drugset / Trial / NCT02508441
Phase 1 Safety and Tolerability Study of Andes-1537 for Injection in Patients With Advanced Unresectable Solid Tumors
NaSingle-groupOpen-labelTreatment
Summary
This is a first-in-human, open-label, dose escalation and expansion, 2-part study to determine the safety, tolerability, and maximum tolerated dose of Andes-1537 for Injection in patients with advanced unresectable solid tumors that are refractory to standard therapy or for which no standard therapy is available.
Timeline
- Start
- 2015-12-08
- Primary completion
- 2017-11-13
- Completion
- 2017-11-13
Outcome
Outcome not reported
Stopped: “Part 1 of the study was completed and the maximum tolerated dose determined. Part 2 of the study was terminated and will be conducted under a new protocol.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MULNITORSEN | Unknown | 100 mg | Subcutaneous |
| Subject | MULNITORSEN | Unknown | 1000 mg | Subcutaneous |
Indications
No indication recorded.