DMT63
Comparable Ofatumumab Treatment Outcomes in Patients across Racial/Ethnic Groups in the Asclepios I/II and Apolitos Studies

Tuesday, October 26, 2021
Exhibit Hall (Rosen Shingle Creek)
Silvia Delgado, MD , Neurology, University of Miami Miller School of Medicine, Miami, FL
Mitzi J Williams, MD , Joi Life Wellness MS Center, Atlanta, GA
Morten Bagger, PhD , Novartis Pharma AG, Basel, Switzerland
Gordon Graham, PhD , Novartis Pharma AG, Basel, Switzerland
Etienne Pigeolet, PhD , Novartis Pharma AG, Basel, Switzerland
Huixin Yu, PhD , Novartis Pharma AG, Basel, Switzerland
Dieter A. Haering, PhD , Novartis Pharma AG, Basel, Switzerland
Roman Willi, PhD , Novartis Pharma AG, Basel, Switzerland
Cecile Kerloeguen, MSc , Novartis Pharma AG, Basel, Switzerland
Chao Xu, PhD , China Novartis Institute of Biomedical Research, Shanghai, China
Masaru Hirano, PhD , Novartis Pharmaceutics, K.K., Tokyo, Japan
Dee Stoneman, MPharm , Novartis Pharma AG, Basel, Switzerland
Wendy Su, PhD , Autoimmune, TG Therapeutics, Inc, New York, NY
Krishnan Ramanathan, PhD , Novartis Pharma AG, Basel, Switzerland
Jin Nakahara, MD, PhD , Department of Neurology, Keio University School of Medicine, Tokyo, Japan



Background:

Ofatumumab is a fully human anti-CD20 monoclonal antibody approved by the FDA for treatment of adults with relapsing multiple sclerosis (RMS). The RMS disease course and treatment response may vary across different racial/ethnic groups.

Objectives:

To compare outcomes across different racial/ethnic patient groups with RMS following ofatumumab treatment.

Methods:

This post hoc analysis included data from patients treated with ofatumumab 20 mg subcutaneously in the Phase 3 ASCLEPIOS I/II studies (n=935; White [n=829], Black/African-American [n=28], Asian [n=36], other [n=42]) and Phase 2 APOLITOS study (n=43; White [n=22], Asian [n=21, Japanese]). We compared efficacy, pharmacokinetics (PK), pharmacodynamics (PD), and safety outcomes for ofatumumab by these patient groups.

Results:

In ASCLEPIOS I/II, annualized relapse rates (95%CI) were similar in White (0.13 [0.11; 0.15]), Black/African-American (0.07 [0.02; 0.22], Asian (0.08 [0.03; 0.24]), and other (0.08 [0.03; 0.18]) patients treated with ofatumumab. As per PK analysis, ofatumumab trough concentrations (median [95%CI]) were comparable in White (0.438 [0.05; 2.53] μg/mL), Black/African-American (0.106 [0.05; 1.67] μg/mL), Asian (0.127 [0.05; 1.20] μg/mL) and other (0.453 [0.05; 2.25] μg/mL) patients in ASCLEPIOS I/II, with numerically higher concentrations (0.713 [0.142; 2.00] μg/mL) observed in Asian patients in APOLITOS. A population-PK analysis demonstrated a statistically significant difference between Japanese and Caucasian PK parameters but no clinically significant difference for maximum serum concentrations and area under the curve in these two populations. In APOLITOS, ofatumumab was associated with a consistent depletion of CD19+ B-cells and CD3+CD20+ T-cells in Asian and White patients, indicating similar PD response. No meaningful differences were observed in the incidence of adverse events (AEs) in ASCLEPIOS I/II (White [84.9%], Black/African-American [92.9%], Asian [66.7%], other [69.8%]) nor in APOLITOS. Overall pattern, incidence rate and severity of AEs across the groups was consistent with the overall population with no discernible trends/safety signals.

Conclusions:

Results revealed no clinically relevant differences in outcomes for RMS patients of different racial/ethnic groups treated with ofatumumab 20 mg subcutaneously, suggesting dose adjustment may not be necessary across these groups.