the development, medicines, receive treatment with, a standard of care, a placebo, detaild information, objectives, risks, ethical.

日本語の文章： 「治験に参加することは、新しい医薬品の開発に貢献する一環となります。治験では、患者は試験薬、標準治療、またはプラシーボのいずれかを受けます。研究の目的やリスク、利益についての詳細な情報を受け取り、自発的な同意を提供することが求められます。治験は患者の権利、安全、福祉を守るために厳格な倫理的原則に基づいて行われます。」

Participate in clinical trials contributes to development of new medicine. In clinical trials, patients are to treated either Investigational product, a standard of care, or placebo. Patients should be received the detail of an objective of study, risk and benefits, also should be provide voluntary consent. Clinical trials are conducted based on strict ethic principals in order to protect the rights, safety, welfare of patients.

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Participating in clinical trials contributes to the development of new medicines. In these trials, patients may receive treatment with either an investigational product, a standard of care, or a placebo. Patients should receive detailed information about the study's objectives, risks, and benefits, and they must provide voluntary consent. Clinical trials are conducted based on strict ethical principles to protect the rights, safety, and welfare of patients.