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Active Not RecruitingNCT06783881

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

A Phase 1 Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Doses of Kylo-12 in Healthy Subjects

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Kylonova (Xiamen) Biopharma co., LTD. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGKylo-12Administered SC.
DRUGPlaceboAdministered SC.

Timeline

Start date
2025-03-12
Primary completion
2025-12-19
Completion
2026-08-30
First posted
2025-01-20
Last updated
2026-03-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06783881. Inclusion in this directory is not an endorsement.