Condition: Locally Advanced or Metastatic Solid Tumors · Colorectal Cancer · Gastric Cancer · Sponsor: ArriVent BioPharma, Inc.
This is an open-label, multi-center, phase I study to evaluate the safety, tolerability, efficacy, and pharmacokinetics of MRG007 (ARR-217) in patients with unresectable locally advanced or metastatic solid tumors.
This description comes directly from the study's public registry record.
Clinical Trials · (888) 622-2827 · ClinicalTrials.gov@ArriVent.com
Always discuss trial participation with your own doctor first.
| ULCA | Los Angeles, California, United States | Recruiting |
| UCSF | San Francisco, California, United States | Recruiting |
| University of Colorado | Aurora, Colorado, United States | Recruiting |
| Sarah Cannon Research Institute | Denver, Colorado, United States | Recruiting |
| Sarah Cannon Research Institute | Sarasota, Florida, United States | Recruiting |
| Sarah Cannon Research Institute | Nashville, Tennessee, United States | Recruiting |
| MD Anderson Cancer Center | Houston, Texas, United States | Recruiting |
| NEXT Dallas | Irving, Texas, United States | Recruiting |
| NEXT Virginia | Fairfax, Virginia, United States | Recruiting |
| Fred Hutchinson Cancer Center | Seattle, Washington, United States | Recruiting |
| Peking University Cancer Hospital | Beijing, Beijing Municipality, China | Recruiting |
| Beijing Gobroad Hospital | Beijing, Beijing Municipality, China | Recruiting |
+ 9 more locations — full list on the registry record.
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07066657