Iron Isomaltoside 1000 (Monofer®) in Non-Dialysis Dependent Chronic Kidney Disease and With Renal-Related Anaemia

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by:
Pharmacosmos A/S
ClinicalTrials.gov Identifier:
NCT01102413
First received: March 26, 2010
Last updated: March 21, 2014
Last verified: March 2014

March 26, 2010
March 21, 2014
April 2010
May 2014   (final data collection date for primary outcome measure)
Change in hemoglobin (Hb) concentration from baseline to week 4. [ Time Frame: Baseline, 4 weeks ] [ Designated as safety issue: No ]
Change in hemoglobin (Hb) concentration from baseline to week 8. [ Time Frame: Baseline, 8 weeks ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT01102413 on ClinicalTrials.gov Archive Site
1. Number of subjects who have change in Hb concentration ≥ 1.0 g/dL from baseline to week 2, 4 or 8. [ Time Frame: Baseline to week 8 ] [ Designated as safety issue: No ]
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Not Provided
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Iron Isomaltoside 1000 (Monofer®) in Non-Dialysis Dependent Chronic Kidney Disease and With Renal-Related Anaemia
A Phase III, Randomized, Comparative, Open-label Study of Intravenous Iron Isomaltoside 1000 (Monofer®) Administered by Infusions or Repeated Bolus Injections in Comparison With Oral Iron Sulphate in Subjects With Non-Dialysis Dependent Chronic Kidney Disease and With Renal-Related Anaemia

The study is designed to determine the effects of an investigational drug Monofer in subjects with non-dialysis dependent chronic kidney disease (NDD-CKD) subjects and with iron deficiency anaemia (IDA).

Not Provided
Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Iron Deficiency Anemia
  • Chronic Kidney Disease
  • Drug: Monofer
    Infusion or injections
  • Drug: Iron Sulphate
    Oral intake
  • Experimental: Monofer
    Injections or infusions
    Intervention: Drug: Monofer
  • Active Comparator: Iron Sulphate
    Oral intake
    Intervention: Drug: Iron Sulphate
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
350
June 2014
May 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Men and women, aged more than 18 years.
  2. Subjects diagnosed with NDD-CKD with MDRD calculated eGFR between 15-59 mL/min.
  3. Hb < 11.0 g/dL (6.80 mmol/L)
  4. Either or both of the following iron stores indicators below target {Serum ferritin < 100 ug/l and Transferrin saturation (TfS)<20%}.
  5. Life expectancy beyond 12 months by Principal Investigator's judgement.
  6. Willingness to participate after informed consent and any authorization as required by local law ( e.g. Protected Health Information [PHI] for North America).

Exclusion Criteria:

  1. Anaemia predominantly caused by factors other than renal impairment or iron deficiency (according to Principal Investigator's judgment).
  2. Iron overload or disturbances in utilisation of iron (e.g. haemochromatosis and haemosiderosis).
  3. Drug hypersensitivity (i.e. previous hypersensitivity to Iron Dextran or iron mono- or disaccharide complexes or to iron sulphate or any excipients of the study drug.
  4. Subjects with history of multiple allergies.
  5. Decompensated liver cirrhosis or active hepatitis (Alanine Aminotransferase (ALT) > 3 times upper normal limit).
  6. Active acute or chronic infections ((assessed by clinical judgment), supplied with White Blood Cells (WBC) and C-Reactive Protein (CRP)).
  7. Rheumatoid arthritis with symptoms or signs of active joint inflammation.
  8. Pregnancy and nursing (To avoid pregnancy, women have to be postmenopausal (at least 12 months must have elapsed since last menstruation), surgically sterile, or women of child bearing potential must use one of the following contraceptives during the whole study period and after the study has ended for at least 5 times plasma biological half-life of the investigational medicinal product (5 days): Contraceptive pills, intrauterine devices (IUD), contraceptive depot injections (prolonged-release gestagen), subdermal implantation, vaginal ring, and transdermal patches).
  9. Extensive active bleeding necessitating blood transfusion.
  10. Planned elective surgery during the study.
  11. Participation in any other clinical study within 3 months prior to screening.
  12. Known intolerance to oral iron treatment.
  13. Untreated B12 or folate deficiency.
  14. I.V. or oral iron treatment or blood transfusion within 4 weeks prior to screening visit.
  15. ESA treatment within 8 weeks prior to screening visit.
  16. Serum ferritin > 500 µg/L.
  17. Any other medical condition that, in the opinion of Principal Investigator, may cause the subject to be unsuitable for the completion of the study or place the subject at potential risk from being in the study or interfere with study drug evaluation. Example, Uncontrolled Hypertension, Unstable Ischemic Heart Disease or Uncontrolled Diabetes Mellitus.
  18. Body weight < 30 kilograms.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT01102413
P-Monofer-CKD-02
Yes
Chief Midical Officer, Pharmacosmos A/S
Pharmacosmos A/S
Not Provided
Not Provided
Pharmacosmos A/S
March 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP