Saturday, July 11, 2026

Drug profile · INN

denosumab-bbdz

denosumab-bbdz (JUBBONTI) is a tumor necrosis factor ligand superfamily member 11 inhibitor. Route of administration: subcutaneous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 1
News articles 0
Drug details — denosumab-bbdz
US status
approved
Class
Route
SUBCUTANEOUS
Patents
0
Programs
1
Data quality
0.84

Quick answer

denosumab-bbdz (JUBBONTI) is a tumor necrosis factor ligand superfamily member 11 inhibitor. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN denosumab-bbdz
Brand JUBBONTI
Mechanism Tumor necrosis factor ligand superfamily member 11 inhibitor
Target Tumor necrosis factor ligand superfamily member 11
Route SUBCUTANEOUS
Formulation INJECTABLE

Mechanism of action

Tumor necrosis factor ligand superfamily member 11 inhibitor

Primary target: Tumor necrosis factor ligand superfamily member 11

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. BoNT A Phase 2 · United Therapeutics Europe · Traumatic Brain Injury

Related & competitor drugs

  1. denosumab Musculo-skeletal system (M05)
  2. prolia Tumor necrosis factor ligand superfamily member 11 inhibitor

Frequently asked questions

What is denosumab-bbdz?

denosumab-bbdz (JUBBONTI) is a tumor necrosis factor ligand superfamily member 11 inhibitor. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for denosumab-bbdz?

JUBBONTI is a marketed brand name for denosumab-bbdz. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of denosumab-bbdz?

denosumab-bbdz has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.