Study of Gefitinib, Trametinib, Disulfiram, and Sunitinib with Chemotherapy for Osteosarcoma

This study is investigating if adding the drugs gefitinib, trametinib, disulfiram, and sunitinib to standard chemotherapy (methotrexate, doxorubicin, cisplatin) is a more effective and safe treatment for people with osteosarcoma (a type of bone cancer) that has spread (metastasis). Researchers will also learn how osteosarcoma survives chemotherapy by studying tumor samples. The study aims to enroll 45 participants between 6 and 49 years old who have newly diagnosed, metastatic osteosarcoma. Success will be measured by how long participants live without their cancer getting worse (progression-free survival) at 12 months, and how long they live overall (overall survival) at 24 months. The current status of this study is unclear.

Study design
This study is an interventional study with a planned enrollment of 45 participants. It is not specified if it is randomized or blinded.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed to measure progression-free survival at 12 months and overall survival at 24 months.

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NCT07477457

A Study of Gefitinib, Trametinib, Disulfiram, and Sunitinib in Addition to Standard Chemotherapy in People With Osteosarcoma

Recruiting
PHASE2Ages 6–49InterventionalTreatment
Memorial Sloan Kettering Cancer Center
~45 participants
Updated 2026-03-17 on ClinicalTrials.gov
What's tested:MethotrexateDoxorubicinCisplatinGefitinibTrametinibDisulfiram

At a glance

Recruiting sites
7 of 7 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
12-month progression free survival (PFS) (cohort 1)
Measured over 12 months
+1 more outcome measured
Osteosarcoma
Metastasis
7 sites across 2 states
New York4
New Jersey3
  • Damon Reed, MD · PRINCIPAL_INVESTIGATOR · Memorial Sloan Kettering Cancer Center

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  • 12-month progression free survival (PFS) (cohort 1)12 months

    Response will be determined by the investigator and progression will be guided by RECIST 1.1 criteria

  • 24-month overall survival (OS) (cohort 2)24 months

    Response will be determined by the investigator and progression will be guided by RECIST 1.1 criteria