drugset / Trial / NCT06999720

Study of HX15001 in Adult Healthy Volunteers.

NCT06999720 ↗

Phase 1 Recruiting 62 enrolled Helixon Biotechnology (Suzhou) Co., Ltd
RandomizedSequentialDouble-blindTreatment

Summary

This is a phase I, randomized, double-blinded, placebo-controlled, single and multiple dose escalation study to evaluate the safety, tolerability, pharmacokinetic characteristics and pharmacodynamics of HX15001 in adult healthy participants. The study consists of two parts: Part A involves single-dose escalation (Cohorts 1-7), and Part B involves multiple-dose escalation (Cohorts 8-9). The primary objective of this study is to characterize the safety and tolerability of single and multiple doses of HX15001 in healthy subjects.

Timeline

Start
2025-06-11
Primary completion
2026-09-30
Completion
2026-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HX15001 Unknown — Subcutaneous

Indications

No indication recorded.