TheraRadar
Data updated: May 26, 2026

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) (avutometinib potassium)

Genetic Support
First-in-Class Orphan Drug Breakthrough Therapy Priority Review Accelerated Approval
Oncology Approved 2025-05-08

The AVMAPKI FAKZYNJA co-pack treats adults with a specific form of recurrent low-grade serous ovarian cancer that carries a KRAS mutation. It helps patients who have already received prior systemic therapy for their cancer. This combination therapy is used to manage the disease by targeting specific proteins that allow tumor cells to grow and survive.

Source: FDA Label • VERASTEM INC

How AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Works

This medication works by blocking multiple signals within the MAPK pathway that cancer cells use to multiply. Avutometinib prevents the activation of proteins called MEK and RAF, while defactinib inhibits focal adhesion kinase (FAK) to further disrupt tumor cell proliferation. By targeting these different pathways simultaneously, the combination increases the overall anti-tumor activity.

1
Indication
--
Phase 3 Trials
1
Priority Reviews
1
Years on Market

Details

Status
Prescription
First Approved
2025-05-08
Patent Cliff
2042

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Routes
ORAL
Dosage Forms
CAPSULE, TABLET

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Approval History

2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2025 to 2025
May 2025 ORIGINAL Priority
New Drug · Type 1 - New Molecular Entity

What AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Treats

1 indications

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) is approved for 1 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Ovarian Cancer
Source: FDA Label

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Target & Pathway

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Target

MEK (Mitogen-Activated Protein Kinase Kinase) Serine/Threonine Kinase

A kinase downstream of BRAF in the MAPK pathway. MEK inhibitors are often combined with BRAF inhibitors to provide more complete pathway blockade and delay resistance. This combination is standard treatment for BRAF-mutant melanoma.

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

What's emerging in AVMAPKI FAKZYNJA CO-PACK (COPACKAGED)'s indications

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Phase 3 candidates targeting molecules with no FDA-approved drug, in indications AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) treats. First-in-class if their pivotal trials read out positive.

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Active Pipeline

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Key Completed Trials

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) FDA Label Details

Indications & Usage

FDA Label (PDF)

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) is indicated for the treatment of Ovarian Cancer.

View full patent landscape →
7 OB patents · 5 families · 185 international docs across 47 countries

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Patents & Exclusivity

Latest Patent: Dec 2042
Exclusivity: May 2032

Patents (7 active)

US11873296 Expires Dec 29, 2042
US12509450 Expires Dec 29, 2042
US11517573 Expires Sep 11, 2040
US11400090 Expires Oct 29, 2038
US7928109 Expires Aug 21, 2029
US8247411 Expires Apr 17, 2028
US7897792 Expires Feb 9, 2027

Exclusivity

ODE-525 Until May 2032
Source: FDA Orange Book

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Revenue Insights

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Patent Timeline

  • Cliff: 2042
  • 8 active patents

Trial Analysis

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Competitive Landscape

  • 11 similar drugs
  • Same target/indication analysis
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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.