drugset / Trial / NCT07427680
Study of TGM-312-SC01 in Healthy Participants and Adults With MASH
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamic (PD) effects of single ascending doses of TGM-312-SC01 in healthy adults and multiple ascending doses in patients with metabolic dysfunction-associated steatohepatitis (MASH).
Timeline
- Start
- 2026-03-03
- Primary completion
- 2028-03
- Completion
- 2028-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TGM-312-SC01 | Unknown | — | Subcutaneous |