Telotristat ethyl

(Xermelo®)

Xermelo®

Drug updated on 10/30/2024

Dosage FormTablet (oral: 250 mg)
Drug ClassTryptophan hydroxylase Inhibitors
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of carcinoid syndrome diarrhea in combination with somatostatin analog (SSA) therapy in adults inadequately controlled by SSA therapy.

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Summary
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  • This summary is based on the review of one systematic review(s)/meta-analysis(es). [1]
  • The study does not provide specific effectiveness data for telotristat ethyl (Xermelo) in treating carcinoid syndrome (CS) but highlights economic and quality-of-life impacts for patients with neuroendocrine tumors and CS.
  • Patients with uncontrolled CS symptoms experienced 23-92% higher costs compared to those with controlled symptoms, with ambulatory/outpatient services being the main cost driver.
  • Quality of life (QOL) is notably impaired in patients with CS, although the study does not detail how different population types or subgroups were affected by telotristat ethyl.
  • There is no safety information available in the reviewed studies.
  • There is no population types or subgroups information available in the reviewed studies.

Product Monograph / Prescribing Information

Document TitleYearSource
Xermelo (telotristat ethyl) Prescribing Information.2022Lexicon Pharmaceuticals, Inc., The Woodlands, TX

Systematic Reviews / Meta-Analyses