The first-in-human Phase 1/Phase 2a study described herein will evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of ADX-038 in both healthy participants (HP) and in patients with paroxysmal nocturnal hemoglobinuria (PNH).
The clinical study described in this protocol is a Phase 1/Phase 2a study evaluating safety, tolerability, PK, and PD of ADX-038. The study consists of 2 parts: 1. Phase 1 - Randomized, double-blind, placebo-controlled, parallel group, single ascending dose (SAD) in HP with up to 5 dose cohorts. 2. Phase 2a - Open label, single-arm (ADX-038), 2 dose study in participants with paroxysmal nocturnal hemoglobinuria (PNH) and residual anemia on a standard-of-care (SOC) anti-C5 regimen of ravulizumab or eculizumab.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
50
Nucleus Network Brisbane
Brisbane, Queensland, Australia
Peter MacCallum Cancer Centre
Melbourne, Victoria, Australia
Royal Melbourne Hospital
Parkville, Victoria, Australia
Richmond Pharmacology Ltd
London, London, United Kingdom
Safety in Healthy Volunteers
To evaluate the safety and tolerability of ADX-038 in HVs by incidence, relationship, and severity of adverse events and serious adverse events
Time frame: 365 days
Safety in Paroxysmal Nocturnal Hemoglobinuria Participants
Evaluate the safety and tolerability of ADX-038 by incidence, relationship, and treatment-emergent adverse events and serious adverse events.
Time frame: 365 days
Pharmacokinetics in Healthy Participants
To characterize the Pharmacokinetics of ADX-038 in HPs by measuring the Maximum observed plasma concentration (Cmax)
Time frame: 8 days
Pharmacodynamics in Healthy Participants
Change from base in plasma concentrations over time in Complement factor B (CFB) protein via assay measurement
Time frame: 365 days
Pharmacodynamics in Paraxysmal Nocturnal Hemoglobinuria
Evaluate the changes in hemoglobin concentrations
Time frame: 365 days
Pharmacodynamics in Paraxysmal Nocturnal Hemoglobinuria
Characterize the changes in serum concentration of complement factor B (CFB) protein and complement alternative pathway activity level.
Time frame: 365 days
Pharmacodynamics in Healthy Participants
Change in complement alternative pathway activity via assay measurement
Time frame: 365 days
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