drugset / Trial / NCT06755450
Study Evaluating Safety Pharmacokinetics and Pharmacodynamics of AUR112 in Patients With Relapsed Advanced Lymphoma
NaSequentialOpen-labelTreatment
Summary
A Phase 1, Open Label, Dose Escalation, Multicenter, First-in-Human (FIH) Study Evaluating the Safety, Pharmacokinetics and Pharmacodynamics of Oral AUR112 in Patients with Relapsed Advanced Lymphoma (ADITI-1)
Timeline
- Start
- 2025-01-15
- Primary completion
- 2027-01-15
- Completion
- 2028-01-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | AUR112 | Unknown | 100 mg | Oral |
| Subject | AUR112 | Unknown | 200 mg | Oral |
| Subject | AUR112 | Unknown | 400 mg | Oral |
| Subject | AUR112 | Unknown | 600 mg | Oral |
| Subject | AUR112 | Unknown | 900 mg | Oral |
| Subject | AUR112 | Unknown | 1200 mg | Oral |
Indications
No indication recorded.