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FOR PROVIDERSAlnylam Sponsored ThirdParty Genetic Testing and Counseling Programs for Primary Hyperoxaluria Type 1 (PH1)Lucy, living with PH1The Alnilam Act program was developed to reduce barriers
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Who needs ph1 - alnylam pharmaceuticals?

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PH1 - Alnylam Pharmaceuticals is needed by individuals who are participating in clinical trials or research studies conducted by Alnylam Pharmaceuticals.
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PH1 refers to a Phase 1 clinical trial conducted by Alnylam Pharmaceuticals, which focuses on developing and evaluating new drug candidates in a small group of healthy volunteers to assess safety, dosage, and side effects.
Typically, the sponsor of the clinical trial, in this case, Alnylam Pharmaceuticals, is required to file the necessary documentation for the Phase 1 trial including regulatory submissions and study results.
Filling out PH1 forms usually involves providing details about the trial design, participant criteria, methods of assessment, and expected outcomes. It is typically done by the research team adhering to regulatory guidelines.
The purpose of PH1 clinical trials by Alnylam Pharmaceuticals is to determine the safety, tolerability, pharmacokinetics, and pharmacodynamics of their new drug candidates in healthy subjects.
Information that must be reported typically includes the trial protocol, participant demographics, adverse events, efficacy outcomes, and compliance with regulatory requirements.
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