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NCT03270007

Research of Intensive Treatment in Hormone Receptor<10% and Human Epidermal Growth Factor Receptor-2 Negative Breast Cancer Patients With Positive Lymph Node Residual Disease After Neoadjuvant Chemotherapy

Status unknown Phase 4 Last updated 28 October 2020
What this trial tests

Phase 4 trial testing Vinorelbine in Primary Breast Cancer in 304 participants. Status unknown.

Timeline
10 November 2017
Primary endpoint
30 June 2024
31 December 2024

Quick facts

Lead sponsorTao OUYANG
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment304
Start date10 November 2017
Primary completion30 June 2024
Estimated completion31 December 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Tao OUYANG — full company profile →

Who can join

Adults 18 to 66, female only, with Primary Breast Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase IV, single-center, prospective, open-label, randomized,controlled study

Publications & conference data

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

  1. Intensive treatment of triple negative breast cancer with residual positive axillary lymph node after neoadjuvant chemotherapy.
    Wang X, He Y, Li J, Wang T, et al · · 2024 · PMID 39604957 · DOI 10.1186/s12905-024-03441-0

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Other trials of Vinorelbine

Trials testing the same drug.

Other Tao OUYANG trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03270007.

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