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Treatment of Iron Overload Requiring Chelation Therapy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01927913
Recruitment Status : Withdrawn (This study was withdrawn until the evaluation of the nonclinical rat findings is complete.)
First Posted : August 23, 2013
Last Update Posted : June 2, 2021
Information provided by (Responsible Party):
Takeda ( Shire )

Brief Summary:
The purpose of this open-label study is to assess liver iron concentration using MRI imaging in subjects with beta-thalassemia when administered with either SPD602 or deferasirox for the treatment of chronic transfusional iron overload.

Condition or disease Intervention/treatment Phase
Transfusional Iron Overload Iron Overload Iron Chelation Beta-thalassemia Transfusional Hemosiderosis Iron Metabolism Disorders Metabolic Diseases Drug: SPD602 Drug: Deferasirox Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A 48-week, Open-label, 2-arm, Parallel-group, Randomized Exploratory Study to Assess Liver Iron Concentration Measured by FerriScan® (R2) Magnetic Resonance Imaging in B-thalassemia Subjects Administered SPD602 (SSP-004184AQ) or Exjade® (Deferasirox) for Treatment of Chronic Transfusional Iron Overload
Estimated Study Start Date : November 20, 2014
Estimated Primary Completion Date : October 30, 2015
Estimated Study Completion Date : October 30, 2015

Arm Intervention/treatment
Experimental: SPD602 Drug: SPD602
32, 50 or 75 mg/kg/day BID, capsule
Other Name: SSP-004184AQ

Active Comparator: Deferasirox Drug: Deferasirox
Per approved country specific label
Other Name: Exjade®

Primary Outcome Measures :
  1. Change in Liver Iron Concentration (LIC) from Baseline Utilizing R2 Magnetic Resonance Imaging (MRI) [ Time Frame: 48 Weeks ]

Secondary Outcome Measures :
  1. Response Rate Utilizing R2* MRI [ Time Frame: 48 weeks ]
  2. Change in Cardiac Iron Concentration (CIC) from baseline Utilizing T2* MRI [ Time Frame: 48 weeks ]
  3. Change in Serum Ferritin Levels from Baseline [ Time Frame: 48 weeks ]
  4. Change in Pancreas Iron Concentration (PIC) from Baseline Utilizing R2* MRI [ Time Frame: 48 weeks ]
  5. Left Ventricular Ejection Fraction (LVEF) Utilizing MRI [ Time Frame: 48 weeks ]
  6. Gastrointestinal Symptom Rating Scale [ Time Frame: 48 weeks ]
  7. Total Neuropathy Score nurse (TNSn) [ Time Frame: 48 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

These criteria are to be met at the Screening Visit (Visit 1), the Washout Visit (Visit 2), and the Baseline Visit (Visit 3), if reassessed.

  • An understanding, ability, and willingness to fully comply with study procedures and restrictions.
  • Ability to voluntarily provide written, signed, and dated (personally or via a legally authorized representative) informed consent as applicable to participate in the study before completing any study-related procedures.
  • Subjects 18 years of age or older at the time of signing consent.
  • Female subjects should be one of the following:

    1. Post-menopausal (12 consecutive months of spontaneous amenorrhea)
    2. Surgically sterile, or
    3. Females of child-bearing potential must have a negative serum Beta-HCG pregnancy test at the Screening Visit (Visit 1) and a negative urine pregnancy test at the Baseline Visit (Visit 3). Females of child-bearing potential must agree to abstain from sexual activity that could result in pregnancy or agree to use acceptable methods of contraception.
  • Subjects with beta-thalassemia who have received at least 100mL/kg of packed red blood cells (or >20 transfusion units) and who have iron overload (transfusional hemosiderosis) requiring chronic treatment with an iron chelator.
  • Serum ferritin >500µg/L at the Screening Visit (Visit 1).
  • Baseline LIC (last MRI assessment prior to Day 1) greater than or equal to 2.0mg and less than 30.0mg iron per g (equivalent dry weight, liver) determined by FerriScan® R2 MRI.

    8. Mean of the previous 3 pre-transfusion hemoglobin concentrations greater than or equal to 7.5g/dL assessed at the Screening Visit (Visit 1) (1 value from clinical laboratory tests taken at the Screening Visit [Visit 1] and the previous 2 historical values available).

Exclusion Criteria:

  • Severe iron overload including: (a) cardiac T2* MRI less than 10.0ms; or (b) LIC by FerriScan® R2 MRI greater than or equal to 30.0mg/g liver (dw) as assessed at the Screening Visit (Visit 1).
  • Iron overload from causes other than transfusional siderosis.
  • Subjects with thalassemia intermedia
  • Unable to undergo MRI assessment.
  • Cardiac LVEF less than 50% at baseline testing by MRI.
  • Subjects with documented liver failure (presence of portal hypertension, hepatic edema, ascites, cirrhosis), Child-Pugh C hepatic impairment, or biliary disorder.
  • Platelet count <100 x 109/L at the Screening Visit (Visit 1).
  • Absolute neutrophils counts of <1500mm3 at the Screening Visit (Visit 1).
  • Evidence of renal insufficiency eg, creatinine clearance <60mL/min or serum creatinine >1.5x ULN at the Screening Visit (Visit 1).
  • Clinically significant laboratory assessments at the Screening Visit (Visit 1).
  • Significant proteinuria: urinary protein/creatinine ratio >1.0 in a non-first void urine sample at the Screening Visit (Visit 1).
  • Current or recurrent disease that could affect the action, absorption, or disposition of the investigational product, or clinical or laboratory assessments.
  • Current or relevant history of physical or psychiatric illness, any medical disorder that may require treatment or make the subject unlikely to fully complete the study, or any condition, including pregnancy, that presents undue risk from the investigational product or procedures.
  • Current use of any medication contraindicated in the deferasirox prescribing information/SmPC.
  • Known or suspected intolerance or hypersensitivity to SSP-004184AQ, deferasirox, closely-related compounds, or any of the stated ingredients in either medication.
  • Known history of alcohol or other substance abuse within the last year.
  • Within 30 days prior to the Baseline Visit (Visit 3):

    1. Have used an investigational product
    2. Have been enrolled in a clinical study (including vaccine studies) that, in the investigator's opinion, may impact this study.
  • History of malignancy within the past 5 years, with the exception of basal cell or squamous cell skin carcinoma or cervical carcinoma in situ or completely resected colon carcinoma in situ.
  • Insufficient venous access that precludes prescribed blood draws for safety laboratory assessments.
  • Pregnant or lactating females.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01927913

Sponsors and Collaborators
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Study Director: Study Director Takeda
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Responsible Party: Shire
ClinicalTrials.gov Identifier: NCT01927913    
Other Study ID Numbers: SPD602-204
FBS0701 (SSP-004184)
2013-000743-33 ( EudraCT Number )
First Posted: August 23, 2013    Key Record Dates
Last Update Posted: June 2, 2021
Last Verified: May 2021
Additional relevant MeSH terms:
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Metabolic Diseases
Iron Overload
Iron Metabolism Disorders
Anemia, Hemolytic, Congenital
Anemia, Hemolytic
Hematologic Diseases
Genetic Diseases, Inborn
Iron Chelating Agents
Chelating Agents
Sequestering Agents
Molecular Mechanisms of Pharmacological Action