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Study identifier: NCT05568212 Synced from ClinicalTrials.gov · July 29, 2026
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Randomized Trial Comparing Standard of Care Versus Immune- Based Combination in Relapsed Stage III Non-small-cell Lung Cancer (NSCLC) Pretreated With Chemoradiotherapy and Durvalumab

Condition: Non-small-cell Lung Cancer Patients  ·  Sponsor: Fondazione Ricerca Traslazionale

PhasePhase 2
Planned participants176
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a randomized, non-comparative, phase II study investigating whether: 1) the addition of durvalumab to investigator's choice second line chemotherapy prolongs survival versus investigator's choice second line chemotherapy in NSCLC patients with locally advanced disease progressing on durvalumab given after concomitant chemoradiotherapy; 2) whether the addition of olaparib to durvalumab improves survival over durvalumab alone after induction chemoimmunotherapy in patients relapsing after completing durvalumab maintenance therapy for stage III disease. After evaluation of inclusion and exclusion criteria and after consent form signature, all eligible patients progressing during durvalumab therapy will be in the Part A of the trial randomized to in a 1:1 ratio to investigator's choice single-agent chemotherapy plus durvalumab (Arm A: experimental arm) or to investigator's choice single-agent chemotherapy (Arm B: standard arm). In the clinical trial's Part B, patients progressing after completion of durvalumab therapy will be further randomized in a 1:1.7 ratio to investigator's choice platinum doublet chemotherapy plus durvalumab for 4 cycles followed by maintenance durvalumab plus olaparib (Arm C: experimental arm) or to investigator's choice platinum doublet chemotherapy plus durvalumab for 4 cycles followed by durvalumab (Arm D: experimental arm). Therapy will be continued up to disease progression, toxicity or patient refusal.

This description comes directly from the study's public registry record.

Talk to the study team

Federico Cappuzzo, MD  ·  06.5266.5698  ·  federico.cappuzzo@ifo.it

Lorenza Landi, MD  ·  3397728272  ·  lorenza.landi@ifo.it

Always discuss trial participation with your own doctor first.

Locations (1)

Istituti Fisioterapici Ospitalieri- Ifo - Istituto Regina ElenaRoma, RM, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT05568212