AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) (avutometinib potassium)
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.
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.
Details
- Status
- Prescription
- First Approved
- 2025-05-08
- Patent Cliff
- 2042
- Routes
- ORAL
- Dosage Forms
- CAPSULE, TABLET
Companies
AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Approval History
What AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Treats
1 indicationsAVMAPKI 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
AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Target & Pathway
ProTarget
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
ProThree rings of competition based on shared molecular targets and treated indications.
MoA expansion candidates
Same target(s), different indications — where else is this mechanism being explored?
Indication competitors
Same indication, different mechanism — what else might this patient receive?
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
See all emerging drugs →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.
Drugs Similar to AVMAPKI FAKZYNJA CO-PACK (COPACKAGED)
3 of 11FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
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.
AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Patents & Exclusivity
Patents (7 active)
Exclusivity
Pro Intelligence Preview
Deep insights for AVMAPKI FAKZYNJA CO-PACK (COPACKAGED)
Revenue Insights
- • Quarterly revenue tracking
- • Historical trend analysis
Patent Timeline
- • Cliff: 2042
- • 8 active patents
Trial Analysis
- • Clinical trial tracking
- • Development stage analysis
Competitive Landscape
- • 11 similar drugs
- • Same target/indication analysis
Full approval history • All patents • Revenue trends • Competitor analysis
Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.