drugset / Trial / NCT06667141

Phase 1 Study of ACR-2316 in Specific Advanced Solid Tumors

NCT06667141 ↗

Phase 1 Recruiting 100 enrolled Acrivon Therapeutics
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a first in-human, Open-label Phase 1 study to assess the safety of ACR-2316 for the treatment of subjects with specific, histologically confirmed, locally advanced, recurrent or metastatic solid tumors.

Timeline

Start
2024-10-08
Primary completion
2026-08-12
Completion
2026-12-12

Drugs

EvaluationDrugModalityDoseRoute
Subject ACR-2316 Unknown — —

Indications

No indication recorded.