Clinical Trials Directory

Trials / Terminated

TerminatedNCT02261805

A Phase I/II Study of Ganetespib in Combination With Doxorubicin

A Phase I/II Study of Ganetespib in Combination With Doxorubicin in Solid Tumors (Phase I) and Refractory Small Cell Lung Cancer (Safety Dose Expansion, Phase II)

Status
Terminated
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
11 (actual)
Sponsor
Georgetown University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a Phase I/safety dose expansion study of the combination of the drug ganetespib and doxorubicin in patients with advanced solid tumors. The purpose of the Phase I part of the study is to determine the recommended phase II dose of ganetespib when given in combination with doxorubicin. The recommended Phase II dose determined at the end of the dose escalation phase will be used to conduct a safety dose expansion phase in relapsed/refractory small cell lung cancer to determine if there is a signal of efficacy in this population.

Detailed description

The dose escalation phase of the study will follow a standard 3+ 3 dose escalation scheme with two dose levels of ganetespib (1-- mg/m2 and 150 mg/m2) administered weekly on Days 1 and 8 of a 21-day cycle, in combination with a fixed dose of doxorubicin at 50 mg/m2 administered on Day 1 alone. After 4-6 cycles of combination therapy, continuation of single agent ganetespib will be permitted for subjects who are deriving clinical benefit. Pharmacokinetic samples for plasma drug levels of ganetespib will be collected pre-dose and 4 hours after completion of treatment on Day 1 and Day 8 of cycle 1 only in subjects in the dose escalation phase. The recommended Phase II dose determined at the end of the dose escalation phase will be used to conduct a safety dose expansion phase in relapsed/ refractory small cell lung cancer to determine if there is a signal of efficacy in this population.

Conditions

Interventions

TypeNameDescription
DRUGGanetespib
DRUGDoxorubicin

Timeline

Start date
2014-10-01
Primary completion
2016-10-01
Completion
2016-10-01
First posted
2014-10-10
Last updated
2018-04-23
Results posted
2018-02-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02261805. Inclusion in this directory is not an endorsement.