Your session is about to expire
← Back to Search
Bisphosphonate
Zoledronic Acid for Parkinson's Disease (TOPAZ Trial)
Phase 4
Recruiting
Led By Steve Cummings, MD
Research Sponsored by California Pacific Medical Center Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Men and women age 60 years or older
Current Parkinson's Disease diagnosis or neurodegenerative parkinsonism diagnosis based on an expert assessment (neurologist diagnosis via medical records confirmation or Telemedicine Screening Assessment)
Must not have
Non-ambulatory, i.e., unable to walk without assistance of another person
Tooth extraction or invasive dental procedures within the past 30 days or planned/scheduled extraction/procedure in the next 12 months
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 years
Awards & highlights
Drug Has Already Been Approved
Pivotal Trial
Summary
This trial is testing whether a single infusion of zoledronic acid can help prevent fractures in people with Parkinson's disease or parkinsonism. A total of 3500 participants will be enrolled in the United States.
Who is the study for?
This trial is for men and women aged 60 or older with Parkinson's disease or parkinsonism, who can follow the study for at least 2 years. They must be able to consent and have a neurologist-confirmed diagnosis. People using bisphosphonates in the last year, those with recent or planned dental procedures, on osteoporosis treatments within 6 months, undergoing dialysis, non-ambulatory individuals, or with certain other diseases are excluded.
What is being tested?
The study tests if a single infusion of Zoledronic Acid (ZA) can prevent fractures compared to a placebo in patients with Parkinson's-related conditions. It's randomized and blinded—meaning neither participants nor researchers know who gets ZA or placebo—and involves over three thousand participants across the U.S.
What are the potential side effects?
Zoledronic Acid may cause flu-like symptoms such as fever and chills, pain at the injection site, nausea, anemia (low red blood cell count), headache, dizziness; rarely it might lead to jaw bone problems (osteonecrosis) or unusual thigh bone fractures.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 60 years old or older.
Select...
I have been diagnosed with Parkinson's Disease or parkinsonism by a neurologist.
Select...
I have been diagnosed with Parkinson's Disease or a similar condition by a specialist.
Select...
I have been diagnosed with Parkinson's Disease or a similar condition by a neurologist.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I need someone's help to walk.
Select...
I haven't had nor plan to have any tooth extractions or major dental work soon.
Select...
I am currently receiving kidney dialysis.
Select...
I have been diagnosed with multiple myeloma or Paget's disease.
Select...
I haven't taken any osteoporosis treatments in the last 6 months.
Select...
I have had a hip fracture in the past.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Number of Participants with Clinical Fractures
Secondary study objectives
Mortality
Number of Participants Hip Fractures
Awards & Highlights
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Zoledronic acid (ZA)Active Control1 Intervention
A single intravenous infusion of Zoledronic acid (5 mg) infused over 45 minutes
Group II: PlaceboPlacebo Group1 Intervention
A single intravenous infusion of placebo infused over 45 minutes
Find a Location
Who is running the clinical trial?
California Pacific Medical Center Research InstituteLead Sponsor
43 Previous Clinical Trials
7,981 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,785 Previous Clinical Trials
28,181,264 Total Patients Enrolled
University of California, San FranciscoOTHER
2,585 Previous Clinical Trials
15,080,689 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I need someone's help to walk.I am 60 years old or older.I have been diagnosed with Parkinson's Disease or parkinsonism by a neurologist.I haven't had nor plan to have any tooth extractions or major dental work soon.The study staff decides that you are not suitable for the study, for example, if you have an uncontrolled drug or alcohol addiction.I have been diagnosed with Parkinson's Disease or a similar condition by a specialist.I have been diagnosed with Parkinson's Disease or a similar condition by a neurologist.I have not taken bisphosphonate drugs in the last year.I am currently receiving kidney dialysis.I have been diagnosed with multiple myeloma or Paget's disease.I haven't taken any osteoporosis treatments in the last 6 months.I have had a hip fracture in the past.
Research Study Groups:
This trial has the following groups:- Group 1: Zoledronic acid (ZA)
- Group 2: Placebo
Awards:
This trial has 2 awards, including:- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Overactive Bladder Patient Testimony for trial: Trial Name: NCT03924414 — Phase 4
Share this study with friends
Copy Link
Messenger