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再発性多発性硬化症患者におけるオファツムマブの長期安全性、忍容性および有効性試験

基本情報

NCT ID
NCT03650114
ステータス
実施中(募集終了)
試験のフェーズ
第3相
試験タイプ
介入
目標被験者数
1,882
治験依頼者名
Novartis

概要

The purpose of this study is to collect long-term safety, tolerability, effectiveness and health outcomes data in eligible subjects who have participated in a Novartis ofatumumab clinical MS study. Vaccination sub-study The purpose of this research sub-study is to find out the effects of ofatumumab on the development of antibody responses to selected vaccines and keyhole limpet hemocyanin (KLH) neo-antigen in subjects with relapsing multiple sclerosis (RMS). COVID-19 sub-study: The purpose of this research sub-study is to explore the immune response following Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) vaccination in a subset of subjects on long-term ofatumumab 20 mg sc. Note: Novartis is not supplying the SARS-CoV-2 vaccine.

対象疾患

Relapsing Multiple Sclerosis

介入

Ofatumumab(BIOLOGICAL)
Tetanus toxoid (TT) containing vaccine (Td, Tdap)(BIOLOGICAL)
13-valent pneumococcal conjugate vaccine (13-PCV)(BIOLOGICAL)
23-valent pneumococcal polysaccharide vaccine (23-PPV)(BIOLOGICAL)
Seasonal Quadrivalent influenza vaccine(BIOLOGICAL)
Keyhole limpet hemocyanin (KLH) neo-antigen(BIOLOGICAL)

依頼者(Sponsor)