase II AntiPD1 Epigenetic Therapy Study in NSCLC NCT01928576 4/14/2021Date: April 14, 2021 Principal Investigator: Julie Brahmer, MD Application No.: NA_0084192 Approved April 14, 2021 If appropriate

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How to fill out informed consent to take

01

Read the informed consent form carefully.

02

Understand the purpose of the study or procedure.

03

Review the risks and benefits outlined in the form.

04

Ask any questions to clarify doubts with the researcher or healthcare provider.

05

Ensure that you are comfortable and willing to participate.

06

Sign and date the form to indicate your consent.

Who needs informed consent to take?

01

Patients participating in medical research.

02

Participants in clinical trials.

03

Individuals undergoing medical procedures.

04

Subjects in psychological studies.

05

Volunteers for experimental treatments.

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What is informed consent to take?

Informed consent to take refers to the process by which an individual voluntarily agrees to participate in a study or treatment after being fully informed about the potential risks, benefits, and implications of participating.

Who is required to file informed consent to take?

Researchers, clinicians, or organizations conducting studies or treatments that involve human subjects are typically required to obtain and file informed consent.

How to fill out informed consent to take?

To fill out informed consent to take, individuals must review the provided information about the study or treatment, ask questions if needed, and then sign the consent form indicating their understanding and willingness to participate.

What is the purpose of informed consent to take?

The purpose of informed consent to take is to ensure that participants are aware of what they are consenting to and to protect their autonomy by enabling them to make an informed decision about their participation.

What information must be reported on informed consent to take?

Informed consent forms must report information such as the purpose of the study, procedures involved, potential risks and benefits, confidentiality measures, and the right to withdraw from the study at any time.

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