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Study identifier: NCT05880667 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Adaptive Radiation for Abdominopelvic Metastases

Condition: Neoplasm - Soft Tissue Pelvis Malignant Secondary · Malignant Neoplasm of Stomach  ·  Sponsor: Fox Chase Cancer Center

PhasePhase 1
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Single arm Phase I trial of adaptive stereotactic body radiation (SBRT) for abdominopelvic metastases. Adaptive SBRT will allow for escalation of the prescription dose and target coverage while maintaining grade 3+ toxicity no greater than 10%. Subjects with metastatic cancer to the abdomen or pelvis requiring local control or palliation will be enrolled.

This description comes directly from the study's public registry record.

Talk to the study team

Tanu Singh  ·  12152141439  ·  tanu.singh@fccc.edu

Joshua Meyer, MD  ·  215-728-2667  ·  Joshua.Meyer@fccc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Fox Chase Cancer CenterPhiladelphia, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05880667