This is a single-arm, open-label, multicenter, Phase 1 study evaluating the safety and efficacy of CTX130 in subjects with relapsed or refractory renal cell carcinoma.
The study may enroll approximately 107subjects in total.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
19
CTX130 CD70-directed T-cell immunotherapy comprised of allogeneic T cells genetically modified ex vivo using CRISPR-Cas9 gene editing components.
Research Site 2
Duarte, California, United States
Research Site 5
Hartford, Connecticut, United States
Research Site 4
Houston, Texas, United States
Research Site 3
Salt Lake City, Utah, United States
Part A (dose escalation): Incidence of adverse events
Adverse events defined as dose-limiting toxicities
Time frame: From CTX130 infusion up to 28 days post-infusion
Part B (cohort expansion): Objective response rate
Objective response rate per Response Evaluation Criteria In Solid Tumors (RECIST) v1.1
Time frame: From CTX130 infusion up to 60 months post-infusion]
Progression Free Survival
Time frame: From date of CTX130 infusion until date of disease progression or death due to any cause, assessed up to 60 months
Overall Survival
Time frame: From date of CTX130 until date of death due to any cause, assessed up to 60 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Site 1
Melbourne, Victoria, Australia
Research Site 6
Toronto, Ontario, Canada
Research Site 7
Amsterdam, North Holland, Netherlands