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Not Yet RecruitingNCT06221072

A Study to Assess the Prevention of Bone-related Events in Patients With Bone Metastases From Malignant Solid Tumors Treated With JMT103 Compared to Zoledronic Acid

A Phase III, Multicenter, Randomized, Double-blind Clinical Trail to Assess JMT103 Compared to Azoledronic Acid for the Prevention of Bone-related Events in Patients With Bone Metastases From Malignant Solid Tumors

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
1,360 (estimated)
Sponsor
Shanghai JMT-Bio Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a phase Ⅲ, multicenter, randomized, double-blind, study to evaluate the efficacy and safety of JMT103 in patients with bone metastases from malignant solid tumors. The purpose of this study is to determine if JMT103 is non-inferior to zoledronic acid.

Conditions

Interventions

TypeNameDescription
DRUGJMT103120 mg by subcutaneous injection every 4 weeks
DRUGzoledronic acid4 mg by intravenous drip (100mL:4mg) every 4 weeks

Timeline

Start date
2024-04-05
Primary completion
2027-05-31
Completion
2028-05-31
First posted
2024-01-24
Last updated
2024-01-24

Source: ClinicalTrials.gov record NCT06221072. Inclusion in this directory is not an endorsement.

A Study to Assess the Prevention of Bone-related Events in Patients With Bone Metastases From Malignant Solid Tumors Tre (NCT06221072) · Clinical Trials Directory