Geneva, Feb. 13 -- International Clinical Trials Registry received information related to the study (ACTRN12626000154303) titled 'A Study on the Safety, Tolerability, Bioavailability and Mechanism of Action of subcutaneous NAV-242 in adults with Hidradenitis Suppurativa' on Feb. 6.
Study Type: Interventional
Study Design:
Purpose: Treatment
Allocation: Non-randomised trial
Masking: Open (masking not used)
Type of endpoint: Safety/efficacy
Primary Sponsor: Navigator Medicines
Condition:
Hidradenitis Suppurativa
Hidradenitis Suppurativa
Inflammatory and Immune System - Autoimmune diseases
Intervention:
This is a Phase 1 open label study to evaluate the safety, tolerability, Pharmacokinetics (PK), Pharmacodynamic(PD), and immunogenic...