An official website of the United States government
A Study of ZL-1310 Versus Investigator's Choice of Therapy in Participants With Relapsed Small Cell Lung Cancer (DLLEVATE)
Trial Status: active
The purpose of this study is to evaluate the efficacy and safety of ZL-1310 compared to
Investigator's Choice Therapy in participants with relapsed Small Cell Lung Cancer.
Inclusion Criteria
Age >/= 18 years, or considered an adult by local regulations, at the time of consent
Signed informed consent
Histologically or cytologically confirmed SCLC. Received 1L platinum-based systemic therapy and had documented disease progression during or after the most recent systemic therapy. Or received 2L tarlatamab is allowed.
Measurable disease according to RECIST v1.1 as assessed by the investigator.
Participants with a history of treated and stable or untreated and asymptomatic CNS metastases based on criteria per protocol.
Adequate organ and marrow function
Eastern Cooperative Group (ECOG) performance status of 0 or 1
Life expectancy of at least 3 months
Participants must be willing to undergo a tumor biopsy or provide archived tumor tissue sample at Screening
Participants must be willing and able to comply with protocol for the duration of the study
Exclusion Criteria
Received more than one line of systemic therapy for Extensive-Stage SCLC.
Received any prior ADC with topoisomerase 1 inhibitor payload
Participants with another known malignancy with exceptions defined in the protocol.
History or suspected ILD/pneumonitis based on criteria per protocol
Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses.
Receipt of anti-cancer treatment known to treat cancers within 3 weeks before the first dose of study treatment.
Prior radiotherapy before study treatment based on criteria per protocol
Unresolved toxicity of Grade >/= 2 from previous anti-cancer treatment, except for alopecia and skin pigmentation.
Known infection or active infection defined in the protocol.
Clinically significant active cardiovascular disease or history of arterial thromboembolic event within 6 months prior to the first dose of study treatment based on criteria per protocol.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07218146.
Locations matching your search criteria
United States
Connecticut
New Haven
Yale University
Status: Active
Name Not Available
North Haven
Yale-New Haven Hospital North Haven Medical Center
Status: Active
Name Not Available
Trumbull
Smilow Cancer Hospital Care Center-Trumbull
Status: Active
Name Not Available
Iowa
Iowa City
University of Iowa/Holden Comprehensive Cancer Center