CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 265 enrolled
Drug / intervention
fruquintinib+sintilimab +2 moredrug
Likely dose
fruquintinib+sintilimab 5 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05522231
NCT05522231Phase 3Active

A Phase II/III Clinical Study to Evaluate the Efficacy and Safety of Fruquintinib in Combination With Sintilimab Versus Axitinib or Everolimus as Second-line Treatment for Locally Advanced or Metastatic Renal Cell Carcinoma (FRUSICA-2)

Hutchmed·interventional·Posted Aug 30, 2022·Updated Jan 3, 2025

In Brief

A Phase 3 clinical trial evaluating fruquintinib+sintilimab, axitinib / everolimus, and 1 other intervention for Advanced Renal Cell Carcinoma. Active but no longer recruiting, targeting 265 participants across 48 sites.

Detailed Summary

The study consists of two parts, the first part is a randomized, open-label, active-controlled study to evaluate the efficacy and safety of fruquintinib in combination with sintilimab versus axitinib or everolimus monotherapy as second-line treatment for locally advanced or metastatic renal cell carcinoma. The second part is a fruquintinib monotherapy factorial cohort study to evaluate the efficacy and safety of fruquintinib monotherapy as for second-line treatment of locally advanced or metastatic renal cell carcinoma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3ActiveOverdue
2023202420252026
First PostedAug 30, 2022
Enrollment StartOct 27, 2022
Primary CompletionJan 1, 2025
Study CompletionMar 1, 2025
TodayJul 1, 2026
Enrollment to primary: 2.2 yearsPosted 3.8 years ago

Interventions

fruquintinib+sintilimabdrug

fruquintinib, 5 mg, QD, PO, 2 weeks on/1 week off, 3 weeks/cycle; sintilimab, 200 mg, IV infusion, Q3W, 3 weeks/cycle.

axitinib / everolimusdrug

axitinib, 5 mg, twice daily (BID), PO, 3 weeks/cycle, dose escalation will be at the investigator 's discretion based on clinical; everolimus, 10 mg, QD, PO, 3 weeks/cycle.

fruquintinibdrug

fruquintinib, 5 mg, QD, PO, 3 weeks on/ 1 week off, 4 weeks/cycle.