Narlumosbart clinical trials
Also written JMT103.
How each study uses narlumosbart is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
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Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
Studies by the year they started
8 studies that test it; most in 2020 (2)
| Year | Studies |
|---|---|
| 2020 | 2 |
| 2022 | 2 |
| 2023 | 1 |
| 2024 | 2 |
| 2025 | 1 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 6 · Other 2
Shanghai JMT-Bio Inc. (6) · RenJi Hospital (1) · Fudan University (1)
Often tested with
Tested in the same studies.
Coming up
From the study records. Dates are the sponsors’ own estimates and often move.
Reaching primary completion within a year · 2, 1 in phase 3
Studies that test narlumosbart, phase 3 first.
- May 2027A Study to Assess the Prevention of Bone-related Events in Patients With Bone Metastases From Malignant Solid Tumors Treated With JMT103 Compared to Zoledronic AcidPhase 3 · Shanghai JMT-Bio Inc.
- Dec 2026The Efficacy and Safety of Narlumosbart in Combination With Stereotactic Body Radiation Therapy to Improve the Efficacy of First-line Chemotherapy Combined With Immunotherapy in Patients With Bone Metastases From Advanced Non-small Cell Lung CancerPhase 2 · Fudan University
Studies
Open first, then newest update. How each study uses narlumosbart is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 8
- The Efficacy and Safety of Narlumosbart in Combination With Stereotactic Body Radiation Therapy to Improve the Efficacy of First-line Chemotherapy Combined With Immunotherapy in Patients With Bone Metastases From Advanced Non-small Cell Lung CancerRecruitingPhase 2Fudan UniversityNCT06738160Written as Narlumosbart
- Narlumosbart Compared With Denosumab in Patients With Multiple Myeloma Bone DiseaseNot yet recruitingPhase 3RenJi HospitalNCT06314698Written as Narlumosbart
- A Study to Assess the Prevention of Bone-related Events in Patients With Bone Metastases From Malignant Solid Tumors Treated With JMT103 Compared to Zoledronic AcidNot yet recruitingPhase 3Shanghai JMT-Bio Inc.NCT06221072Written as JMT103
- A Study to Evaluate the Efficacy and Safety of Narlumosbart (JMT103) in Patients With Giant Cell Tumor of BoneNot yet recruitingPhase 3Shanghai JMT-Bio Inc.NCT05813665Written as Narlumosbart
- A Clinical Trial to Assess the Efficacy and Safety of JMT103 in Patients With Refractory HCMTerminatedPhase 1/2Shanghai JMT-Bio Inc.NCT04198480Written as JMT103
- Efficacy and Safety of JMT103 in Patients With Bone Metastases From Solid TumorsCompletedPhase 1Shanghai JMT-Bio Inc.NCT04630522Written as Drug: JMT103- 120 mg SC Q4W
- Efficacy and Safety of JMT103 in the Treatment of Postmenopausal Women With OsteoporosisStatus unknownPhase 2Shanghai JMT-Bio Inc.NCT05278338Written as JMT103
- Efficacy and Safety of JMT103 in the Treatment of Glucocorticoid Induced OsteoporosisStatus unknownPhase 2Shanghai JMT-Bio Inc.NCT05397938Written as JMT103
Codes
What other systems call narlumosbart · ClinicalTrials.gg INT016903
- UNII (FDA) J38KT46AH8NARLUMOSBARTOne source FDA
- NCI Thesaurus C190458NarlumosbartOne source FDA
| System | Code | Name there | Checked by |
|---|---|---|---|
| UNII (FDA) | J38KT46AH8 | NARLUMOSBART | One source FDA |
| NCI Thesaurus | C190458 | Narlumosbart | One source FDA |
“Confirmed” means two independent publishers link the code to this drug; “one source”, one does and its name agrees.