CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 116 target
Drug / intervention
Neoadjuvant chemo-immunotherapy +3 moredrug
Likely dose
Neoadjuvant chemo-immunotherapy 200 mgfrom 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/NCT05468242
NCT05468242Phase 2RecruitingUpdate OverdueUpdated 20mo ago · Completion was 18mo ago
Enrollment Stalled
Long Recruiting
Update Overdue

A Phase II Trial of Tislelizumab as Consolidation Therapy in Patients With Locally Advanced Non-Small Cell Lung Cancer Who Have Not Progressed Following Neoadjuvant Chemotherapy Plus Tislelizumab ± Bevacizumab and Definitive Concurrent Chemoradiation Therapy

Sun Yat-sen University·interventional·Posted Jul 21, 2022·Updated Oct 30, 2024

In Brief

A Phase 2 clinical trial evaluating Neoadjuvant chemo-immunotherapy, Bevacizumab, and 2 other interventions for Stage III Non-small Cell Lung Cancer. Currently recruiting, targeting 116 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

The phase II Study is to explore the efficacy and safety of Tislelizumab as consolidation therapy in patients with locally advanced non-small cell lung cancer who have not progressed following neoadjuvant chemotherapy plus Tislelizumab ± Bevacizumab and definitive concurrent chemoradiation therapy.

Study Details

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

Timeline

Phase 2RecruitingOverdue
20222023202420252026
First PostedJul 21, 2022
Enrollment StartJan 1, 2022
Primary CompletionDec 30, 2024
TodayJul 1, 2026
Enrollment to primary: 3.0 yearsPosted 3.9 years ago

Interventions

Neoadjuvant chemo-immunotherapydrug

The neoadjuvant chemo-immunotherapy before radiotherapy comprised of chemotherapy plus Tislelizumab \[200 mg, once every 3 weeks (Q3W)\].

Bevacizumabdrug

The Bevacizumab was administrated concurrently with neoadjuvant chemo-immunotherapy (7.5mg/kg) once every 3 weeks (Q3W).

Radiotherapyradiation

Definitive radiotherapy to the thoracic lesions.

Tislelizumabdrug

Tislelizumab consolidation (200 mg) is performed once every 3 weeks after the neoadjuvant therapy and concurrent chemo-radiotherapy, and will continue on a Q3W schedule for a maximum duration of 12 months.