Advanced or Metastatic Breast Cancer

3

Review clinical trials related to Advanced or Metastatic Breast Cancer. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study of AND019 in Women With ER Positive HER2 Negative Advanced or Metastatic Breast Cancer

This is a first in human dose escalation and expansion study to evaluate the safety, tolerability, pharmacokinetic (PK), pharmacodynamic (PD) activity, and preliminary anti-tumor activity of AND019 in postmenopausal women with advanced or metastatic estrogen receptor (ER)-positive (human epidermal growth factor receptor 2 \[HER2\]-negative) breast cancer.

Participants needed: 61
Trial details
Phase: Phase 1Age: 18+Biological sex: FemaleType: InterventionalSponsor: Kind Pharmaceuticals LLCUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Postmenopausal women defined as NCCN guideline at the time of informed consent. [+7]

Previous treatment with any SERDs. [+19]

Status: Recruiting

Evaluating the Addition of Elacestrant (Oral SERD) to Olaparib (PARP-inhibitor) in Patients With Advanced/Metastatic HR+/HER2- Breast Cancer

Trial design: Phase II, prospective, multi-center, randomized, open label, parallel group study in patients with HR-positive, HER2-negative locally advanced or metastatic breast cancer with gBRCA1/2 mutation, with 2:1 randomization into Arm A (olaparib + elacestrant) or arm B (olaparib). Treatment in either arm will be given until disease progression, unacceptable toxicity, withdrawal of patient´s consent to study participation, or end of study. Trial population: Patients with HR-positive, HER2-negative locally advanced or metastatic breast cancer with gBRCA1/2 mutation, with an indication for standard-of-care PARP inhibitor therapy and planned treatment with olaparib, an ECOG performance status of 0-2 and life expectancy of \> 6 months, with normal bone marrow and kidney functions and no active or newly diagnosed central nervous system (CNS) metastases or symptomatic metastatic visceral disease at risk of life-threatening complications. Interventions: Patients randomized to Arm A will receive 600 mg olaparib daily and 400 mg elacestrant daily, while patients randomized to Arm B will receive 600 mg olaparib daily. Blood tests (hematology, biochemistry) will be performed at the beginning of every cycle, and imaging for tumor assessment (chest and abdominopelvic imaging) as well as QoL assessments will be performed every three months and in case of suspicion of progression/end of study.

Participants needed: 176
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: GBG Forschungs GmbHUpdated: Dec 1, 2025Locations: 36
Eligibility criteria

Written informed consent prior to beginning specific protocol procedures, includ... [+10]

Known hypersensitivity reaction to one of the compounds, excipients, or substanc... [+25]

Status: Not yet recruiting

The Efficacy of Oral Cryotherapy in Preventing TROP2-ADC-Induced Oral Mucositis in Patients With Advanced Breast Cancer

The incidence of oral mucositis associated with TROP2-ADC therapy in patients with advanced breast cancer is notably high. Identifying effective preventive and therapeutic strategies is essential for enhancing patient quality of life and optimizing treatment outcomes. Oral cryotherapy has been demonstrated to be efficacious in mitigating oral mucositis induced by radiotherapy and chemotherapy. Consequently, this study seeks to investigate the potential preventive efficacy of oral cryotherapy on TROP2-ADC-induced oral mucositis in patients with advanced breast cancer

Participants needed: 124
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Henan Cancer HospitalUpdated: Apr 18, 2025Locations: 1
Eligibility criteria

Participants voluntarily enrolled in the study, signed the informed consent form... [+10]

Prior TROP2-targeted treatment was administered. [+3]