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Iberdomide Capsules 0.75 mg, 1 mg Suppliers & Bulk Manufacturers

Available Forms: Capsules

Available Strengths: 0.75 mg, 1 mg

Reference Brands: Zenbexus (Bristol Myers Squibb)

Category: Oncology Cancer Care

Iberdomide (Zenbexus, Bristol Myers Squibb) is an oral CELMoD for multiple myeloma, used with daratumumab and dexamethasone. The US FDA approved it in August 2026. PharmaTradz handles enquiries for authorised supply of the originator product (named-patient and import-permit orders), and connects developers, API makers and licensees preparing for patent expiry.

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Product Description:

Iberdomide is a cereblon E3 ligase modulator (CELMoD), a successor to lenalidomide and pomalidomide. It binds cereblon much more strongly and causes faster, deeper breakdown of Ikaros and Aiolos, two proteins myeloma cells depend on. It also stimulates the immune system against the tumour, and it can work in myeloma that has become resistant to the older drugs.

The US FDA granted iberdomide accelerated approval as Zenbexus in August 2026 for adults with multiple myeloma who have had at least one prior line of therapy, in combination with subcutaneous daratumumab and dexamethasone. It is supplied as 0.75 mg and 1 mg capsules. Like other drugs in its family it can harm an unborn baby, so pregnancy prevention is required.

Sourcing and licensing notes. Iberdomide is patented and made only by Bristol Myers Squibb; there is no generic. Generic lenalidomide and pomalidomide are widely available, and we supply those too. We handle enquiries for authorised supply of Zenbexus and connect developers and licensees interested in the molecule ahead of patent expiry.

How Iberdomide Capsules 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

Multiple myeloma after at least one prior treatment, together with daratumumab and dexamethasone.

Zenbexus, from Bristol Myers Squibb. The US FDA approved it in August 2026.

All three act on cereblon. Iberdomide binds it more strongly and is designed to work where the older drugs have stopped working.

No. It is patented. We handle authorised-supply enquiries and connect developers and licensees preparing for patent expiry.

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