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A Phase I/IIa, Sequential Cohort, Dose Escalation Trial to Determine the Safety, Tolerability and Maximum Tolerated Dose of AP23573 [deforolimus] When Administered Orally in Patients With Refractory or Advanced Malignancies

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A Phase I/IIa, Sequential Cohort, Dose Escalation Trial to Determine the Safety, Tolerability and Maximum Tolerated Dose of AP23573 [deforolimus] When Administered Orally in Patients With Refractory or Advanced Malignancies

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 May 2022

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At a glance

  • Drugs Ridaforolimus (Primary)
  • Indications Cancer
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors ARIAD Pharmaceuticals; Merck Sharp & Dohme Corp.

    • Most Recent Events

    • 29 May 2013 Primary endpoints added as reported by ClinicalTrials.gov.
    • 12 May 2009 Actual end date (Mar 2009) added as reported by ClinicalTrials.gov.
    • 12 May 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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