Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Soft Tissue Sarcoma
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Primary Objectives: 1) Assess whether the rate of clinical benefit is sufficiently high to merit promise for further study Secondary Objectives: Characterize the 6-month progression-free survival rate Assess whether the treatment yields a reasonably safe and tolerable profile

Primary Objectives: 1) Assess whether the rate of clinical benefit is sufficiently high to merit promise for further study Secondary Objectives: Characterize the 6-month progression-free survival rate Assess whether the treatment yields a reasonably safe and tolerable profile

Tracking Information

NCT #
NCT04118166
Collaborators
Bristol-Myers Squibb
Investigators
Principal Investigator: Kristen Ganjoo, MD Stanford University