drugset / Trial / NCT06783881

Single-ascending Dose Study of Kylo-12 in Healthy Subjects

NCT06783881 ↗

Phase 1 Active not recruiting 50 enrolled Kylonova (Xiamen) Biopharma co., LTD.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a first-in-human, randomized, double-blind, placebo-controlled, single ascending dose study in healthy volunteers. Kylo-12 will be evaluated in approximately 50 subjects to assess safety, tolerability, pharmacokinetics and pharmacodynamic effects.

Timeline

Start
2025-03-12
Primary completion
2025-12-19
Completion
2026-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Kylo-12 Unknown — Subcutaneous

Indications