Under construction – not a live service
Sign in
Not yet taking people in DenmarkPhase 3

Zoledronic acid to protect bones from steroid damage in people with lymphoma

Tests zoledronic acid for bone protection in adults with lymphoma receiving steroids.

Key facts

Who runs it
Region Nordjylland
Where
Aalborg, Aarhus N, Copenhagen Oe, Herning, Odense C, Roskilde, and Vejle, DenmarkSee the 7 sites
Registry title
Zoledronic acid as prophylaxis against glucocorticoid-induced osteoporosis in lymphoma
Status
Not yet recruiting
Phase
Phase 3
People taking part
132 people, planned
Started
1 Sept 2026
Expected to end
31 Mar 2030
Type of study
Interventional
Record updated
7 September 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with certain lymphomas who are about to start steroid-containing chemotherapy. It tests zoledronic acid to protect bones from steroid-induced bone thinning.

Age
18 years or older
Sex
Women and men can join
Disease stage
Large B-cell lymphoma, transformed indolent B-cell lymphoma, mantle cell lymphoma, follicular lymphoma, Burkitt lymphoma or T-cell lymphoma. Planned for at least 6 cycles of a steroid-containing chemotherapy such as (R-)CHOP, usually as 1st line treatment. ECOG performance status 0-2. Life expectancy of at least 2 years.
Earlier treatment
Indolent lymphoma may also be in 2nd line, if more than 24 months have passed since the first diagnosis and none of the listed regimens were given in 1st line. Prednisone (or equivalent) of at least 60mg/day is planned. No glucocorticoid treatment for more than four weeks at screening.

Main reasons for not taking part

  • Cannot take bisphosphonates
  • Treatment with bone-protecting medicines such as bisphosphonates, denosumab or teriparatide, or ongoing lithium or anticonvulsants
  • eGFR below 35ml/min
  • Pregnant or breastfeeding
  • Planned radiation to hips or lower back, or planned autologous stem cell transplantation

The registry criteria, word for word

Show all 18 criteriaShow less

Who can take part

  • Age ≥18
  • Capable of reading and understanding Danish language
  • Diagnosed with Large B-cell lymphomas, transformations of indolent B-cell lymphomas, mantle cell lymphoma, follicular lymphoma, Burkitt lymphoma and T-cell lymphomas planned for treatment with a glucocorticoid-containing chemotherapy regimen (The 5th edition of the World Health Organization classification of haematolymphoid tumours: lymphoid neoplasms)
  • Planned for ≥6 cycles of treatment with (Rituximab), Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-)CHOP), CHOP, CVP, R-CVP, mini-CHOP, R-mini-CHOP, CEOP, R-CEOP, CHOEP, R-CHOEP, DA-EPOCH, R-DA-EPOCH) in 1st line with exception of patients with indolent lymphoma, who may also receive the listed treatments in 2nd line, if more than 24 months have passed between first lymphoma diagnosis and 2nd line treatment and if none of the above treatments were given as 1 st line treatment. Rituximab is however, being part of many treatment regimens, allowed for both 1st Line and 2nd line treatment. Minimum dose of prednisone (or equivalent) must be 60mg/day (ex. for mini-CHOP 60mgx1 for day 1-5). Patients who are planned to receive central nervous system prophylaxis or radiation therapy in addition to (R-)CHOP (-like) chemotherapy are also eligible
  • Willingness to comply with protocol specific procedures
  • Minimum estimated life expectancy for participants 2 year
  • ECOG Performance status 0-2

Who cannot take part

  • Planned radiation therapy against hips and/or lower back region (columna lumbalis)
  • On treatment with antiresorptive or anabolic medications including hormone replacement therapy (such as bisphosphonates, denosumab, strontium ranelate, selective estrogen receptor modulators (SERMs), estrogen used to treat symptoms associated with female menopause, teriparatide), received ongoing lithium or anticonvulsants treatment
  • Glucocorticoid treatment for more than four weeks at the time of screening start. (Local estrogen therapy (e.g., estradiol vaginal inserts) is permitted regardless of duration)
  • Planned autologous stem cell transplantation consolidation
  • Patients diagnosed with a pathological fracture at baseline related to lymphoma (as assessed on baseline routine pre-therapy imaging with CT or PET/CT)
  • Previous lower back surgery or hip surgery making DXA impossible to assess
  • Poor dental status (need of invasive dental procedures and/or infections) on inspection by study physician
  • eGFR <35ml/min (screening blood tests or in blood tests obtained up till 3 weeks before screening if available)
  • Contraindications to bisphosphonates
  • Patients with an ECOG Performance status >2
  • Pregnant and lactating women

Where in Denmark

  • Region NordjyllandAalborg, DenmarkNot yet recruiting
  • Region MidtjyllandAarhus N, DenmarkNot yet recruiting
  • Region HovedstadenCopenhagen Oe, DenmarkNot yet recruiting
  • Region MidtjyllandHerning, DenmarkNot yet recruiting
  • Region SyddanmarkOdense C, DenmarkNot yet recruiting
  • Region SjaellandRoskilde, DenmarkNot yet recruiting
  • Lillebaelt HospitalVejle, DenmarkNot yet recruiting

About the trial

What the trial wants to find out

The objective of the trial is to determine if intravenous zoledronic acid (ZOL) as prophylaxis is safe and effective against glucocorticoid-induced osteoporosis (GIO) in lymphoma patients.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record

Print a page for my doctor

Data and sources

Registry record
Listed on the EU's official list of trials (CTIS).
Official title
Zoledronic acid as prophylaxis against glucocorticoid-induced osteoporosis in lymphoma
Plain-language title
Zoledronic acid to protect bones from steroid damage in people with lymphomaGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 9 November 2026.
Record updated
7 September 2026