CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 168 enrolled / 168 target
Drug / intervention
Cisplatin +4 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00887159
NCT00887159Phase 2CompletedMonitor (0.8/mo)Completion was 115mo ago

A Randomized Phase II Study of Cisplatin and Etoposide in Combination With Either Hedgehog Inhibitor GDC-0449 or IGF-1R MOAB IMC-A12 for Patients With Extensive Stage Small Cell Lung Cancer

National Cancer Institute (NCI)·interventional·Posted Apr 23, 2009·Updated Jun 24, 2026

In Brief

A Phase 2 clinical trial evaluating Cisplatin, Cixutumumab, and 3 other interventions for Extensive Stage Small Cell Lung Carcinoma and Recurrent Small Cell Lung Carcinoma. Completed, enrolled 168 participants across 301 sites.

Signals

Enrolling slower than its timeline implies

Detailed Summary

This randomized phase II trial studies cisplatin and etoposide to see how well they work when given with or without Hedgehog inhibitor GDC-0449 (vismodegib) or IGF-1R MOAB IMC-A12 (cixutumumab) in treating patients with extensive-stage small cell lung cancer. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Etoposide may slow the growth of tumor cells by blocking some of the enzymes needed for cell growth. Vismodegib may slow the growth of tumor cells. Monoclonal antibodies, such as cixutumumab, may interfere with the ability of tumor cells to grow and spread. It is not yet known whether giving cisplatin and etoposide are more effective when given together with vismodegib or cixutumumab in treating small cell lung cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedApr 23, 2009
Enrollment StartJul 16, 2009
Primary CompletionNov 15, 2016
TodayJul 2, 2026
Enrollment to primary: 7.3 yearsPosted 17.2 years ago

Arms & Interventions

Arm A (CE)active_comparator

Patients receive cisplatin IV over 1-2 hours on day 1 and etoposide IV over 1-2 hours on days 1-3. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity.

Drug: CisplatinDrug: EtoposideOther: Laboratory Biomarker Analysis
Arm B (CE + GDC-0449)experimental

Patients receive cisplatin and etoposide as in Arm A and vismodegib PO QD on days 1-21. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity. Patients then receive vismodegib alone QD in the absence of disease progression or unacceptable toxicity.

Drug: CisplatinDrug: EtoposideOther: Laboratory Biomarker AnalysisDrug: Vismodegib
Arm C (CE + IMC-A12)experimental

Patients receive cisplatin and etoposide as in Arm A and cixutumumab IV over 1 hour on days 1, 8, and 15. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity. Patients then receive cixutumumab alone once weekly in the absence of disease progression or unacceptable toxicity.

Drug: CisplatinBiological: CixutumumabDrug: EtoposideOther: Laboratory Biomarker Analysis

Interventions

Cisplatindrug

Given IV

Cixutumumabbiological

Given IV

Etoposidedrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Vismodegibdrug

Given PO