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IFCT-2201 ADAPTABLE A non-comparative randomized phase II trial evaluating the combination of paclitaxel-bevacizumab ± atezolizumab in patients with advanced non-squamous NSCLC progressing after immunotherapy and chemotherapy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-502103-30-00
Acronym
IFCT-2201
Enrollment
156
Registered
2023-02-16
Start date
2023-04-25
Completion date
Unknown
Last updated
2024-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

advanced non-squamous non-small cell lung cancer

Brief summary

Progression free survival (PFS) at 6 months as determined by independent reviewer.

Detailed description

PFS at 6 months as determined by investigator assessment, Objective response rate (ORR), Overall survival, PFS, Incidence, nature, and severity of adverse events, graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, Version 5.0 (NCI CTCAE v5.0), Clinically significant changes in symptoms, function, and HRQoL scales from the patient-completed European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30 LC13); overall health status will also be assessed using the EQ-5D-5L including visual analogue scale (VAS).

Interventions

DRUGBEVACIZUMAB
DRUGPACLITAXEL

Sponsors

Intergroupe Francophone de Cancerologie Thoracique
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Progression free survival (PFS) at 6 months as determined by independent reviewer.

Secondary

MeasureTime frame
PFS at 6 months as determined by investigator assessment, Objective response rate (ORR), Overall survival, PFS, Incidence, nature, and severity of adverse events, graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, Version 5.0 (NCI CTCAE v5.0), Clinically significant changes in symptoms, function, and HRQoL scales from the patient-completed European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30 LC13); overall health status will also be assessed using the EQ-5D-5L including visual analogue scale (VAS).

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026