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OncoMatch/Clinical Trials/NCT05905887

Rivoceranib Plus Paclitaxel in Patients With Gastrointestinal Stromal Tumor

Is NCT05905887 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Rivoceranib Mesylate, Paclitaxel for gastrointestinal stromal tumors.

Phase 2RecruitingAsan Medical CenterNCT05905887Data as of Jun 2026Location: South Korea

Treatment: Rivoceranib Mesylate, PaclitaxelThe 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.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

Rivoceranib Mesylate, Paclitaxel

Cancer type

Gastrointestinal Stromal Tumor

Biomarker criteria

Required: KIT mutation

mutation in KIT or PDGFRα gene

Required: PDGFRA mutation

mutation in KIT or PDGFRα gene

Required: KIT overexpression (CD117+) (CD117(+))

CD117(+)

Required: ABCB1 overexpression (P-glycoprotein IHC score > 3) (IHC score > 3)

P-glycoprotin IHC score > 3

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≥ 20

Prior therapy

Min 3 prior lines

Must have received: tyrosine kinase inhibitor (imatinib, sunitinib, regorafenib)

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

Lab requirements

Blood counts

Neutrophil >1,500/mm3; Platelet > 100,000/mm3; Hemoglobin >8.0 g/dL

Kidney function

Creatinine <1.5 x ULN

Liver function

Total bilirubin < 1.5 x ULN; AST/ALT < 2.5 x ULN

Adequate bone marrow, hepatic, renal, and other organ functions Neutrophil >1,500/mm3 Platelet > 100,000/mm3 Hemoglobin >8.0 g/dL Total bilirubin < 1.5 x upper limit of normal (ULN) AST/ALT < 2.5 x ULN Creatinine <1.5 x ULN

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05905887 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received tyrosine kinase inhibitor.

Does this trial require KIT?

Yes, KIT mutation is a required biomarker for enrollment.

Does this trial require PDGFRA?

Yes, PDGFRA mutation is a required biomarker for enrollment.

Does this trial require KIT?

Yes, KIT overexpression (CD117+) is a required biomarker for enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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