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A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Ascending, Multidose Study To Determine Safety and Tolerability of Orally Administered LX1606 in Subjects With Symptomatic Carcinoid Syndrome Refractory to Stable-Dose Octreotide Long-Acting Release Depot Therapy

Trial Profile

A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Ascending, Multidose Study To Determine Safety and Tolerability of Orally Administered LX1606 in Subjects With Symptomatic Carcinoid Syndrome Refractory to Stable-Dose Octreotide Long-Acting Release Depot Therapy

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 02 Jan 2019

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At a glance

  • Drugs Telotristat etiprate (Primary)
  • Indications Malignant carcinoid syndrome
  • Focus Adverse reactions
  • Sponsors Lexicon Pharmaceuticals
  • Most Recent Events

    • 31 Aug 2018 Biomarkers information updated
    • 12 Sep 2017 Results of pooled analysis of 5 trials (NCT02026063, NCT02063659, NCT01677910, NCT01104415, NCT00853047) presented at the 42nd European Society for Medical Oncology Congress
    • 31 Mar 2016 Results from the qualitative interview study (n=11) published in the Clinical Therapeutics.
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