Crohn's DiseasePhase 3NCT01444092
Safety Study of Entocort for Children With Crohn's Disease
A Phase 3 study testing Entocort in people with Crohn's Disease, run by Padagis LLC at 24 sites in 5 countries.
Trial summary
A Safety Study using Entocort EC for children with mild to moderate Crohn's Disease Read more about this study
- Who is it for?
- Ages 5 to 17 years
- Conditions the study is for
- Crohn's Disease
- What is being tested?
- Entocort
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 123 participants
- Where
- 24 sitesin 5 countries
- Study dates
- Nov 2011to Sep 2014
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 5 to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- All male and female subjects must be aged 5 to 17, inclusive, and must not have reached their 18th birthday by the estimated final office visit.
- Subject must be diagnosed with active Crohn's disease of the ileum and/or ascending colon confirmed by endoscopic and/or radiographic evidence, and/or evidence of mucosal erosions and/or histology.
- Subjects with mild to moderate Crohn's disease.
- All subjects must have a stool analysis negative for Clostridium difficile toxin, Yersinia enterolytica, Campylobacter jejuni, Salmonella, Shigella, within the 30 days prior to visit 1.
- All subjects must have had laboratory assessments within 7 days prior to visit 1.
- All subjects must weigh >= 15 kg at time of enrollment
Who cannot join
- Subjects who have had any previous intestinal resection proximal to and including the ascending colon
- Subjects with evidence of severe active Crohn's disease and/or, stricturing and prestenotic dilatation, clinical evidence of obstruction, perirectal abscess, perirectal disease with active draining fistulas, perforation, or any septic complications
- Subjects who do not have a negative stool analysis, within the 30 days prior to visit 1
- Subjects who have been screened/or enrolled in this study previously within the last 30 days
- Subjects with morning cortisol level <150 nmol/l (5.4 ug/dl) or DHEA-S below normal range for age and gender
Trial locations and contacts
24 sites in 5 countries.
24 sites in 5 countries
United States11 sites
Research Site
Atlanta, Georgia
Research Site
Aurora, Colorado
Research Site
Boston, Massachusetts
Research Site
Buffalo, New York
Research Site
Chicago, Illinois
Research Site
Greenville, North Carolina
Research Site
Mays Landing, New Jersey
Research Site
Morristown, New Jersey
Research Site
Nashville, Tennessee
Research Site
Oak Lawn, Illinois
Research Site
Saint Paul, Minnesota
Poland5 sites
Research Site
Krakow
Research Site
Lodz
Research Site
Rzeszów
Research Site
Warsaw
Research Site
Wroclaw
Italy4 sites
Research Site
Florence
Research Site
Messina
Research Site
Naples
Research Site
Roma
Canada3 sites
Research Site
Halifax, Nova Scotia
Research Site
London, Ontario
Research Site
Toronto, Ontario
About this study
Official title: A Multicenter, Open Label, Non-comparative Study to Evaluate the Safety of Entocort EC for the Treatment of Crohn's Disease in Paediatric Subjects Aged 5 to 17 Years, Inclusive
A Safety Study using Entocort EC for children with mild to moderate Crohn's Disease
Read the detailed description
A Multicenter, Open label, Non-comparative Study to Evaluate the Safety of Entocort EC for the Treatment of Crohn's Disease in Paediatric Subjects Aged 5 to 17 Years, Inclusive
- Conditions
- Crohn's Disease
- Being tested
- Entocort
- Medical subject headings
- Crohn Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
EntocortDrug
Entocort capsules, oral
| Study group | Role | What they receive |
|---|---|---|
| Entocort | Experimental | Study Medication Receives: Drug: Entocort |
What is being measured
The primary outcome is the main question the study is designed to answer.
Adverse Event
Number of patients with at least one adverse event
Measured: 12 weeks
Secondary outcomes (2)
PCDAI
Paediatric Crohn's Disease Activity Index. Range from 0 (best) to 100 (worst).
Measured: Baseline to 8 weeks
IMPACT 3
IMPACT 3 is a self-administered QoL form. The score ranges from 35 (poor) to 175 (best).
Measured: Baseline to 8 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Sep 2011 (estimated)
- Study startNov 2011
- Primary completionSep 2014
- Study completionSep 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Crohn's 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
- 123 participants (actual)
Sponsor and investigators
- Lead sponsor
- Padagis LLC
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Stanley Cohen, MD, Principal investigator, Children's Center for Digestive Healthcare, LLC, Atlanta, Georgia, USA and Emory University School of Medicine, Atlanta, Georgia, USAStefan Eklund, MD, Study director, AstraZeneca Pharmaceuticals, Mölndal, Sweden
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01444092
- Sponsor's protocol ID
- D9422C00001
- Status last verified
- Jan 2022
- First submitted
- 28 Sep 2011
- Last updated
- 6 Jan 2022
- Results posted
- Yes, on ClinicalTrials.gov
Publications
Cohen SA, Aloi M, Arumugam R, Baker R, Bax K, Kierkus J, Koletzko S, Lionetti P, Persson T, Eklund S. Enteric-coated budesonide for the induction and maintenance of remission of Crohn's disease in children. Curr Med Res Opin. 2017 Jul;33(7):1261-1268. doi: 10.1080/03007995.2017.1313213. Epub 2017 Apr 19.
PubMed 28420280
Study at a glance
From the registry record, last updated by the sponsor on 6 Jan 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multicenter, Open Label, Non-comparative Study to Evaluate the Safety of Entocort EC for the Treatment of Crohn's Disease in Paediatric Subjects Aged 5 to 17 Years, Inclusive
- ClinicalTrials.gov ID
- NCT01444092
- Acronym / sponsor ID
- D9422C00001
- Conditions
- Crohn's Disease
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 123 participants (actual)
- Lead sponsor
- Padagis LLCIndustry (pharma, biotech, devices)
- Study start
- Nov 2011
- Primary completion
- Sep 2014 (actual)
- Study completion
- Sep 2014 (actual)
- First posted
- 30 Sep 2011 (estimated)
- Results
- Posted 11 Aug 2016
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A Safety Study using Entocort EC for children with mild to moderate Crohn's Disease
Detailed description
A Multicenter, Open label, Non-comparative Study to Evaluate the Safety of Entocort EC for the Treatment of Crohn's Disease in Paediatric Subjects Aged 5 to 17 Years, Inclusive
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Entocort | Experimental | Drug: EntocortStudy Medication |
Who may qualify
- Ages
- 5 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (6 listed)
- All male and female subjects must be aged 5 to 17, inclusive, and must not have reached their 18th birthday by the estimated final office visit.
- Subject must be diagnosed with active Crohn's disease of the ileum and/or ascending colon confirmed by endoscopic and/or radiographic evidence, and/or evidence of mucosal erosions and/or histology.
- Subjects with mild to moderate Crohn's disease.
- All subjects must have a stool analysis negative for Clostridium difficile toxin, Yersinia enterolytica, Campylobacter jejuni, Salmonella, Shigella, within the 30 days prior to visit 1.
- All subjects must have had laboratory assessments within 7 days prior to visit 1.
Key exclusion criteria (5 listed)
- Subjects who have had any previous intestinal resection proximal to and including the ascending colon
- Subjects with evidence of severe active Crohn's disease and/or, stricturing and prestenotic dilatation, clinical evidence of obstruction, perirectal abscess, perirectal disease with active draining fistulas, perforation, or any septic complications
- Subjects who do not have a negative stool analysis, within the 30 days prior to visit 1
- Subjects who have been screened/or enrolled in this study previously within the last 30 days
- Subjects with morning cortisol level <150 nmol/l (5.4 ug/dl) or DHEA-S below normal range for age and gender
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 |
|---|---|---|
| EntocortEntocort capsules, oral | Drug | Entocort |
Primary outcome
Adverse Event
Time frame: 12 weeks
Number of patients with at least one adverse event
2 secondary outcomes
PCDAI
Time frame: Baseline to 8 weeks
IMPACT 3
Time frame: Baseline to 8 weeks
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jan 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 28420280Cohen SA, Aloi M, Arumugam R, Baker R, Bax K, Kierkus J, Koletzko S, Lionetti P, Persson T, Eklund S. Enteric-coated budesonide for the induction and maintenance of remission of Crohn's disease in children. Curr Med Res Opin. 2017 Jul;33(7):1261-1268. doi: 10.1080/03007995.2017.1313213. Epub 2017 Apr 19.
- CSR SynopsisLink provided by the sponsor.
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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.
Stanley Cohen, MD principal investigator
Children's Center for Digestive Healthcare, LLC, Atlanta, Georgia, USA and Emory University School of Medicine, Atlanta, Georgia, USA
Stefan Eklund, MD study director
AstraZeneca Pharmaceuticals, Mölndal, Sweden
24 sites in 5 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Entocort in people with Crohn's Disease, run by Padagis LLC at 24 sites in 5 countries.
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 6 inclusion and 5 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 6 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 24 sites in United States, Poland, Italy, Canada, Germany. 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?
Yes. Results are posted in the registry (first posted 11 Aug 2016). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Adverse Event (time frame: 12 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01444092, which also lists 1 linked publication.
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 6 Jan 2022.