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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

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Jean Minjoz Hospital, Dermatology department
Coordinator of this site? Confirm its status
BesançonFranceUnknown status
Caen Hospital, Clinical haematology department
Coordinator of this site? Confirm its status
CaenFranceUnknown status
Estaing Hospital, Cellular therapy and clinical haematology department
Coordinator of this site? Confirm its status
Clermont-FerrandFranceUnknown status
Lille CHRU Hospital, Internal medicine and clinical immunology department
Coordinator of this site? Confirm its status
LilleFranceUnknown status
La Timone Hospital, Dermatology and cutaneous oncology department
Coordinator of this site? Confirm its status
MarseilleFranceUnknown status
Lapeyronie Hospital, Rheumatology and Immunology department
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status
Necker Hospital, Adult haematology department
Coordinator of this site? Confirm its status
ParisFranceUnknown status
La Pitié-Salpêtrière Hospital, Internal medicine and clinical immunology department
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Cochin Hospital, Rheumatology department
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Strasbourg Hospital, Rheumatology department
Coordinator of this site? Confirm its status
StrasbourgFranceUnknown status
Toulouse Hospital, Dermatology department
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.