TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED)

AVUTOMETINIB POTASSIUM
Oncology Approved 2025-05-08
1
Indication
--
Phase 3 Trials
1
Priority Reviews
0
Years on Market

Details

Status
Prescription
First Approved
2025-05-08
Routes
ORAL
Dosage Forms
CAPSULE, TABLET

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Approval History

Loading approval history...

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

Pro

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.

๐Ÿ”ฌ

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...
โญ

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
๐Ÿ“Š

Trial Timeline

Full development history with FDA approval milestones

Loading...
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

Pro

Indications & Usage

FDA Label (PDF)

AVMAPKI FAKZYNJA CO-PACK is indicated for the treatment of adult patients with KRAS -mutated recurrent low-grade serous ovarian cancer (LGSOC) who have received prior systemic therapy. This indication is approved under accelerated approval based on tumor response rate and duration of response [see Clinical Studies ]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. AVMAPKI FAKZYNJA CO-PACK, a combination of avutometinib and defactinib, each kinase inhibitors, is indicated for the treatment of adult patients ...

AVMAPKI FAKZYNJA CO-PACK (COPACKAGED) Patents & Exclusivity

Latest Patent: Dec 2042
Exclusivity: May 2030

Patents (8 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

NCE Until May 2030
Source: FDA Orange Book

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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