ClinicalTrials.gov record
Recruiting Phase 3 Interventional

Phase III Trial of Anlotinib, Catequentinib in Advanced Alveolar Soft Part Sarcoma, Leiomyosarcoma, Synovial Sarcoma (APROMISS)

ClinicalTrials.gov ID: NCT03016819

Public ClinicalTrials.gov record NCT03016819. 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 May 18, 2026, 4:37 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 III Study of AL3818 (Anlotinib, Catequentinib) Hydrochloride Monotherapy in Subjects With Metastatic or Advanced Alveolar Soft Part Sarcoma, Leiomyosarcoma and Synovial Sarcoma

Study identification

NCT ID
NCT03016819
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Advenchen Laboratories, LLC
Industry
Enrollment
325 participants

Conditions and interventions

Interventions

  • AL3818 Drug
  • AL3818 or placebo Drug
  • Dacarbazine Drug
  • Digoxin (0.25mg) Drug
  • Midazolam 2 mg for CYP3A4 phenotyping Drug
  • Rosuvastatin 10 mg tablet. Drug

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
Aug 14, 2017
Primary completion
Nov 30, 2027
Completion
Nov 30, 2028
Last update posted
Feb 24, 2026

2017 – 2028

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Mayo Clinic Arizona Phoenix Arizona 85054 Completed
University of California Los Angeles Los Angeles California 90404 Completed
Sarcoma Oncology Center Santa Monica California 90403 Recruiting
Stanford Medicine Cancer Institute Stanford California 94305 Completed
University of Colorado Denver Aurora Colorado 80045 Completed
Mayo Clinic Jacksonville Jacksonville Florida 32224 Completed
University of Miami Sylvester Comprehensive Cancer Center Miami Florida 33136 Completed
Northwestern University Chicago Illinois 60611 Completed
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109 Completed
Mayo Clinic Rochester Rochester Minnesota 55905 Completed
Washington University St. Louis St Louis Missouri 63130 Completed
Columbia University Medical Center New York New York 10032 Withdrawn
Thomas Jefferson Hospital - Sidney Kimmel Cancer Center Philadelphia Pennsylvania 19107 Completed
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15219 Completed
Vanderbilt University Nashville Tennessee 37203 Completed
MD Anderson Cancer Center Houston Texas 77030 Completed
UW Medicine-Seattle Cancer Care Alliance Seattle Washington 98109 Completed

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03016819, 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 Feb 24, 2026 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03016819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →