Avutometinib Potassium 0.8 mg Suppliers & Bulk Manufacturers
Available Forms: Capsules
Available Strengths: 0.8 mg
Reference Brands: Avmapki (USA), Fakzynja (USA)
Category: Oncology Cancer Care
Avutometinib 0.8 mg capsules, an oral RAF/MEK clamp used with defactinib for KRAS-mutated recurrent low-grade serous ovarian cancer. For hospital pharmacies and importers arranging named-patient supply.
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Product Description:
Avutometinib is an oral RAF/MEK clamp, a kinase inhibitor that holds RAF and MEK together in an inactive complex so the MAPK growth signal cannot pass down the chain. Unlike classic MEK inhibitors, it also stops RAF from switching MEK back on, an escape route that matters in KRAS-driven tumours. It is a potassium salt in 0.8 mg capsules. The 200 mg figure shown with it belongs to defactinib, a focal adhesion kinase inhibitor tablet packed and taken alongside it.
The pairing holds accelerated approval in the United States for adults with KRAS-mutated recurrent low-grade serous ovarian cancer after prior systemic treatment. Avutometinib is taken twice a week and defactinib twice a day, for three weeks of every four-week cycle, so a dosing calendar helps. Eye disorders, including blurred vision, are a known effect, and eye examinations are scheduled before and during use. Rash, raised liver enzymes and raised creatine phosphokinase are watched for. Both drugs can harm an unborn child.
Sourcing notes. This is a newly approved innovator therapy with very narrow registration, so most demand moves through named-patient or special-access import against an oncologist's prescription. Make clear whether you need the co-pack or the capsules alone, since the regimen is built on both. Keep capsules in the original container as the carton directs. Ask for the batch CoA, a traceable chain back to the authorisation holder, serialised packs with the approved leaflet and the import licence your regulator issues for unregistered medicines. Pharmacy teams apply their usual precautions for oral anticancer drugs.
How Avutometinib Potassium is supplied today, and licensing ahead of patent expiry
Where avutometinib with defactinib is approved
Checked 3 Oct 2026| Market | Status | Brand · regulator · date |
|---|---|---|
| United States | Approved | Avmapki Fakzynja Co-Pack · FDA · May 2025 (accelerated) |
| 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
It is used, as part of combination therapy with defactinib, to treat KRAS-mutated recurrent low-grade serous ovarian cancer in adults after prior systemic therapy.
Avutometinib potassium is a kinase inhibitor, a potassium salt of a small molecule designed to inhibit RAF and MEK kinases, with the molecular formula C₂₁H₁₇FKN₅O₅S.
Avmapki Fakzynja Co‑Pack (co-packaged with defactinib).
Manufactured by Verastem Oncology under regulated pharmaceutical standards.
Avutometinib potassium
Avmapki Fakzynja Co‑Pack
Manufactured under regulated standards by Verastem Oncology and supply partners in the United States.
Avmapki Fakzynja Co-Pack (Avutometinib + Defactinib) is developed and sold by Verastem 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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