drugset / Trial / NCT04762225
RPTR-168 in Patients With Human Papillomavirus Strain 16 (HPV-16) E6/E7 Positive Tumors and Melanoma
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to assess the safety and tolerability of escalating doses of RPTR-168 as a monotherapy in patients with HPV-16 E6/E7 positive tumors (HNSCC, cervical) and melanoma.
Timeline
- Start
- 2021-05-10
- Primary completion
- 2022-09-14
- Completion
- 2022-10-11
Outcome
Outcome not reported
Stopped: “Development program terminated”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RPTR-168 | Unknown | — | Intravenous |