Clinical Trials Directory

Trials / Unknown

UnknownNCT03568097

Immunotherapy in Combination With Chemotherapy in Small-cell Lung Cancer

Phased Avelumab Combined With Chemotherapy as First-line Treatment for Patients With Advanced Small-cell Lung Cancer (SCLC)

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
55 (estimated)
Sponsor
Hellenic Cooperative Oncology Group · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

PAVE(Phased Avelumab combined with chemotherapy as first-line treatment for patients with advanced small-cell lung cancer) is a Greek, investigator- initiated, single arm open- label phase II study of Avelumab in combination with cisplatin or carboplatin/ etoposide. The study will include an initial safety run-in, open-label, singlearm part (Part 1), and the actual phase II study (Part 2). The total number of patients will not change (the safety run-in patients will be included in the final total number of participants). The safety run-in period will not alter the total study timelines, as phase II accrual will follow immediately after the safety run-in.

Detailed description

Advanced small cell lung cancer (SCLC) remains a disease with dismal prognosis and new therapeutics are urgently needed. SCLC is notably chemosensitive and first-line chemotherapy with platinum analogs and etoposide is associated with high rates of initial objective responses that unfortunately do not last long. The primary endpoint for study design is 1-year PFS rate, where according to RECIST v1.1 PFS is determined as the time from the date of study entry to the date of progression, death from any cause or date of last contact.Secondary End Point is the evaluation of efficacy of the study treatment in terms of Overall Survival (OS), Best Overall Response (BOR), Objective Response Rate (ORR) and Duration of Response (DOR). Evaluation of the safety of the study treatment by assessing Treatment-Emergent Adverse Events (TEAEs). Evaluation of the Quality of Life of patients receiving the study the study treatment. Evaluation of potential biomarkers on fresh or archival sample,of formalin-fixed paraffin embedded tumor tissue block or a minimum of 10 unstained tumor tissue sections. Moreover 10 ml of EDTA-stored blood sample will be collected as well.

Conditions

Interventions

TypeNameDescription
DRUGAvelumab10 mg/kg will be given as intravenous infusion (IV) every two weeks (q 2 weeks) until disease progression.

Timeline

Start date
2018-09-16
Primary completion
2022-03-30
Completion
2024-04-01
First posted
2018-06-26
Last updated
2023-06-02

Locations

6 sites across 1 country: Greece

Source: ClinicalTrials.gov record NCT03568097. Inclusion in this directory is not an endorsement.