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NCT04775069COMPLETEDanonymous

A Prospective Study Comparing the Antibody Response of Subjects With Chronic Liver Disease to mRNA, Inactivated Virus and Adenovirus Vector COVID-19 Vaccines

Sponsor

Source record

Humanity & Health Medical Group Limited

Phase

Source record

Phase 4

Modality

AI-normalized

protein therapy

Target

AI-normalized

Antibody response to SARS-CoV-2 in patients with chronic liver disease, specifically evaluating the immunogenicity of mRNA, inactivated virus, and adenovirus vector COVID-19 vaccines.

Indication / condition

AI-normalized

Chronic Liver Disease

Intervention

Source record

BNT162b2, CoronaVac, AZD1222

Source & freshness

Source record

NCT ID

NCT04775069

Original source

ClinicalTrials.gov

Source last updated

Oct 04, 2023

Ingested at

Jun 17, 2026

Internal sync

Jun 17, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT04775069

Title

A Prospective Study Comparing the Antibody Response of Subjects With Chronic Liver Disease to mRNA, Inactivated Virus and Adenovirus Vector COVID-19 Vaccines

Sponsor

Humanity & Health Medical Group Limited

Status

COMPLETED

Phase

Phase 4

Condition raw

Chronic Liver Disease

Condition normalized

Chronic Liver Disease

Modality raw

protein therapy

Modality normalized

protein therapy

Target raw

Antibody response to SARS-CoV-2 in patients with chronic liver disease, specifically evaluating the immunogenicity of mRNA, inactivated virus, and adenovirus vector COVID-19 vaccines.

Target normalized

Antibody response to SARS-CoV-2 in patients with chronic liver disease, specifically evaluating the immunogenicity of mRNA, inactivated virus, and adenovirus vector COVID-19 vaccines.

Interventions

BNT162b2, CoronaVac, AZD1222

Public preview

Source record

The study conducted by Humanity & Health Medical Group Limited aims to assess the antibody response in chronic liver disease (CLD) patients to three different COVID-19 vaccines available in Hong Kong. Given the unique immune challenges faced by CLD patients, this research could provide critical insights into vaccine efficacy in this vulnerable population. The findings may influence vaccination strategies and guidelines, potentially leading to increased market demand for tailored vaccine solutions. Furthermore, the results could enhance the competitive positioning of the involved vaccine manufacturers (Pfizer-BioNTech, Sinovac, AstraZeneca) by demonstrating their products' effectiveness in a specific patient demographic. The completion of this study may also attract interest from healthcare providers and policymakers focused on improving vaccination outcomes in high-risk groups.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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