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Terminated Phase 2 Interventional Results available

A Safety and Efficacy Study of XERMELO® + First-line Chemotherapy in Patients With Advanced Biliary Tract Cancer

ClinicalTrials.gov ID: NCT03790111

Public ClinicalTrials.gov record NCT03790111. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 5:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter, Open-label, Safety and Efficacy Study of XERMELO® (Telotristat Ethyl) Plus First-line Chemotherapy in Patients With Locally Advanced, Unresectable, Recurrent or Metastatic Biliary Tract Cancer (BTC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A Phase 2, multicenter, open-label, 2-stage study to assess the safety, tolerability, and efficacy of XERMELO in combination with first-line (1L) therapy (cisplatin \[cis\] plus gemcitabine \[gem\])

Study identification

NCT ID
NCT03790111
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
TerSera Therapeutics LLC
Industry
Enrollment
53 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 12, 2019
Primary completion
Jan 12, 2022
Completion
Jan 12, 2022
Last update posted
Apr 18, 2023

2019 – 2022

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
TerSera Investigational Site Gilbert Arizona 85234
TerSera Investigational Site Fullerton California 92835
TerSera Investigational Site Gainesville Florida 32610
TerSera Investigational Site Tampa Florida 33612
TerSera Investigational Site Chicago Illinois 60637
TerSera Investigational Site Westwood Kansas 66205
TerSera Investigational Site Lexington Kentucky 40536
TerSera Investigational Site Boston Massachusetts 02118
TerSera Investigational Site Grand Rapids Michigan 49503
TerSera Investigational Site Buffalo New York 14263
TerSera Investigational Site Lake Success New York 11042
TerSera Investigational Site Charlotte North Carolina 28204
TerSera Investigational Site Oklahoma City Oklahoma 73104
TerSera Investigational Site San Antonio Texas 78229

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03790111, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 18, 2023 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03790111 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →