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A Study to Evaluate ALN-AGT01 RVR in Adult Healthy Volunteers

OverviewStructured DataIssuesContributors

Contents

clinicaltrials.gov/study/NCT06675565
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT066755650
Trial Recruitment Size
780
Trial Sponsor
Alnylam Pharmaceuticals
Alnylam Pharmaceuticals
0
Clinical Trial Start Date
November 5, 2024
0
Primary Completion Date
August 5, 2025
0
Study Completion Date
August 5, 2025
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Drug0
Interventional Trial Phase
Phase 10
Official Name
A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of ALN-AGT01 RVR in Adult Healthy Volunteers0
Last Updated
November 5, 2024
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Triple0
Masked Party
Investigator0
Care Provider0
Participant0

Other attributes

Intervention Treatment
ALN-AGT01 RVR0
Placebo0
Study summary

The purpose of this study is to evaluate the safety, tolerability and PK of single ascending doses of ALN-AGT01 RVR.

Timeline

No Timeline data yet.

Further Resources

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References

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