Condition: Locally Advanced / Metastatic Solid Tumors · Sponsor: Crescent Biopharma, Inc.
The purpose of this study is to determine the safety and tolerability of monotherapy CR-001 and identify the maximum tolerated dose (MTD), and/or optimal biologic dose and Recommended Phase 2 Dose(s) (RP2D) in participants with locally advanced or metastatic solid tumors.
This description comes directly from the study's public registry record.
Crescent Clinical Trials · 617-430-5595 · clinicaltrials@crescentbiopharma.com
Always discuss trial participation with your own doctor first.
| Clinical Study Site | Birmingham, Alabama, United States | Recruiting |
| Clinical Study Site | Los Angeles, California, United States | Recruiting |
| Clinical Study Site | Denver, Colorado, United States | Recruiting |
| Clinical Study Site | Orlando, Florida, United States | Recruiting |
| Clinical Study Site | Sarasota, Florida, United States | Recruiting |
| Clinical Study Site | Detroit, Michigan, United States | Recruiting |
| Clinical Study Site | Grand Rapids, Michigan, United States | Recruiting |
| Clinical Study Site | New York, New York, United States | Recruiting |
| Clinical Study Site | Columbus, Ohio, United States | Recruiting |
| Clinical Study Site | Pittsburgh, Pennsylvania, United States | Recruiting |
| Clinical Study Site | Nashville, Tennessee, United States | Recruiting |
| Clinical Study Site | Dallas, Texas, United States | Recruiting |
+ 13 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07335497