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Life sciences · Phase 1 Trial
ClinicalTrials.gov · September 14, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 1 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT05403723). This is a study registration, not published results. Lead sponsor: University of Maryland, Baltimore. Recruitment status: SUSPENDED. Phase: PHASE1. Study type: INTERVENTIONAL. Enrollment: 50 participants (ESTIMATED). Conditions: Extensive-stage Small-cell Lung Cancer. Interventions: DRUG: Durvalumab 50 MG/1 ML Intravenous Solution; DRUG: Etoposide Injection; DRUG: Cisplatin; DRUG: Carboplatin; DEVICE: Stereotactic Body Radiotherapy. Primary outcome measures: Incidence of treatment-related adverse events (AEs) , Up to 2.5 years. Brief summary: This is trial studying the safety of adaptive stereotactic body radiotherapy (SBRT) combined with durvalumab immunotherapy, platinum chemotherapy, and etoposide chemotherapy in platinum refractory extensive stage small cell lung cancer (SCLC).