A Study to Evaluate the Safety and Tolerability of AB680 in Participants With Gastrointestinal Malignancies (NCT04104672)
A Phase 1 Study to Evaluate the Safety and Tolerability of AB680 Combination Therapy in Participants With Gastrointestinal Malignancies
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a Phase 1, open-label, dose-escalation, and dose-expansion, with a gated randomization portion, study to evaluate the safety, tolerability, pharmacokinetic, pharmacodynamic and clinical activity of AB680 in combination with zimberelimab (AB122), nab-paclitaxel and gemcitabine in participants with advanced pancreatic cancer.
Who can join: Review the eligibility criteria below.
Location: Research Site โ Santa Monica, California
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (9 Sites)
- Research Site โ Santa Monica, California
- Research Site โ St Louis, Missouri
- Research Site โ New York, New York
- Research Site โ New York, New York
- Research Site โ Philadelphia, Pennsylvania
- Research Site โ Pittsburgh, Pennsylvania
- Research Site โ Houston, Texas
- Research Site โ San Antonio, Texas
- Research Site โ Madison, Wisconsin
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.