Clinical Trials Directory

Trials / Completed

CompletedNCT05494580

Pamiparib Plus Surufatinib in Patients With Platinum-resistant Ovarian Cancer

Pamiparib in Combination With Surufatinib in Patients With Platinum-resistant Ovarian Cancer Who Received Prior Poly (ADP-ribose) Polymerase (PARP) Inhibitors: a Multicenter, Single-arm, Phase Ib/II Trial

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
29 (actual)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

A number of studies suggest that the combination of PARP inhibitors and antiangiogenic agents produce synergistic activities. Pamiparib is a small molecule inhibitor selectivity for both PARP1 and PARP2. Surufatinib is a novel small-molecule inhibitor that simultaneously targets tumor angiogenesis (via Vascular Endothelial Growth Factor Receptor \[VEGFR\]1, VEGFR 2, VEGFR3 and Fibroblast Growth Factor Receptor 1 \[FGFR1\]) and immune evasion (via Colony Stimulating Factor 1 Receptor \[CSF1R\]). In this trial, we aimed to evaluate the efficacy, safety and tolerability of pamiparib in combination with surufatinib in patients with platinum-resistant ovarian cancer who received prior PARP inhibitors.

Conditions

Interventions

TypeNameDescription
DRUGPamiparibOral
DRUGSurufatinibOral

Timeline

Start date
2022-09-22
Primary completion
2024-06-20
Completion
2026-01-31
First posted
2022-08-10
Last updated
2026-03-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05494580. Inclusion in this directory is not an endorsement.