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Zidesamtinib Tablets 25 mg, 100 mg Suppliers & Bulk Manufacturers

Available Forms: Tablets

Available Strengths: 25 mg, 100 mg

Reference Brands: Jideytro (Nuvalent)

Category: Oncology Cancer Care

Zidesamtinib (Jideytro, Nuvalent) is a ROS1-selective kinase inhibitor for ROS1-positive non-small cell lung cancer after a previous ROS1 inhibitor, approved by the US FDA in July 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:

Zidesamtinib blocks the ROS1 kinase, including the G2032R resistance mutation that stops earlier drugs such as crizotinib and entrectinib from working. It crosses into the brain, where ROS1-positive lung cancer often spreads, and it was designed not to inhibit the related TRK kinases. TRK inhibition causes the dizziness, weight gain and falls seen with some other ROS1 drugs.

The US FDA approved zidesamtinib as Jideytro in July 2026 for adults with ROS1-positive, locally advanced or metastatic non-small cell lung cancer previously treated with a ROS1 tyrosine kinase inhibitor. It is supplied as 25 mg and 100 mg tablets.

Sourcing and licensing notes. Zidesamtinib is patented and made only by Nuvalent; there is no generic. Other ROS1 options on PharmaTradz include crizotinib, entrectinib, repotrectinib and taletrectinib. We handle enquiries for authorised supply of Jideytro and connect developers and licensees interested in the molecule ahead of patent expiry.

How Zidesamtinib 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

ROS1-positive advanced non-small cell lung cancer in adults already treated with a ROS1 inhibitor.

Jideytro, from Nuvalent. The US FDA approved it in July 2026.

Yes. It was designed to block ROS1 with the G2032R resistance mutation and to reach the brain.

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

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