HealthyPhase 1NCT02531204
A Study of ASP1585 to Evaluate the Bioequivalence Between ASP1585 Granules and ASP1585 Capsules
A Phase 1 study testing ASP1585 in people with Healthy and Urine Phosphorus Excretion, run by Astellas Pharma Inc at 1 site in Japan.
Trial summary
The purpose of this study is to assess the bioequivalence between ASP1585 granules and ASP1585 capsules after repeated oral administration of ASP1585 granules or ASP1585 capsules under open-label conditions in non-elderly healthy male subjects. In addition, the safety of these products is assessed. Read more about this study
- Who is it for?
- Ages 20 to 44 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Healthy, Urine Phosphorus Excretion
- 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
- 60 participants
- Where
- 1 siteJapan
- Study dates
- Aug 2014to Feb 2015
- Phase
- Phase 1
- 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 to 44 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Body weight (at screening) ≥ 50.0 kg and < 80.0 kg
- Body mass index (BMI) (at screening) ≥ 17.6 kg/m2 and < 26.4 kg/m2
- Healthy, as judged by the investigator/sub-investigator based on medical history and the results of physical examination (subjective symptoms and objective findings) and all tests obtained at screening and during the period from hospital admission to immediately before study medication in 1st period.
Who cannot join
- Received or scheduled to receive any investigational drugs in other clinical trials, post-marketing studies, or clinical studies within 120 days before the screening or during the period from the screening to 1st hospitalization.
- Donated or scheduled to donate 400 mL of whole blood within 90 days before the screening or during the period from the screening to 1st hospitalization, 200 mL of whole blood within 30 days before the screening or during the period from the screening to 1st hospitalization, or blood components within 14 days before the screening or during the period from the screening to 1st hospitalization.
- Any deviation of the laboratory tests at screening or 1st hospitalization.
- A deviation from the normal range of blood pressure, pulse rate, or body temperature at screening or 1st hospitalization
- Sitting blood pressure: Systolic blood pressure: ≥90 mmHg, ≤140 mmHg; Diastolic blood pressure: ≥40 mmHg, ≤90 mmHg
- Sitting pulse rate; ≥40 bpm, ≤99 bpm
Show all 17Show fewer
- Axillary body temperature; ≥35.0°C, ≤37.0°C
- History of drug allergies
- Upper gastrointestinal disease (e.g., nausea, vomiting, and stomachache) within 7 days before 1st hospitalization
- Concurrent or previous hepatic disease (e.g., viral hepatitis, drug-induced liver injury, and hepatic impairment)
- Concurrent or previous heart disease (e.g., congestive heart failure, angina pectoris, and arrhythmia requiring treatment)
- Concurrent or previous GI disease (e.g., ileus paralytic, gastric atony, intestinal atony, colitis ulcerative, peptic ulcer and gastroesophageal reflux esophagitis; except for a history of appendicitis).
- Concurrent or previous renal disease (e.g., acute renal failure, glomerulonephritis, and interstitial nephritis)
- Concurrent or previous renal disease (e.g., acute renal failure, glomerulonephritis, and interstitial nephritis)
- Concurrent or previous cerebrovascular disorder (e.g., cerebral infarction)
- Previous use of bixalomer
- Excessive smoking or drinking habit
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Pharmacodynamic Study of ASP1585 - Verification of Bioequivalence Between ASP1585 Granules and ASP1585 Capsules
The purpose of this study is to assess the bioequivalence between ASP1585 granules and ASP1585 capsules after repeated oral administration of ASP1585 granules or ASP1585 capsules under open-label conditions in non-elderly healthy male subjects. In addition, the safety of these products is assessed.
- Conditions
- Healthy, Urine Phosphorus Excretion
- Being tested
- ASP1585
- Keywords
- ASP1585, Bioequivalence, Pharmacodynamic, Phosphate binder, Bixalomer, urinary phosphorus excretion
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ASP1585Drug
Also called Bixalomer, Kiklin
oral
| Study group | Role | What they receive |
|---|---|---|
| ASP1585 granules preceding group | Experimental | Not described Receives: Drug: ASP1585 |
| ASP1585 capsules preceding group | Active comparator | Not described Receives: Drug: ASP1585 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Average daily amount of urine phosphorus change from baseline
Average daily amount of urine phosphorus on Day 5 to Day 8 was compared with that on Day -4 to Day 1 (baseline)
Measured: Day 5 to Day 8 after start of each dosing
Secondary outcomes (1)
Safety profile assessed by the incidence of adverse events, vital signs, clinical laboratory tests, and 12-lead ECG
ECG: Electrocardiogram
Measured: Up to Day 17 on Period 2
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Aug 2015 (estimated)
- Study startAug 2014
- Primary completionFeb 2015
- Study completionFeb 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HealthyStudies 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 1
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Astellas Pharma Inc
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Medical Director, Study director, Astellas Pharma Inc
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02531204
- Sponsor's protocol ID
- 1585-CL-0201
- Status last verified
- Aug 2015
- First submitted
- 12 Aug 2015
- Last updated
- 24 Aug 2015
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Aug 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pharmacodynamic Study of ASP1585 - Verification of Bioequivalence Between ASP1585 Granules and ASP1585 Capsules
- ClinicalTrials.gov ID
- NCT02531204
- Acronym / sponsor ID
- 1585-CL-0201
- Conditions
- Healthy, Urine Phosphorus Excretion
- Keywords
- ASP1585, Bioequivalence, Pharmacodynamic, Phosphate binder, Bixalomer, urinary phosphorus excretion
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Astellas Pharma IncIndustry (pharma, biotech, devices)
- Study start
- Aug 2014
- Primary completion
- Feb 2015 (actual)
- Study completion
- Feb 2015 (actual)
- First posted
- 24 Aug 2015 (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.
The purpose of this study is to assess the bioequivalence between ASP1585 granules and ASP1585 capsules after repeated oral administration of ASP1585 granules or ASP1585 capsules under open-label conditions in non-elderly healthy male subjects. In addition, the safety of these products is assessed.
Study design
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ASP1585 granules preceding group | Experimental | Drug: ASP1585 |
| ASP1585 capsules preceding group | Active comparator | Drug: ASP1585 |
Who may qualify
- Ages
- 20 to 44 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Body weight (at screening) ≥ 50.0 kg and < 80.0 kg
- Body mass index (BMI) (at screening) ≥ 17.6 kg/m2 and < 26.4 kg/m2
- Healthy, as judged by the investigator/sub-investigator based on medical history and the results of physical examination (subjective symptoms and objective findings) and all tests obtained at screening and during the period from hospital admission to immediately before study medication in 1st period.
Key exclusion criteria (17 listed)
- Received or scheduled to receive any investigational drugs in other clinical trials, post-marketing studies, or clinical studies within 120 days before the screening or during the period from the screening to 1st hospitalization.
- Donated or scheduled to donate 400 mL of whole blood within 90 days before the screening or during the period from the screening to 1st hospitalization, 200 mL of whole blood within 30 days before the screening or during the period from the screening to 1st hospitalization, or blood components within 14 days before the screening or during the period from the screening to 1st hospitalization.
- Any deviation of the laboratory tests at screening or 1st hospitalization.
- A deviation from the normal range of blood pressure, pulse rate, or body temperature at screening or 1st hospitalization
- History of drug allergies
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: Bixalomer, Kiklinoral | Drug | ASP1585 capsules preceding group, ASP1585 granules preceding group |
Primary outcome
Average daily amount of urine phosphorus change from baseline
Time frame: Day 5 to Day 8 after start of each dosing
Average daily amount of urine phosphorus on Day 5 to Day 8 was compared with that on Day -4 to Day 1 (baseline)
1 secondary outcome
Safety profile assessed by the incidence of adverse events, vital signs, clinical laboratory tests, and 12-lead ECG
Time frame: Up to Day 17 on Period 2
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 24 Aug 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.
Medical Director study director
Astellas Pharma Inc
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing ASP1585 in people with Healthy and Urine Phosphorus Excretion, run by Astellas Pharma Inc at 1 site 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 17 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 24 Aug 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site 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 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
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?
Average daily amount of urine phosphorus change from baseline (time frame: Day 5 to Day 8 after start of each dosing). 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 24 Aug 2015.