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Siltuximab

Alternative Names: siltuximab, cnto 328, sylvant, CNTO-328, CNTO328
Latest Update: 2024-12-19
Latest Update Note: Clinical Trial Update

Product Description

Siltuximab is recommended by international consensus as a first-line treatment for idiopathic multicentric Castleman disease on the basis of durable efficacy and safety data. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/32027862/)

Mechanisms of Action: IL6 Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Approved

Approved Countries: Australia | Austria | Belgium | Brazil | Canada | Croatia | Cyprus | Czech | Denmark | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hong Kong | Hungary | Iceland | Ireland | Israel | Italy | Korea | Latvia | Lithuania | Luxembourg | Malaysia | Netherlands | New Zealand | Norway | Philippines | Poland | Portugal | Romania | Singapore | Slovakia | Slovenia | Spain | Sweden | Switzerland | Taiwan | Turkey | United Kingdom | United States | Vietnam

Approved Indications: None

Known Adverse Events: None

Company: EUSA Pharma
Company Location:
Company CEO:
Additonal Commercial Interests: BeiGene

Clinical Description

Map of Global Clinical Trials for Siltuximab

Countries in Clinic: United States

Active Clinical Trial Count: 3

Highest Development Phases

Phase 2: Adenocarcinoma|Amyloidosis|Multiple Myeloma|Pancreatic Cancer

Phase 1: Cytokine Release Syndrome|Lymphoma, Non-Hodgkin

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

CASE1424

P1

Not yet recruiting

Lymphoma, Non-Hodgkin|Cytokine Release Syndrome

2028-09-01

NCT03315026

P2

Active, not recruiting

Multiple Myeloma|Amyloidosis

2025-10-01

IRB00105616

P2

Completed

Pancreatic Cancer|Adenocarcinoma

2023-04-05

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