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Sarilumab bulk supplier for pharma manufacturers

Sarilumab Suppliers & Bulk Manufacturers

Available Forms: injection (prefilled syringe)

Available Strengths: 150 mg/1.14 mL, 200 mg/1.14 mL

Reference Brands: Kevzara (USA/EU)

Category: Immune Disorder

Sarilumab is a fully human monoclonal antibody that targets the interleukin‑6 (IL‑6) receptor (both membrane‑bound and soluble forms). By blocking IL‑6 from binding to its receptor, sarilumab inhibits the IL-6 mediated inflammatory signaling pathway. This reduces inflammation, immune‑mediated damage, and other symptoms associated with autoimmune inflammatory diseases such as rheumatoid arthritis and polymyalgia rheumatica.

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Product Description:

Sarilumab is a fully human monoclonal antibody that binds both the soluble and membrane-bound forms of the interleukin-6 receptor, blocking IL-6 signalling. IL-6 drives the systemic features of inflammatory disease — the acute phase response, anaemia of chronic disease, fatigue — as well as joint destruction, which is why blocking it produces a clinical picture different from TNF inhibition.

It is used for moderate to severe rheumatoid arthritis in adults who have responded inadequately to other disease-modifying drugs, and for polymyalgia rheumatica in patients who cannot taper off corticosteroids — an indication that matters because PMR is common in older people and long-term steroid use causes fractures, diabetes and infection. It is given by subcutaneous injection every two weeks. Blocking IL-6 suppresses the acute phase response, so CRP and fever can be absent during a serious infection, which delays recognition. Neutropenia, raised transaminases and raised lipids require monitoring, and gastrointestinal perforation is a recognised risk in patients with diverticulitis.

Sourcing notes. Originator biologic, on patent, no biosimilar. Cold chain, with a defined room-temperature period. Prefilled syringe and pen are separate presentations. It competes directly with tocilizumab, which now has biosimilars — a significant pricing pressure.

How Sarilumab is supplied today, and licensing ahead of patent expiry

Named-patient import Where a patient needs the product in a market where it is not registered, named-patient import is the lawful route. It requires the treating physician's documentation and authorisation from the destination regulator. We handle this pathway. Named-patient access
Authorised distribution For registered markets, supply runs through the manufacturer's authorised distribution channel. We can identify the authorised route for your market and tell you whether the product is registered there at all. Innovator sourcing
A genericised alternative Where the clinical requirement is the drug class rather than this specific molecule, there is often an off-patent alternative that is faster to register and materially cheaper. Tell us the indication and target market and we will say plainly whether one exists. Discuss alternatives
Licensing and generic development Patents expire country by country, and in many countries development and dossier filing can start before expiry under research and regulatory-review exemptions. We connect manufacturers developing this molecule, dossier holders, licensees and tech-transfer partners for markets where it is, or will become, off-patent. Partner on this molecule
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Frequently Asked Questions

Sarilumab is used to treat moderate to severe rheumatoid arthritis in adults who have not responded adequately to other disease-modifying antirheumatic drugs (DMARDs). It works as an interleukin-6 (IL-6) receptor antagonist, reducing inflammation and slowing joint damage.

Sarilumab is made from a human monoclonal antibody that specifically targets and blocks the IL-6 receptor, preventing the inflammatory effects of IL-6.

The trade name is Kevzara.

Kevzara is manufactured by Regeneron Pharmaceuticals in collaboration with Sanofi.

The generic name is sarilumab.

The primary brand name is Kevzara.

It is manufactured in approved biopharmaceutical facilities in the USA and Europe.

Kevzara (Sarilumab) is developed and sold by Sanofi and Regeneron. PharmaTradz handles enquiries for authorised supply of the originator product, named-patient import where it is not registered, and licensing or development work ahead of patent expiry.

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