Clinical Trials Directory

Trials / Completed

CompletedNCT02044120

ESP1/SARC025 Global Collaboration: A Phase I Study of a Combination of the PARP Inhibitor, Niraparib and Temozolomide and/or Irinotecan Patients With Previously Treated, Incurable Ewing Sarcoma

ESP1/SARC025 Global Collaboration: A Phase I Study of a Combination of the PARP Inhibitor, Niraparib and Temozolomide and/or Irinotecan in Patients With Previously Treated,Incurable Ewing Sarcoma

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Sarcoma Alliance for Research through Collaboration · Academic / Other
Sex
All
Age
13 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to define the dose-limiting toxicities and maximum tolerated dose of the poly ADP-ribose polymerase inhibitor niraparib and escalating doses of temozolomide and/or irinotecan in patients with pre-treated incurable Ewing sarcoma.

Conditions

Interventions

TypeNameDescription
DRUGniraparib
DRUGTemozolomide
DRUGIrinotecan

Timeline

Start date
2014-05-01
Primary completion
2021-01-01
Completion
2021-01-01
First posted
2014-01-23
Last updated
2021-01-12

Locations

5 sites across 2 countries: United States, United Kingdom

Source: ClinicalTrials.gov record NCT02044120. Inclusion in this directory is not an endorsement.

ESP1/SARC025 Global Collaboration: A Phase I Study of a Combination of the PARP Inhibitor, Niraparib and Temozolomide an (NCT02044120) · Clinical Trials Directory