drugset / Trial / NCT06259903

Subcutaneous Administration of MD-18 in Healthy Subjects

NCT06259903 ↗

Phase 1 Unknown 35 enrolled Cohen Global, Ltd.
RandomizedSequentialDouble-blindTreatment

Summary

A Single Center, Single Dose, Double-blind, Randomized, Placebo-controlled Dose-Escalating Study to Evaluate Safety, Tolerability and Pharmacokinetics of Subcutaneously Administered MD-18 in healthy subjects.

Timeline

Start
2024-05-07
Primary completion
2024-12
Completion
2025-04

Drugs

EvaluationDrugModalityDoseRoute
Subject MD-18 Unknown 40 mg Subcutaneous
Subject MD-18 Unknown 80 mg Subcutaneous
Subject MD-18 Unknown 160 mg Subcutaneous
Subject MD-18 Unknown 240 mg Subcutaneous
Subject MD-18 Unknown 320 mg Subcutaneous

Indications

No indication recorded.