Phase 1 Trial in Patients With Human Papillomavirus (HPV)-Associated Cancer
Completed · Phase 1
Conditions studied: HPV Associated Cancers
In brief
This is an open-label, non-randomized, Phase I, dose escalation/dose expansion study in cohorts of patients with relapsed, resistant, or metastatic HPV-associated cancers. The Expansion Phase will begin in parallel one dose level lower than the highest dose deemed safe in the Dose Escalation in combination with a PD-1 checkpoint blockade.
Key facts
- Study ID
- NCT05826275
- Run by
- Toragen, Inc.
- People needed
- 28
- Starts
- 2023-06-20
- Expected to finish
- 2025-06-28
- Last updated by the study team
- 2025-09-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Prior histologically confirmed HPV-associated squamous cell carcinoma, which is relapsed, resistant, or metastatic
- Life expectancy of at least 3 months
- Dose Escalation Phase: patients who have experienced disease progression on Standard of Care Therapies
You may not qualify if…
- Active CNS metastases
- Have any history of seizure disorder or are taking prophylactic seizure medication
- Have an active viral, bacterial, or fungal infection
Where it is running
- City of Hope — Duarte, California, United States
- UCSD Moores Cancer Center — La Jolla, California, United States
- Yale University — New Haven, Connecticut, United States
- Icahn School of Medicine at Mount Sinai — New York, New York, United States
- MD Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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