Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00395629 · ClinicalTrials.gov registry record · Phase 1

Safety and Efficacy of Deferasirox (ICL670) in Patients With Iron Overload Resulting From Hereditary Hemochromatosis

A Phase 1 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
49
Enrollment target

NCT00395629: Completed Phase 1 study, sponsored by Novartis Pharmaceuticals.

NCT00395629 is a Phase 1 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 49 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00395629, a Phase 1 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
49 participants
Enrollment target

Study Summary

Brief Summary: This study was designed to explore a safe dose and characterize the preliminary safety and efficacy of ICL670 in adult patients with previously documented history of homozygous C282Y.

Primary Outcome

Mean absolute change in serum ferritin from baseline to the end of the extension study.

Interventions

  • DRUG Deferasirox (ICL670)

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2006-08
Est. Completion 2009-03
Phase Phase 1
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT00395629 record still lists

NCT00395629 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower).

The record links to 0 conditions, and to 1 intervention - of which Deferasirox (ICL670) is the first listed.

NCT00395629 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00395629 about?

NCT00395629 is a clinical study titled "Safety and Efficacy of Deferasirox (ICL670) in Patients With Iron Overload Resulting From Hereditary Hemochromatosis". Brief Summary: This study was designed to explore a safe dose and characterize the preliminary safety and efficacy of ICL670 in adult patients with previously documented history of homozygous C282Y.

What is the current status of trial NCT00395629?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2006-08. Estimated completion is 2009-03.

What interventions are being tested in trial NCT00395629?

The interventions under investigation include: Deferasirox (ICL670) (DRUG).

Who is sponsoring clinical trial NCT00395629?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00395629's enrollment target sits among peer trials

49 1017th of 2000 higher than 976 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02704858 · 49 participants · Phase 1

    Safety and Efficacy Study in Recurrent or Progressive Grade III or IV IDH1 Mutated Glioma

  • NCT03516708 · 49 participants · Phase 1

    Epacadostat (INCB024360) Added to Preoperative Chemoradiation in Patients With Locally Advanced Rectal Cancer

  • NCT03692429 · 49 participants · Phase 1

    alloSHRINK - Standard cHemotherapy Regimen and Immunotherapy With Allogeneic NKG2D-based CYAD-101 Chimeric Antigen Receptor T-cells

  • NCT04329494 · 49 participants · Phase 1

    PIPAC for the Treatment of Peritoneal Carcinomatosis in Patients With Ovarian, Uterine, Appendiceal, Colorectal, or Gastric Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00395629, the US trial registry maintained by the National Library of Medicine. NCT00395629 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.