Zoledronic acid
Regulatory milestones approvals, filings & regulatory actions · 8 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansions (4) | US (FDA) | RECLAST | — | 2008-06-03 – 2009-05-29 | fda.gov ↗ |
| Label expansions (2) | US (FDA) | ZOMETA | — | 2004-02-27 – 2008-03-20 | fda.gov ↗ |
| Approved | US (FDA) | ZOMETA | — | 2001-08-20 | fda.gov ↗ |
| Approved | EU (EMA) | Zometa | — | 2001-03-20 | europa.eu ↗ |
Trials 240 · started per year
Also used as a comparator or background therapy in 86 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 16 trials | ||||||
| Phase 1 | NCT06513624 Background | Dec 2024 → Dec 2026 expected | — | National University Hospital, Singapore | Recruiting | No outcome recorded |
| Phase 1 | NCT02517918 Background | Feb 2015 → Sep 2016 | osteosarcoma | Institut Bergonié | Completed | No outcome recorded |
| Phase 1 | NCT01721993 Comparator | Jan 2013 → Jul 2014 | — | Thar Pharmaceuticals, Inc | Completed | No outcome recorded |
| Phase 1 | NCT00741377 Background | Jan 2009 → Dec 2011 | plasma cell myeloma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 1 | NCT00415779 Background | Jul 2006 → Dec 2008 | metastatic prostate carcinoma | National Cancer Institute, Naples | Completed | No outcome recorded |
| Phase 1 | NCT00258258 Background | Aug 2005 → Mar 2009 | plasma cell myeloma | Roswell Park Cancer Institute | Terminated | No outcome recorded |
| Phase 1/22 trials | ||||||
| Phase 1/2 | NCT06374459 Comparator | Jan 2025 → May 2032 expected | hormone receptor-positive breast cancer | Washington University School of Medicine | Recruiting | No outcome recorded |
| Phase 1/2 | NCT04279392 Comparator | Sep 2020 → Dec 2022 | bone resorption disease | University of Nebraska | Completed | No outcome recorded |
| Phase 224 trials | ||||||
| Phase 2 | NCT07043608 Background | May 2026 → Feb 2029 expected | clear cell renal carcinoma, metastatic carcinoma in the bone | Kelly Fitzgerald, MD | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT05677152 Comparator | Aug 2022 → Jul 2025 overdue | — | AUVA Traumazentrum Vienna Site UKH Meidling | Recruiting | No outcome recorded |
| Phase 2 | NCT05328154 Comparator | Jun 2022 → Dec 2024 | postmenopausal osteoporosis | University Hospital, Clermont-Ferrand | Completed | No outcome recorded |
| Phase 2 | NCT04608630 Comparator | Jul 2021 → Feb 2027 expected | osteoporosis | Australian and New Zealand Intensive Care Research Centre | Recruiting | No outcome recorded |
| Phase 2 | NCT04325776 Comparator | Sep 2020 → May 2021 | non-small cell lung carcinoma | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Unknown | No outcome recorded |
| Phase 2 | NCT03396315 Comparator | Jan 2018 → Jun 2023 | osteoporosis | Columbia University | Completed | No outcome recorded |
| Phase 2 | NCT03183557 Comparator | Oct 2017 → Dec 2022 | osteoporosis | Shinshu University | Unknown | No outcome recorded |
| Phase 2 | NCT03118570 Background | Sep 2017 → Oct 2019 | osteogenesis imperfecta type 1, osteogenesis imperfecta type 3, osteogenesis imperfecta type 4 | Ultragenyx Pharmaceutical Inc | Completed | No outcome recorded |
| Phase 2 | NCT03127319 Comparator | Jul 2017 → Apr 2019 | non-small cell lung carcinoma | Affiliated Hospital of Hebei University | Unknown | No outcome recorded |
| Phase 2 | NCT02632916 Comparator | Aug 2016 → Feb 2020 | osteoporosis | Children's Hospital of Eastern Ontario | Completed | No outcome recorded |
| Phase 2 | NCT01951586 Comparator | Dec 2013 → Jul 2016 | non-small cell lung carcinoma | Amgen | Completed | No outcome recorded |
| Phase 2 | NCT01788176 Comparator | Dec 2013 → Dec 2015 | complex regional pain syndrome | University of Sao Paulo General Hospital | Unknown | No outcome recorded |
| Phase 2 | NCT01215344 Background | Nov 2010 → Nov 2015 | plasma cell myeloma | Vanderbilt-Ingram Cancer Center | Completed | No outcome recorded |
| Phase 2 | NCT00781261 Comparator | Aug 2009 → Dec 2013 | osteonecrosis | University of Sydney | Unknown | No outcome recorded |
| Phase 2 | NCT00903162 Background | May 2009 → Jul 2014 | female breast carcinoma | Dana-Farber Cancer Institute | Completed | No outcome recorded |
| Phase 2 | NCT01330238 Comparator | Dec 2008 → Mar 2011 | — | University of Oulu | Completed | No outcome recorded |
| Phase 2 | NCT00399802 Comparator | Nov 2006 → Dec 2007 | breast cancer, metastatic carcinoma in the bone | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 2 | NCT00216151 Comparator | Jun 2005 → Mar 2007 | plasma cell myeloma | Hoosier Cancer Research Network | Terminated | No outcome recorded |
| Phase 2 | NCT00091832 Comparator | Sep 2004 → Nov 2005 | breast cancer, metastatic neoplasm | Amgen | Completed | No outcome recorded |
| Phase 2 | NCT00081159 Background | Jul 2004 → Sep 2014 | metastatic malignant neoplasm, prostate cancer | M.D. Anderson Cancer Center | Completed | No outcome recorded |
| Phase 2 | NCT00072930 Background | Dec 2003 → Apr 2007 | prostate cancer | MedImmune LLC | Completed | No outcome recorded |
| Phase 2 | NCT00181584 Comparator | Sep 2003 → Feb 2006 | bone resorption disease, prostate cancer | Massachusetts General Hospital | Completed | No outcome recorded |
| Phase 2 | NCT00582556 Comparator | Apr 2003 → Mar 2011 | prostate cancer | University of Wisconsin, Madison | Completed | No outcome recorded |
| Phase 2 | NCT01341262 Background | Mar 2002 → Oct 2007 | plasma cell myeloma | IRCCS Azienda Ospedaliero-Universitaria di Bologna | Completed | No outcome recorded |
| Phase 2/32 trials | ||||||
| Phase 2/3 | NCT01006395 Comparator | Jan 2011 → Apr 2019 | prostate cancer | Austin Health | Completed | No outcome recorded |
| Phase 2/3 | NCT00524849 Comparator | Nov 2006 → Aug 2008 | breast cancer, metastatic carcinoma in the bone | Fudan University | Completed | No outcome recorded |
| Phase 322 trials | ||||||
| Phase 3 | NCT07056478 Comparator | Jan 2026 → Jan 2028 expected | pelvic muscle wasting | Prince of Wales Hospital, Shatin, Hong Kong | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT06533865 Background | Mar 2025 → Oct 2028 expected | functional hypothalamic amenorrhea | Massachusetts General Hospital | Recruiting | No outcome recorded |
| Phase 3 | NCT04779216 Background | Sep 2021 → Oct 2024 | anorexia nervosa, osteoporosis | Karen Klahr Miller, MD | Completed | No outcome recorded |
| Phase 3 | NCT04303026 Comparator | Mar 2020 → Jun 2023 | osteoarthritis, hip | Vestre Viken Hospital Trust | Unknown | No outcome recorded |
| Phase 3 | NCT04034199 Comparator | Aug 2019 → Dec 2020 | idiopathic inflammatory myopathy, osteoporosis | Kwong Wah Hospital | Unknown | No outcome recorded |
| Phase 3 | NCT03930992 Background | Apr 2019 → Oct 2022 | osteoporosis | University of Guadalajara | Completed | No outcome recorded |
| Phase 3 | NCT03040765 Comparator | May 2018 → Apr 2019 | beta-thalassemia major, osteoporosis | Hamad Medical Corporation | Terminated | No outcome recorded |
| Phase 3 | NCT02123264 Comparator | May 2014 → Jun 2018 | rheumatoid arthritis | Carmen Gómez-Vaquero | Terminated | No outcome recorded |
| Phase 3 | NCT01802658 Comparator | Nov 2012 → Dec 2016 | abnormal mineralization disorder | Nantes University Hospital | Terminated | No outcome recorded |
| Phase 3 | NCT01345019 Comparator | May 2012 → Jul 2016 | lytic metastatic bone lesion, plasma cell myeloma | Amgen | Completed | No outcome recorded |
| Phase 3 | NCT01348269 Comparator | May 2011 → Aug 2015 | bone marrow disorder | Wuerzburg University Hospital | Completed | No outcome recorded |
| Phase 3 | NCT00330759 Comparator | Jun 2006 → Apr 2009 | lytic metastatic bone lesion | Amgen | Completed | No outcome recorded |
| Phase 3 | NCT00321620 Comparator | Apr 2006 → Oct 2009 | metastatic carcinoma in the bone | Amgen | Completed | No outcome recorded |
| Phase 3 | NCT00321464 Comparator | Apr 2006 → Jul 2009 | metastatic carcinoma in the bone | Amgen | Completed | No outcome recorded |
| Phase 3 | NCT00326820 Comparator | Jan 2006 → Dec 2012 | breast cancer, humoral hypercalcemia of malignancy, metastatic malignant neoplasm | Wales Cancer Trials Unit | Unknown | No outcome recorded |
| Phase 3 | NCT00099177 Comparator | Aug 2005 → Dec 2007 | bone neoplasm, metastatic malignant neoplasm | Hoffmann-La Roche | Terminated | No outcome recorded |
| Phase 3 | NCT00099203 Comparator | Jul 2005 → Dec 2007 | bone neoplasm, metastatic neoplasm | Hoffmann-La Roche | Terminated | No outcome recorded |
| Phase 3 | NCT00512993 Comparator | Dec 2004 → Nov 2013 | breast cancer | GBG Forschungs GmbH | Completed | No outcome recorded |
| Phase 3 | NCT00145275 Background | Dec 2004 → Oct 2005 | — | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00215943 Comparator | Jun 2003 → Aug 2012 | plasma cell myeloma | H. Lee Moffitt Cancer Center and Research Institute | Terminated | No outcome recorded |
| Phase 3 | NCT00033332 Background | Apr 2002 → Mar 2006 | plasma cell myeloma | National Cancer Institute (NCI) | Completed | No outcome recorded |
| Phase 3 | NCT00295646 Comparator | Jun 1999 → Mar 2008 | breast cancer | Austrian Breast & Colorectal Cancer Study Group | Completed | No outcome recorded |
| Phase 427 trials | ||||||
| Phase 4 | NCT07406685 Comparator | Mar 2026 → Mar 2030 expected | postmenopausal osteoporosis | National Taiwan University Hospital | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT06859580 Comparator | Mar 2025 → Feb 2028 expected | primary hyperparathyroidism | University of Aarhus | Recruiting | No outcome recorded |
| Phase 4 | NCT06643780 Comparator | Apr 2024 → Apr 2027 expected | pelvic muscle wasting | Prince of Wales Hospital, Shatin, Hong Kong | Recruiting | No outcome recorded |
| Phase 4 | NCT06118905 Comparator | Feb 2024 → Feb 2029 expected | osteoporosis | Susan L. Greenspan | Recruiting | No outcome recorded |
| Phase 4 | NCT06135298 Background | Dec 2023 → Jul 2025 | osteoporosis | Aksaray University | Completed | No outcome recorded |
| Phase 4 | NCT05666310 Comparator | Feb 2023 → Jan 2026 overdue | muscular atrophy, osteoporosis | Nami Safai Haeri | Active not recruiting | No outcome recorded |
| Phase 4 | NCT05361408 Comparator | Feb 2022 → Feb 2024 | osteoporosis | Yonsei University | Completed | No outcome recorded |
| Phase 4 | NCT05058976 Background | Sep 2021 → Mar 2027 expected | postmenopausal osteoporosis | Susan L. Greenspan | Active not recruiting | No outcome recorded |
| Phase 4 | NCT05598606 Comparator | Jan 2021 → Jan 2023 | drug pseudoallergy | Shenzhen People's Hospital | Completed | No outcome recorded |
| Phase 4 | NCT04597931 Comparator | Nov 2020 → Nov 2023 | osteoporosis, spinal cord injury | Sheba Medical Center | Unknown | No outcome recorded |
| Phase 4 | NCT04087096 Background | Aug 2020 → Aug 2024 | disease of bone structure | Massachusetts General Hospital | Completed | No outcome recorded |
| Phase 4 | NCT04177940 Comparator | Aug 2020 → Jul 2024 | osteoporosis | University of Alabama at Birmingham | Completed | No outcome recorded |
| Phase 4 | NCT03924414 Comparator | Nov 2019 → Feb 2026 | Lewy body dementia, Parkinson disease, extrapyramidal and movement disease, multiple system atrophy +3 | California Pacific Medical Center Research Institute | Completed | No outcome recorded |
| Phase 4 | NCT02480634 Background | Jun 2019 → Sep 2021 | metastatic carcinoma in the bone, non-small cell lung carcinoma | Daping Hospital and the Research Institute of Surgery of the Third Military Medical University | Unknown | No outcome recorded |
| Phase 4 | NCT04085419 Comparator | May 2019 → May 2023 | osteoporosis, primary hyperparathyroidism | University Medical Centre Ljubljana | Unknown | No outcome recorded |
| Phase 4 | NCT03576599 Comparator | Jun 2017 → Jun 2019 | bone disorder | Oslo University Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT03087851 Comparator | Mar 2017 → Aug 2020 | osteoporosis | Aarhus University Hospital | Completed | No outcome recorded |
| Phase 4 | NCT03735537 Comparator | Nov 2016 → Feb 2025 | osteogenesis imperfecta | University of Edinburgh | Completed | No outcome recorded |
| Phase 4 | NCT02286830 Comparator | Jan 2015 → Feb 2023 | plasma cell myeloma | Thomas Lund | Completed | No outcome recorded |
| Phase 4 | NCT02176382 Comparator | Aug 2014 → Feb 2020 | postmenopausal osteoporosis | Massachusetts General Hospital | Completed | No outcome recorded |
| Phase 4 | NCT01732770 Comparator | Nov 2012 → Jan 2015 | postmenopausal osteoporosis | Amgen | Completed | No outcome recorded |
| Phase 4 | NCT01907880 Comparator | Aug 2012 → Jan 2016 | breast cancer | Ottawa Hospital Research Institute | Completed | No outcome recorded |
| Phase 4 | NCT00927186 Comparator | Jul 2009 → Oct 2010 | postmenopausal osteoporosis | Eli Lilly and Company | Completed | No outcome recorded |
| Phase 4 | NCT00765687 Comparator | Aug 2008 → May 2012 | metastatic carcinoma in the bone, non-small cell lung carcinoma | Sun Yat-sen University | Completed | No outcome recorded |
| Phase 4 | NCT01153425 Comparator | Jul 2008 → Dec 2012 | osteoporosis | University of Pennsylvania | Completed | No outcome recorded |
| Phase 4 | NCT00431444 Comparator | Jan 2007 → Jul 2008 | osteoporosis | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00733538 Comparator | Dec 2004 → Nov 2009 | plasma cell myeloma | Centre Hospitalier Universitaire de Nice | Completed | No outcome recorded |
| Phase not applicable3 trials | ||||||
| — | NCT05906056 Background | May 2023 → Apr 2026 overdue | spinal cord injury, stroke disorder, traumatic brain injury | University of Ioannina | Recruiting | No outcome recorded |
| — | NCT00580047 Comparator | Dec 2003 → Jul 2014 | impaired renal function disease | University of Nebraska | Completed | No outcome recorded |
| — | NCT00520052 Comparator | Aug 2003 → Aug 2005 | osteoporosis | Wirral University Teaching Hospital NHS Trust | Completed | No outcome recorded |
Press releases naming this drug 1 release
| Date | Issuer | Release |
|---|---|---|
| 2015-10-11 | Amgen | New Data Show Greater Bone Mineral Density Gains With Prolia® (Denosumab) Compared With Zoledronic Acid amgen.com ↗ |
Evidence & citations 21 cited values
Every value below carries the sentence it was read from. 337 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | zoledronic acid | “The purpose of this study is to assess the effect of zoledronic acid on bone mineral density in prostatic cancer patients currently receiving androgen deprivation therapy.” NCT00489905 ↗312“The use of zoledronic acid (Zometa) has an established place in the management of malignancies with a predilection for skeletal involvement (in particular metastasis).” NCT01367288 ↗ “Zometa (zoledronic acid) will be administered by infusion on Day 1 of a 3-week cycle followed by tumor assessment from CT and/or PET scans every 2 cycles.” NCT01204203 ↗ “Zoledronic acid, Aclasta® 5 mg will be administered intravenously according to standard management criteria in order to obtain an homogeneous population.” NCT05328154 ↗ “Zoledronic acid (zoledronate) for postmenopausal women with early breast cancer receiving adjuvant letrozole (ZO-FAST study): final 60-month results.” PMID 23047045 ↗ Oct 2012 “Commercially available intravenous (IV) bisphosphonates administered per package insert, included pamidronate, ibandronic acid, and zoledronic acid” NCT00091832 ↗ “Patients with no bone metastasis (n=150) will receive Standard therapy plus Zoledronic acid administration 4 mg IV monthly during Months 1-18.” NCT01129336 ↗ “IV Bisphosphonate (eg pamidronate or zoledronic acid) every 4 weeks for 6 doses as described by package insert during the treatment phase.” NCT00104650 ↗ “Zoledronic Acid (Zometa), a new generation, highly potent bisphosphonate used to treat osteoporosis and hypercalcemia of malignancy” NCT00206388 ↗ “5mg intravenous Zoledronic Acid (100mL solution) once yearly and subcutaneous placebo (1mL normal saline) every 6 months” NCT06643780 ↗ “2.5 mg/day oral letrozole for approximately 6.5 months neoadjuvant treatment plus zoledronic acid 4 mg i.v. q4w” NCT00375752 ↗ “1 Arm (HIV+): will receive Zoledronic acid 4mg and colaren ® (vitamin D, magnesium, phosphate, calcium).” NCT03930992 ↗ “Zometa® (zoledronic acid) in 100ml of calcium free solution i.v. as a 15 minute infusion every 3 months” NCT00294437 ↗ “zoledronic acid 5 mg (Aclasta®) administered as single intravenous infusion (100 ml): Verum” NCT05677152 ↗ “One intravenous infusion of zoledronic acid 4 mg every 4 weeks, according to labelled use.” NCT03408652 ↗ “Zoledronic acid by IB or pamidronate by IV can be used as per standard of care.” NCT01215344 ↗ “intravenous (I.V.) zoledronic acid (ZA) 4 mg given once at study initiation” PMID 21147688 ↗ Dec 2010 “Intravenous zoledronic acid 5 mg plus subcutaneous placebo every 12 months” NCT05598606 ↗ “Using aclasta: intravenous infusion of 5 mg of zoledronic acid once a year” NCT04149405 ↗ “Treatment with zoledronic acid will be initiated during hospitalization” NCT01564121 ↗ “alternating use of Prolia (Denosumab) and Aclasta (Zoledronic acid)” NCT05091086 ↗ “ZOMETA 4 mg (zoledronic acid for injection in 100mg solution )” NCT00035997 ↗ “Tumor Associated Macrophage Targeted Therapy (Zoledronic Acid)” NCT05053750 ↗ “Aclasta® (Zoledronic acid 5mg/100ml) is given intravenously” NCT02838121 ↗ “Zoledronic Acid will be administrated by infusion (IV).” NCT02517918 ↗ “Intravenous injection of zoledronic acid” NCT05493267 ↗ “DMAB to "Early" Zoledronic Acid (ZA)” NCT04177940 ↗ “Reclast (ZOL446, zoledronic acid)” NCT00668200 ↗ “Zoledronic acid” NCT01204203 ↗ “Zoledronic acid” NCT07043608 ↗ |
| Known as | 4 Herbs Formula | ClinicalTrials.gov intervention name — accepted as the source's own label NCT06023420 ↗ |
| Known as | acid zoledronique | “The investigators offer a study phase 2 of the effectiveness of N-BP (acid zoledronique) on the prevention of the local recurrence” NCT01564121 ↗ |
| Known as | Acide zoledronic | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01219790 ↗ |
| Known as | Acide Zoledronique | ClinicalTrials.gov intervention name — accepted as the source's own label NCT02739555 ↗ |
| Known as | Aclasta | “Zoledronic acid, Aclasta® 5 mg will be administered intravenously according to standard management criteria in order to obtain an homogeneous population.” NCT05328154 ↗10“Group 1: Experimental group 30 cases, Aclasta® (Zoledronic acid 5mg/100ml) is given intravenously on the 4th postoperative day” NCT02838121 ↗ “Patients will be randomised 1:1 to receive either one infusion aclasta (5 mg zolendronic acid, n=40) or placebo (n=40).” NCT04115397 ↗ “Novartis Pharmaceuticals Australia provided ampoules of zoledronic acid (Aclasta®) and matching placebo without cost.” PMID 34104395 ↗ May 2021 “Zoledronic acid (Aclasta) is a drug known for its protective effect in some bone diseases (tumors, paget).” NCT00100620 ↗ “zoledronic acid 5 mg (Aclasta®) administered as single intravenous infusion (100 ml): Verum” NCT05677152 ↗ “Plus a single dose of zoledronic acid (Aclasta) once the diagnosis of HO is made.” NCT05906056 ↗ “alternating use of Prolia (Denosumab) and Aclasta (Zoledronic acid)” NCT05091086 ↗ “Zoledronic acide (Aclasta)” NCT07056478 ↗ “zoledronic acid (aclasta)” NCT00939900 ↗ |
| Known as | AK156 | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01522521 ↗ |
| Known as | CGP42446 | “Zoledronic acid (Zometa®, CGP42446) is a member of a class of compounds known as bisphosphonates.” NCT00264420 ↗1“Zoledronic acid (Zometa®, CGP42446) is the most potent clinically available bisphosphonates” NCT00216151 ↗ |
| Known as | Reclast | ClinicalTrials.gov intervention name — accepted as the source's own label NCT00668200 ↗ |
| Known as | ZLD | “Bisphosphonates such as zoledronic acid (ZLD) reduce skeletal events in MM” PMID 22902362 ↗ Aug 2012 |
| Known as | ZOL | “We randomized 63 nonosteoporotic, ART-naive adults with HIV initiating ART with atazanavir/ritonavir + tenofovir/emtricitabine to a single zoledronic acid (ZOL) infusion (5 mg)...” PMID 27193748 ↗ May 20168“This study is a randomized, double-blinded, placebo-controlled trial investigating the effects of zoledronic acid (ZOL) versus placebo in patients with primary...” NCT06859580 ↗ “A post hoc analysis of the HORIZON Recurrent Fracture Trial was done to determine the effect of zoledronic acid (ZOL) on total hip (TH) and femoral neck (FN) BMD in subgroups...” PMID 24839241 ↗ Dec 2014 “The AZURE trial is an ongoing phase III, academic, multi-centre, randomised trial designed to evaluate the role of zoledronic acid (ZOL) in the adjuvant therapy of women with...” PMID 21394500 ↗ Mar 2011 “A single infusion of zoledronic acid (ZOL) after acute spinal cord injury (SCI) attenuates bone loss at the hip (proximal femur) and knee (distal femur and proximal tibia) for...” PMID 34278611 ↗ Jul 2021 “To develop a pharmacometric model to predict jawbone zoledronic acid (Zol) concentrations in oncologic patients” NCT02069340 ↗ “three bisphosphonate (BP) treatments: risedronate (RIS), alendronate (ALN), and zoledronic acid (ZOL)” PMID 36602607 ↗ Jan 2023 “neoadjuvant chemotherapy +/- zoledronic acid (ZOL) in invasive breast cancer” PMID 23515409 ↗ Mar 2013 “treated with 5 milligrams of zoledronic acid (ZOL) once yearly” PMID 21037195 ↗ Nov 2010 |
| Known as | ZOL446 | “Reclast (ZOL446, zoledronic acid)” NCT00668200 ↗ |
| Known as | Zoledronate | “The purpose of the HOBOE study, Version 1, was to compare the adjuvant hormonal therapy treatments of Tamoxifen, Letrozole and Letrozole + Zoledronate for their effects on bone...” NCT00412022 ↗6“Zoledronate is a third generation aminobiphosphonate (BP), probably the most powerful among the available compounds which received market clearance authorisation in MM with bone damage.” NCT00733538 ↗ “Zoledronic acid (zoledronate) for postmenopausal women with early breast cancer receiving adjuvant letrozole (ZO-FAST study): final 60-month results.” PMID 23047045 ↗ Oct 2012 “The aim of this study was to compare zoledronic acid (zoledronate) and alendronate for prevention of transplantation bone loss.” PMID 23024190 ↗ Sep 2012 “Zoledronate, which is licensed for use, is administered intravenously once a year which should be easier to administer.” NCT01702415 ↗ “patients receive zoledronate IV over at least 15 minutes once every 3 months during months 1-24” NCT00022087 ↗ “Group 1: Zoledronate plus calcium and vit D supplementation” NCT00114556 ↗ |
| Known as | zoledronic | ClinicalTrials.gov intervention name — accepted as the source's own label NCT03127319 ↗ |
| Known as | Zoledronic acid (Zometa, Reclast, Zomera) | “Zoledronic acid (Zometa, Reclast, Zomera)” NCT01332617 ↗ |
| Known as | Zoledronic Acid Injection | “Drug: Zoledronic Acid Injection” NCT04325776 ↗1“Drug: Zoledronic Acid Injection” NCT04719650 ↗ |
| Known as | Zolendronic acid | “Patients will be randomised 1:1 to receive either one infusion aclasta (5 mg zolendronic acid, n=40) or placebo (n=40).” NCT04115397 ↗ |
| Known as | Zometa | “Patients will be randomized to receive either 4 herbs formula plus Zometa or Zometa alone after all the eligibility criteria have been fulfilled and informed consent has been signed.” NCT06023420 ↗24“The use of zoledronic acid (Zometa) has an established place in the management of malignancies with a predilection for skeletal involvement (in particular metastasis).” NCT01367288 ↗ “Zometa (zoledronic acid) will be administered by infusion on Day 1 of a 3-week cycle followed by tumor assessment from CT and/or PET scans every 2 cycles.” NCT01204203 ↗ “Efficacy and Tolerability of Intravenous Zometa® (Zoledronic Acid) 4 mg in Primary Breast Cancer Patients With Disseminated Tumor Cells in Bone Marrow.” NCT00172068 ↗ “the study drugs thalidomide and Zometa (zoledronic acid) were provided by Celgene Pharmaceuticals and Novartis Oncology, respectively” PMID 22902362 ↗ Aug 2012 “Patients will be treated every 3 weeks with 4 mg zoledronic acid (Zometa), administered by a 15 min. intravenous infusion.” NCT00287261 ↗ “six cycles of docetaxel (Taxotere®), Adriamycin® (endoxan) and Cyclofosfamide (TAC) and zoledronic acid (Zometa)” NCT01099436 ↗ “Intravenous Paricalcitol (ZEMPLAR™) [19-NOR-1 ALPHA, 25 - (OH)D] With Zoledronic Acid (Zometa™)” NCT00258258 ↗ “Zometa is administered at a dose of 4 mg by continuous infusion every two weeks for 2 months.” NCT00083382 ↗ “Zoledronic acid (Zometa®, CGP42446) is the most potent clinically available bisphosphonates” NCT00216151 ↗ “Zoledronic acid (Zometa) belongs to a class of drugs called bisphosphonates.” NCT00264420 ↗ “Co-administration with Zometa: Calcium 500 mg + vitamin D 400-500 IU daily” NCT00765687 ↗ “4 mg of zoledronic acid (Zometa) will be added to each bag of bone cement” NCT03295981 ↗ “Zoledronic Acid (Zometa®) Plus Strontium-89” NCT00554918 ↗ “Zometa (zoledronic acid)” NCT00697619 ↗ “Zoledronic acid (Zometa)” NCT00126386 ↗ “zoledronic acid (Zometa)” NCT00966992 ↗ |
| Action | Inhibit | “The mechanism of action of nitrogen-containing bisphosphonates such as pamidronate and zoledronic acid appears to involve inhibition of the mevalonate pathway” NCT00295867 ↗ |
| Modality | Other / unclassified | “Bisphosphonates reduce bone metastases in postmenopausal women with early-stage breast cancer” PMID 32929540 ↗ Sep 2020 |
| Route | Intravenous | “zoledronate IV monthly” NCT00004928 ↗ |