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A Clinical Study to Investigate the Efficacy and Safety of an Investigational Combination Therapy With BNT324 and BNT327 in Patients With Advanced Lung Cancer
NCT06892548 · View on ClinicalTrials.gov ↗
Study Summary
This study aims to investigate the combination of BNT324, a B7-H3 antibody-drug conjugate (ADC) with BNT327, a programmed death-ligand 1 (PD-L1) and vascular endothelial growth factor (VEGF) bispecific antibody, in participants with advanced/metastatic or relapsed/progressive small cell lung cancer (SCLC) and non small cell lung cancer (NSCLC).
Conditions Studied
Interventions
- BIOLOGICAL BNT324
- BIOLOGICAL BNT327
Study Locations (20)
California
- Precision NextGen Oncology and Research Center — Beverly Hills
- Cedars Sinai Medical Center — Los Angeles
- UCLA - David Geffen School of Medicine — Santa Monica
Texas
- Texas Oncology - DFW — Dallas
- MD Anderson Cancer Center — Houston
- Texas Oncology - Northeast — Tyler
Victoria
- Bendigo Hospital — Bendigo
- Barwon Health — Geelong
- Sunshine Hospital — Saint Albans
New York
- Memorial Sloan Kettering Cancer Center (MSKCC) — New York
- Icahn School of Medicine at Mount Sinai PRIME — New York
Arizona
- Mayo Clinic Arizona — Phoenix
Florida
- Mayo Clinic in Florida — Jacksonville
Iowa
- University of Iowa Hospitals & Clinics PARENT — Iowa City
Minnesota
- Mayo Clinic-Rochester — Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 594 participants |
| Start Date | 2025-05-02 |
| Est. Completion | 2031-06 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06892548
The ClinicalTrials.gov registry entry for NCT06892548 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 594 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BioNTech SE, which has 123 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Advanced Lung Cancer appearing as the primary indexed condition, and to 2 interventions — of which BNT324 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06892548 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Texas, Victoria. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06892548 about?
NCT06892548 is a clinical study titled "A Clinical Study to Investigate the Efficacy and Safety of an Investigational Combination Therapy With BNT324 and BNT327 in Patients With Advanced Lung Cancer". This study aims to investigate the combination of BNT324, a B7-H3 antibody-drug conjugate (ADC) with BNT327, a programmed death-ligand 1 (PD-L1) and vascular endothelial growth factor (VEGF) bispecific antibody, in participants with advanced/metastatic or relapsed/progressive small cell lung cancer ...
What is the current status of trial NCT06892548?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 594 participants. The study started on 2025-05-02. Estimated completion is 2031-06.
What conditions does trial NCT06892548 study?
This clinical trial studies the following conditions: Advanced Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06892548?
The interventions under investigation include: BNT324 (BIOLOGICAL), BNT327 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06892548?
This trial is sponsored by BioNTech SE, which has 123 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06892548 being conducted?
This trial has 20 study locations across Arizona, California, Florida, Iowa, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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