drugset / Trial / NCT06213259

A Study of KD6005 in Healthy Participants and Participants With Rheumatoid Arthritis (RA)

NCT06213259 ↗

Phase 1 Completed 73 enrolled Shanghai Kanda Biotechnology Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This phase 1 study will consist of two parts: Phase 1a is a single-dose study, and will evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary pharmacodynamics (PD) in healthy participants. Phase 1b is a multiple doses study, and will evaluate the safety, tolerability, PK and preliminary PD in participants with rheumatoid arthritis (RA).

Timeline

Start
2024-01-06
Primary completion
2025-01-10
Completion
2025-01-10

Drugs

EvaluationDrugModalityDoseRoute
Subject KD6005 Unknown — Subcutaneous

Indications