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Clinical Trial GFT505B2161 Protocol V3.0 04 December 2017NCT03124108TITLE PRECLINICAL PROTOCOL PHASE 2 Protocol N GFT505B2161 Extract N201600381780 IND number: 132202 Final 3.0 Release date 04 December

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What is clinical trial gft505b-216-1?

Clinical trial gft505b-216-1 is a specific clinical study aimed at evaluating the safety, efficacy, and possible side effects of the experimental drug GFT505 under controlled conditions.

Who is required to file clinical trial gft505b-216-1?

The sponsor or the organization conducting the clinical trial, typically a pharmaceutical company or a research institution, is required to file clinical trial gft505b-216-1.

How to fill out clinical trial gft505b-216-1?

To fill out clinical trial gft505b-216-1, the sponsor must provide detailed information regarding the trial design, objectives, methodology, treatment regimens, participant criteria, and data collection procedures, ensuring compliance with regulatory standards.

What is the purpose of clinical trial gft505b-216-1?

The purpose of clinical trial gft505b-216-1 is to investigate the therapeutic effects of GFT505 on specific medical conditions, assess its safety profile, and gather data that supports regulatory approval and clinical usage.

What information must be reported on clinical trial gft505b-216-1?

The information that must be reported includes the trial's objectives, design, methodology, participant demographics, results, and any adverse events that occurred during the study.

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