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PEDAL
Trial ProtocolProspective Evaluation of Measurable Residual Disease in Intensively
Treated Patients with Acute Myeloid Leukemia (AML) as Surrogate
Endpoint for Survival
Trial Code:
Therapeutic
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Anyone conducting a clinical trial and using the clinicaltrialsgov platform needs to fill out Berschrift 1.
02
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Individuals or entities seeking to register and publish details about their clinical trials on a public platform will require Berschrift 1 completion.
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What is berschrift 1 - clinicaltrialsgov?
Berschrift 1 - clinicaltrialsgov is a section of the clinicaltrialsgov website where information about clinical trials is submitted and made publicly available.
Who is required to file berschrift 1 - clinicaltrialsgov?
All sponsors or investigators conducting clinical trials are required to file berschrift 1 - clinicaltrialsgov.
How to fill out berschrift 1 - clinicaltrialsgov?
Berschrift 1 - clinicaltrialsgov can be filled out by providing information about the clinical trial, including study objectives, methods, eligibility criteria, and contact information.
What is the purpose of berschrift 1 - clinicaltrialsgov?
The purpose of berschrift 1 - clinicaltrialsgov is to provide transparency and access to information about clinical trials to the public and research community.
What information must be reported on berschrift 1 - clinicaltrialsgov?
Information such as study title, protocol summary, recruitment status, location, and key dates must be reported on berschrift 1 - clinicaltrialsgov.
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