About this trial

This study is to evaluate the safety and tolerability of JAB-2485 monotherapy in adult participants with advanced solid tumors.

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • JAB-2485 (Aurora A inhibitor)
  • JAB-2485 (Aurora A inhibitor)

Treatment groups

102 Participants
are divided into 2 treatment groups

Locations

8
China
Cancer Hospital Chinese Academy of Medical Sciences100101, BeijingBeijing Municipality, China
Peking University Third Hospital100101, BeijingBeijing Municipality, China
Jilin Cancer Hospital130000, ChangchunJilin, China
Shandong Cancer Hospital250117, JinanShandong, China

Sponsors and collaborators

Jacobio Pharmaceuticals Co., Ltd.

Lead sponsor