TheraRadar
Data updated: May 26, 2026

RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj)

Genetically Validated
Oncology Approved 2025-12-17

RYBREVANT FASPRO is indicated for the treatment of Non-Small Cell Lung Cancer.

Source: FDA Label • Johnson & Johnson • Endoglycosidase

How RYBREVANT FASPRO Works

Amivantamab is a bispecific antibody that binds to the extracellular domains of EGFR and MET to disrupt signaling and induce receptor degradation. By binding to these receptors on the surface of tumor cells, it also targets them for destruction by immune effector cells through antibody-dependent cellular cytotoxicity and trogocytosis. The hyaluronidase component acts as an endoglycosidase that transiently depolymerizes hyaluronan in the subcutaneous tissue. This increases tissue permeability to facilitate the local delivery and absorption of the treatment.

2
Indications
--
Phase 3 Trials
1
Priority Reviews
0
Years on Market

Details

Status
Prescription
First Approved
2025-12-17
Routes
SINGLE-USE
Dosage Forms
INJECTION, VIAL

RYBREVANT FASPRO Approval History

2026
Original
New Indication
New Form
Label Update
6 FDA actions from 2025 to 2026
Feb 2026 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer
Dec 2025 ORIGINAL Priority
Update · Type 5 - New Formulation or New Manufacturer

What RYBREVANT FASPRO Treats

1 indications

RYBREVANT FASPRO is approved for 1 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Non-Small Cell Lung Cancer
Source: FDA Label

RYBREVANT FASPRO Target & Pathway

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Target

EGFR (Epidermal Growth Factor Receptor) Growth Factor Receptor

A receptor that triggers cell growth, proliferation, and survival when activated. Mutations or overexpression of EGFR drive many cancers, particularly lung cancer. Blocking EGFR stops the growth signals that fuel tumor progression.

RYBREVANT FASPRO 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.

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Active Pipeline

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Key Completed Trials

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Completed studies with published results, ranked by significance

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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.

RYBREVANT FASPRO FDA Label Details

Indications & Usage

FDA Label (PDF)

RYBREVANT FASPRO is indicated for the treatment of Non-Small Cell Lung Cancer.

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Data Sources

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