drugset / Trial / NCT04430348
PTX-35 in Patients With Advanced Solid Tumors
Non-randomizedSequentialOpen-labelTreatment
Summary
A Phase I, First-in-Human, Dose-Escalation Study to Evaluate the Safety of the Monoclonal Antibody PTX-35 in Patients with Advanced Solid Tumors Refractory to Standard of Care
Timeline
- Start
- 2020-06-04
- Primary completion
- 2022-11-02
- Completion
- 2023-06-15
Outcome
Outcome not reported
Stopped: “Absence of immunological response”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PTX-35 | Monoclonal antibody | 0.01 mg/kg | Intravenous |
| Subject | PTX-35 | Monoclonal antibody | 0.03 mg/kg | Intravenous |
| Subject | PTX-35 | Monoclonal antibody | 0.1 mg/kg | Intravenous |
| Subject | PTX-35 | Monoclonal antibody | 0.3 mg/kg | Intravenous |
| Subject | PTX-35 | Monoclonal antibody | 1 mg/kg | Intravenous |
| Subject | PTX-35 | Monoclonal antibody | 3 mg/kg | Intravenous |