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Vepdegestrant Tablets 100 mg, 200 mg Suppliers & Bulk Manufacturers

Available Forms: Tablets

Available Strengths: 100 mg, 200 mg

Reference Brands: Veppanu (Arvinas)

Category: Oncology Cancer Care

Vepdegestrant (Veppanu, Arvinas) is a once-daily tablet for ER-positive, HER2-negative, ESR1-mutated advanced breast cancer, approved by the US FDA in May 2026. It is the first approved PROTAC protein degrader. 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:

Vepdegestrant is a PROTAC (proteolysis-targeting chimera). One end of the molecule binds the oestrogen receptor and the other recruits the cell's own protein-disposal machinery, so the receptor is tagged and destroyed rather than just blocked. It is the first medicine of this type to be approved, and it works against the ESR1-mutant receptors that make breast cancer resistant to aromatase inhibitors.

The US FDA approved vepdegestrant as Veppanu in May 2026 for adults with ER-positive, HER2-negative, ESR1-mutated advanced or metastatic breast cancer that has progressed after at least one endocrine therapy. An ESR1 mutation test is needed before treatment. It is taken as a 200 mg tablet once a day.

Sourcing and licensing notes. Vepdegestrant is patented and there is no generic. We confirm registration status for each destination before quoting. We handle authorised-supply enquiries and connect developers and licensees interested in the molecule and the PROTAC class ahead of patent expiry.

How Vepdegestrant Tablets 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

ER-positive, HER2-negative, ESR1-mutated advanced or metastatic breast cancer after at least one endocrine therapy.

Veppanu, from Arvinas. The US FDA approved it in May 2026.

A molecule that makes the cell destroy a target protein instead of just blocking it. Vepdegestrant destroys the oestrogen receptor and is the first PROTAC to be approved.

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

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