TheraRadar
Data updated: May 26, 2026

BILDYOS (denosumab-nxxp)

RANK Ligand Blocking Activity
Oncology Approved 2025-08-29

Bildyos (denosumab-nxxp) is a RANK ligand inhibitor indicated to treat osteoporosis and increase bone mass in patients at high risk for fracture. The medication is used for postmenopausal women and men with osteoporosis, as well as individuals with glucocorticoid-induced osteoporosis. It is also indicated for patients undergoing specific oncological treatments, including men receiving androgen deprivation therapy for nonmetastatic prostate cancer and women receiving aromatase inhibitor therapy for breast cancer.

Source: FDA Label • SHANGHAI HENLIUS BIOTECH • RANK Ligand Inhibitor

How BILDYOS Works

Bildyos binds to RANKL, a protein essential for the formation, function, and survival of osteoclasts, which are the cells responsible for bone resorption. By preventing RANKL from activating its receptor on the surface of osteoclasts and their precursors, the drug inhibits bone breakdown. This reduction in resorption increases bone mass and strength in both cortical and trabecular bone.

2
Indications
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-08-29
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: DENOSUMAB-NXXP

BILDYOS Approval History

2026
Original
New Indication
New Form
Label Update
2 FDA actions from 2025 to 2025 · 1 indication expansions
Oct 2025 ORIGINAL
Efficacy
Aug 2025 ORIGINAL
Update

What BILDYOS Treats

4 indications

BILDYOS is approved for 4 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Osteoporosis
  • Glucocorticoid-Induced Osteoporosis
  • Prostate Cancer
  • Breast Cancer
Source: FDA Label

BILDYOS Boxed Warning

SEVERE HYPOCALCEMIA IN PATIENTS WITH ADVANCED KIDNEY DISEASE Patients with advanced chronic kidney disease (eGFR < 30 mL/min/1.73 m 2 ), including dialysis dependent patients, are at greater risk of severe hypocalcemia following denosumab products administration. Severe hypocalcemia resulting in hospitalization, life-threatening events and fatal cases have been reported [see Warnings and Precautions ( 5.1 )] . The presence of chronic kidney disease-mineral bone disorder (CKD-MBD) markedly increa...

Auto-substitute OK for Prolia

Pharmacists can substitute BILDYOS for Prolia without calling the prescriber. This is a lower-cost alternative with no clinically meaningful differences.

BILDYOS 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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Phase 3 candidates targeting molecules with no FDA-approved drug, in indications BILDYOS treats. First-in-class if their pivotal trials read out positive.

Drugs Similar to BILDYOS

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CONEXXENCE
DENOSUMAB-BNHT
4 shared
Fresenius Kabi
Shared indications:
OsteoporosisGlucocorticoid-Induced OsteoporosisProstate Cancer +1 more
JUBBONTI
DENOSUMAB-BBDZ
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Novartis
Shared indications:
OsteoporosisGlucocorticoid-Induced OsteoporosisProstate Cancer +1 more
OSPOMYV
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SAMSUNG BIOEPIS CO LTD
Shared indications:
OsteoporosisGlucocorticoid-Induced OsteoporosisProstate Cancer +1 more
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Key Completed Trials

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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.

BILDYOS FDA Label Details

Indications & Usage

FDA Label (PDF)

BILDYOS is indicated for the treatment of Osteoporosis; Glucocorticoid-Induced Osteoporosis; Prostate Cancer; Breast Cancer.

⚠️ BOXED WARNING

WARNING: SEVERE HYPOCALCEMIA IN PATIENTS WITH ADVANCED KIDNEY DISEASE Patients with advanced chronic kidney disease (eGFR < 30 mL/min/1.73 m 2 ), including dialysis dependent patients, are at greater risk of severe hypocalcemia following denosumab products administration. Severe hypocalcemia resulti...

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Data Sources

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