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STATUS Recruiting

Study of Sacituzumab Govitecan in Patients With Solid Tumor

LAST UPDATED

April 12, 2024

Clinicaltrials.gov ID

NCT05119907

OVERVIEW

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

PROTOCOL SUMMARY

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

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Participation Requirements

Calendar

Age

18 Years +

Condition

Sex

All

Healthy Icon

Healthy Volunteers

No

Study Details

Medical Condition

Solid Tumor

Gender

N/A

Date

October 2021 - December 2025

Study Type

Interventional

Study Phase

Phase 2

Product

Sacituzumab Govitecan-hziy

Eligibility Information

Inclusion

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.
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Exclusion

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.
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Locations

Locations (15)
Recruiting

Beijing Obstetrics and Gynecology Hospital, Capital Medical University

Beijing, China, 100006

Recruiting

Chinese Academy of Medical Sciences Cancer Hospital

Beijing, China, 100021

Recruiting

Beijing Cancer Hospital

Beijing, China, 100142

Recruiting

The First Hospital of Jilin University

Changchun, China, 130021

Recruiting

Fujian Cancer Hospital

Fuzhou, China, 350014

Study Complete

Fujian Cancer Hospital

Fuzhou, China, 350014

Recruiting

The Sixth Affiliated Hospital, Sun Yat-Sen University

Guangzhou, China, 510655

Recruiting

The First Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, China, 310003

Recruiting

Zhejiang Cancer Hospital

Hangzhou, China, 310022

Recruiting

Harbin Medical University Cancer Hospital

Harbin, China, 150076

Recruiting

Anhui Provincial Hospital

Hefei, China, 230001

Recruiting

Jiangsu Province Hospital

Nanjing, China, 210029

Recruiting

Union Hospital Tongji Medical College Huazhong University of Science and Technology

Wuhan, China, 43006

Study Complete

Union Hospital Tongji Medical College Huazhong University of Science and Technology

Wuhan, China, 43006

Recruiting

Henan Cancer Hospital

Zhengzhou, China, 450000