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Clinical Trial Detail

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NCT ID NCT05821777
Title A Study to Evaluate Safety, Tolerability and Preliminary Activity of LB101 in Participants With Advanced Solid Tumors
Recruitment Active, not recruiting
Gender both
Phase Phase Ib/II
Variant Requirements Yes
Sponsors Centessa Pharmaceuticals (UK) Limited
Indications
Therapies
Age Groups: adult | senior
Covered Countries USA | FRA

Facility Status City State Zip Country Details
Sarah Cannon Research Institute at HealthONE. Denver Colorado 80218 United States Details
Sarah Cannon Research Institute at Florida Cancer Specialists Sarasota Florida 34232 United States Details
Memorial Sloan Kettering Cancer Center New York New York 10065 United States Details
Sarah Cannon Research Institute at Tennessee Oncology Nashville Nashville Tennessee 37203 United States Details
NEXT Oncology - Dallas Irving Texas 75039 United States Details
NEXT Oncology San Antonio Texas 78229 United States Details
Institut Gustave Roussy Villejuif 94805 France Details
*Shaded cells indicate that there was no data available from clinicaltrials.gov for the field