Rivoceranib Plus Paclitaxel in Patients With Gastrointestinal Stromal Tumor

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age20+
SponsorAsan Medical Center

About this trial

The purpose of this study is to evaluate the efficacy and safety of rivoceranib and paclitaxel combination therapy in patients with P-glycoprotein overexpressing GIST who failed standard treatment with imatinib, sunitinib, and regorafenib.

Eligibility criteria

Qualifiers

Age 20 years or older, at the time of acquisition of informed consent

Histologically confirmed metastatic and/or advanced GIST with CD117(+), DOG-1(+), or mutation in KIT or PDGFRα gene

P-glycoprotin IHC score > 3 (Tumor tissue with disease progression after regorafenib treatment)

Failed (progressed and/or intolerable) after prior treatments for GIST, including at least imatinib and sunitinib, regorafenib.

Disqualifiers

Women of child-bearing potential who are pregnant or breast feeding

Women or men who are not willing to use effective contraception entering the study period or until at least 3 months after the last study drug administration.

If any of the following applies within ≤ 6 months prior to starting study enrollment : Myocardial Infarction, severe instable angina, coronary/peripheral bypass, NYHA class III or IV congestive heart failure, stroke or transient ischemic attack, treatment required severe arrhythmia.

Uncontrolled infection

Trial design

Treatments tested in this trial

  • Rivoceranib Mesylate, Paclitaxel

Treatment groups

48 Participants
are divided into 1 treatment group

Sponsors and collaborators