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Indication

HER2-Positive Breast Cancer

Clinical and regulatory intelligence for HER2-Positive Breast Cancer with 9 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
9
Catalysts
0
Assets
2

Relevant assets

Exploratory →
Tucatinib →

Relevant companies

SHR-A1811 →

Recent signals(9)

CompetitiveAugust 4, 2026

RO7771950 Shows Promise Against Tucatinib in HER2-Positive Breast Cancer Trial

A clinical trial is underway to evaluate RO7771950 in combination with trastuzumab and capecitabine against tucatinib with the same regimen.

ClinicalAugust 2, 2026

Exploratory Study of SHR-A1811 in HER2-Positive Advanced Breast Cancer

The study evaluates the efficacy and safety of SHR-A1811 administered through various routes in patients with HER2-positive advanced breast cancer.

RegulatoryJuly 28, 2026

FDA Accepts Supplement for PERJETA (Pertuzumab) by Genentech

The FDA has accepted a supplemental Biologics License Application for PERJETA (pertuzumab) from Genentech.

RegulatoryJuly 26, 2026

FDA Submission Update for ONTRUZANT (BLA761100) by Samsung Bioepis

The FDA has received a supplemental application (BLA761100) for ONTRUZANT, an HER2-targeting biosimilar.

RegulatoryJuly 19, 2026

FDA Approves HERCEPTIN HYLECTA Supplement Application

The FDA has approved the supplemental application for HERCEPTIN HYLECTA, which combines trastuzumab and hyaluronidase.

RegulatoryJuly 19, 2026

FDA Approves PHESGO Supplement for Genentech's Combination Therapy

The FDA has approved a supplemental application for PHESGO, a combination of pertuzumab, trastuzumab, and hyaluronidase-zzxf.

ClinicalJuly 3, 2026

Phase 2 Study of Zanidatamab with Chemotherapy in HER2-positive Breast Cancer

A Phase 2 study is underway to evaluate the safety and efficacy of zanidatamab combined with chemotherapy in HER2-positive breast cancer.

ClinicalJune 17, 2026

Phase III Trial Compares 6 vs. 12 Months of HER2-Targeted Therapy in Breast Cancer

A phase III trial is investigating whether 6 months of HER2-targeted therapy is more effective than 12 months for HER2-positive breast cancer patients who achieved a pathologic complete response after neoadjuvant chemotherapy.

RegulatoryJune 16, 2026

Enhertu Gains FDA Approval for Two New HER2+ Early Breast Cancer Indications

Enhertu has received FDA approval for two new indications in HER2-positive early breast cancer, both before and after surgery.

Upcoming catalysts

No catalysts indexed for this entity yet.

Therapeutic areas

HER2-Positive Breast Cancer →
Oncology →

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