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Trial record 8 of 36 for:    pharmacosmos

Open-label PK Study of Iron Isomaltoside 1000 (Monofer) Administered by 500 mg IV Injection or 1000 mg IV Infusion to Patients With Inflammatory Bowel Disease

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. Identifier: NCT01213680
Recruitment Status : Completed
First Posted : October 4, 2010
Last Update Posted : November 14, 2013
Information provided by (Responsible Party):
Pharmacosmos A/S

Brief Summary:
The purpose of this study is to assess the pharmakokinetic properties of higher doses (500 mg and 1000 mg) of Monofer(R)in patients suffering from inflammatory bowel disease

Condition or disease Intervention/treatment Phase
Inflammatory Bowel Disease Drug: Monofer (iron isomaltoside 1000) Drug: Monofer Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 16 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Open-label Pharmakokinetic Study of Iron Isomaltoside 1000 (Monofer)Administered by 500 mg IV Injection or 1000 mg Intravenous Infusion to Patients With Inflammatory Bowel Disease (PK-IBD-02)
Study Start Date : February 2012
Actual Primary Completion Date : August 2012
Actual Study Completion Date : November 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Iron

Arm Intervention/treatment
Active Comparator: 1000 mg iron isomaltoside as intravenous infusion Drug: Monofer (iron isomaltoside 1000)
1000 mg iron isomaltoside administered as a infusion over 15 minutes

Active Comparator: 500 mg iron isomaltoside 1000 as bolus injection Drug: Monofer
500 mg iron isomaltoside 1000 given as bolus injection over 2 minutes

Primary Outcome Measures :
  1. Total serum iron pharmakokinetic parameters [ Time Frame: 24, 48 and72 hours ]

Secondary Outcome Measures :
  1. Total urine-iron pharmakokinetic parameters [ Time Frame: 24, 48 and 72 hours ]

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:

  1. Men and women, aged more than 18 years
  2. Subjects diagnosed with inflammatory bowel disease and mild to moderate disease activity (defined as a score of less than or equal to 5 on the Harvey-Bradshaw index for Crohn's disease and a Mayo score (subscore without endoscopy) of less than or equal to 6 for ulcerative colitis)
  3. Weight above 50 kg
  4. Hb <12 g/dL (7.45 mmol/L)
  5. Transferrin saturation (TfS) <20%
  6. Life expectancy beyond 12 months by investigator's judgment
  7. Willingness to participate after informed consent -

Exclusion Criteria:

  1. Anaemia predominantly caused by other factors than iron deficiency anaemia
  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)
  4. Known hypersensitivity to any excipients in the investigational drug products
  5. Subjects with a history of multiple allergies
  6. Active Intestinal Tuberculosis
  7. Active intestinal amoebic infections
  8. Decompensated liver cirrhosis and hepatitis (Alanine Aminotransferase (ALT) > 3 times upper limit normal)
  9. History of immunocompromise and/or history of Hepatitis B and/or C
  10. Acute infections (assessed by clinical judgment), supported by white blood cells (WBC) and C-reactive protein (CRP))
  11. Rheumatoid arthritis with symptoms or signs of active joint inflammation
  12. 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: Contraceptive pills, intrauterine devices (IUD), contraceptive depot injections (prolonged-release gestagen), subdermal implantation, vaginal ring, and transdermal patches)
  13. Extensive active bleeding necessitating blood transfusion
  14. Planned elective surgery during the study
  15. Participation in any other clinical study within 3 months prior to screening
  16. Untreated B12 or folate deficiency
  17. Other I.V. or oral iron treatment or blood transfusion within 4 weeks prior to screening visit
  18. Erythropoietin treatment within 4 weeks prior to screening visit
  19. Any other medical condition that, in the opinion of Investigator, may cause the patient to be unsuitable for the completion of the study or place the patient at potential risk from being in the study. Example: Uncontrolled Hypertension, Unstable Ischemic Heart Disease or Uncontrolled Diabetes Mellitus

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 identifier (NCT number): NCT01213680

Sponsors and Collaborators
Pharmacosmos A/S
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Study Chair: Lars Lykke Thomsen, MD Pharmacosmos A/S

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Responsible Party: Pharmacosmos A/S Identifier: NCT01213680     History of Changes
Other Study ID Numbers: P-Monofer-PK-IBD-02
First Posted: October 4, 2010    Key Record Dates
Last Update Posted: November 14, 2013
Last Verified: November 2013
Keywords provided by Pharmacosmos A/S:
Inflammatory Bowel Disease, IBD
Additional relevant MeSH terms:
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Intestinal Diseases
Inflammatory Bowel Diseases
Gastrointestinal Diseases
Digestive System Diseases
Ferric Compounds
Iron isomaltoside 1000
Trace Elements
Growth Substances
Physiological Effects of Drugs