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NCT00434239

A Pilot Study of the Combination of Lenalidomide (Revlimid®) With Two Different Dose Levels of Short Term Administration of Recombinant Human Stem Cell Factor (rhSCF; Ancestim) for Myelodysplasia.

Status unknown EARLY_PHASE1 Last updated 8 January 2013
What this trial tests

EARLY_PHASE1 trial testing Lenalidomide + Ancestim in Myelodysplasia in 25 participants. Status unknown.

Timeline
1 February 2007
Primary endpoint
1 May 2011
1 May 2014

Quick facts

Lead sponsorPeter MacCallum Cancer Centre, Australia
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment25
Start date1 February 2007
Primary completion1 May 2011
Estimated completion1 May 2014
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Peter MacCallum Cancer Centre, Australia — full company profile →

Who can join

18 and older, any sex, with Myelodysplasia. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This study is mainly assessing the safety of Revlimid in combination with Ancestim (recombinant human stem cell factor) in patients with symptomatic myelodysplasia. Of those two compounds, Revlimid has been shown to be an active drug in myelodysplasia. Clinical responses will also be assessed.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Myelodysplasia

Currently open trials in the same condition.

Other Peter MacCallum Cancer Centre, Australia trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00434239.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing