First in Human Study of TORL-1-23 in Participants With Advanced Cancer

This first-in-human study will evaluate the safety, tolerability, pharmacokinetics, and antitumor activity of TORL-1-23 in patients with advanced cancer

Trial Details

NCT ID
NCT05103683
Phase
PHASE1
Sponsor
TORL Biotherapeutics, LLC
Status
RECRUITING
Cancer Type
Uterine Cancer
Interventions
  • TORL-1-23
Locations (sample)
  • Fullerton, California, United States|33.87029,-117.92534
  • Los Angeles, California, United States|34.05223,-118.24368
  • Lexington, Kentucky, United States|37.98869,-84.47772
  • Minneapolis, Minnesota, United States|44.97997,-93.26384
  • Rochester, Minnesota, United States|44.02163,-92.4699

Key Eligibility Criteria

  • Advanced solid tumor
  • Measurable disease, per RECIST v1.1
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  • Adequate organ function

For full eligibility, visit ClinicalTrials.gov.

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