Ziftomenib 200 mg Suppliers & Bulk Manufacturers
Available Forms: Capsules
Available Strengths: 200 mg
Reference Brands: Komzifti (USA)
Category: Oncology Cancer Care
Ziftomenib is a small‑molecule menin inhibitor. It blocks the interaction between menin and MLL proteins, disrupting a pathway critical for the survival and proliferation of certain leukemia cells, especially those with NPM1 mutation or MLL rearrangement. It is used in adult patients with relapsed or refractory AML who have no satisfactory alternative treatment options.
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Product Description:
Ziftomenib inhibits menin, a scaffold protein that is not itself an oncogene but is indispensable to one. In leukaemias driven by KMT2A rearrangement or NPM1 mutation, menin anchors the leukaemogenic complex to chromatin and keeps a set of developmental genes switched on, locking the cell in an immature, self-renewing state. Breaking the menin interaction releases that block and the cells differentiate into mature myeloid cells rather than simply dying.
It is used for relapsed or refractory acute myeloid leukaemia with the relevant mutations, where outcomes have been poor and few options exist. Because the mechanism is differentiation rather than cytotoxicity, the characteristic risk is differentiation syndrome — fever, dyspnoea, hypoxia, effusions and oedema as a large mass of blasts matures at once — which requires prompt recognition and corticosteroid treatment. QT prolongation requires ECG monitoring; cytopenias and infection occur.
Sourcing notes. Recently approved originator product, on patent, with registration so far in a limited number of territories — verify before quoting. Requires NPM1 or KMT2A testing at the destination. Treating centres need familiarity with differentiation syndrome, which is otherwise easily mistaken for sepsis or fluid overload. Oral capsules, room temperature.
How Ziftomenib is supplied today, and licensing ahead of patent expiry
Where ziftomenib is approved
Checked 3 Oct 2026| Market | Status | Brand · regulator · date |
|---|---|---|
| United States | Approved | Komzifti · FDA · Nov 2025 |
| Generic / biosimilar | None | None approved as of the check date |
Not approved in your country? A hospital or doctor can often still import it for a named patient, through a special-access, import-permit or compassionate-use route. We confirm which route applies in your country and the documents needed before quoting. Ask about named-patient supply →
Frequently Asked Questions
Ziftomenib is used to treat adult patients with relapsed or refractory acute myeloid leukemia (AML) who have an NPM1 mutation and have no satisfactory alternative treatment options. It works by targeting the genetic pathway driving the leukemia to slow disease progression.
It is made from the active pharmaceutical ingredient ziftomenib, a small-molecule menin inhibitor that disrupts the interaction between the Menin protein and KMT2A (MLL), which helps prevent the growth of leukemia cells.
The trade name is Komzifti.
Komzifti is manufactured by Kura Oncology in collaboration with Kyowa Kirin.
The generic name is ziftomenib.
The brand name is Komzifti.
It is manufactured in approved pharmaceutical facilities in the USA and Japan, with distribution depending on regulatory approvals.
Komzifti (Ziftomenib) is developed and sold by Kura Oncology. 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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