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Monoclonal Antibodies

Lurbinectedin + Atezolizumab for Small Cell Lung Cancer (IMforte Trial)

Phase 3
Waitlist Available
Research Sponsored by Hoffmann-La Roche
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Histologically or cytologically confirmed ES-SCLC
No prior systemic therapy for ES-SCLC
Must not have
Treatment with therapeutic oral or IV antibiotics at the time of randomization
Receiving consolidative chest radiation
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months and 12 months after randomization
Awards & highlights
No Placebo-Only Group
Pivotal Trial

Summary

This trial is testing lurbinectedin in combination with atezolizumab compared to atezolizumab alone as maintenance therapy in people with small-cell lung cancer.

Who is the study for?
This trial is for adults with extensive-stage small-cell lung cancer who've responded well or have stable disease after initial treatment with carboplatin, etoposide, and atezolizumab. They should be in good physical condition (ECOG PS of 0 or 1), have no prior systemic therapy for ES-SCLC, no active infections like HIV or hepatitis, and no history of certain autoimmune diseases or other cancers within the last five years.
What is being tested?
The study tests if adding lurbinectedin to atezolizumab as a maintenance therapy offers more benefits compared to using atezolizumab alone after first-line induction therapy. Participants are randomly assigned to one of these two options following their initial response to treatment.
What are the potential side effects?
Potential side effects include immune-related reactions due to atezolizumab such as inflammation in various organs, infusion reactions from both drugs, possible blood disorders, fatigue, digestive issues like nausea and diarrhea, and increased risk of infection.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My cancer is confirmed as small cell lung cancer through a biopsy.
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I have not had any treatment for my small cell lung cancer.
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I am fully active or restricted in physically strenuous activity but can do light work.
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My blood and organs are healthy enough for specific cancer treatment.
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I haven't had chemo or radiotherapy for my small cell lung cancer in the last 6 months.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am currently taking antibiotics through pills or IV.
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I am undergoing radiation therapy focused on my chest.
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I have had lung conditions like pulmonary fibrosis or pneumonitis.
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I have previously been treated with specific immune therapies or lurbinectedin/trabectedin.
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I have or had cancer spread to my brain or spinal cord.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months and 12 months after randomization
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months and 12 months after randomization for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
IRF-Assessed Progression-Free Survival (PFS)
Overall Survival (OS)
Secondary study objectives
Confirmed Objective Response Rate (ORR) as Determined by the IRF
Confirmed Objective Response Rate (ORR) as Determined by the Investigator
Duration of Response (DOR) as Determined by the IRF
+8 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Arm A: Atezolizumab+LurbinectedinExperimental Treatment4 Interventions
Induction phase: participants will receive standard of care atezolizumab on Day 1 of each 21-day cycle in combination with carboplatin on Day 1 and etoposide on Days 1, 2, and 3 of each 21-day cycle for 4 cycles. Maintenance phase: participants will receive atezolizumab on Day 1 of each 21-day cycle in combination with lurbinectedin on Day 1 of each 21-day cycle.
Group II: Arm B: AtezolizumabActive Control3 Interventions
Induction phase: participants will receive standard of care atezolizumab on Day 1 of each 21-day cycle in combination with carboplatin on Day 1 and etoposide on Days 1, 2, and 3 of each 21-day cycle for 4 cycles. Maintenance phase: participants will receive atezolizumab on Day 1 of each 21-day cycle.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Atezolizumab
2016
Completed Phase 3
~5860
Carboplatin
2014
Completed Phase 3
~6120
Etoposide
2010
Completed Phase 3
~2960
Lurbinectedin
2022
Completed Phase 3
~780

Find a Location

Who is running the clinical trial?

Hoffmann-La RocheLead Sponsor
2,456 Previous Clinical Trials
1,096,952 Total Patients Enrolled
Jazz PharmaceuticalsIndustry Sponsor
249 Previous Clinical Trials
34,150 Total Patients Enrolled
Clinical TrialsStudy DirectorHoffmann-La Roche
2,225 Previous Clinical Trials
895,700 Total Patients Enrolled

Media Library

Atezolizumab (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT05091567 — Phase 3
Small Cell Lung Cancer Research Study Groups: Arm A: Atezolizumab+Lurbinectedin, Arm B: Atezolizumab
Small Cell Lung Cancer Clinical Trial 2023: Atezolizumab Highlights & Side Effects. Trial Name: NCT05091567 — Phase 3
Atezolizumab (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05091567 — Phase 3
~84 spots leftby Apr 2025