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Myelodysplastic SyndromesNCT01026376

An Expanded Access Program for Decitabine in Patients With Myelodysplastic Syndrome (MDS)

A study testing decitabine in people with Myelodysplastic Syndromes, run by Janssen-Cilag Farmaceutica Ltda. at 11 sites in 3 countries.

No Longer Available

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this study is to provide Decitabine to patients with Myelodysplastic syndrome (MDS) of all FAB (French-American-British) subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups, including both previously treated and untreated patients. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Myelodysplastic Syndromes
What is being tested?
decitabine
Type of treatment
Injection or infusion
How many people
Not given
Where
11 sitesin 3 countries
Study dates
Jun 2008to Nov 2011
Phase
Expanded access
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

  • Must have a diagnosis of MDS (de novo / primary or secondary) of all FAB subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups
  • Has an Eastern Oncology Cooperative Group (ECOG) performance status of 0-2
  • Adequate hepatic and renal function as measured by the following pre-treatment laboratory criteria within 21 days of starting treatment with Decitabine (laboratory measure of liver function no more than 2.5 times the upper limit of normal, laboratory measure of total bilirubin and serum creatinine no more than 1.5 times the upper limit of normal)
  • Female patients must be postmenopausal, or surgically sterile, or abstinent, or, if sexually active, be practicing an effective method of birth control (e.g., prescription oral contraceptives, contraceptive injections, intrauterine device, double-barrier method, contraceptive patch, male partner sterilization) before entry and throughout the study
  • Have a negative serum or urine pregnancy test at screening
  • Male subjects should be advised not father a child while on or within 2 months of completion of Decitabine therapy

Who cannot join

  • Have a diagnosis of AML (>20% bone marrow blasts) or other progressive malignant disease
  • has previously been treated with Azacitidine or Decitabine
  • Have uncontrolled heart disease or uncontrolled congestive heart failure
  • Have uncontrolled restrictive or obstructive pulmonary disease
  • Have active viral or bacterial infection
  • Have known positive serology for HIV
Show all 9Show fewer
  • Have a mental illness or any other condition that could prevent full cooperation with the treatment and monitoring requirements of the study
  • Have known hypersensitivity to any of the excipients of decitabine
  • Are pregnant or breast-feeding

Trial locations and contacts

11 sites in 3 countries.

11 sites in 3 countries

Brazil9 sites
  • Study site

    Belo Horizonte

  • Study site

    Botucatu

  • Study site

    Brasília

  • Study site

    Campinas

  • Study site

    Fortaleza

  • Study site

    Pinheiros

  • Study site

    Rio de Janeiro

  • Study site

    São Paulo

  • Study site

    São Paulol

Other trials in Brazil

Hong Kong1 site
  • Study site

    Hong Kong

Other trials in Hong Kong

Thailand1 site
  • Study site

    Bangkok

Other trials in Thailand

About this study

The purpose of this study is to provide Decitabine to patients with Myelodysplastic syndrome (MDS) of all FAB (French-American-British) subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups, including both previously treated and untreated patients.

Read the detailed description

Myelodysplastic Syndromes (MDS), which includes a diverse group of bone marrow disorders that result in ineffective production of blood cells, frequently occurs in elderly patients. Historically, the available treatments for MDS have been symptomatic and supportive, and have not been shown to be effective in producing sustained improvement in hematopoiesis (production of all types of blood cells ) or in delaying leukemic evolution (leukemia is a serious disease in which too many white blood cells are produced, causing weakness and sometimes death). This project is an open-label (all people involved know the identity of the intervention), multicenter, international single arm, Phase 3b study to provide expanded access to Decitabine for patients with myelodysplastic syndromes (MDS). The purpose of this study is to provide Decitabine to patients with Myelodysplastic syndrome (MDS) according some medical classifications: FAB (French-American-British) subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups, including previously treated and untreated for MDS. The secondary objectives are to evaluate the safety and tolerability of Decitabine, as well as the overall response rate according to the International Working Group (IWG) 2000 and IWG 2006 response criteria, hematologic improvement, cytogenetic response rates (evaluation based on genetic), time to acute myeloid leukemia progression or death (evaluate the length of time that passes prior to onset of leukemia progression and/or death), blood product transfusion requirements per patient (with corresponding dates to collect the number of transfusion independent days), days in the hospital (including reason for hospitalization and the ward within the hospital where the hospitalizations occur) and, optionally, quality of life assessment (EORTC QLQ C-30). 3-day cycle: Decitabine will be administered as a 15mg/m2 administered by continuous infusion over 3 hours repeated every 8 hours for 3 days. 5-day cycle: Another optional schedule could be adopted (at discretion of investigators), Decitabine at a dose of 20mg/m² administered intravenously over 1 hour, once daily for 5 consecutive days, of a 4-week cycle. Treatment may be continued as long as the patient continues to benefit.

Being tested
decitabine
Keywords
Myelodysplastic Syndromes, Decitabine
Medical subject headings
Myelodysplastic Syndromes

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • decitabineDrug

    Cycles of 15mg/m2 infusion during 3h, 3 times a day, per 3 days

  • decitabineDrug

    Cycles of 20mg/m2 infusion during 1h, once a day, per 5 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Dec 2009 (estimated)
  2. Study startJun 2008
  3. Primary completionNov 2011
  4. Study completionNov 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Expanded access
IDs, dates and publications
ClinicalTrials.gov ID
NCT01026376
Sponsor's protocol ID
CR015037
Other IDs
DACOGENMYE3001
Status last verified
Apr 2013
First submitted
3 Dec 2009
Last updated
18 Apr 2013
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing decitabine in people with Myelodysplastic Syndromes, run by Janssen-Cilag Farmaceutica Ltda. at 11 sites in 3 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 9 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: status not confirmed, as of the sponsor's last update on 18 Apr 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 11 sites in Brazil, Hong Kong, Thailand. 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.

Are results available for this study?

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.

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 18 Apr 2013.

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Clinical Trial NCT01026376 | AzTrials