Changeflow GovPing Healthcare & Life Sciences VC005 Tablets Phase 1 Hepatic Impairment PK Study
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VC005 Tablets Phase 1 Hepatic Impairment PK Study

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Summary

A Phase 1 clinical trial (NCT07551557) registered on ClinicalTrials.gov evaluating the pharmacokinetics and safety of a single 25 mg oral dose of VC005 tablets in participants with mild and moderate hepatic impairment compared to participants with normal hepatic function. The study is single-dose, open-label in design and includes both hepatic impairment and healthy female participants. VC005 is an investigational drug tablet under clinical development.

“This study is a Phase I, single-dose, open-label trial designed to evaluate the pharmacokinetics and safety of a single oral dose of 25 mg VC005 tablets in participants with mild and moderate hepatic impairment compared to participants with normal hepatic function.”

NIH , verbatim from source
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About this source

ClinicalTrials.gov is the NIH-run registry of every clinical trial conducted in the United States, plus most international trials sponsored by US-based companies or institutions. By federal law, sponsors must register Phase 2 through Phase 4 studies before enrolling patients and post results within a year of completion. This feed tracks every new trial registration and study update, around 700 a month: drug interventions, device studies, behavioral protocols, observational research. Watch this if you scout drug candidates moving into mid or late-stage development, monitor competitor pipelines, or follow rare disease research where new trials signal patient hope. GovPing parses sponsor, phase, intervention, and target indication on each entry.

What changed

This document is a clinical trial registry entry for NCT07551557, a Phase 1 pharmacokinetics study of VC005 tablets. The trial will assess a single 25 mg oral dose in participants with mild and moderate hepatic impairment compared to healthy participants with normal hepatic function.

Affected parties include clinical investigators conducting the study, pharmaceutical companies developing VC005, and patients meeting hepatic impairment criteria. The registry entry establishes the study parameters and inclusion/exclusion framework but does not impose compliance obligations on external parties.

Archived snapshot

Apr 27, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

Pharmacokinetics of VC005 Tablets in Subjects With Hepatic Impairment and Normal Hepatic Function

Phase 1 NCT07551557 Kind: PHASE1 Apr 27, 2026

Abstract

This study is a Phase I, single-dose, open-label trial designed to evaluate the pharmacokinetics and safety of a single oral dose of 25 mg VC005 tablets in participants with mild and moderate hepatic impairment compared to participants with normal hepatic function.

Conditions: Hepatic Impairment and Healthy Female

Interventions: VC005 Tablets

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Last updated

Classification

Agency
NIH
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Clinical investigators Pharmaceutical companies Patients
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Clinical trial conduct Drug development
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Compliance frameworks
GxP
Topics
Pharmaceuticals Public Health

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