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NCT06740474

A Study to Assess the Safety, Tolerability and Pharmacokinetics of ABI-6250 in Healthy Participants

Completed Phase 1 Last updated 4 December 2025
What this trial tests

Phase 1 trial testing ABI-6250 in Hepatitis Delta Virus in 40 participants. Completed in 8 July 2025.

Timeline
31 January 2025
Primary endpoint
8 July 2025
8 July 2025

Quick facts

Lead sponsorAssembly Biosciences
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment40
Start date31 January 2025
Primary completion8 July 2025
Estimated completion8 July 2025
Sites1 location across New Zealand

Drugs / interventions tested

Conditions studied

Sponsor

Assembly Biosciences — full company profile →

Who can join

Adults 18 to 60, any sex, with Hepatitis Delta Virus or Hepatitis D. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is designed to assess safety, tolerability, and pharmacokinetics of single ascending doses (SAD) and multiple-ascending doses (MAD) of ABI-6250 in healthy participants. Effect of food will also be evaluated in Part A.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Assembly Biosciences trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06740474.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing