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NCT05856513

Pharmacokinetics of ZSP1273 in Participants With Hepatic Impairment

Completed Phase 1 Last updated 1 December 2023
What this trial tests

Phase 1 trial testing ZSP1273 in Hepatic Impairment in 24 participants. Completed in 4 July 2023.

Timeline
15 June 2023
Primary endpoint
4 July 2023
4 July 2023

Quick facts

Lead sponsorGuangdong Raynovent Biotech Co., Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposebasic science
Enrollment24
Start date15 June 2023
Primary completion4 July 2023
Estimated completion4 July 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Guangdong Raynovent Biotech Co., Ltd — full company profile →

Who can join

Adults 18 to 68, any sex, with Hepatic Impairment or Pharmacokinetics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will assess the effect of hepatic impairment on the pharmacokinetics (PK), safety and tolerability of ZSP1273.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Single-Dose Tolerability and Pharmacokinetics of Onradivir in Chinese Patients with Hepatic Impairment and Healthy Matched Controls.
    Li C, Li H, Mai J, Zhang H, et al · · 2025 · cited 5× · PMID 39287964 · DOI 10.1002/jcph.6134
  2. Anti-influenza drugs targeting trimeric RNA polymerase complex: From development to clinics.
    Li Y, Zhang J, He F, Cao C, et al · · 2026 · PMID 41685158 · DOI 10.1016/j.apsb.2025.11.033

Verify or expand the search:

Other trials of ZSP1273

Trials testing the same drug.

Other recruiting trials for Hepatic Impairment

Currently open trials in the same condition.

Other Guangdong Raynovent Biotech Co., Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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