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NCT06711055: TaxHER

Taxane Combined Targeted Therapy for Low-risk HER2 Positive and Lymph Node Negative Breast Cancer

Recruiting now Last updated 2 December 2024
What this trial tests

trial in HER2-positive Breast Cancer in 285 participants. Currently enrolling.

Timeline
1 January 2015
Primary endpoint
31 December 2031
31 December 2031

Quick facts

Lead sponsorShu Wang
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment285
Start date1 January 2015
Primary completion31 December 2031
Estimated completion31 December 2031
Sites1 location across China

Conditions studied

Sponsor

Shu Wang

Who can join

Eligibility, female only, with HER2-positive Breast Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Human epidermal growth factor receptor 2 (HER2) positive breast cancer is a molecular subtype with high malignancy and high risk of recurrence and metastasis. HER2 targeted drugs has greatly improved the prognosis and survival of such patients. At present, for HER2 positive breast cancer patients with negative lymph nodes, chemotherapy drugs combined with trastuzumab is the current standard treatment scheme, and in most cases, chemotherapy uses a combination of two drugs, while the main beneficiaries of the trastuzumab and paltuzumab are concentrated in the group of patients with positive lymph nodes. Can targeted therapy be used to reduce the progression of chemotherapy and further achieve efficient and low toxicity strategies. To explore the efficacy and safety of adjuvant therapy of taxane chemotherapy combined with trastuzumab targeting therapy for low-risk HER2 positive and lymph node negative early breast cancer.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for HER2-positive Breast Cancer

Currently open trials in the same condition.

Other Shu Wang trials

Trials by the same sponsor.

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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/NCT06711055.

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