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Study identifier: NCT07673601 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Assess the Absolute Bioavailability and How Adimanebart SC Moves Through the Body in Healthy Adult Participants

Condition: Healthy Volunteers (HV) · Healthy Volunteer  ·  Sponsor: argenx

PhasePhase 1
Planned participants52
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

This study aims to find out how much adimanebart gets into the blood circulation of healthy adults. Researchers will measure the amount of adimanebart in blood over time to learn how it moves through the body. The drug's safety will also be assessed. The participants will be assigned to one of 3 parts of the study: part 1 investigates the absolute bioavailability; part 2 investigates the effect of different body weights on adimanebart in blood after subcutaneous (SC) dosing; part 3 investigates formulation adaptations. Participants will be in the study for approximately up to 24 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Sabine Coppieters, MD  ·  857-350-4834  ·  clinicaltrials@argenx.com

Always discuss trial participation with your own doctor first.

Locations (1)

AltasciencesMontreal, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07673601