drugset / Trial / NCT04143789
Evaluation of AP-002 in Patients With Solid Tumors
SequentialOpen-labelTreatment
Summary
The purpose of this trial is to define an effective and safe dose of AP-002 in advanced or recurrent solid tumors for which there are no standard therapies to use in subsequent studies in advanced or recurrent breast, non-small cell lung cancer (NSCLC) or prostate cancers.
Timeline
- Start
- 2019-09-27
- Primary completion
- 2021-03
- Completion
- 2021-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 8 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 16 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 32 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 64 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 84 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 108 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 140 mg | Oral |
| Subject | TRIS(8-HYDROXYQUINOLINATO)GALLIUM | Unknown | 180 mg | Oral |