JAB-2485 Activity in Adult Patients With Advanced Solid Tumors
This study is to evaluate the safety and tolerability of JAB-2485 monotherapy in adult participants with advanced solid tumors.
Checked against the public recordLast updated Jan 9, 2026 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1 / Phase 2
- Sponsor
- Jacobio Pharmaceuticals Co., Ltd.
- Interventions being studied
- Drug: JAB-2485 (Aurora A inhibitor); Drug: JAB-2485 (Aurora A inhibitor)
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: * Must have Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 * Must be able to provide an archived tumor sample * Must have histologically or cytologically confirmed metastatic or locally advanced solid tumor * Dose Expansion phase cohorts must meet specific expression or gene mutation where indicated * Must be refractory to or become intolerant of existing therapy(ies) known to provide clinical benefit for their condition * Must have at least 1 measurable lesion per RECIST v1.1 * Must have adequate organ functions * Must be able to swallow and retain orally administered medication Exclusion Criteria: * Has central nervous system (CNS) metastases or carcinomatous meningitis, except if CNS metastases treated and no evidence of radiographic progression or hemorrhage for at least 28 days * Active infection requiring systemic treatment within 7 days * Active hepatitis B virus (HBV), hepatitis C virus (HCV), or HIV * Any severe and/or uncontrolled medical conditions * left ventricular ejection fraction (LVEF) ≤50% assessed by echocardiogram (ECHO) or multigated acquisition scan (MUGA) * QT interval using Fridericia's formula (QTcF) interval \>470 msec * Experiencing unresolved CTCAE 5.0 Grade \>1 toxicities * Clinically significant eye disorders
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Henry Ford Health SystemDetroit, Michigan
- Washington UniversitySt Louis, Missouri
- Mary Crowley Cancer ResearchDallas, Texas
- University of Utah Huntsman Cancer InstituteSalt Lake City, Utah
- Cancer Hospital Chinese Academy of Medical SciencesBeijing, Beijing Municipality
- Peking University Third HospitalBeijing, Beijing Municipality
- Jilin Cancer HospitalChangchun, Jilin
- Shandong Cancer HospitalJinan, Shandong
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jan 9, 2026. Always confirm current availability with the study team.