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This document serves as an informed consent form for participants in a clinical research study sponsored by Suzhou Connect Biopharmaceuticals. The study aims to evaluate the efficacy, safety, pharmacokinetics, and pharmacodynamics of the investigational drug CBP-201 for treating moderate to severe atopic dermatitis. The consent form outlines the purpose, procedures, risks, benefits, and participants\' rights regarding their involvement in the study.
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How to fill out informed consent form for

01
Start by reading the informed consent form carefully to understand the information provided.
02
Provide your personal information, including your name and contact details, in the designated sections.
03
Review the purpose of the study or treatment being conducted.
04
Understand any potential risks or benefits associated with participation.
05
Ask any questions you may have regarding the procedure or study to the researcher or healthcare professional.
06
Confirm your understanding and willingness to participate by signing and dating the form.
07
Keep a copy of the signed form for your records.

Who needs informed consent form for?

01
Individuals participating in clinical trials or research studies.
02
Patients receiving treatment that involves significant risks.
03
Participants in educational programs that require personal information disclosure.
04
Anyone involved in studies that could influence their welfare or rights.
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An informed consent form is a document that provides information about a study or medical procedure, ensuring that participants understand what participation entails and that they agree to take part voluntarily.
Researchers, healthcare providers, or organizations conducting studies or medical procedures involving human subjects are required to file an informed consent form.
To fill out an informed consent form, participants must read the document carefully, understand the information provided, sign it indicating their willingness to participate, and date it appropriately.
The purpose of an informed consent form is to ensure that participants are fully informed about the risks and benefits of the study or procedure and to protect their autonomy in making a decision.
The informed consent form must report information such as the purpose of the study, procedures involved, risks and benefits, confidentiality assurances, and the right to withdraw at any time.
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Relevant keywords

clinical trial informed consent CBP-201 atopic dermatitis biopharmaceuticals placebo-controlled randomized study pharmacokinetics safety evaluation investigational drug

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