An Efficacy and Safety Study of Trabectedin Versus Doxorubicin-Based Chemotherapy in Participants With Translocation-Related Sarcomas (TRS)

Completed · Phase 3

Conditions studied: Sarcoma

In brief

The purpose of this study is to evaluate the efficacy and safety of trabectedin compared to standard doxorubicin in participants with advanced translocation-related sarcomas (cancer of connective tissue cells) (TRS).

Key facts

Study ID

NCT00796120

Run by

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

People needed

121

Starts

2008-11-01

Expected to finish

2014-08-01

Last updated by the study team

2015-12-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Pathological diagnosis of translocation-related sarcomas (TRS) including the following subtypes: alveolar soft part sarcoma, angiomatoid fibrous histiocytoma, clear cell sarcoma, desmoplastic small round cell tumor, low grade endometrial stromal sarcoma (prior hormone therapy allowed), low grade fibromyxoid sarcoma, myxoid chondrosarcoma, myxoid/round cell liposarcoma (MRCL) and synovial sarcoma
• Participants must have unresectable locally advanced or metastatic progressive disease prior to enrolment
• Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) score of 0-2
• Adequate cardiac function, defined as left ventricular ejection fraction (LVEF) within normal limits according to institutional standards, as shown by echocardiography or scintigraphy multiple-gated acquisition scan [MUGA]
• Measurable disease as defined by the radiological (computed tomography [CT] scan and magnetic resonance imaging [MRI]) Response Evaluation Criteria in Solid Tumors (RECIST v.1.0) guidelines

You may not qualify if…

• Known hypersensitivity to any components of the intravenous formulation of trabectedin or the comparators
• Prior chemotherapy treatment or irradiation of the lesion if only one target lesion is available
• Brain metastases and/or leptomeningeal metastases, even if treated
• Pregnant or lactating women or men and women of reproductive potential who are not using effective contraceptive methods
• History of another neoplastic disease (except basal cell carcinoma or cervical carcinoma in situ adequately treated) unless in remission for five years or more

Where it is running

• Study site — Santa Monica, California, United States
• Study site — Boston, Massachusetts, United States
• Study site — Albuquerque, New Mexico, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Houston, Texas, United States
• Study site — Salt Lake City, Utah, United States
• Study site — Boreaux, France
• Study site — Lille, France
• Study site — Lyon, France
• Study site — Paris, France
• Study site — Villejuif, France
• Study site — Bad Saarow, Germany
• Study site — Cologne, Germany
• Study site — Mannheim, Germany
• Study site — Barcelona, Spain
• Study site — Palma, Spain
• Study site — Valencia, Spain
• Study site — Edinburgh, United Kingdom
• Study site — Glasgow, United Kingdom
• Study site — London, United Kingdom
• Study site — Manchester, United Kingdom

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.