A Phase II Clinical Study of Surufatinib Combined With Sintilimab in the Treatment of Advanced Gastric Cancer

NCT05235906 | Unknown Phase 2

• 1 other identifier: HMPL-012-SPRING-G104
• Study Type: interventional
• Target: 61
• Locations: 1 country
• Sites: 1

Brief Summary

The efficacy and safety of the use of Surufatinib in combination with Sintilimab.

Conditions

Gastric Adenocarcinoma

Outcome Measures

Primary Outcomes (1)

• Objective response rate (ORR)

  Objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumours (RECIST) version. 1.1, and immune-related (ir) RECIST

  up to 12 months

Secondary Outcomes (3)

• Disease control rate (DCR)

  up to 12 months

• Progression-free survival (PFS)

  up to 12 months

• Overall survival (OS)

  up to 24 months

Study Arms (1)

Surufatinib + Sintilimab

EXPERIMENTAL

Drug: Surufatinib+Sintilimab

Interventions

Surufatinib+Sintilimab DRUG

Surufatinib at a dose of 250mg Qd, with humanized anti-PD-1 monoclonal antibody Sintilimab injected intravenously 200mg per 3 weeks until disease progresses or unacceptable tolerability occurs.

Surufatinib + Sintilimab

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients must have the ability to understand and voluntarily sign informed consent;
• Age: 18-75 years old;
• Patients have histologically or cytologically confirmed advanced or recurrent gastric or gastroesophageal junction adenocarcinoma;
• NO previous therapy for advanced/metastatic disease of GC/GEJ and CPS≥1;
• Patients have measurable disease as defined by RECIST 1.1 as determined by investigator;
• Eastern Cooperative Group (ECOG) performance status of 0 to 2;
• Has adequate organ function;
• Expected survival period ≥ 3 months;
• Patients who not received a blood transfusion within 7 days of registration;
• Patients have recovered adverse events associated with chemotherapy, radiation and surgical operation as pretreatment to Grade 1 or lower with CTCAE v5.0 excluding stable symptoms (eg alopecia, peripheral sensory neuropathy, skin hyperpigmentation, dysgeusia etc.).
• Patients capable of taking oral medication;
• Female of childbearing potential who are negative in a pregnancy test within 7 days before enrollment. Both male and female patients should agree to use an adequate method of contraception (total abstinence, an intrauterine device or hormone releasing system, an contraceptive implant and an oral contraceptive) starting with the first dose of study therapy through 6 months after the last dose of study therapy. Duration will be determined when the subject is assigned to treatment.

You may not qualify if:

• Patients who received prior anticancer treatment within 14 days (or 5 times the half-life time, whichever is shorter) or any investigational agent within 28 days prior to the first dose of study drugs.
• Patients who have undergone surgical treatment and radiotherapy with in 2 weeks before enrollment.
• Patients with a history of prior treatment with Lenvatinib or any anti-programmed death 1 (anti-PD-1), anti-programmed ligand death 1 (anti-PD-L1), or anti-programmed ligand death 2 (anti-PD-L2 agent).
• Patients with symptomatic brain metastasis.
• Patients with hypertension that is difficult to control (systolic blood pressure ≥150 mmHg and diastolic blood pressure ≥100 mmHg) despite treatment with several hypotensive agents.
• Those who have received live vaccination within 4 weeks before the start of treatment.
• Patients with active hepatitis.
• Patients with a history of human immunodeficiency virus (HIV).
• Patients were judged unsuitable as subject of this trial by investigator.

Sponsors & Collaborators

• Sun Yat-sen University: lead

Study Sites (1)

Cancer center of SunYat-sen University

Guangzhou, Guangdong, 510060, China

RECRUITING

Central Study Contacts

Dongsheng Zhang, PhD

CONTACT

86-2087343795; zhangdsh@sysucc.org.cn

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: February 9, 2022
• First Posted: February 11, 2022
• Study Start: August 16, 2022
• Primary Completion: March 31, 2024
• Study Completion: March 31, 2025
• Last Updated: August 9, 2023

Record last verified: 2023-08

Locations

CN (1)