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A Phase II Study of Combination Oral CC-5013 Lenalidomide (Revlimid™), Oral Sunitinib (Sutent™) and Low Dose Oral Metronomic Cyclophosphamide for the Treatment of Stage IV Ocular Melanoma

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00482911
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:36:38.215840+00:00
Published At
2012-11-14T00:00:00+00:00
Record Updated At
2017-03-27
Results Posted At
2012-11-14
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Intraocular Melanoma", "Malignant Conjunctival Neoplasm"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2017-03-27"
protocolSection.identificationModule.nctId
"NCT00482911"
protocolSection.identificationModule.officialTitle
"A Phase II Study of Combination Oral CC-5013 Lenalidomide (Revlimid\u2122), Oral Sunitinib (Sutent\u2122) and Low Dose Oral Metronomic Cyclophosphamide for the Treatment of Stage IV Ocular Melanoma"
protocolSection.statusModule.overallStatus
"TERMINATED"
protocolSection.designModule.phases
["PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2012-11-14"

Study condition terms

  • Intraocular Melanoma (protocolSection.conditionsModule.conditions)
  • Malignant Conjunctival Neoplasm (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.