CI

At a glance

ClinicalIndex Comparison Record
Phase 3Unknown· 200 target
Drug / intervention
Nimotuzumab +4 moredrug
Likely dose
Nimotuzumab 400mgfrom 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/NCT02409186
NCT02409186Phase 3Unknown

A Randomized, Controlled, Double-blind Study to Evaluate Efficacy and Survival of Combining Nimotuzumab Plus Concurrent Chemo-radiotherapy in Loco-regional Esophageal Squamous Cell Carcinoma

Shandong Cancer Hospital and Institute·interventional·Posted Apr 6, 2015·Updated Apr 21, 2016

In Brief

A Phase 3 clinical trial evaluating Nimotuzumab, radiotherapy, and 3 other interventions for Prosthesis Survival. Targeting 200 participants across 14 sites.

Detailed Summary

Esophageal cancer is the sixth leading cause of cancer death in worldwide. Over the past 2 decades, well-designed clinical trials have documented the clinical benefits of combination of chemotherapy and radiation for localized esophageal cancer, either as primary therapy or in neoadjuvant setting. Paclitaxel, a radiation sensitizer, has important single-agent activity in esophageal cancer. Paclitaxel-based chemoradiation has been the framework for the recent Radiation Therapy Oncology Group (RTOG) trials of nonoperative management of esophageal cancer. Accumulating clinical evidence suggests that Epidermal Growth Factor Receptor (EGFR) represents a viable target in the treatment of esophageal cancer. EGFR expression is associated with poor prognosis. Nimotuzumab binds specifically to EGFR on both normal and tumor cells and competitively inhibits the binding of Epidermal Growth Factor (EGF) and other ligands, such as Transforming Growth Factor-α (TGF-α). Preclinical models have suggested synergy between nimotuzumab, paclitaxel, cisplatin and radiation. For our phase II study in locally advanced esophageal squamous cell carcinoma (ESCC), the combination of cetuximab and chemoradiotherapy has demonstrated both response and survival benefits. Myara et al reported that nimotuzumab plus concurrent chemoradiation therapy (CCRT) was safe and provided statistically significant objective response (47.8%) and disease control rate (60.9%) in nonresectable ESCC. With all these, the investigators plan to study phase III trial.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3UnknownOverdue
201520162017201820192020202120222023202420252026
First PostedApr 6, 2015
Enrollment StartMar 1, 2015
Primary CompletionDec 1, 2017
Study CompletionDec 1, 2021
TodayJul 1, 2026
Enrollment to primary: 2.8 yearsPosted 11.2 years ago

Interventions

Nimotuzumabdrug

400mg/w,d1, week 1-7

radiotherapyradiation

Three dimensional conformal RT(3DCRT)/IntensityModulatedRadiationTherapy(IMRT):1.8 Gy/f/day, T59.4 Gy/33f,week 1-7

chemoradiotherapy Paclitaxeldrug

45 mg/m2, d1, week 1-7

chemoradiotherapy Cisplatindrug

20 mg/m2, d1, week 1-7

placeboother

400mg/w,d1, week 1-7