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Active Not RecruitingNCT05781048

A Phase I Clinical Study of the Safety, Tolerability,Pharmacokinetics, and Initial Efficacy of HRS-6209 Monotherapy in Patients With Advanced Solid Tumors

An Open-label, Multi-center Phase I Study of Safety, Tolerability, Pharmacokinetics, and Initial Efficacy of HRS-6209 Monotherapy in Patients With Advanced Solid Tumors

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Jiangsu HengRui Medicine Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study is being conducted to evaluate the efficacy, andsafety of HRS-6209in subjects with advanced solid tumors.To explore the reasonable dosage of HRS-6209.This study also preliminarily evaluated the efficacy of HRS-6209 in patients with advanced solid tumors.

Conditions

Interventions

TypeNameDescription
DRUGHRS-6209HRS-6209

Timeline

Start date
2023-03-23
Primary completion
2026-12-30
Completion
2026-12-30
First posted
2023-03-23
Last updated
2026-03-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05781048. Inclusion in this directory is not an endorsement.

A Phase I Clinical Study of the Safety, Tolerability,Pharmacokinetics, and Initial Efficacy of HRS-6209 Monotherapy in P (NCT05781048) · Clinical Trials Directory