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Protocol No. DCL10001A Phase 1, Multimeter, OpenTable, Dose Escalation Study of I131CLR1404 in Subjects with Relapsed or Refractory Advanced Solid Malignancies05 May 2010 Version 00Cellectar, Inc. 3301
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Gather all the necessary information and documents required for the phase 1 multi-center.
02
Identify the principal investigator and collaborating investigators for the study.
03
Determine the study design and objectives.
04
Develop the study protocol, including study procedures and interventions.
05
Obtain ethical approval from the appropriate research ethics committee.
06
Identify and select the participating study centers based on their suitability and capability.
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Train the study staff at each center on the study protocol and procedures.
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Conduct pre-study visits to ensure that each center meets the necessary requirements.
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Initiate the study by recruiting participants at each center.
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Monitor and manage the study progress, ensuring adherence to the study protocol.
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Collect and analyze the data obtained from each center.
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Prepare and submit the study report to the relevant authorities.

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A phase 1 multi-center is a research study that involves multiple research sites collaborating on a single clinical trial.
Any organization or individual conducting a phase 1 multi-center study is required to file the necessary paperwork.
To fill out a phase 1 multi-center, you must gather all required information and submit it according to the guidelines provided by the regulatory authorities.
The purpose of a phase 1 multi-center is to gather data from multiple research sites to increase the generalizability of the study findings.
Information such as study protocol, informed consent forms, recruitment strategies, and study timeline must be reported on a phase 1 multi-center.
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