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NCT00425555 · ClinicalTrials.gov registry record · Phase 2

Study of Oral LBH589 in Adult Patients With Refractory Cutaneous T-Cell Lymphoma

A Phase 2 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
139
Enrollment target

NCT00425555: Completed Phase 2 study, sponsored by Novartis Pharmaceuticals.

NCT00425555 is a Phase 2 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 139 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00425555, a Phase 2 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
139 participants
Enrollment target

Study Summary

This study will evaluate the safety and efficacy of LBH489B in adult patients with refractory Cutaneous T-Cell Lymphoma.

Primary Outcome

Skin response was primarily classified based on an assessment using mSWAT, provided there was documented evidence of stable disease or better in lymph node/viscera.The mSWAT is a tool specifically developed to evaluate the extent of skin disease in CTCL (Olsen et al 2007). Responses in the skin based on SWAT are defined as: * Complete Response (CR): no evidence of skin disease * Partial Response (PR): ≥ 50% decrease of the modified SWAT score compared with baseline * Stable Disease (SD): Neith

Interventions

  • DRUG Panobinostat

Trial Details

FieldValue
Enrollment Target 139 participants
Start Date 2007-01
Est. Completion 2013-06
Phase Phase 2
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT00425555 record still lists

NCT00425555 is an interventional study that assigns participants to a tested intervention. The registered 139 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which Panobinostat is the first listed.

NCT00425555 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00425555 about?

NCT00425555 is a clinical study titled "Study of Oral LBH589 in Adult Patients With Refractory Cutaneous T-Cell Lymphoma". This study will evaluate the safety and efficacy of LBH489B in adult patients with refractory Cutaneous T-Cell Lymphoma.

What is the current status of trial NCT00425555?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 139 participants. The study started on 2007-01. Estimated completion is 2013-06.

What interventions are being tested in trial NCT00425555?

The interventions under investigation include: Panobinostat (DRUG).

Who is sponsoring clinical trial NCT00425555?

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 NCT00425555's enrollment target sits among peer trials

139 525th of 2000 higher than 1,476 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT00425555, the US trial registry maintained by the National Library of Medicine. NCT00425555 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.