Chronic Kidney DiseasePhase 3NCT00892749
Long-term Study in Patients With Chronic Kidney Disease and Hyperphosphatemia on Hemodialysis
A Phase 3 study testing ASP1585 in people with Chronic Kidney Disease and Renal Dialysis, run by Astellas Pharma Inc at 4 sites in Japan.
Trial summary
This is a multi-center, open-labeled, non-comparative study to examine the safety and efficacy of ASP1585 for long-term dosing in chronic kidney disease and hyperphosphatemia patients on hemodialysis. Read more about this study
- Who is it for?
- Ages 20 years and older
- Conditions the study is for
- Chronic Kidney Disease, Renal Dialysis, Renal Insufficiency
- What is being tested?
- ASP1585
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 248 participants
- Where
- 4 sitesJapan
- Study dates
- May 2009to Sep 2010
- Phase
- Phase 3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Chronic kidney disease patients on hemodialysis
- Hyperphosphatemia
- Written informed consent
Who cannot join
- Patients with gastrointestinal surgery or enterectomy
- Severe cardiac disease patients
- Patients with severe constipation or diarrhea
- Patients with a complication of malignant tumors
- Patients with uncontrolled hypertension
- Patients treated with parathyroid intervention
Trial locations and contacts
4 sites in 1 country.
Japan4 sites
Study site
Chūbu
Study site
Chugoku
Study site
Kansai
Study site
Kantou
About this study
Official title: A Phase 3, Long-term Study in Patients With Chronic Kidney Disease (CKD) and Hyperphosphatemia on Hemodialysis
This is a multi-center, open-labeled, non-comparative study to examine the safety and efficacy of ASP1585 for long-term dosing in chronic kidney disease and hyperphosphatemia patients on hemodialysis.
- Being tested
- ASP1585
- Keywords
- hyperphosphatemia, hemodialysis, CKD, ASP1585
- Medical subject headings
- Renal Insufficiency, Chronic, Renal Insufficiency, Hyperphosphatemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ASP1585Drug
Also called ILY101, AMG223
oral
| Study group | Role | What they receive |
|---|---|---|
| 1. ASP1585 | Experimental | Not described Receives: Drug: ASP1585 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in serum Phosphorus level
Measured: After 48 weeks
Secondary outcomes (4)
Percent of the patients meeting the target range of serum Phosphorus levels
Measured: During the treatment
Changes in serum Calcium level
Measured: After 48 weeks
Changes in serum Ca x P
Measured: After 48 weeks
Changes in intact PTH level
Measured: After 48 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 May 2009 (estimated)
- Study startMay 2009
- Primary completionSep 2010
- Study completionSep 2010
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Kidney DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 248 participants (actual)
Sponsor and investigators
- Lead sponsor
- Astellas Pharma Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Use Central Contact, Study chair, Astellas Pharma Inc
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00892749
- Sponsor's protocol ID
- 1585-CL-0004
- Status last verified
- Apr 2015
- First submitted
- 30 Apr 2009
- Last updated
- 4 May 2015
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 May 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 3, Long-term Study in Patients With Chronic Kidney Disease (CKD) and Hyperphosphatemia on Hemodialysis
- ClinicalTrials.gov ID
- NCT00892749
- Acronym / sponsor ID
- 1585-CL-0004
- Keywords
- hyperphosphatemia, hemodialysis, CKD, ASP1585
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 248 participants (actual)
- Lead sponsor
- Astellas Pharma IncIndustry (pharma, biotech, devices)
- Study start
- May 2009
- Primary completion
- Sep 2010 (actual)
- Study completion
- Sep 2010 (actual)
- First posted
- 4 May 2009 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a multi-center, open-labeled, non-comparative study to examine the safety and efficacy of ASP1585 for long-term dosing in chronic kidney disease and hyperphosphatemia patients on hemodialysis.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 1. ASP1585 | Experimental | Drug: ASP1585 |
Who may qualify
- Ages
- 20 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Chronic kidney disease patients on hemodialysis
- Hyperphosphatemia
- Written informed consent
Key exclusion criteria (6 listed)
- Patients with gastrointestinal surgery or enterectomy
- Severe cardiac disease patients
- Patients with severe constipation or diarrhea
- Patients with a complication of malignant tumors
- Patients with uncontrolled hypertension
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ASP1585Also: ILY101, AMG223oral | Drug | 1. ASP1585 |
Primary outcome
Changes in serum Phosphorus level
Time frame: After 48 weeks
4 secondary outcomes
Percent of the patients meeting the target range of serum Phosphorus levels
Time frame: During the treatment
Changes in serum Calcium level
Time frame: After 48 weeks
Changes in serum Ca x P
Time frame: After 48 weeks
Changes in intact PTH level
Time frame: After 48 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 May 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Use Central Contact study chair
Astellas Pharma Inc
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing ASP1585 in people with Chronic Kidney Disease and Renal Dialysis, run by Astellas Pharma Inc at 4 sites in Japan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 May 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in Japan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in serum Phosphorus level (time frame: After 48 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 May 2015.