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NCT03511391COMPLETEDanonymous

CHEckpoint Inhibition in Combination With an Immunoboost of External Beam Radiotherapy in Solid Tumors: CHEERS-trial

Sponsor

Source record

University Hospital, Ghent

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Checkpoint inhibitors targeting PD-1/PD-L1 pathways in combination with stereotactic body radiotherapy (SBRT).

Indication / condition

AI-normalized

Urothelial Carcinoma

Intervention

Source record

Nivolumab or Pembrolizumab or Atezolizumab, SBRT

Source & freshness

Source record

NCT ID

NCT03511391

Original source

ClinicalTrials.gov

Source last updated

Jan 23, 2024

Ingested at

Jun 18, 2026

Internal sync

Jun 18, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT03511391

Title

CHEckpoint Inhibition in Combination With an Immunoboost of External Beam Radiotherapy in Solid Tumors: CHEERS-trial

Sponsor

University Hospital, Ghent

Status

COMPLETED

Phase

Phase 2

Condition raw

Urothelial Carcinoma, Melanoma, Renal Cell Carcinoma, Non-small Cell Lung Cancer, Head and Neck Cancer

Condition normalized

Urothelial Carcinoma, Melanoma, Renal Cell Carcinoma, Non-small Cell Lung Cancer, Head and Neck Cancer

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Checkpoint inhibitors targeting PD-1/PD-L1 pathways in combination with stereotactic body radiotherapy (SBRT).

Target normalized

Checkpoint inhibitors targeting PD-1/PD-L1 pathways in combination with stereotactic body radiotherapy (SBRT).

Interventions

Nivolumab or Pembrolizumab or Atezolizumab, SBRT

Public preview

Source record

The CHEERS trial, sponsored by University Hospital Ghent, investigates the efficacy of combining SBRT with checkpoint inhibitors (Nivolumab, Pembrolizumab, Atezolizumab) in patients with advanced solid tumors. Given the increasing use of immunotherapy in oncology, this trial addresses a significant unmet need in enhancing progression-free survival (PFS) in non-small-cell lung carcinoma, urothelial carcinoma, renal cell carcinoma, melanoma, and head-and-neck carcinoma. The results could position the combination therapy favorably in a competitive landscape dominated by monotherapies, potentially leading to expanded indications and market opportunities. The trial's completion in January 2024 and subsequent publication of results will be critical for assessing the commercial viability and strategic partnerships for further development.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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