Dry Eye With Sjögren's SyndromePhase 3NCT02503176
An Extension Study of KCT-0809 in Dry Eye Patients With Sjögren's Syndrome
A Phase 3 study testing KCT-0809 ophthalmic solution in people with Dry Eye With Sjögren's Syndrome, run by Kissei Pharmaceutical Co., Ltd. at 1 site in Japan.
Trial summary
The purpose of this study is to evaluate of the long-term safety and efficacy of KCT-0809 in dry eye patients with Sjögren's syndrome. Read more about this study
- Who is it for?
- Ages 20 years and older
- Conditions the study is for
- Dry Eye With Sjögren's Syndrome
- What is being tested?
- KCT-0809 ophthalmic solution
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- Not given
- Where
- 1 siteJapan
- Study dates
- Start not givento 29 May 2017
- 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
- Adult, Older adult
Who may be able to join
- Dry eye patients with Sjögren's syndrome finished KCT1301 study
Who cannot join
- Patients with poor adherence to medication of study drug in KCT1301 study
Trial locations and contacts
1 site in 1 country.
About this study
The purpose of this study is to evaluate of the long-term safety and efficacy of KCT-0809 in dry eye patients with Sjögren's syndrome.
- Conditions
- Dry Eye With Sjögren's Syndrome
- Being tested
- KCT-0809 ophthalmic solution
- Keywords
- Dry eye syndromes, Corneal diseases, Conjunctival diseases
- Medical subject headings
- Dry Eye Syndromes, Corneal Diseases, Conjunctival Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
KCT-0809 ophthalmic solutionDrug
| Study group | Role | What they receive |
|---|---|---|
| KCT-0809 | Experimental | Not described Receives: Drug: KCT-0809 ophthalmic solution |
What is being measured
The primary outcome is the main question the study is designed to answer.
Incidences of adverse events
Measured: 52 weeks
Secondary outcomes (1)
Score of the corneal staining
Measured: 52 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2015 (estimated)
- Primary completion29 May 2017
Why it stopped: Discontinuation of the development
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dry Eye With Sjögren's SyndromeStudies 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
Sponsor and investigators
- Lead sponsor
- Kissei Pharmaceutical Co., Ltd.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02503176
- Sponsor's protocol ID
- KCT1302
- Status last verified
- Mar 2018
- First submitted
- 17 Jul 2015
- Last updated
- 5 Mar 2018
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Mar 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Extension Study of KCT-0809 in Dry Eye Patients With Sjögren's Syndrome
- ClinicalTrials.gov ID
- NCT02503176
- Acronym / sponsor ID
- KCT1302
- Conditions
- Dry Eye With Sjögren's Syndrome
- Keywords
- Dry eye syndromes, Corneal diseases, Conjunctival diseases
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Discontinuation of the development
- Lead sponsor
- Kissei Pharmaceutical Co., Ltd.Industry (pharma, biotech, devices)
- Primary completion
- 29 May 2017 (actual)
- First posted
- 20 Jul 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 evaluate of the long-term safety and efficacy of KCT-0809 in dry eye patients with Sjögren's syndrome.
Study design
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| KCT-0809 | Experimental | Drug: KCT-0809 ophthalmic solution |
Who may qualify
- Ages
- 20 years and older
- Sex
- All
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Dry eye patients with Sjögren's syndrome finished KCT1301 study
Key exclusion criteria (1 listed)
- Patients with poor adherence to medication of study drug in KCT1301 study
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 |
|---|---|---|
| KCT-0809 ophthalmic solution | Drug | KCT-0809 |
Primary outcome
Incidences of adverse events
Time frame: 52 weeks
1 secondary outcome
Score of the corneal staining
Time frame: 52 weeks
Results and safety
The study was stopped early (reason given: Discontinuation of the development). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Mar 2018.
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing KCT-0809 ophthalmic solution in people with Dry Eye With Sjögren's Syndrome, run by Kissei Pharmaceutical Co., Ltd. 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 1 inclusion and 1 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: stopped early, as of the sponsor's last update on 5 Mar 2018. 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 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 was stopped early (reason given: Discontinuation of the development). Results are not available in the source record.
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?
Incidences of adverse events (time frame: 52 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 5 Mar 2018.