Myelodysplastic SyndromePhase 2MDSAZA0706NCT00897130
5-Azacitidine in Low-risk Myelodysplastic Syndromes (MDSs)
A Phase 2 study testing Azacytidine in people with Myelodysplastic Syndrome, run by Università degli Studi di Brescia at 7 sites in Italy.
Trial summary
Azacitidine will be given at a dose of 75 mg/sqm (s.c) daily for 5 consecutive days every 28 days (every month) for a total of 8 courses to low risk MDSs according to IPSS scoring system. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Myelodysplastic Syndrome
- What is being tested?
- Azacytidine
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 28 participants
- Where
- 7 sitesItaly
- Study dates
- Aug 2008to Dec 2014
- Phase
- Phase 2
- 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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients with low-risk (IPSS 0-INT1) MDS according to WHO classification, presenting one or more of the followings:
- Symptomatic anemia requiring RBC transfusion supportive therapy previously unresponsive to EPO or not expected to respond to EPO
- Thrombocytopenia requiring platelet transfusion with or without muco-cutaneous haemorrhagic syndrome
- Persistent (> 3 months) absolute neutrophil count less then 1,5 x 109/L, with or without infections, requiring or not myeloid growth factor therapy
- ≥ 18 years old.
- Life expectancy ≥ 3 months.
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- ECOG performance Status Grade 0-2.
- Serum bilirubin levels ≤ 1.5 upper limit of the normal (ULN)
- Serum GOT and GPT levels ≤ 2x UNL.
- Creatinine levels ≤ 1.5x UNL.
- Negative serum β-human chorionic gonadotropin (β-HCG) pregnancy test 24 hours prior to beginning of therapy with 5-AZA, for fertile women.
- Written informed consent.
Who cannot join
- Patients with MDS according to WHO classification with INT-2 or high IPSS risk.
- Life expectancy < 3 months.
- ECOG performance Status Grade > 2.
- Serum bilirubin levels >1.5 upper limit of the normal (ULN).
- Serum GOT and GPT levels > 2 x UNL.
- Creatinine levels >1.5 x UNL.
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- Pregnancy or breast feeding.
- Insulin-dependent diabetes and uncontrolled non insulin-dependent diabetes.
- Severe cardiac or pulmonary disease incompatible with the conduction of the protocol.
- Patient with a clear indication to receive long-term anticoagulant therapy.
- Other active hematologic or solid tumors.
- Severe CNS disease.
- Malignant hepatic tumors.
- Hypersensitivity to mannitol or azacitidine.
- No written informed consent.
Trial locations and contacts
7 sites in 1 country.
7 sites in 1 country
Italy7 sites
University of Bologna
Bologna
Chair of Haematology, Bone Marrow Transplant Unit
Brescia, 25123
Cremona
Cremona
University of Genova
Genova
Mantova
Mantua
University of Siena
Siena
University of Udine
Udine
About this study
Official title: Clinical and Biological Effects of 5-Azacitidine Five Days/Monthly Schedule in Symptomatic Low-risk Myelodysplastic Syndromes (MDSs)
Azacitidine will be given at a dose of 75 mg/sqm (s.c) daily for 5 consecutive days every 28 days (every month) for a total of 8 courses to low risk MDSs according to IPSS scoring system. In fact, several studies produced high rates of trilineage responses, reduces the risk of progression to acute myeloid leukemia (AML) in high-risk MDS and improves the quality of life (QoL). The use of 5-Aza in the earlier phases of MDS could reduce the proliferative advantage of MDS clone and favour the regrowth of normal hematopoiesis.
Read the detailed description
5-Azacitidine(5-AZA) is the most promising drug for treatment MDSs. When administered at a dose of 75mg/m2/day subcutaneously for 7 days, every 28 days (every month), 5-Aza produces high rates of trilineage responses, reduces the risk of progression to AML in high-risk MDS and improves the QoL. The use of 5-Aza in the earlier phases of MDS could reduce the proliferative advantage of MDS clone and favour the regrowth of normal hematopoiesis. Other doses or schedules could improve its efficacy. Gene expression profile studies in MDS patients who are sensitive or resistant to 5-AZA are lacking and data coming from these studies could be useful to clarify the mechanisms of 5-azacitidine and optimize the therapy.
Objectives of the study
Primary:
- To evaluate the efficacy (hematologic response) and toxicity of 5-Aza five days monthly treatment schedule in patients with low-risk MDS (IPSS 0-INT1)
Secondary:
- To evaluate QoL by the FACT-An questionnaire
- To evaluate time to progression of MDS;
- To evaluate the gene expression profile of MDS patients sensitive or resistant to 5-AZA;
- To evaluate oncostatin M, interleukin-6 and interleukin-11 levels in the responders and non responders.
Azacitidine will be given at a dose of 75mg/sqm subcutaneous daily for 5 consecutive days every 28 days (every month) for a total of 8 courses. 5-Aza dosages will be adjusted as follows:
Patients' care and other medications
- RBC are transfused to maintain a Hb level > 90 g/L, or whenever indicated.
- Platelets are transfused if platelet count is < 20 x 109/L, or whenever indicated.
- EPO is not allowed during the trial time (8 months= 8 courses of 5-AZA therapy)
- Granulocyte or granulocyte-monocyte colony stimulating factor (G-CSF or GM-CSF) are allowed in case of severe neutropenia and/or systemic infection.
- Antibiotics and antifungals per os are given in prophylaxis if neutrophils <0.5 x 109 /L.
- Antibiotics are given i.v. in case of fever (> 38°C for > 24 h) or whenever indicated.
- Antifungals are given i.v. in case of fever persisting for more than 5 days of antibiotics i.v. or whenever indicated.
- Other experimental drugs or agents are not allowed.
- If another experimental drug or agent will be administered, the patient must discontinue the treatment with 5-AZA, and goes off-study.
Definition of Response
The response to treatment will be assessed according to IWG 2006 criteria, as reported by Cheson et al.(28) (Appendix F)
Response criteria for altering natural history of MDS:
- Complete remission (CR) Bone marrow: ≤5% myeloblasts with normal maturation of all cell lines Persistent dysplasia will be notes Peripheral blood: Hgb ≥ 11g/dl, Platelets ≥ 100 x 109/l, Neutrophils ≥ 1.0 x 109/l, Blasts 0%
- Partial remission (PR)
All CR criteria if abnormal before treatment except:
Bone marrow blasts decreased by ≥50% over pretreatment but still >5% Cellularity and morphology not relevant
- Marrow CR Bone marrow ≤ 5% myeloblasts and decrease by ≥ 50% over pretreatment Peripheral blood: if HI response, they will be noted in addition to marrow CR
- Stable disease Failure to achieve at least PR, but no evidence of progression for >8 weeks
- Failure Death during treatment or disease progression characterized by worsening of cytopenias, increase in the percentage bone marrow blasts, or progression to a more advanced MDS FAB subtype than pretreatment.
- Relapse after CR or PR
At least one of the following:
- Return to pretreatment bone marrow blast percentage
- Decrement of ≥ 50% from maximum remission/response levels in granulocytes or platelets
- Reduction in Hgb concentration by ≥ 1.5 g/dl or transfusion dependence
- Cytogenetic Response
- Complete Disappearance of the chromosomal abnormality without appearance of new ones
- Partial At least 50% reduction of the chromosomal abnormality
- Disease progression For patients with Less than 5% blasts: ≥50% increase in blasts to > 5% blasts 5%-10% blasts: ≥50% increase to >10% blasts 10%-20% blasts: ≥ 50% increase to > 20% blasts 20%-30% blasts: ≥50% increase to >30% blasts Any of the following At least 50% decrement from maximum remission/response in granulocytes or platelets Reduction in Hgb by ≥ 2g/dl Transfusion dependence
Survival
Endpoints:
Overall: death from any cause Event free: failure or death from any cause PFS: disease progression or death form MDS DFS: time to relapse Cause-specific death: death related to MDS
Response criteria for hematologic improvement (HI)
- Erythroid response (HI-E) (pretreatment, <11 g/dl) Hgb increase by ≥1.5 g/dl Relevant reduction on units of RBC transfusion by an absolute number of at least 4 RBC transfusions/8 weeks compared with the pretreatment transfusion number in the previous 8 weeks. Only RBC transfusions given for a Hgb of ≤ 9.0 g/dl pretreatment will count in the RBC transfusion response evaluation
- Platelet response (HI-P)(pretreatment, <100 x 109/l) Absolute increase of ≥ 30 x 109/l for patients starting with >20 x 109/l platelets Increase from < 20 x 109/l to >20 x 109/l and by at least 100%
- Neutrophil response (HI-N) (pretreatment, <1.0 x 109/l) At least 100% increase and an absolute increase > 0.5 x 109/l
- Progression or relapse after HI
- At least one of the following:
- At least 50% decrement from maximum response levels in granulocytes or platelets
- Reduction in Hgb by ≥ 1.5 g/dl Transfusion dependence
Quality of Life (QoL) QoL will be assessed by the FACT-An score before treatment and monthly during the study, at the end of each cycle of treatment. The FACT-An questionnaire will be performed as outpatient interviews by one trained nurse The QoL battery, according to FACT-An questionnaire, consists of items including physical, functional, emotional, social spiritual symptoms
Patient evaluation
- Physical examination (at entry and every month).
- Peripheral blood count and differential (at entry and every two weeks).
- Bone marrow biopsy (at entry; at the end of the 4th course; at the end of study-8th course).
- Bone marrow aspirate (at entry; at the end of the 4th course; at the end of study-8th course).
- Cytogenetics (at entry; at end of the 4th course; at the end of study -8th course).
- Blood biochemistry profile (at entry and every month).
- HBV, HCV, HIV (at entry).
- Gene Profile (at entry; at the end of the 4th course; at the end of study-8th course).
- Cytokines, Onc.M, IL6, IL11 (at entry; at the end of the 4th course; at the end of study-8th course).
- FACT-an (at entry; at the end of each course).
- Conditions
- Myelodysplastic Syndrome
- Being tested
- Azacytidine
- Keywords
- low-risk (IPSS 0-INT1) MDS according to WHO classification
- Medical subject headings
- Myelodysplastic Syndromes
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AzacytidineDrug
Azacitidine will be given at a dose of 75mg/sqm subcutaneous daily for 5 consecutive days every 28 days (every month) for a total of 8 courses. 5-Aza dosages will be adjusted
| Study group | Role | What they receive |
|---|---|---|
| Azacytidine | Experimental | Azacitidine will be given at a dose of 75mg/sqm subcutaneous daily for 5 consecutive days every 28 days (every month) for a total of 8 courses. 5-Aza dosages will be adjusted. Receives: Drug: Azacytidine |
What is being measured
The primary outcome is the main question the study is designed to answer.
To evaluate the efficacy (hematologic response) of five days monthly 5-Aza treatment schedule in patients with low-risk MDS (IPSS 0-1).
Measured: 36 months
To evaluate the toxicity of five days monthly 5-Aza treatment schedule in patients with low-risk MDS (IPSS 0-1).
Measured: 36 months
Secondary outcomes (1)
To evaluate the QoL by the FACT-An questionnaire
Measured: 36 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 May 2009 (estimated)
- Study startAug 2008
- Primary completionDec 2009
- Study completionDec 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Myelodysplastic 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 2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 28 participants (actual)
Sponsor and investigators
- Lead sponsor
- Università degli Studi di Brescia
- Sponsor type
- University, hospital or other
- Collaborators
- University of Udine, University of Bologna, University of Genova, University of Siena, Cremona, Mantova
- Responsible party
- Principal investigator, Domenico Russo, Università degli Studi di Brescia
- Investigators
- Prof Domenico Russo, MD, Principal investigator, Chair of Haematology, Brescia University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00897130
- Sponsor's protocol ID
- 2007-003943-55
- Acronym
- MDSAZA0706
- Status last verified
- Dec 2014
- First submitted
- 8 May 2009
- Last updated
- 3 Dec 2014
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Abdulhaq H, Rossetti JM. The role of azacitidine in the treatment of myelodysplastic syndromes. Expert Opin Investig Drugs. 2007 Dec;16(12):1967-75. doi: 10.1517/13543784.16.12.1967.
PubMed 18042004
Study at a glance
From the registry record, last updated by the sponsor on 3 Dec 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical and Biological Effects of 5-Azacitidine Five Days/Monthly Schedule in Symptomatic Low-risk Myelodysplastic Syndromes (MDSs)
- ClinicalTrials.gov ID
- NCT00897130
- Acronym / sponsor ID
- MDSAZA0706 / 2007-003943-55
- Conditions
- Myelodysplastic Syndrome
- Keywords
- low-risk (IPSS 0-INT1) MDS according to WHO classification
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 28 participants (actual)
- Lead sponsor
- Università degli Studi di BresciaUniversity, hospital or other
- Collaborators
- University of Udine, University of Bologna, University of Genova, University of Siena, Cremona, Mantova
- Study start
- Aug 2008
- Primary completion
- Dec 2009 (actual)
- Study completion
- Dec 2014 (actual)
- First posted
- 12 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.
Azacitidine will be given at a dose of 75 mg/sqm (s.c) daily for 5 consecutive days every 28 days (every month) for a total of 8 courses to low risk MDSs according to IPSS scoring system. In fact, several studies produced high rates of trilineage responses, reduces the risk of progression to acute myeloid leukemia (AML) in high-risk MDS and improves the quality of life (QoL). The use of 5-Aza in the earlier phases of MDS could reduce the proliferative advantage of MDS clone and favour the regrowth of normal hematopoiesis.
Detailed description
5-Azacitidine(5-AZA) is the most promising drug for treatment MDSs. When administered at a dose of 75mg/m2/day subcutaneously for 7 days, every 28 days (every month), 5-Aza produces high rates of trilineage responses, reduces the risk of progression to AML in high-risk MDS and improves the QoL. The use of 5-Aza in the earlier phases of MDS could reduce the proliferative advantage of MDS clone and favour the regrowth of normal hematopoiesis. Other doses or schedules could improve its efficacy. Gene expression profile studies in MDS patients who are sensitive or resistant to 5-AZA are lacking and data coming from these studies could be useful to clarify the mechanisms of 5-azacitidine and optimize the therapy.
Objectives of the study
Primary:
- To evaluate the efficacy (hematologic response) and toxicity of 5-Aza five days monthly treatment schedule in patients with low-risk MDS (IPSS 0-INT1)
Secondary:
- To evaluate QoL by the FACT-An questionnaire
- To evaluate time to progression of MDS;
- To evaluate the gene expression profile of MDS patients sensitive or resistant to 5-AZA;
- To evaluate oncostatin M, interleukin-6 and interleukin-11 levels in the responders and non responders.
Azacitidine will be given at a dose of 75mg/sqm subcutaneous daily for 5 consecutive days every 28 days (every month) for a total of 8 courses. 5-Aza dosages will be adjusted as follows:
Patients' care and other medications
- RBC are transfused to maintain a Hb level > 90 g/L, or whenever indicated.
- Platelets are transfused if platelet count is < 20 x 109/L, or whenever indicated.
- EPO is not allowed during the trial time (8 months= 8 courses of 5-AZA therapy)
- Granulocyte or granulocyte-monocyte colony stimulating factor (G-CSF or GM-CSF) are allowed in case of severe neutropenia and/or systemic infection.
- Antibiotics and antifungals per os are given in prophylaxis if neutrophils <0.5 x 109 /L.
- Antibiotics are given i.v. in case of fever (> 38°C for > 24 h) or whenever indicated.
- Antifungals are given i.v. in case of fever persisting for more than 5 days of antibiotics i.v. or whenever indicated.
- Other experimental drugs or agents are not allowed.
- If another experimental drug or agent will be administered, the patient must discontinue the treatment with 5-AZA, and goes off-study.
Definition of Response
The response to treatment will be assessed according to IWG 2006 criteria, as reported by Cheson et al.(28) (Appendix F)
Response criteria for altering natural history of MDS:
- Complete remission (CR) Bone marrow: ≤5% myeloblasts with normal maturation of all cell lines Persistent dysplasia will be notes Peripheral blood: Hgb ≥ 11g/dl, Platelets ≥ 100 x 109/l, Neutrophils ≥ 1.0 x 109/l, Blasts 0%
- Partial remission (PR)
All CR criteria if abnormal before treatment except:
Bone marrow blasts decreased by ≥50% over pretreatment but still >5% Cellularity and morphology not relevant
- Marrow CR Bone marrow ≤ 5% myeloblasts and decrease by ≥ 50% over pretreatment Peripheral blood: if HI response, they will be noted in addition to marrow CR
- Stable disease Failure to achieve at least PR, but no evidence of progression for >8 weeks
- Failure Death during treatment or disease progression characterized by worsening of cytopenias, increase in the percentage bone marrow blasts, or progression to a more advanced MDS FAB subtype than pretreatment.
- Relapse after CR or PR
At least one of the following:
- Return to pretreatment bone marrow blast percentage
- Decrement of ≥ 50% from maximum remission/response levels in granulocytes or platelets
- Reduction in Hgb concentration by ≥ 1.5 g/dl or transfusion dependence
- Cytogenetic Response
- Complete Disappearance of the chromosomal abnormality without appearance of new ones
- Partial At least 50% reduction of the chromosomal abnormality
- Disease progression For patients with Less than 5% blasts: ≥50% increase in blasts to > 5% blasts 5%-10% blasts: ≥50% increase to >10% blasts 10%-20% blasts: ≥ 50% increase to > 20% blasts 20%-30% blasts: ≥50% increase to >30% blasts Any of the following At least 50% decrement from maximum remission/response in granulocytes or platelets Reduction in Hgb by ≥ 2g/dl Transfusion dependence
Survival
Endpoints:
Overall: death from any cause Event free: failure or death from any cause PFS: disease progression or death form MDS DFS: time to relapse Cause-specific death: death related to MDS
Response criteria for hematologic improvement (HI)
- Erythroid response (HI-E) (pretreatment, <11 g/dl) Hgb increase by ≥1.5 g/dl Relevant reduction on units of RBC transfusion by an absolute number of at least 4 RBC transfusions/8 weeks compared with the pretreatment transfusion number in the previous 8 weeks. Only RBC transfusions given for a Hgb of ≤ 9.0 g/dl pretreatment will count in the RBC transfusion response evaluation
- Platelet response (HI-P)(pretreatment, <100 x 109/l) Absolute increase of ≥ 30 x 109/l for patients starting with >20 x 109/l platelets Increase from < 20 x 109/l to >20 x 109/l and by at least 100%
- Neutrophil response (HI-N) (pretreatment, <1.0 x 109/l) At least 100% increase and an absolute increase > 0.5 x 109/l
- Progression or relapse after HI
- At least one of the following:
- At least 50% decrement from maximum response levels in granulocytes or platelets
- Reduction in Hgb by ≥ 1.5 g/dl Transfusion dependence
Quality of Life (QoL) QoL will be assessed by the FACT-An score before treatment and monthly during the study, at the end of each cycle of treatment. The FACT-An questionnaire will be performed as outpatient interviews by one trained nurse The QoL battery, according to FACT-An questionnaire, consists of items including physical, functional, emotional, social spiritual symptoms
Patient evaluation
- Physical examination (at entry and every month).
- Peripheral blood count and differential (at entry and every two weeks).
- Bone marrow biopsy (at entry; at the end of the 4th course; at the end of study-8th course).
- Bone marrow aspirate (at entry; at the end of the 4th course; at the end of study-8th course).
- Cytogenetics (at entry; at end of the 4th course; at the end of study -8th course).
- Blood biochemistry profile (at entry and every month).
- HBV, HCV, HIV (at entry).
- Gene Profile (at entry; at the end of the 4th course; at the end of study-8th course).
- Cytokines, Onc.M, IL6, IL11 (at entry; at the end of the 4th course; at the end of study-8th course).
- FACT-an (at entry; at the end of each course).
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Azacytidine | Experimental | Drug: AzacytidineAzacitidine will be given at a dose of 75mg/sqm subcutaneous daily for 5 consecutive days every 28 days (every month) for a total of 8 courses. 5-Aza dosages will be adjusted. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (12 listed)
- Patients with low-risk (IPSS 0-INT1) MDS according to WHO classification, presenting one or more of the followings:
- ≥ 18 years old.
- Life expectancy ≥ 3 months.
- ECOG performance Status Grade 0-2.
- Serum bilirubin levels ≤ 1.5 upper limit of the normal (ULN)
Key exclusion criteria (15 listed)
- Patients with MDS according to WHO classification with INT-2 or high IPSS risk.
- Life expectancy < 3 months.
- ECOG performance Status Grade > 2.
- Serum bilirubin levels >1.5 upper limit of the normal (ULN).
- Serum GOT and GPT levels > 2 x UNL.
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 |
|---|---|---|
| AzacytidineAzacitidine will be given at a dose of 75mg/sqm subcutaneous daily for 5 consecutive days every 28 days (every month) for a total of 8 courses. 5-Aza dosages will be adjusted | Drug | Azacytidine |
Primary outcome
To evaluate the efficacy (hematologic response) of five days monthly 5-Aza treatment schedule in patients with low-risk MDS (IPSS 0-1).
Time frame: 36 months
To evaluate the toxicity of five days monthly 5-Aza treatment schedule in patients with low-risk MDS (IPSS 0-1).
Time frame: 36 months
1 secondary outcome
To evaluate the QoL by the FACT-An questionnaire
Time frame: 36 months
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 3 Dec 2014.
- Results publication: PubMed 18042004Abdulhaq H, Rossetti JM. The role of azacitidine in the treatment of myelodysplastic syndromes. Expert Opin Investig Drugs. 2007 Dec;16(12):1967-75. doi: 10.1517/13543784.16.12.1967.
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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.
Prof Domenico Russo, MD principal investigator
Chair of Haematology, Brescia University
7 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Azacytidine in people with Myelodysplastic Syndrome, run by Università degli Studi di Brescia at 7 sites in Italy.
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 12 inclusion and 15 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 3 Dec 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 7 sites in Italy. 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
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?
To evaluate the efficacy (hematologic response) of five days monthly 5-Aza treatment schedule in patients with low-risk MDS (IPSS 0-1). (time frame: 36 months). The study lists 2 primary outcomes in all. 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 NCT00897130, 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 3 Dec 2014.