This study will evaluate the safety and tolerability of LYL797, a ROR1-targeted CAR
T-cell therapy, in patients with ROR1+ relapsed or refractory triple negative breast
cancer (TNBC), non-small cell lung cancer (NSCLC), platinum-resistant epithelial ovarian
cancer/ fallopian tube cancer/ primary peritoneal cancer (Ovarian cancer), or Endometrial
cancer. The first part of the study will determine the safe dose for the next part of the
study, and will enroll patients with TNBC, NSCLC, Ovarian or Endometrial cancer. The
second part of the study will test that dose in additional patients with TNBC, NSCLC,
Ovarian or Endometrial cancer.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05274451.
Locations matching your search criteria
United States
Texas
Houston
M D Anderson Cancer CenterStatus: Active
Name Not Available
This Phase 1, single-arm, open-label, multi-center, dose-escalation and expansion study
will evaluate the safety and tolerability of LYL797, ROR1- targeted CAR T cells, in
adults with relapsed and/or refractory ROR1+ triple negative breast cancer (TNBC),
non-small cell lung cancer (NSCLC), Ovarian cancer, or endometrial cancer. The
dose-escalation phase includes patients with TNBC, NSCLC, Ovarian, or Endometrial cancer,
and will investigate multiple dose levels to identify the recommended Phase 2 dose
(RP2D). The dose-expansion phase will enroll patients with TNBC, NSCLC, Ovarian, or
Endometrial cancer at the RP2D.
Lead OrganizationLyell Immunopharma Inc