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Terminated Phase 1Phase 2 Interventional Results available

Surufatinib in Combination With Tislelizumab in Subjects With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT04579757

Public ClinicalTrials.gov record NCT04579757. 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 Oct 26, 2026, 7:26 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

An Open-Label Phase Ib/II Study of Surufatinib in Combination With Tislelizumab in Subjects With Advanced Solid Tumors

Brief summary

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

This open-label, phase Ib/II study of surufatinib in combination with tislelizumab will evaluate the safety, tolerability, PK and efficacy in patients with advanced solid tumors. The study consists of 2 parts - dose finding (Part 1) and dose expansion (Part 2).

Study identification

NCT ID
NCT04579757
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Hutchmed
Industry
Enrollment
87 participants

Conditions and interventions

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 5, 2021 (Actual)
Primary completion
Apr 30, 2024 (Actual)
Completion
Aug 27, 2024 (Actual)
Last update posted
May 8, 2025

2021 – 2024

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Arizona Oncology Associated, PC-HOPE Tucson Arizona 85711 —
City of Hope Duarte California 91010 —
Rocky Mountain Cancer Centers Midtown Denver Colorado 80218 —
Johns Hopkins University - Sibley Memorial Hospital Washington D.C. District of Columbia 20016 —
Emory University - Winship Cancer Institute Atlanta Georgia 30322 —
Holden Comprehensive Cancer Center, University of Iowa Iowa City Iowa 52242 —
Memorial Sloan Kettering Cancer Center New York New York 10021 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
University of Pennsylvania, Perelman Center for Advanced Medicine Philadelphia Pennsylvania 19104 —
Prisma Health - Upstate (ITOR) Greenville South Carolina 29605 —
Sarah Cannon Nashville Tennessee 37203 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
Mary Crowley Cancer Research Dallas Texas 75230 —
Texas Oncology - Baylor Charles A. Sammons Cancer Center Dallas Texas 75246 —
Texas Oncology, P.A. Fort Worth Texas 76104 —
The University of Texas MD Anderson Cancer Center Houston Texas 77079 —
Texas Oncology, P.A. Tyler Texas 75702 —
Virginia Cancer Specialists, PC Fairfax Virginia 22031 —

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 NCT04579757, 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 May 8, 2025 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04579757 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →