Study of Sacituzumab Govitecan in Patients With Solid Tumor

Solid Tumor Clinical Trial

Official title:

A Phase II Open Label Study of Sacituzumab Govitecan in Patients With Solid Tumor

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05119907
• Other study ID #: EVER-132-003
• Secondary ID: CTR20210912
• Status: Recruiting
• Phase: Phase 2
• Start date: October 12, 2021
• Est. completion date: December 2025

Study information

• Verified date: April 2024
• Source: Gilead Sciences
• Contact: Gilead Clinical Study Information Center
• Phone: 1-833-445-3230 (GILEAD-0)
• Email: GileadClinicalTrials[@]gilead.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this study is to learn more about the study drug, sacituzumab govitecan-hziy, in participants with solid tumor.

Description:

Only Cohort C: Cervical Cancer (CC) is enrolling at this time.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 300
• Est. completion date: December 2025
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Key Inclusion Criteria:

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
• Histologically or cytologically-documented, incurable locally advanced or metastatic

solid tumor of one of the following types:

• Cohort A: oesophageal squamous-cell carcinoma that was refractory or intolerant to fluoropyrimidine-based, platinum-based, and taxane-based chemotherapy.
• Cohort B: gastric adenocarcinoma that was refractory or intolerant to fluoropyrimidine-based, platinum-based, and taxane-based chemotherapy.
• Cohort C: cervical cancer that was refractory or intolerant to platinum-based and taxane-based chemotherapy.
• Cohort D: biliary tract cancer, including intrahepatic cholangiocarcinoma (IHCC), extrahepatic cholangiocarcinoma (EHCC), and gallbladder cancer (GBC), with exception of ampullary carcinoma, progressed during or after first line platinum-based or fluoropyrimidine-based chemotherapy.
• Cohort E: lung adenocarcinoma with activating genomic alterations (EGFR/ ALK/ ROS1/ BRAF/ MET/ RET) that was refractory or intolerant to targeted tyrosine kinase inhibitors (TKIs) and had not received platinum-based chemotherapy for unresectable local advanced or metastatic disease, and no suitable or willing to receive platinum-based chemotherapy.
• Measurable disease by computed tomography (CT) or magnetic resonance imaging (MRI) in accordance with RECIST v 1.1, bone-only disease is not measurable and is not permitted.
• Availability of archival tumor tissue or newly acquired biopsy (unstaining tumor slides, recommended from metastasis sites).
• Adequate bone marrow, hepatic and renal function.
• Recovered from all prior treatment-related toxicities to Grade 1 or less by NCI-CTCAE v 5.0 (except alopecia or peripheral neuropathy that may be Grade 2 or less).
• Individuals must have completed all prior cancer treatments at least 2 weeks prior to the first dose including chemotherapy , radiotherapy and major surgery. Prior antibody treatment for cancer must have been completed at least 3 weeks prior to the first dose.
• Individuals must have at least a 3-month life expectancy.

Key Exclusion Criteria:

• Previous treatment with topoisomerase I inhibitors as a free form or as other formulations.
• Previous treatment with Trop-2 targeted therapy.
• Individuals with a history of or current central nervous system (CNS) metastases.
• Known additional malignancy within 3 years prior to enrollment with the exception of curatively treated basal cell carcinoma of the skin, squamous cell carcinoma of the skin and/or curatively resected in situ cancers.
• Individuals known to be human immunodeficiency virus positive.
• Individuals with active hepatitis B virus (HBV), or hepatitis C virus (HCV) infection. Hepatitis B core antibody (HBcAb) testing is required and if positive, then HBV DNA testing will be performed and if positive the individual will be excluded.
• Known history of unstable angina, myocardial infarction (MI), or chronic heart failure present within 6 months of first dose or clinically significant cardiac arrhythmia (other than stable atrial fibrillation) requiring anti-arrhythmia therapy or left ventricular ejection fraction < 50%.
• Known history of clinically significant active chronic obstructive pulmonary disease, or other moderate-to-severe chronic respiratory illness present within 6 months of the first dose.
• Infection requiring systematic antibiotic use within 1 week of the first dose.
• Individuals with active chronic inflammatory bowel disease (ulcerative colitis, Crohn disease) and individuals with a history of bowel obstruction or gastrointestinal (GI) perforation.
• High dose systemic corticosteroids within 2 weeks prior to the first dose (however, low dose corticosteroids = 10 mg prednisone or equivalent daily are permitted provided the dose is stable for 4 weeks).
• Individuals who have received a live vaccine within 30 days of first dose. Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Related Conditions & MeSH terms

• Neoplasms
• Solid Tumor

Intervention

Drug:
• Sacituzumab Govitecan-hziy
Administered intravenously

Locations

Country	Name	City	State
China	Beijing Cancer Hospital	Beijing
China	Beijing Obstetrics and Gynecology Hospital, Capital Medical University	Beijing
China	Chinese Academy of Medical Sciences Cancer Hospital	Beijing
China	The First Hospital of Jilin University	Changchun
China	Fujian Cancer Hospital	Fuzhou
China	Fujian Cancer Hospital	Fuzhou
China	The Sixth Affiliated Hospital, Sun Yat-Sen University	Guangzhou
China	The First Affiliated Hospital, Zhejiang University School of Medicine	Hangzhou
China	Zhejiang Cancer Hospital	Hangzhou
China	Harbin Medical University Cancer Hospital	Harbin
China	Anhui Provincial Hospital	Hefei
China	Jiangsu Province Hospital	Nanjing
China	Union Hospital Tongji Medical College Huazhong University of Science and Technology	Wuhan
China	Union Hospital Tongji Medical College Huazhong University of Science and Technology	Wuhan
China	Henan Cancer Hospital	Zhengzhou

Sponsors (1)

Lead Sponsor	Collaborator
Gilead Sciences

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v 1.1) By Investigator Assessment	ORR is defined as the proportion of participants who achieve a complete response (CR) or partial response (PR).	Up to 4 years
Secondary	Duration of Response (DOR)	DOR is defined as the time from the first documentation of CR or PR to the earlier of the first documentation of definitive progressive disease (PD) or death from any cause (whichever comes first).	Up to 4 years
Secondary	Disease Control Rate (DCR)	DCR is defined as the proportion of participants who achieve CR, PR, or stable disease (SD).	Up to 4 years
Secondary	Progression-free Survival (PFS)	PFS is defined as the time from the first dose of sacituzumab govitecan-hziy (SG) until the date of objective PD, or death (whichever comes first).	Up to 4 years
Secondary	Overall Survival (OS)	OS is defined as the time from the first dose of SG until death due to any cause.	Up to 4 years
Secondary	Percentage of Participants Experiencing Adverse Events (AEs) According to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0		First dose date up to 4 years plus 30 days
Secondary	Percentage of Participants Experiencing Serious Adverse Events (SAEs) According to NCI CTCAE Version 5.0		First dose date up to 4 years plus 30 days
Secondary	Pharmacokinetic (PK) Parameter: Cmax of Sacituzumab Govitecan-hziy and Free SN-38	Cmax is defined as the maximum observed concentration of drug.	Up to 4 years
Secondary	PK Parameter: Tmax of Sacituzumab Govitecan-hziy and Free SN-38	Tmax is defined as the time (observed time point) of Cmax.	Up to 4 years
Secondary	PK Parameter: Ctrough of Sacituzumab Govitecan-hziy and Free SN-38	Ctrough is defined as the concentration of drug at the end of the dosing interval.	Up to 4 years
Secondary	Percentage of Participants Who Developed Anti-Drug Antibodies (ADAs) Against SG		Up to 4 years

External Links

•   Gilead Clinical Trials Website