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JAB-30355 in Patients With Advanced Solid Tumors Harboring TP53 Y220C Mutation
RECRUITINGPhase 1/2Sponsored by Jacobio Pharmaceuticals Co., Ltd.
Actively Recruiting
PhasePhase 1/2
SponsorJacobio Pharmaceuticals Co., Ltd.
Started2024-07-24
Est. completion2027-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations7 sites
View on ClinicalTrials.gov →
NCT06386146
Summary
This study is to evaluate the efficacy and safety of JAB-30355 in adult participants with advanced solid tumors harboring TP53 Y220C mutation.
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: * Written informed consent. * Participant must be ≥18 years of age at the time of signing the Informed Consent Form (ICF). * ECOG performance status score of 0 or 1. * Has been treated with at least one line of systemic therapy for that tumor type and stage. * Have documentation of confirmed TP53 Y220C mutation. * At least 1 measurable lesion per RECIST v1.1. * Adequate hematological, renal and hepatic function and appropriate coagulation condition. * Able to swallow and retain orally administered medication. Exclusion Criteria: * Active brain or spinal metastases or primary CNS tumor. * Active infection requiring systemic treatment within 7 days. * Active HBV or HCV. * Any severe and/or uncontrolled medical conditions. * LVEF ≤50% assessed by ECHO or MUGA. * QTcF\>470 msec.
Conditions2
CancerSolid Tumors
Locations7 sites
Research Site
Denver, Colorado, 80218
Research site
Lake Mary, Florida, 32771
Research site
St Louis, Missouri, 63110
Research site
Canton, Ohio, 44718
Research site
Cleveland, Ohio, 44195
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Actively Recruiting
PhasePhase 1/2
SponsorJacobio Pharmaceuticals Co., Ltd.
Started2024-07-24
Est. completion2027-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations7 sites
View on ClinicalTrials.gov →
NCT06386146