The study is for patients with advanced melanoma who are eligible for standard therapy with Pembrolizumab.
A First-in-human, Clinical Trial Assessing the Safety of ES2B-C001-S01 With or Without [Adjuvant] in Patients With HER2-expressing Metastatic Breast Cancer.
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
This trial is no longer recruiting — here are similar active trials
Matched by cancer type/biomarker, currently recruiting.
This study, known as LUNAR-2, aims to investigate the effectiveness and safety of using TTFields, delivered by the NovoTTF-200T device, concomitantly administered with pembrolizumab and platinum-based chemotherapy for patients with advanced non-small cell lung cancer that has spread to other parts of the body. The primary goals of the study are to assess overall survival and progression-free survival. Secondary objectives include analyzing outcomes based on the specific histology (subtype) of the lung cancer.
The goal of this randomized, double-blind, multi-regional phase 3 study of cadonilimab combined with chemotherapy versus chemotherapy in combination with or without nivolumab for the first-line treatment of participants with HER2-negative, previously untreated, unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma trial is to compare OS between cadonilimab combined with chemotherapy and chemotherapy in combination with or without nivolumab in the ITT population.
Metastatic colorectal cancer or mCRC is a cancer that starts in the parts of the large intestine (the colon or rectum) and has already spread to other parts of the body. This cancer can be hard to treat because it can behave differently from one person to another. Over time, treatments may stop working, and side effects can build up. In later treatment stages, there are only a few standard medicine options available. Because of this, studies often look at both how long people live and how treatment affects quality of life. The main aim of this study is to see how long adults in Poland with mCRC live without their cancer getting worse (progression-free survival or PFS) when they receive fruquintinib after at least two previous treatments. Fruquintinib (TAK 113) is a medicine taken by mouth that is designed to slow tumor growth. Other aim is to find out how long adults in Poland with mCRC live while being treated with fruquintinib (overall survival or OS). The study also wants to record how fruquintinib is used in routine care in adults with mCRC in Poland (for example when treatment starts, changes in doses, and how long treatment continues). Another aim is to learn about people with mCRC, such as their medical history and past treatment as well as their quality of life while they are in the study. The study will look at data already existing in the participants' medical charts.
About the trial
The trial is a first-in-human, phase I, open-label, dose-escalating trial to assess the safety and tolerability of ES2B-C001 combined with or without \[adjuvant\], in patients with human epidermal growth factor receptor 2 (HER2) expressing metastatic breast cancer.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Osoby w wieku 18 lat lub starsze.
- •Zdiagnozowany rozsiany rak piersi z obecnością białka HER2 (po co najmniej 2-3 wcześniejszych terapiach antynowotworowych).
- •Przewidywana długość życia co najmniej 3 miesiące.
- •Ogólny stan zdrowia pozwalający na normalną aktywność (stopień 0-2 w skali ECOG).
- •Dobra praca narządów wewnętrznych (serca, płuc, nerek, wątroby) i szpiku kostnego.
- •Kobiety niebędące w ciąży i stosujące skuteczną antykoncepcję lub po menopauzie; mężczyźni stosujący skuteczną antykoncepcję lub po sterylizacji.
✗ Disqualifies
- •Planowana lub niedawno zakończona (w ciągu ostatniego miesiąca) chemioterapia lub stosowanie leków wpływających na układ odpornościowy, jeśli występuje neutropenia (niski poziom białych krwinek).
- •Aktywne przerzuty do mózgu wymagające wysokich dawek sterydów w ciągu ostatnich 14 dni.
- •Uczestnictwo w innym badaniu klinicznym w ciągu ostatnich 21 dni.
- •Poważne, niekontrolowane choroby (niezwiązane z rakiem), które mogą zagrażać bezpieczeństwu pacjenta lub wpłynąć na wyniki badania.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- September 18, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (3)
Medical University of Graz
Graz, Austria
Ordensklinikum Linz GmbH Barmherzige Schwestern
Linz, Austria
Medical University Of Vienna
Vienna, Austria
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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