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Anti-tumor antibiotic

Study to Investigate the Safety and Activity of Aldoxorubicin Plus Ifosfamide/Mesna in Subjects With Metastatic Soft Tissue Sarcoma

Santa Monica, CA
Phase 1 & 2
Waitlist Available
Research Sponsored by ImmunityBio, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 17 months
Awards & highlights
No Placebo-Only Group

Summary

This is a Phase 1 open-label study to study the safety and activity of aldoxorubicin with ifosfamide/mesna in subjects with metastatic, advanced, unresectable soft tissue sarcoma.

Eligible Conditions
  • Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~17 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 17 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Number of Adverse Events in Participants
Secondary study objectives
Tumor Response

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: 250 mg/m2 aldoxorubicinExperimental Treatment1 Intervention
Group II: 170 mg/m2 aldoxorubicinExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
170 mg/m2 aldoxorubicin
2014
Completed Phase 2
~70
250 mg/m2 aldoxorubicin
2014
Completed Phase 2
~100

Find a Location

Closest Location:Sarcoma Oncology Center· Santa Monica, CA

Who is running the clinical trial?

ImmunityBio, Inc.Lead Sponsor
74 Previous Clinical Trials
4,824 Total Patients Enrolled
CytRxLead Sponsor
21 Previous Clinical Trials
1,521 Total Patients Enrolled
Dan Levitt, M.D.Study DirectorCytRx Coporation
1 Previous Clinical Trials
30 Total Patients Enrolled
~6 spots leftby Mar 2026