Study to Evaluate the Safety and Tolerability of Andecaliximab as Monotherapy and in Combination With Chemotherapy in Participants With Advanced Solid Tumors
The primary objective of the study is to determine the maximum tolerated dose of andecaliximab monotherapy and to evaluate the safety and tolerability of andecaliximab (formerly GS-5745) alone and in combination with chemotherapy. The study consists of 2 parts (Parts A and B). Participants can only qualify for and participate in 1 part. Part A is a sequential dose escalation to determine the maximum tolerated dose of andecaliximab in participants with advanced solid tumors that are refractory to or intolerant to standard therapy or for which no standard therapy exists. In Part A, participants will receive andecaliximab only. Part B is a dose expansion to obtain additional safety and tolerability data for andecaliximab in participants with advanced pancreatic adenocarcinoma, lung adenocarcinoma, lung squamous cell carcinoma, esophagogastric adenocarcinoma, colorectal cancer, or breast cancer. In Part B, participants will receive andecaliximab in combination with standard-of-care chemotherapy.
Ask AI to explain this studyKey things to know
This describes the study’s primary purpose.
Plus 9 other study approaches.
These are broad labels—not an eligibility decision.
Checked against the public recordLast updated Jun 2, 2020 · Source: ClinicalTrials.gov
Ask the study team to confirm whether enrollment is open.
Interventional
Locations may change over time.
Study sponsor
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1
- Sponsor
- Gilead Sciences
- Interventions being studied
- Drug: Andecaliximab; Drug: Gemcitabine; Drug: Nab-paclitaxel; Drug: Carboplatin; Drug: Pemetrexed; Drug: Leucovorin; Drug: Oxaliplatin; Drug: 5-FU; Drug: Bevacizumab; Drug: Irinotecan; Drug: Paclitaxel
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.
- Key
- Part A: histologically or cytologically confirmed advanced malignant solid tumor that is refractory to or intolerant of standard therapy or for which no standard therapy is available
- Part B: Pancreatic Adenocarcinoma
- Presence of histologically confirmed inoperable locally advanced or metastatic pancreatic adenocarcinoma
- Part B: NSCLC
- Stage IIIB with malignant pleural effusion/pleural seeding or stage IV histologically confirmed NSCLC
- Absence of known epidermal growth factor receptor (EGFR) mutation
- Absence of known translocation or inversion events involving the ALK gene locus (resulting in EML4-ALK fusion)
- Part B: Esophagogastric Adenocarcinoma:
- Histologically confirmed inoperable advanced gastric adenocarcinoma (including adenocarcinoma of the gastrooesophageal junction) or relapsed gastric adenocarcinoma
- Human epidermal growth factor receptor 2 (HER2)-negative tumor (primary tumor or metastatic lesion)
- Part B: First-Line Colorectal Cancer
- Histologically confirmed inoperable advanced adenocarcinoma of the colon or rectum
- Radiographically measureable disease
- No prior cytotoxic chemotherapy to treat their metastatic disease
- Part B: Second-Line Colorectal Cancer
- Histologically confirmed inoperable advanced adenocarcinoma of the colon or rectum
- Radiographically measureable disease
- Received first-line combination therapy containing oxaliplatin and fluoropyrimidine with or without bevacizumab for metastatic disease with documented evidence of disease progression during or after treatment completion
- Part B: Breast Cancer
- Histologically or cytologically confirmed metastatic breast cancer
- Radiographically measureable disease
- Previous hormonal therapy for metastatic breast cancer or cytotoxic adjuvant chemotherapy is allowed
- Treatment with weekly single-agent paclitaxel is appropriate in the opinion of the treating physician
- HER-2 negative tumor (primary tumor or metastatic lesion)
- Adequate organ function Key
- Pregnant or lactating
- Individuals with known central nervous system (CNS) metastases, unless metastases are treated and stable and the individual does not require systemic steroids
- Myocardial infarction, symptomatic congestive heart failure, unstable angina, or serious uncontrolled cardiac arrhythmia within the last 6 months
- Anti-tumor therapy within 28 days of study drug dosing; concurrent use of hormone therapy for breast or prostate cancer is permitted Note: Other protocol defined Inclusion/
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Alabama OncologyBirmingham, Alabama
- Pinnacle Oncology HematologyScottsdale, Arizona
- Comprehensive Blood and Cancer CenterBakersfield, California
- San Diego Pacific Oncology and Hematology Associates, Inc.Encinitas, California
- University of Southern California (USC)Los Angeles, California
- California Pacific Medical CenterSan Francisco, California
- UCLA Medical CenterSanta Monica, California
- Florida Cancer SpecialistsSarasota, Florida
- Parkview Research CenterFort Wayne, Indiana
- Indiana University Health Goshen Center for Cancer CareGoshen, Indiana
- Washington University School of MedicineSt Louis, Missouri
- Cornell UniversityNew York, New York
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jun 2, 2020. Always confirm current availability with the study team.