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CompletedNCT00349453Updated Dec 12, 2011

Study Using Deferiprone Alone or in Combination With Desferrioxamine in Iron Overloaded Transfusion-dependent Patients

A Phase 2 interventional study of Deferiprone (L1) and Deferiprone (L1) in Hemochromatosis, sponsored by Lipomed. Completed at 13 sites in Switzerland. Open to participants aged 4 Years and older. Per ClinicalTrials.gov, last updated 2011-12-12.

Sponsored by Lipomed · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
24
Allocation
Non-randomized
Ages
4 Years and older
Sex
All
01

Study summary

Systematical (retro- and prospective) investigation of the long-term safety (toxicity assessment according to CTCAE v3.0) and efficacy of deferiprone either given alone or in combination with desferrioxamine

Read the detailed description

Patients with refractory anemias requiring regular blood transfusions accumulate iron at the rate of approximately 0.5 mg/kg/day, which may lead to serious organ toxicity, e.g. to the heart, liver and endocrine organs. The human body has no active mechanism for the excretion of excess iron. Therefore multiply transfused patients will develop a secondary hemosiderosis, if excess iron is not excreted by a chelating agent. Symptoms of iron-overload occur when body iron stores reach 10-20 g. At higher levels severe, even fatal complications, particularly cardiac failure, may develop.

Desferrioxamine (DFO, Desferal) is the established and commonly used iron-chelating drug, but is expensive and must be given by slow subcutaneous or intravenous infusion for 8-12 hours a day during 5-7 days weekly at a dosage of 40-50 mg/kg body weight/day. This often leads to failure of compliance of the patient and therefore to inefficient iron chelation. Further, some patients are hypersensitive to desferrioxamine and others suffer from toxicity, e.g. to the ears or eyes.

Deferiprone (L1; CP20; 1,2 dimethyl-3-hydroxypyrid-4-one) is an orally active iron chelator investigated in various clinical trials since 1987. Dosages of 75 - 100 mg/kg body weight/day of L1 have been considered effective to maintain stable iron balance (urinary iron excretion of 0.5 mg/kg/day) and to reduce serum ferritin levels between 6% and 25% within one year of treatment in iron-overloaded thalassemic patients. There exists long-term experience with patients who have received deferiprone continuously for more than 10 years so far. The main side effects encountered during a deferiprone therapy are arthropathy, gastrointestinal symptoms, headache, and mild zinc deficiency. These adverse reactions are usually reversed on reducing the dose or discontinuing the drug. Except for severe joint symptoms in few patients, most of the subjects in different clinical trials have been able to continue with L1 therapy for a long term. The most severe, but rare complication following administration of deferiprone is agranulocytosis or neutropenia.

A new treatment regimen combining deferiprone with desferrioxamine is currently being investigated in many countries. Preliminary data have demonstrated that the combined use of both drugs is highly active showing an additive or even synergistic effect (significant decrease of serum ferritin and hepatic iron content, increase of urinary iron excretion). This synergism could be explained by the different mode of action of the two drugs. It could be demonstrated that patients who were not sufficiently chelated with desferrioxamine or deferiprone, could achieve a negative iron balance with the combination treatment of both drugs. The combined regimen was generally well tolerated. It has been speculated that the individual toxicity profile of both drugs can be positively influenced by the simultaneous administration of L1 and DFO. The daily treatment with L1 tablets combined with at least twice a week administration of parenteral desferrioxamine is more patient-convenient and therefore may enhance the patient's compliance.

The primary aim of this study is to systematically investigate the long-term safety (toxicity assessment according to CTCAE v3.0) of deferiprone either given alone or in combination with desferrioxamine. Further, in patients agreeing to perform annual SQUID analysis of the liver, the annual change of liver iron concentration (LIC) will be examined for four years.

02

Conditions studied

  • Hemochromatosis

Keywords

  • Deferiprone
  • L1
  • Desferrioxamine
  • Hemochromatosis
  • Iron overload
  • Thalassemia
03

In context

Hemochromatosis

67 studies on the registry are indexed under Hemochromatosis; 4 are open to participants now.

This study's enrollment of 24 is below the median of 61 across 42 interventional studies indexed under Hemochromatosis.

Browse Hemochromatosis studies →

Lead sponsor

Lipomed is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Iron overloaded male or female patients with primary or secondary hemochromatosis
  • Age: 4 years and older
  • Patients with desferrioxamine toxicity or allergy (e.g. visual or hearing defects, bone abnormalities, reactions at injection site)
  • Patients unable or unwilling to comply satisfactorily with regular desferrioxamine administration on 5-7 days/week
  • Combination treatment: patients not sufficiently chelated with desferrioxamine or deferiprone monotherapy
  • Patients must be willing to undergo routine screening including medical history, physical examination and hematology, biochemistry and other laboratory tests
  • Written informed consent

Exclusion criteria

Exclusion Criteria:

  • Children under 4 years of age
  • Female and male of reproductive age, sexually active but not taking adequate contraceptive precaution
  • Woman who are pregnant or breast-feeding
  • Patients with HIV
  • Patients with active hepatitis requiring treatment
  • Patients with severe hepatic failure, cirrhosis
  • Patients with neutropenia (neutrophils less than 1.5 exp9/l, MDS: less than 0.5 exp9/l)
  • Patients with thrombocytopenia (platelets less than 100 exp9/l, MDS: less than 20 exp9/l)
  • Patients with decompensated heart failure (LVEF less than 40% or patients under continuous cardiac medication)
  • Patients with severe renal failure
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    Deferiprone (L1) monotherapy

    Deferiprone (L1) monotherapy

    Drug: Deferiprone (L1)

  • Experimental
    Combination therapy

    Deferiprone (L1) and desferrioxamine combination treatment

    Drug: Deferiprone (L1) · Drug: Desferrioxamine

Interventions

  • DrugDeferiprone (L1)

    50-100 mg/kg body weight daily

  • DrugDeferiprone (L1)

    75 mg/kg body weight daily

  • DrugDesferrioxamine

    35-50 mg/kg body weight on 2 or more days per week

06

What researchers measure

Primary outcomes

  1. Liver Iron Concentration (LIC) by SQUID

    Time frame: Yearly

  2. Long-term safety profile

    Time frame: Long-term

Secondary outcomes

  1. Serum ferritin

    Time frame: At quarterly control visits

  2. Urinary Iron Excretion (UIE)

    Time frame: At six-monthly control visits

  3. Heart iron content (optional) by MRI T2* and MRI SIR

    Time frame: Yearly

07

Study locations

13 sites
  • Cantonal Hospital, Children's Clinic
    Aarau, Aargau 5001, Switzerland
  • Cantonal Hospital
    Aarau, Aargau 5001, Switzerland
  • Cantonal Hospital Graubünden
    Chur, Graubünden 7000, Switzerland
  • Private practice
    Arzo, Ticino 6864, Switzerland
  • Private practice
    Lugano, Ticino 6900, Switzerland
  • Regional Hospital
    Lugano, Ticino 6900, Switzerland
  • Private practice
    Riva San Vitale, Ticino 6826, Switzerland
  • Private children's practice
    Brig, Wallis 3900, Switzerland
  • Private practice
    Oerlikon, Zurich 8050, Switzerland
  • Private children's practice
    Bern, 3014, Switzerland
  • Children's Hospital of Eastern Switzerland
    St. Gallen, 9006, Switzerland
  • University Children's Hospital
    Zurich, 8032, Switzerland
  • University Hospital
    Zurich, 8091, Switzerland
08

References and documents

Publications

  • Tondury P, Zimmermann A, Nielsen P, Hirt A. Liver iron and fibrosis during long-term treatment with deferiprone in Swiss thalassaemic patients. Br J Haematol. 1998 Jun;101(3):413-5. doi: 10.1046/j.1365-2141.1998.00725.x. PubMed 9633879 ↗
  • Tondury P, Kontoghiorghes GJ, Ridolfi-Luthy A, Hirt A, Hoffbrand AV, Lottenbach AM, Sonderegger T, Wagner HP. L1 (1,2-dimethyl-3-hydroxypyrid-4-one) for oral iron chelation in patients with beta-thalassaemia major. Br J Haematol. 1990 Dec;76(4):550-3. doi: 10.1111/j.1365-2141.1990.tb07915.x. PubMed 2265118 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 12, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00349453
Lead sponsor
Lipomed
Responsible party
Sponsor
First posted
Jul 7, 2006
Start date
Mar 2005
Primary completion
May 2011
Completion
May 2011
Last update
Dec 12, 2011

Study contacts

Petrign FG Töndury, MD
principal investigator
Markus Schmugge Liner, MD
principal investigator · University Children's Hospital, Zurich

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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