drugset / Trial / NCT05498597
AMT-151 in Patients With Selected Advanced Solid Tumours
NaSingle-groupOpen-labelTreatment
Summary
This first-in-human study will evaluate the Maximum Tolerated Dose (MTD) / the Recommended Phase 2 Dose (RP2D), safety, tolerability, anti-tumor activity, pharmacokinetics, pharmacodynamics and immunogenicity of AMT-151, a novel antibody-drug conjugate against folate receptor alpha, in patients with selected advanced solid tumors.
Timeline
- Start
- 2023-01-25
- Primary completion
- 2024-01-01
- Completion
- 2024-10-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | AMT-151 | Unknown | — | Intravenous |
Indications
endometrial clear cell adenocarcinoma
endometrial endometrioid adenocarcinoma
endometrial serous adenocarcinoma
lung adenocarcinoma
malignant pleural mesothelioma
ovarian clear cell adenocarcinoma
ovarian endometrioid adenocarcinoma
ovarian mucinous adenocarcinoma
pancreatic ductal adenocarcinoma
triple-negative breast carcinoma