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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
Interventions1
Locations7 sites
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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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