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The effect of Jadenu with Exjade in reducing serum ferritin levels in patients with beta thalassemia major and intermedia

Comparison the effect deferasirox swallow form (Jadenu®) with deferasirox granule (Exjade®) in reduce of serum ferritin in patients with major and intermedia beta thalassemia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210831052350N1
Enrollment
66
Registered
2021-11-20
Start date
2021-11-15
Completion date
Unknown
Last updated
2021-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: major thalasemia. Condition 2: intermedia thalasemia. Beta thalassemia Beta thalassemia

Interventions

Intervention 1: Intervention group: The group that receives Jadenu. Jadenu is part of the drug class deferasirox . 33 people are being treated with Deferasirox (Jadenu®) for 6 months. This drug will b

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age over 2 years Patients diagnosed with thalassemia major and intermedia Having conscious satisfaction Serum ferritin above 1000 µg / mL

Exclusion criteria

Exclusion criteria: Existence of contraindications to the studied drugs (Exjade®) and (Jadenu®) Patients with GFR ?40 mL / min / 1.73 m2 Patients with stunted growth Patients at high risk for myelodysplasia syndrome (MDS) Advanced cancer Platelets below 50 x 109 / L Patients with knowledge of sensitivity to drugs of the defrazirox group Patients with liver failure Patients with gastrointestinal bleeding Patients with renal insufficiency Simultaneous use of other iron chelators

Design outcomes

Primary

MeasureTime frame
Serum ferritin. Timepoint: Sampling every two months. Method of measurement: The patient's serum is separated by centrifuge and given to an auto-analyzer.;Serum creatinine. Timepoint: Sampling every two months. Method of measurement: The patient's serum is separated by centrifuge and given to an auto-analyzer.;Serum BUN. Timepoint: Sampling every two months. Method of measurement: The patient's serum is separated by centrifuge and given to an auto-analyzer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahid Falahati

Arak University of Medical Sciences

fateme_zarei1995@yahoo.com+98 86 7723 2853

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026