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NCT00639002 · ClinicalTrials.gov registry record · Phase 2

A Study to Determine the Effect and Safety of an Oral Janus Kinase 2 (JAK2)-Inhibitor (Ruxolitinib; INBC018424) in Patients With Multiple Myeloma

A Phase 2 study, sponsored by Incyte Corporation.

Completed
Registry status
Phase 2
Development phase
13
Enrollment target

NCT00639002: Completed Phase 2 study, sponsored by Incyte Corporation.

NCT00639002 is a Phase 2 study that has completed, run by Incyte Corporation. The registered enrollment target is 13 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00639002, a Phase 2 study, has completed, sponsored by Incyte Corporation.

COMPLETED
Registry status
Phase 2
Development phase
13 participants
Enrollment target

Study Summary

The purpose of this study was to determine clinical efficacy and safety of ruxolitinib (INCB018424), a small molecule Janus kinase 2 (JAK2)-inhibitor, in patients with refractory or relapsed multiple myeloma.

Primary Outcome

A responder is defined as a patient with a complete response (negative immunofixation on the serum and urine and disappearance of any soft tissue plasmacytomas and ≤ 5% plasma cells in bone marrow) or a partial response (≥ 50% reduction of serum M-protein and reduction in 24 h urinary M-protein by ≥ 90% or to \< 200 mg per 24 h).

Interventions

  • DRUG Ruxolitinib 25 mg
  • DRUG Dexamethasone 40 mg

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2008-03
Est. Completion 2010-07
Phase Phase 2
Incyte Corporation

239 total trials

What the finished NCT00639002 record still lists

NCT00639002 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Ruxolitinib 25 mg is the first listed.

NCT00639002 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00639002 about?

NCT00639002 is a clinical study titled "A Study to Determine the Effect and Safety of an Oral Janus Kinase 2 (JAK2)-Inhibitor (Ruxolitinib; INBC018424) in Patients With Multiple Myeloma". The purpose of this study was to determine clinical efficacy and safety of ruxolitinib (INCB018424), a small molecule Janus kinase 2 (JAK2)-inhibitor, in patients with refractory or relapsed multiple myeloma.

What is the current status of trial NCT00639002?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 13 participants. The study started on 2008-03. Estimated completion is 2010-07.

What interventions are being tested in trial NCT00639002?

The interventions under investigation include: Ruxolitinib 25 mg (DRUG), Dexamethasone 40 mg (DRUG).

Who is sponsoring clinical trial NCT00639002?

This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00639002's enrollment target sits among peer trials

13 1947th of 2000 higher than 53 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 NCT00639002, the US trial registry maintained by the National Library of Medicine. NCT00639002 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.