CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 122 enrolled / 122 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/NCT02498613
NCT02498613Phase 2ActiveUpdate Overdue (1.0/mo)Completion was 48mo ago

A Phase 2 Study of Cediranib in Combination With Olaparib in Advanced Solid Tumors

National Cancer Institute (NCI)·interventional·Posted Jul 15, 2015·Updated Jun 17, 2026

In Brief

A Phase 2 clinical trial evaluating 18F-Fluoromisonidazole, Cediranib Maleate, and 3 other interventions for Advanced Malignant Solid Neoplasm and 25 related conditions. Active but no longer recruiting, targeting 122 participants across 16 sites in 2 countries.

Signals

Enrollment appears stalled

Detailed Summary

This phase II trial studies cediranib maleate in combination with olaparib in treating patients with solid tumors that have spread to other parts of the body (advanced/metastatic) or cannot be removed by surgery (unresectable), including breast cancer, non-small cell lung cancer, small cell lung cancer, and pancreatic cancer. Cediranib maleate and olaparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Cediranib maleate may also block the flow of oxygen to the tumor, and may help make the tumor more sensitive to olaparib.

Study Details

Timeline

Phase 2Active
201620172018201920202021202220232024202520262027
First PostedJul 15, 2015
Enrollment StartAug 31, 2016
Primary CompletionJun 22, 2022
Study CompletionApr 10, 2027
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 11.0 years ago

Arms & Interventions

Treatment (cediranib maleate, olaparib)experimental

Patients receive cediranib maleate PO QD on day 1. Patients undergoing FMISO scan also receive olaparib PO BID beginning the day after the second FMISO scan and the rest of the patients receive olaparib PO BID beginning day 4 of cycle 1. Cycles repeat every 28 days (35 days for cycle 1) in the absence of disease progression or unacceptable toxicity.

Other: 18F-FluoromisonidazoleDrug: Cediranib MaleateOther: Laboratory Biomarker AnalysisDrug: OlaparibProcedure: Positron Emission Tomography

Interventions

18F-Fluoromisonidazoleother

Correlative studies

Cediranib Maleatedrug

Given PO

Laboratory Biomarker Analysisother

Correlative studies

Olaparibdrug

Given PO

Positron Emission Tomographyprocedure

Correlative studies