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fruquintinib

Generic: FRUQUINTINIB·Brand: FRUZAQLA, Fruzaqla

fruquintinib: 9 clinical trials tracked.

fruquintinib evidence translation

What we can confirm

9 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about fruquintinib, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 5 study sponsors
Clinical Trials (9)

A Phase II, Open-label, Non-comparative, Randomized Study of Second-line Doublet Chemotherapy (FOLFOX or FOLFIRI) Plus Fruquintinib Versus Doublet Chemotherapy (FOLFOX or FOLFIRI) Plus Bevacizumab in Metastatic Colorectal Cancer

NCT07150403·Phase 2·IGMS
Not yet recruiting

Primary endpoint: Disease Control Rate (DCR)

InterventionalRandomizedopen74 targetStarted 2025-12Completion 2028-1045 sites · FranceFederation Francophone de Cancerologie Digestive

A Phase II Study Investigating Fruquintinib Plus FOLFIRI as Second-Line Treatment for Participants With Metastatic Colorectal Cancer (mCRC)

NCT07011576·Phase 2·IGMS
Recruiting

Primary endpoint: Progression-Free Survival (PFS) rate at 6 months

Interventionalopen60 targetStarted 2025-09Completion 2027-0611 sites · United StatesSCRI Development Innovations, LLC

A Phase 2 Trial of Fruquintinib and Tislelizumab in ctDNA-defined Minimal Residual Disease in Colorectal Cancer After Completion of Adjuvant Chemotherapy

NCT07136077·Phase 2
Recruiting

Primary endpoint: Safety and adverse events (AEs)

Interventionalopen20 targetStarted 2025-09Completion 2028-041 site · United StatesM.D. Anderson Cancer Center

A Single Arm Phase 4 Trial to Evaluate the Safety and Efficacy of Oral Fruquintinib in the Treatment of Refractory Metastatic Colorectal Cancer in Patients From Minority Populations Underrepresented in Prior Fruquintinib Studies

NCT06562543·Phase 4·TAK
Recruiting

Primary endpoint: Number of Participants with Treatment Emergent Grade 3 and Grade 4 Hypertension

Interventionalopen78 targetStarted 2025-01Completion 2027-1045 sites · Puerto Rico, United StatesTakeda

A Phase 1 Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ASKG915 in Patients With Selected Advanced Solid Tumors

NCT05867420·Phase 1/Phase 2
Recruiting

Primary endpoint: Dose limiting toxicities (DLTs)

Interventionalopen594 targetStarted 2023-08Completion 2028-064 sites · China, United StatesAskGene Pharma, Inc.

A Phase 1-2 Dose-escalation and Expansion Study of ST316 in Subjects With Selected Advanced Unresectable and Metastatic Solid Tumors

NCT05848739·Phase 1·IGMS
Recruiting

Primary endpoint: Number of participants with treatment-related adverse events as assessed by CTCAE v5.0

Interventionalopen130 targetStarted 2023-06Completion 2027-0511 sites · United StatesSapience Therapeutics

An Open-Label, Phase 1b/2 Study to Evaluate the Safety and Efficacy of Fruquintinib in Combination With Tislelizumab in Patients With Advanced Solid Tumors

NCT04577963·Phase 1/Phase 2·HMDCF
Terminated

Primary endpoint: Part 1: Number of Patients With Dose-Limiting Toxicities (DLTs)

Interventionalopen52 targetStarted 2021-08Completion 2024-0616 sites · United StatesHutchmed

A Global Multicenter Randomized Placebo-Controlled Phase 3 Trial To Compare The Efficacy And Safety Of Fruquintinib Plus Best Supportive Care To Placebo Plus Best Supportive Care In Patients With Refractory Metastatic Colorectal Cancer

NCT04322539·Phase 3·HCM
Completed

Primary endpoint: Overall Survival (OS)

InterventionalRandomizedquadruple691 enrolledStarted 2020-08Completion 2024-0450 sites · Australia, United StatesHutchison Medipharma Limited

An Open-Label, Multicenter, Long-Term Extension Study of Treatment With Tislelizumab, Pamiparib, and Other Investigational Agents in Patients With Advanced Malignancies

NCT04164199·Phase 3·ONC
Completed

Primary endpoint: Number of Participants with Immune-Mediated Adverse Events, Serious Adverse Events, and Adverse Events Grade 3 or Higher

Interventionalopen404 enrolledStarted 2019-12Completion 2026-0550 sites · Australia, China, United StatesBeOne Medicines