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Active Not RecruitingNCT06993116

A Phase I Study of SHR-4712 in Patients With Advanced Solid Tumors

A Phase I Clinical Study on the Safety, Tolerability, Pharmacokinetics and Efficacy of SHR-4712 in Patients With Advanced Solid Tumors

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Guangdong Hengrui Pharmaceutical Co., Ltd · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a Phase 1, open label, first-in-human study to evaluate safety, tolerability, Pharmacokinetics (PK), Pharmacodynamics (PD), immunogenicity and anti-tumor activity of SHR-4712 in patients with advanced solid tumors. Patients will treat with SHR-4712 until unacceptable toxicity or disease progression.

Conditions

Interventions

TypeNameDescription
DRUGSHR-4712 InjectionSHR-4712 injection.

Timeline

Start date
2025-06-09
Primary completion
2027-05-01
Completion
2027-05-01
First posted
2025-05-28
Last updated
2026-01-28

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06993116. Inclusion in this directory is not an endorsement.

A Phase I Study of SHR-4712 in Patients With Advanced Solid Tumors (NCT06993116) · Clinical Trials Directory