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Pasireotide Diaspartate bulk supplier for pharma manufacturers

Pasireotide Diaspartate Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 0.3 mg/mL, 0.6 mg/mL, 1.2 mg/mL, 10 mg, 20 mg, 30 mg

Reference Brands: Signifor (USA/EU)

Category: Orphan Drugs

Pasireotide Diaspartate is a Orphan Drugs product available as Injection in strengths 0.3 mg/mL, 0.6 mg/mL, 1.2 mg/mL, 10 mg, 20 mg, 30 mg. It corresponds to the reference brand Signifor (USA/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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📘 Sourcing Guide

Product Description:

Pasireotide is an orphan drug used for the treatment of Cushing’s disease in patients who are not candidates for pituitary surgery or have persistent or recurrent disease following surgery. Marketed under the brand name Signifor, Pasireotide was developed by Novartis and has received approval in the United States and European Union for this rare endocrine disorder.

It is a synthetic somatostatin analogue with a uniquely high affinity for somatostatin receptor subtype 5, approximately 40 times greater than other somatostatin analogues. By selectively binding to this receptor, Pasireotide effectively inhibits excess adrenocorticotropic hormone (ACTH) secretion, leading to reduced cortisol production and helping restore hormonal balance in patients with Cushing’s disease.

Pasireotide is available in both short-acting subcutaneous formulations and long-acting intramuscular depot injections, offering flexibility in treatment schedules ranging from daily to monthly dosing. Due to its targeted mechanism of action, patients require monitoring for potential effects on glucose metabolism, liver function, and gallbladder health. As an orphan drug, Pasireotide provides a specialized therapeutic option for managing a rare and challenging endocrine condition.

Pasireotide Diaspartate — third party manufacturing & bulk supply

Pasireotide Diaspartate is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.
Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.
Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

What to include when you enquire

  • Destination market — determines which manufacturers hold the right site-level approvals
  • First order quantity and estimated annual volume
  • Whether you need a registration dossier or the product is already registered
  • Packaging, labelling and language requirements
  • Incoterms and required shelf life

Manufacturers of Pasireotide Diaspartate listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding. Narcotic drugs and controlled substances are supplied strictly against valid import and export permits issued by the competent authorities.

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Frequently Asked Questions

Pasireotide diaspartate is used for the treatment of Cushing’s disease in patients not eligible for surgery or with persistent or recurrent disease, and in selected cases of acromegaly.

Pasireotide diaspartate is a synthetic somatostatin analogue designed to bind multiple somatostatin receptor subtypes to regulate hormone secretion.

The trade name of Pasireotide diaspartate is Signifor.

Pasireotide diaspartate (Signifor) is developed and marketed by Novartis Pharmaceuticals.

The generic name of Signifor is Pasireotide diaspartate.

The brand name of Pasireotide diaspartate is Signifor.

Pasireotide diaspartate is manufactured at Novartis-approved facilities under international GMP and regulatory standards.

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