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Clinical Trial Summary

Multicenter phase II study on trabectedin in patients advanced uterine and ovarian carcinosarcoma. Patients will receive trabectedin until disease progression or unacceptable toxicity. Disease response evaluation will be assessed every 9 weeks.


Clinical Trial Description

This is a Phase II, multi-centre, single arm study aiming at evaluating efficacy and toxicity of Trabectedin in a population of advanced or recurrent ovarian and uterine carcinosarcoma. Trabectedin will be infused at the dose of 1.3 mg/m2 as a 3- hour iv infusion every 3 weeks via a central venous catheter. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02993705
Study type Interventional
Source Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Contact
Status Completed
Phase Phase 2
Start date February 22, 2017
Completion date November 13, 2019

See also
  Status Clinical Trial Phase
Recruiting NCT05537844 - Longitudinal Sample Collection to Investigate Adaptation and Evolution of Ovarian High-grade Serous Carcinoma
Recruiting NCT05500391 - Assessment of Compliance With Monitoring Conducted by a Physician in Person or by a Nurse in Remote Monitoring Phase 2
Active, not recruiting NCT03206177 - Paclitaxel/Carboplatin + Galunisertib for Patients With Carcinosarcoma of the Uterus or Ovary Phase 1