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NCT03684967

Study of Fruquintinib (HMPL-013) in High Risk Patients With Advanced NSCLC

Withdrawn Phase 2 Last updated 19 November 2019
What this trial tests

Phase 2 trial testing Fruquintinib in Lung Cancer. Withdrawn.

Timeline
8 May 2018
Primary endpoint
6 September 2019
6 September 2019

Quick facts

Lead sponsorHutchison Medipharma Limited
PhasePhase 2
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date8 May 2018
Primary completion6 September 2019
Estimated completion6 September 2019
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Hutchison Medipharma Limited — full company profile →

Who can join

18 and older, any sex, with Lung Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Fruquintinib administered at 4 mg once daily in cycle 1 and 5 mg once daily in followed cycles (3 weeks on and 1 week off, 4 weeks as 1 cycle) was well tolerated and demonstrated encouraging preliminary clinical antitumor activity in patients with advanced NSCLC in phase II study. This study is aimed to evaluate the efficacy and safety of Fruquintinib in the treatment of high risk patients with advanced NSCLC who is \> 75 years, or Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) = 2, or without systemic chemotherapy, or with at least three lines systemic chemotherapies.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. AIMedGraph: a comprehensive multi-relational knowledge graph for precision medicine.
    Quan X, Cai W, Xi C, Wang C, et al · · 2023 · cited 7× · PMID 36856726 · DOI 10.1093/database/baad006

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Other trials of Fruquintinib

Trials testing the same drug.

Other recruiting trials for Lung Cancer

Currently open trials in the same condition.

Other Hutchison Medipharma Limited trials

Trials by the same sponsor.

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Data sources for this page

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