TheraRadar
Data updated: Jul 17, 2026

LUNSUMIO VELO (mosunetuzumab-axgb) · Roche

Approved 2022-12-22

LUNSUMIO VELO is FDA-approved to treat 1 condition (same as LUNSUMIO).

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

Details

Status
Prescription
First Approved
2022-12-22
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: MOSUNETUZUMAB-AXGB

LUNSUMIO VELO Approval History

2023
2024
2025
2026
Original
New Indication
New Form
Label Update
8 FDA actions from 2022 to 2026 · 2 indication expansions
Jun 2026 SUPPL
Label · Labeling
Dec 2025 SUPPL
Efficacy
Nov 2024 SUPPL
Efficacy

What LUNSUMIO VELO Treats

1 indications

LUNSUMIO VELO is approved for 1 conditions since its original approval in 2022. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Follicular Lymphoma

Same approved indications as LUNSUMIO (same active ingredient).

Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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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.

LUNSUMIO VELO FDA Label Details

Indications & Usage

FDA Label (PDF)

LUNSUMIO VELO is FDA-approved to treat 1 condition — same approved indications as LUNSUMIO.

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Data Sources

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