RecruitingPhase 2NCT06088381
Selective Adjuvant Therapy for HPV-mediated Oropharynx SCCs Based on Residual Circulating Tumor DNA Levels (SAVAL)
Studying Squamous cell carcinoma of the oropharynx
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Maryland, Baltimore
- Principal Investigator
- Jason K Molitoris, MD, PhDUniversity of Maryland/Maryland Proton Treatment Center
- Intervention
- Experimental Observation(other)
- Enrollment
- 61 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2030
Study locations (5)
- Maryland Proton Treatment Center, Baltimore, Maryland, United States
- University of Maryland Greenebaum Cancer Center, Baltimore, Maryland, United States
- Upper Chesapeake Health, Bel Air, Maryland, United States
- Central Maryland Radiation Oncology, Columbia, Maryland, United States
- Baltimore Washington Medical Center, Glen Burnie, Maryland, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT06088381 on ClinicalTrials.govOther trials for Squamous cell carcinoma of the oropharynx
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