Graft Vs Host DiseasePhase 3NCT00128739
Treatment of Gastro-Intestinal and/or Hepatic Graft Versus Host Disease With Budesonide in Patients Following Peripheral Blood Stem Cell Transplantation
A Phase 3 study testing Budesonide in people with Graft Vs Host Disease, run by Rafa Laboratories at 1 site in Israel.
Trial summary
Twenty-four (2 x 12) patients with intestinal graft versus host disease (GVHD) Grades 2, 3 or 4 will be treated with budesonide 3mg three times daily or placebo for 12 weeks. All of the patients will receive cyclosporine and by mouth (po) prednisone or intravenous (IV) methylprednisone with a starting dose of… Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- Graft Vs Host Disease
- What is being tested?
- Budesonide
- How many people
- 24 participants
- Where
- 1 siteIsrael
- Study dates
- Jan 2001to Aug 2005
- 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 18 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients with clinical and biopsy proven Grades 2, 3 or 4 intestinal GVHD
- Patients with a negative stool culture
- Male or female patients aged between 18 - 70 years
- Signed written informed consent of the patient
Who cannot join
- Uncertain GVHD diagnosis (other causes of intestinal disease are possible)
- Severe other disease which may influence the patient prognosis
- Contraindication to the use of steroids
- Patient's inability to swallow the study medications
- Concurrent use of non-steroidal anti-inflammatory drug (NSAID)
- Known spontaneous or iatrogenic disturbances of thrombocyte aggregation or blood clotting.
Show all 14Show fewer
- Kidney dysfunction with creatinine level higher than 2mg/dl
- Patients on preventative antimicrobial therapy with the exception of Resprim® (sulfamethoxazole and trimethoprim)
- Patients taking somatostatin
- Patients taking anti-GVHD medication with the exception of steroids (maximum dose of prednisone or methylprednisolone 2mg/kg/day) and cyclosporine A or tacrolimus
- Pregnancy or lactation
- Insufficient contraception protection
- Participation in another clinical study within the last 30 days.
- Mental condition rendering the patient unable to understand the nature or scope and possible consequences of the study and/or evidence of an uncooperative attitude.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Phase 3 Study to Evaluate the Place of Budesonide in the Treatment of GVHD
Twenty-four (2 x 12) patients with intestinal graft versus host disease (GVHD) Grades 2, 3 or 4 will be treated with budesonide 3mg three times daily or placebo for 12 weeks. All of the patients will receive cyclosporine and by mouth (po) prednisone or intravenous (IV) methylprednisone with a starting dose of 2mg/kg/day (standard anti-GVHD treatment). Doses of steroids will be decreased by approximately 10% or 10mg per week (depending upon patient's weight) upon response to therapy, defined as a decrease of volume of diarrhea by 50% per day, decrease in abdominal pain and no presence of bloody stool. Patients with Grades 3 or 4 will be withdrawn from the study if there is no response after one week of therapy. Patients with Grade 2 may continue with no decrease in prednisone dose until response is achieved.
Read the detailed description
Graft versus host disease (GVHD) is one of the most common complications of bone marrow transplantation (BMT). Targets of GVHD are the gastro-intestinal tract (GIT) liver and skin, causing severe diarrhea and mucosal aberration and hepatitis that can cause life threatening liver failure. As a result of the mucosal aberration and the general immuno-suppression, caused both by the GVHD process itself and by the anti GVHD therapy, these patients are highly susceptible for severe, life threatening infections that usually originate from the GIT. Systemic steroids are the backbone of anti GVHD therapy. However, in GVHD systemic steroids have to be administered for a prolonged duration and in high doses, thus causing prolonged immune suppression, and exposing the patients to steroid side effects such as hypertension, diabetes, cataract formation etc.
Budesonide is a steroid that combines topical anti-inflammatory activity with high first-pass hepatic extraction. It was shown to be effective in treatment of inflammatory bowel disease with results slightly less then systemic steroids and fewer steroid-related adverse reactions. Except for its influence on the gut, budesonide was also shown to benefit inflammatory hepatic conditions such as primary biliary cirrhosis, liver transplantation and autoimmune hepatitis. Recently, it has been shown that budesonide is an effective treatment in acute GIT GVHD. The investigators propose to evaluate the effect of budesonide in GIT and hepatic GVHD with the following study.
Patients:
Twelve patients after allogenic peripheral blood stem cell transplantation (PBSCT) with grade >= 2 GIT and/or hepatic GVHD will be prospectively compared to 12 placebo controls.
Inclusion Criteria:
- Clinical and biopsy proven grade >/= 2 GIT AND/OR hepatic GVHD.
Exclusion Criteria:
- Preventive antimicrobial treatment (with the exception of Resprim) or somatostatin in the GIT GVHD patients.
- Anti-GVHD treatment other then steroids (maximal dose ≤ 2 mg/kg methylprednisolone) and cyclosporine A or tacrolimus.
Study Protocol:
All patients will be assessed for GVHD scoring (organ and general) according to standard criteria and tested before inclusion for the following parameters -
- Colon and/or liver biopsy GVHD staging (including number of crypt abscesses).
- Liver function tests - blood albumin, AST, ALT, GGTP, Alk Phos, LDH, bilirubin, coagulation function, cholesterol.
- Stool - volume and frequency.
- Radiological - CT scan for mucosal edema, wall thickening and ascites.
- Kidney function tests - blood creatinine, creatinine clearance.
- Blood pressure.
- Fasting blood glucose. If normal - oral glucose tolerance test, glycosylated hemoglobin.
- Ophthalmologist evaluation for cataract formation and IOP.
- GIT absorption assessment - xylose absorption.
- Microbiological - stool culture and stool for CDT, CMV PCR, culture for CMV in blood and urine.
- Bone density - by ultrasound.
After inclusion the patients will be treated with budesonide 9 or 15mg per day in divided doses or placebo. Other anti-GVHD treatment or ursodeoxycholic acid will not be withheld but tapering off will be tried.
Study parameters:
- LFT, albumin, PT, cholesterol, renal function, stool volume and frequency, CMV culture and PCR, clinical GVHD staging - every 2 weeks.
- Xylose test - every month.
- Ophthalmologist evaluation, diabetes control and CT scan - every 3 months.
- GIT and/or liver biopsy for GVHD staging (including number of crypt abscesses) and CMV PCR, bone density - every 6 months
- Blood, urine and stool culture during every febrile episode.
Study duration: 14 weeks.
End points:
- Hospitalizations: due to GVHD and/or due to infections.
- Overall and GIT or hepatic GVHD staging.
- Time to response.
- Maximal daily diarrhea (volume and frequency).
- Weight.
- Liver function tests.
- Cataract formation and IOP.
- TNF level.
- Albumin.
- TPN consumption.
- Bone density.
- Hypertension.
- Diabetes - presence and control.
- Febrile episodes.
- Positive cultures.
- Days of antibiotic therapy.
- Survival.
- Conditions
- Graft Vs Host Disease
- Being tested
- Budesonide
- Medical subject headings
- Graft vs Host Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BudesonideDrug
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Aug 2005 (estimated)
- Study startJan 2001
- Study completionAug 2005
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Graft Vs Host 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
- Randomised
- Intervention model
- Single group
- Masking
- Double blind
- Enrolment
- 24 participants
Sponsor and investigators
- Lead sponsor
- Rafa Laboratories
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Dr. Falk Pharma GmbH
- Investigators
- Michael Y Shapira, MD, Principal investigator, Hadassah Medical Organization
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00128739
- Sponsor's protocol ID
- 25-23/02/01
- Status last verified
- Aug 2005
- First submitted
- 9 Aug 2005
- Last updated
- 29 Aug 2005
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Aug 2005. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 3 Study to Evaluate the Place of Budesonide in the Treatment of GVHD
- ClinicalTrials.gov ID
- NCT00128739
- Acronym / sponsor ID
- 25-23/02/01
- Conditions
- Graft Vs Host Disease
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 24 participants
- Lead sponsor
- Rafa LaboratoriesIndustry (pharma, biotech, devices)
- Collaborators
- Dr. Falk Pharma GmbH
- Study start
- Jan 2001
- Study completion
- Aug 2005
- First posted
- 10 Aug 2005 (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.
Twenty-four (2 x 12) patients with intestinal graft versus host disease (GVHD) Grades 2, 3 or 4 will be treated with budesonide 3mg three times daily or placebo for 12 weeks. All of the patients will receive cyclosporine and by mouth (po) prednisone or intravenous (IV) methylprednisone with a starting dose of 2mg/kg/day (standard anti-GVHD treatment). Doses of steroids will be decreased by approximately 10% or 10mg per week (depending upon patient's weight) upon response to therapy, defined as a decrease of volume of diarrhea by 50% per day, decrease in abdominal pain and no presence of bloody stool. Patients with Grades 3 or 4 will be withdrawn from the study if there is no response after one week of therapy. Patients with Grade 2 may continue with no decrease in prednisone dose until response is achieved.
Detailed description
Graft versus host disease (GVHD) is one of the most common complications of bone marrow transplantation (BMT). Targets of GVHD are the gastro-intestinal tract (GIT) liver and skin, causing severe diarrhea and mucosal aberration and hepatitis that can cause life threatening liver failure. As a result of the mucosal aberration and the general immuno-suppression, caused both by the GVHD process itself and by the anti GVHD therapy, these patients are highly susceptible for severe, life threatening infections that usually originate from the GIT. Systemic steroids are the backbone of anti GVHD therapy. However, in GVHD systemic steroids have to be administered for a prolonged duration and in high doses, thus causing prolonged immune suppression, and exposing the patients to steroid side effects such as hypertension, diabetes, cataract formation etc.
Budesonide is a steroid that combines topical anti-inflammatory activity with high first-pass hepatic extraction. It was shown to be effective in treatment of inflammatory bowel disease with results slightly less then systemic steroids and fewer steroid-related adverse reactions. Except for its influence on the gut, budesonide was also shown to benefit inflammatory hepatic conditions such as primary biliary cirrhosis, liver transplantation and autoimmune hepatitis. Recently, it has been shown that budesonide is an effective treatment in acute GIT GVHD. The investigators propose to evaluate the effect of budesonide in GIT and hepatic GVHD with the following study.
Patients:
Twelve patients after allogenic peripheral blood stem cell transplantation (PBSCT) with grade >= 2 GIT and/or hepatic GVHD will be prospectively compared to 12 placebo controls.
Inclusion Criteria:
- Clinical and biopsy proven grade >/= 2 GIT AND/OR hepatic GVHD.
Exclusion Criteria:
- Preventive antimicrobial treatment (with the exception of Resprim) or somatostatin in the GIT GVHD patients.
- Anti-GVHD treatment other then steroids (maximal dose ≤ 2 mg/kg methylprednisolone) and cyclosporine A or tacrolimus.
Study Protocol:
All patients will be assessed for GVHD scoring (organ and general) according to standard criteria and tested before inclusion for the following parameters -
- Colon and/or liver biopsy GVHD staging (including number of crypt abscesses).
- Liver function tests - blood albumin, AST, ALT, GGTP, Alk Phos, LDH, bilirubin, coagulation function, cholesterol.
- Stool - volume and frequency.
- Radiological - CT scan for mucosal edema, wall thickening and ascites.
- Kidney function tests - blood creatinine, creatinine clearance.
- Blood pressure.
- Fasting blood glucose. If normal - oral glucose tolerance test, glycosylated hemoglobin.
- Ophthalmologist evaluation for cataract formation and IOP.
- GIT absorption assessment - xylose absorption.
- Microbiological - stool culture and stool for CDT, CMV PCR, culture for CMV in blood and urine.
- Bone density - by ultrasound.
After inclusion the patients will be treated with budesonide 9 or 15mg per day in divided doses or placebo. Other anti-GVHD treatment or ursodeoxycholic acid will not be withheld but tapering off will be tried.
Study parameters:
- LFT, albumin, PT, cholesterol, renal function, stool volume and frequency, CMV culture and PCR, clinical GVHD staging - every 2 weeks.
- Xylose test - every month.
- Ophthalmologist evaluation, diabetes control and CT scan - every 3 months.
- GIT and/or liver biopsy for GVHD staging (including number of crypt abscesses) and CMV PCR, bone density - every 6 months
- Blood, urine and stool culture during every febrile episode.
Study duration: 14 weeks.
End points:
- Hospitalizations: due to GVHD and/or due to infections.
- Overall and GIT or hepatic GVHD staging.
- Time to response.
- Maximal daily diarrhea (volume and frequency).
- Weight.
- Liver function tests.
- Cataract formation and IOP.
- TNF level.
- Albumin.
- TPN consumption.
- Bone density.
- Hypertension.
- Diabetes - presence and control.
- Febrile episodes.
- Positive cultures.
- Days of antibiotic therapy.
- Survival.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- Double blind
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Patients with clinical and biopsy proven Grades 2, 3 or 4 intestinal GVHD
- Patients with a negative stool culture
- Male or female patients aged between 18 - 70 years
- Signed written informed consent of the patient
Key exclusion criteria (14 listed)
- Uncertain GVHD diagnosis (other causes of intestinal disease are possible)
- Severe other disease which may influence the patient prognosis
- Contraindication to the use of steroids
- Patient's inability to swallow the study medications
- Concurrent use of non-steroidal anti-inflammatory drug (NSAID)
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 |
|---|---|---|
| Budesonide | Drug | – |
Primary outcome
Not reported in the source record.
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 29 Aug 2005.
Related trials for Graft Vs Host Disease
Active, not recruitingPhase 2
De-escalated Cyclophosphamide (PTCy) and Ruxolitinib for Graft-versus-Host Disease (GVHD) Prophylaxis
Graft-versus-host Disease
RecruitingEarly Phase 1
HMCT/CT2401: Abatacept GVHD Prophylaxis Following Omidubicel HCT
Hematologic Malignancy
RecruitingObservational study
Improved Methods of Cell Selection for Bone Marrow Transplant Alternatives
Graft-Versus-Host Disease, Graft-versus-leukemia
RecruitingPhase 1/2
The Lowest Effective Dose of Post-Transplantation Cyclophosphamide in Combination With Sirolimus and Mycophenolate Mofetil as Graft-Versus-Host Disease Prophylaxis After Reduced Intensity Conditioning and Peripheral Blood Stem Cell Transplantation
Peripheral Blood Stem Cell Transplantation, Hematopoietic Stem Cell Transplantation
RecruitingPhase 1/2
Phase I/II Study of Pacritinib, A JAK2/IRAK1/CSF1R Inhibitor, in Refractory Chronic Graft-Versus-Host Disease (cGVHD) After Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)
Graft vs Host Disease
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.
Michael Y Shapira, MD principal investigator
Hadassah Medical Organization
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 Budesonide in people with Graft Vs Host Disease, run by Rafa Laboratories at 1 site in Israel.
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 4 inclusion and 14 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 29 Aug 2005. 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 Israel. 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.
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 29 Aug 2005.