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NCT05597800: LUNGVIR

Nivolumab/Ipilimumab and Chemotherapy Combination in Advanced NSCLC Patients With HIV, HBV, HCV and Long Covid Syndrome

Not yet recruiting Phase 2 Last updated 28 October 2022
What this trial tests

Phase 2 trial testing Nivolumab and Ipilimumab in NSCLC Stage IV in 105 participants. Not yet recruiting.

Timeline
1 February 2023
Primary endpoint
31 December 2026
30 March 2027

Quick facts

Lead sponsorUniversita di Verona
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment105
Start date1 February 2023
Primary completion31 December 2026
Estimated completion30 March 2027
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Universita di Verona — full company profile →

Who can join

Adults 18 to 75, any sex, with NSCLC Stage IV or HIV. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Study type: Phase 2 - Interventional Trial Number of patients to be enrolled: 105 Participating countries: Italy Study drugs: nivolumab and ipilimumab Cohort A: HBV and HCV patients Cohort B: HIV patients Cohort C: Long COVID syndrome The stratification factors are HBV/HCV positive (cohort A), HIV positive (cohort B), patients with Long Covid syndrome (Cohort C), histology (squamous vs non-squamous histology), and gender (male vs female).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Nivolumab and Ipilimumab

Trials testing the same drug.

Other recruiting trials for NSCLC Stage IV

Currently open trials in the same condition.

Other Universita di Verona trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05597800.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing