Reslizumab 10mg/ml Suppliers & Bulk Manufacturers
Available Forms: Injection
Available Strengths: 10mg/ml
Reference Brands: CINQAIR (USA), CINQAERO (EU)
Category: Immune Disorder
Reslizumab is a Immune Disorder product available as Injection in strengths 10mg/ml. It corresponds to the reference brands CINQAIR (USA), CINQAERO (EU). Verified GMP manufacturers and suppliers on PharmaTradz offer it in bulk for import worldwide, with regulatory documentation and dossier support available on request.
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Product Description:
Reslizumab is a humanised monoclonal antibody that binds circulating interleukin-5 and prevents it reaching its receptor on eosinophils. IL-5 is the cytokine that drives eosinophil production, survival and activation, so neutralising it depletes eosinophils — the cells responsible for the airway inflammation in eosinophilic asthma.
It is used as add-on maintenance treatment for severe asthma with an eosinophilic phenotype in adults whose disease is not controlled by inhaled therapy. In trials it reduced exacerbation rates and improved lung function in patients with raised blood eosinophil counts; patients without that phenotype do not benefit, so a blood eosinophil count is required to select candidates. Unlike the other anti-IL-5 agents, which are subcutaneous, reslizumab is given as an intravenous infusion every four weeks, dosed by body weight — which means clinic attendance rather than home administration. It carries a boxed warning for anaphylaxis, so it is given where that can be managed and patients are observed afterwards.
Sourcing notes. Originator biologic, on patent, no biosimilar. Cold chain. The intravenous route and weight-based dosing make it a hospital and infusion-centre product, competing with subcutaneous alternatives that patients can take at home — the main commercial constraint.
How Reslizumab is supplied today, and licensing ahead of patent expiry
Frequently Asked Questions
Reslizumab is sold as Cinqair and Cinqaero. It is developed and sold by Teva. 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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