Get the free Protocol-RTOG 0132/ACRIN 6665 Amendment 9, 9.10.07 - acrin

RADIATION THERAPY ONCOLOGY GROUP RTCG 0132 A PHASE II TRIAL OF NEOADJUVANT/ADJUVANT STI-571 (NSC #716051) FOR PRIMARY AND RECURRENT OPERABLE MALIGNANT GIST EXPRESSING THE KIT RECEPTOR TYROSINE KINASE

How to fill out protocol-rtog 0132acrin 6665 amendment

How to fill out protocol-rtog 0132acrin 6665 amendment:

1. Start by obtaining a copy of the protocol-rtog 0132acrin 6665 amendment form. This form can typically be found on the official website of the organization or institution responsible for overseeing the protocol.
2. Read the instructions carefully before beginning to fill out the form. This will help ensure that you understand the requirements and can provide accurate information.
3. Begin by providing your personal details, such as your name, contact information, and any relevant identification numbers or codes.
4. Next, provide the necessary information about the protocol for which the amendment is being made. This may include the protocol number, title, and a brief description.
5. Clearly state the specific changes or amendments that need to be made to the protocol. It is important to be concise and precise in describing the modifications.
6. If applicable, provide any additional documentation or supporting materials that may be required or helpful in understanding the proposed changes.
7. Review the completed form before submitting it to ensure that all the necessary information has been provided and all sections have been properly filled out.

Who needs protocol-rtog 0132acrin 6665 amendment:

1. Researchers or medical professionals involved in conducting clinical trials or studies under the protocol-rtog 0132acrin 6665 may need the amendment. This could include principal investigators, study coordinators, or other members of the research team.
2. Institutional review boards (IRBs) or ethics committees responsible for reviewing and approving the protocol may also require the amendment. They ensure that any changes made to the protocol align with ethical guidelines and regulations.
3. Regulatory authorities or agencies overseeing the protocol or clinical trial may request the amendment to ensure compliance with regulatory requirements and standards.
4. Participants or patients enrolled in the protocol-rtog 0132acrin 6665 may indirectly benefit from the amendment, as it aims to improve the quality, safety, or efficacy of the study.

Note: It is important to consult the specific guidelines and regulations governing the protocol-rtog 0132acrin 6665 and seek guidance from the appropriate authorities or professionals when filling out the amendment form.

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