Study of Sacituzumab Govitecan-hziy (IMMU-132) in Adults With Epithelial Cancer
Purpose
The primary objective in Phase I is to evaluate the safety and tolerability of sacituzumab govitecan-hziy (SG) as a single agent administered in 21-day treatment cycles in previously treated participants with advanced epithelial cancer. In Phase II, the primary objective is to evaluate the safety and efficacy of sacituzumab govitecan-hziy administered in 21-day treatment cycles at a dose selected in Phase I. Tumor types in the study will include: cervical, colorectal, endometrial, ovarian, esophageal, gastric adenocarcinoma, glioblastoma multiforme, head and neck cancers- squamous cell, hepatocellular, prostate, non-small-cell lung cancer, pancreatic, renal cell, small-cell lung cancer, non-triple negative breast cancer (non-TNBC), triple-negative breast cancer (TNBC) and metastatic urothelial cancer (mUC).
Conditions
- Gastric Adenocarcinoma
- Esophageal Cancer
- Hepatocellular Carcinoma
- Non-small Cell Lung Cancer
- Small Cell Lung Cancer
- Ovarian Epithelial Cancer
- Carcinoma Breast Stage IV
- Hormone-refractory Prostate Cancer
- Head and Neck Cancers- Squamous Cell
- Renal Cell Cancer
- Urinary Bladder Neoplasms
- Cervical Cancer
- Endometrial Cancer
- Glioblastoma Multiforme
- Triple Negative Breast Cancer
- Pancreatic Cancer
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Individuals able to understand and give written informed consent. - Histologically or cytologically confirmed epithelial cancer of one of the following types: - Gastric adenocarcinoma (GC) - Esophageal cancer (EC) - Hepatocellular carcinoma (HCC) - Non-small-cell lung cancer (NSCLC) - Small-cell lung cancer (SCLC) - Epithelial ovarian cancer (EOC) - Cervical Cancer - Endometrial Cancer - Triple-negative breast cancer (TNBC) - Non-triple-negative breast cancer - Papillary thyroid cancer (excludes follicular, medullary, Hurthle cell, and anaplastic thyroid cancer) - Glioblastoma multiforme (GBM) - Hormone-refractory prostate cancer (HRPC) - Head and neck cancers- squamous cell (SCCHN) - Renal cell cancer (clear cell) (RCC) - Urothelial cancer - Stage IV (metastatic) disease (except for individuals with GBM). - Refractory to or relapsed after at least one prior standard therapeutic regimen - Adequate performance status (ECOG 0 or 1) - Expected survival ≥ 6 months. - Measurable disease by CT or MRI. - At least 2 weeks beyond treatment (chemotherapy, investigational drugs including small molecular inhibitors, immunotherapy and/or radiation therapy) or major surgery and recovered from all acute toxicities to Grade 1 or less (except alopecia). - At least 2 weeks beyond high dose systemic corticosteroids (however, low dose corticosteroids < 20 mg prednisone or equivalent daily are permitted). - Adequate hematology without ongoing transfusional support (hemoglobin > 9 g/dL, absolute neutrophil count (ANC) > 1,500 per mm^3, platelets > 100,000 per mm^3). - Adequate renal and hepatic function (creatinine ≤ 2.0 x institutional upper limit of normal (IULN), bilirubin ≤ 1.5 IULN, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3.0 x IULN or 5 x IULN if know liver metastases). - Otherwise, all toxicity at study entry ≤ Grade 1.
Exclusion Criteria
- Women who are pregnant or lactating. - Women of childbearing potential and fertile men unwilling to use effective contraception during study until conclusion of 12-week post-treatment evaluation period. - Individuals with Gilbert's disease. - Individuals with brain metastases can be enrolled only if treated, non-progressive brain metastases and off high-dose steroids (> 20 mg prednisone or equivalent) for at least 4 weeks. - Presence of bulky disease (defined as any single mass > 7 cm in its greatest dimension). Individuals with a mass over 7 cm, but otherwise eligible, may be considered for enrollment after discussion and approval with the medical monitor. - Individuals with active ≥ grade 2 anorexia, nausea or vomiting, and/or signs of intestinal obstruction. - Individuals with non-melanoma skin cancer or carcinoma in situ of the cervix are eligible, while individuals with other prior malignancies must have had at least a 3-year disease-free interval. - Individuals known to be HIV positive, hepatitis B positive, or hepatitis C positive. - Known history of unstable angina, MI, or CHF present within 6 months or clinically significant cardiac arrhythmia (other than stable atrial fibrillation) requiring anti-arrhythmia therapy. - Known history of clinically significant active COPD, or other moderate-to-severe chronic respiratory illness present within 6 months. - Prior history of clinically significant bleeding, intestinal obstruction, or GI perforation within 6 months of initiation of study treatment. - Infection requiring intravenous antibiotic use within 1 week. - History of an anaphylactic reaction to irinotecan or ≥ Grade 3 GI toxicity to prior irinotecan, - Other concurrent medical or psychiatric conditions that, in the Investigator's opinion, may be likely to confound study interpretation or prevent completion of study procedures and follow-up examinations.
Study Design
- Phase
- Phase 1/Phase 2
- Study Type
- Interventional
- Allocation
- Non-Randomized
- Intervention Model
- Sequential Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Sacituzumab Govitecan-hziy (SG) 8 mg/kg |
Participants will receive sacituzumab govitecan-hziy (SG) 8 mg/kg of body weight via intravenous (IV) infusion on Days 1 and 8 of a 21-day treatment cycle until disease progression or unacceptable toxicity. |
|
|
Experimental SG 10 mg/kg |
Participants will receive SG 10 mg/kg of body weight via intravenous (IV) infusion on Days 1 and 8 of a 21-day treatment cycle until disease progression or unacceptable toxicity. |
|
|
Experimental SG 12 mg/kg |
Participants will receive SG 12 mg/kg of body weight via intravenous (IV) infusion on Days 1 and 8 of a 21-day treatment cycle until disease progression or unacceptable toxicity. |
|
|
Experimental SG 18 mg/kg |
Participants will receive SG 18 mg/kg of body weight via intravenous (IV) infusion on Days 1 and 8 of a 21-day treatment cycle until disease progression or unacceptable toxicity. |
|
More Details
- Status
- Completed
- Sponsor
- Gilead Sciences
Study Contact
Detailed Description
The outcome measures are planned to be assessed up to the data cutoff date. Following the data cutoff date, the participants will either stay on the study and will be followed for safety data collection or rolled into another Gilead-sponsored study. Therefore, only safety data will be collected after the data cutoff date.