CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 903 target
Drug / intervention
Nivolumab +5 morebiological
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/NCT02595944
NCT02595944Phase 3ActiveOn Track

Adjuvant Nivolumab in Resected Lung Cancers (ANVIL)-A Randomized Phase III Study of Nivolumab After Surgical Resection and Adjuvant Chemotherapy in Non-Small Cell Lung Cancers

National Cancer Institute (NCI)·interventional·Posted Nov 4, 2015·Updated Jun 17, 2026

In Brief

A Phase 3 clinical trial evaluating Biospecimen Collection, Computed Tomography, and 4 other interventions for Stage IB Lung Non-Small Cell Carcinoma AJCC v7 and 2 related conditions. Active but no longer recruiting, targeting 903 participants across 885 sites.

Detailed Summary

This phase III ALCHEMIST treatment trial studies how well nivolumab after surgery and chemotherapy work in treating patients with stage IB-IIIA non-small cell lung cancer. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

Study Details

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

Timeline

Phase 3Active
201620172018201920202021202220232024202520262027
First PostedNov 4, 2015
Enrollment StartJul 22, 2016
Primary CompletionDec 31, 2026
TodayJul 2, 2026
Enrollment to primary: 10.4 yearsPosted 10.7 years agoPrimary completion in 6 months

Arms & Interventions

Arm I (nivolumab)experimental

Patients receive nivolumab IV over 30 minutes on day 1 of each cycle. Cycles repeat every 4 weeks for up to 1 year in the absence of disease progression or unacceptable toxicity. Patients also undergo CT and/or PET/CT throughout the trial and blood sample collection during screening and follow-up. Patients may undergo an ECHO as clinically indicated on study.

Procedure: Biospecimen CollectionProcedure: Computed TomographyProcedure: Echocardiography TestBiological: NivolumabProcedure: Positron Emission Tomography
Arm II (observation)active_comparator

Patients are followed serially with CT and/or PET/CT imaging for up to 1 year and then during follow-up. Patients also undergo blood sample collection during screening and follow-up. Patients may undergo an ECHO as clinically indicated on study.

Procedure: Biospecimen CollectionProcedure: Computed TomographyProcedure: Echocardiography TestOther: Observation ActivityProcedure: Positron Emission Tomography

Interventions

Biospecimen Collectionprocedure

Undergo blood sample collection

Computed Tomographyprocedure

Undergo CT

Echocardiography Testprocedure

Undergo ECHO

Nivolumabbiological

Given IV

Observation Activityother

Undergo observation

Positron Emission Tomographyprocedure

Undergo PET-CT