NCT03401060CompletedPhase 3
Interest of Denosumab Treatment in Osteoporosis Associated to Systemic Mastocytosis
Source: ClinicalTrials.gov · Last updated 31 Mar 2026
Brief summary (registry, in English)
The study is looking at the efficacy of subcutaneously administrated denosumab 60 mg every 6 months versus placebo after 3 years, by analyze of lumbar spine bone mineral density (BMD) in systemic mastocytosis. Investigators hypothesize that use of denosumab subcutaneously in patients with osteoporosis related to systemic mastocytosis is effective and safe to improve bone mineral density and prevent new bone events, based on targeted specific RANKL secretion by mast cells and short half-life of denosumab.
- Status (registry)
- Completed
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 24 (actual)
- First submitted
- 4 Jan 2018
- Start date
- 5 Mar 2018
- Primary completion date
- 11 Mar 2024
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Diseases
- Osteoporosis
- NCT number
- NCT03401060
- EudraCT number
- 2016-000596-25
What you commit to
- Study type: Interventional · Phase 3
- Participants enrolled: 24
- From 5 Mar 2018 to the primary completion date, 11 Mar 2024
- 11 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patient previously treated with denosumab
- Patient with hypocalcemia and/or hypo25-hydroxyvitamin D level non substituted prior enrolment
- Patient with dental problem that need any dental surgery within 6 months after enrolment.
Other illness
- Patient with aggressive mastocytosis or/and Associated Hematologic Non-Mastocytosis Disease (AHNMD)
- Patient with conditions that influence bone metabolism (primitive hyperparathyroidism, hyperaldosteronism, hypercorticism, etc …)
- Patient with medical, psychiatric or other conditions that may interfere with patient safety
Lab values
- Patient treated with intravenous bisphosphonate within 1 year prior to enrolment or with any other antiosteoporotic treatment within 3 months before enrolment. (per os bisphosphonate, strontium ranelate) Calcium and vitamin supplementation will be accepted
- Patient with clearance of creatinine less than 30 mL/min/1,73m2 (MDRD) or patient receiving dialysis
Age
- Woman without contraceptive treatment if of childbearing age.
Other
- Pregnant or breastfeeding woman
- Patient with contraindication to denosumab
Who the study is looking for
- Male or female \>/= 18 years of age at time of informed consent
- Willingness and ability to sign informed consent, comply with scheduled visits, treatment plan, laboratory tests and other study procedures.
- Patient with Indolent systemic or cutaneous mastocytosis according to WHO criteria (Appendix 4) with any specific treatment including corticosteroid, chemotherapy and immunomodulating drugs.
- Patient with:
- osteoporosis defined as bone mineral density T score ≤ -2.5 at the lumbar spine, OR
- osteopenia defined as BMD T-score \>-2,5 and ≤ -1 at the lumbar spine and low energy fracture (defined as fractures that are associated with decreased bone mineral density. Are excluded fractures of skull, face, mandible, metacarpals, fingers, or toes, pathologic fracture, and fracture that are associated with severe trauma).
- (in case of osteoarthritis at the lumbar spine, the T score at left femoral neck or total left hip can be used to define osteoporosis or osteopenia)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (11)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Jean Minjoz Hospital, Dermatology department Coordinator of this site? Confirm its status | Besançon | France | Unknown status |
| Caen Hospital, Clinical haematology department Coordinator of this site? Confirm its status | Caen | France | Unknown status |
| Estaing Hospital, Cellular therapy and clinical haematology department Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| Lille CHRU Hospital, Internal medicine and clinical immunology department Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| La Timone Hospital, Dermatology and cutaneous oncology department Coordinator of this site? Confirm its status | Marseille | France | Unknown status |
| Lapeyronie Hospital, Rheumatology and Immunology department Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| Necker Hospital, Adult haematology department Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| La Pitié-Salpêtrière Hospital, Internal medicine and clinical immunology department Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Cochin Hospital, Rheumatology department Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Strasbourg Hospital, Rheumatology department Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
| Toulouse Hospital, Dermatology department Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.