CI

At a glance

ClinicalIndex Comparison Record
Phase 1Active· 117 enrolled / 117 target
Drug / intervention
Cediranib Maleate +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/NCT01064648
NCT01064648Phase 1ActiveUpdate Overdue (0.6/mo)Completion was 97mo ago

A Phase I/Randomized Phase II Study of Cediranib (NSC#732208) Versus Placebo in Combination With Cisplatin and Pemetrexed in Chemonaive Patients With Malignant Pleural Mesothelioma

National Cancer Institute (NCI)·interventional·Posted Feb 8, 2010·Updated Jun 17, 2026

In Brief

A Phase 1 clinical trial evaluating Cediranib Maleate, Cisplatin, and 3 other interventions for Epithelioid Mesothelioma and 3 related conditions. Active but no longer recruiting, targeting 117 participants across 231 sites.

Signals

Enrollment appears stalled

Detailed Summary

This randomized phase I/II trial is studying the side effects and best dose of cediranib maleate when given together with pemetrexed disodium and cisplatin and to see how well it works in treating patients with malignant pleural mesothelioma. Drugs used in chemotherapy, pemetrexed disodium and 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. Cediranib maleate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving pemetrexed disodium and cisplatin together with cediranib maleate may kill more tumor cells.

Study Details

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

Timeline

Phase 1Active
201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 8, 2010
Enrollment StartMar 15, 2010
Primary CompletionJun 1, 2018
Study CompletionMar 31, 2027
TodayJul 2, 2026
Enrollment to primary: 8.2 yearsPosted 16.4 years ago

Arms & Interventions

Arm I (pemetrexed disodium, cisplatin, cediranib maleate))experimental

Patients receive pemetrexed disodium IV over 10 minutes and cisplatin IV over 2 hours on day 1 and cediranib maleate PO QD on days 1-21. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity. Patients then receive cediranib maleate alone PO QD in the absence of disease progression or unacceptable toxicity.

Drug: Cediranib MaleateDrug: CisplatinOther: Laboratory Biomarker AnalysisDrug: Pemetrexed Disodium
Arm II (pemetrexed disodium, cisplatin, placebo)active_comparator

Patients receive pemetrexed disodium and cisplatin as in arm I and placebo PO QD on days 1-21. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity. Patients then receive placebo alone PO QD in the absence of disease progression or unacceptable toxicity.

Drug: CisplatinOther: Laboratory Biomarker AnalysisDrug: Pemetrexed DisodiumOther: Placebo Administration

Interventions

Cediranib Maleatedrug

Given orally

Cisplatindrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Pemetrexed Disodiumdrug

Given IV

Placebo Administrationother

Given orally