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RecruitingNCT05690581

Safety, Tolerability, Pharmacokinetic Characteristics, and Efficacy of CM369 in Advanced Solid Tumors & Hematologic Malignancies

A Nonrandomized, Open-label, Multicenter, Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, and Efficacy of CM369 in Subjects with Advanced Solid Tumors and Hematologic Malignancies

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
146 (estimated)
Sponsor
Beijing InnoCare Pharma Tech Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This is a nonrandomized, open-label, multicenter, phase I clinical trial to evaluate the safety, tolerability, pharmacokinetic characteristics, and efficacy of CM369 in subjects with advanced solid tumors and Hematologic Malignancies.

Conditions

Interventions

TypeNameDescription
DRUGCM369Specified dose on specified days.

Timeline

Start date
2023-02-23
Primary completion
2025-10-30
Completion
2026-02-28
First posted
2023-01-19
Last updated
2024-12-27

Locations

3 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05690581. Inclusion in this directory is not an endorsement.

Safety, Tolerability, Pharmacokinetic Characteristics, and Efficacy of CM369 in Advanced Solid Tumors & Hematologic Mali (NCT05690581) · Clinical Trials Directory