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Clinical Trial Details

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Brief Title A Study of LY2510924 and Durvalumab in Participants With Solid Tumors
Official Title A Phase 1a/1b Study of CXCR4 Peptide Antagonist (LY2510924) Administered in Combination With the Anti-PD-L1 Antibody, Durvalumab (MEDI4736), in Advanced Refractory Solid Tumors
Principal Investigator Kindler, Hedy
Brief Summary The main purpose of this study is to evaluate the safety and tolerability of chemokine (C-X-C Motif) receptor 4 (CXCR4) peptide antagonist LY2510924 and durvalumab for phase 1a and 1b in participants with advanced refractory solid tumors.
Gender Both
Ages 18 Years
Enrollment 45
Accepts Healthy Volunteers No
Lead Sponsor Eli Lilly and CompanyIndustry
Collaborator AstraZenecaIndustry
Study Design Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Study Phase Phase 1
Study Type Interventional
Contact Name Colin Weekes
Contact Phone 1-855-702-8222 (adult trials) or 1-773-702-6808 (pediatric trials)
Condition Solid Tumor
Detail for Health Professional (on clinicaltrials.gov)
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