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.
Immunologic Targeting of ESR1 Receptor for Hormone Receptor 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.
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.
The goal of this clinical trial is to determine the most effective dose of EIK1005 that a person can take safely. Additionally, this study will test how well EIK1005 is tolerated alone and in combination with pembrolizumab in treating patients with advanced cancer.
The purpose of this study is to evaluate the safety and efficacy of Navlimetostat (BMS-986504) monotherapy or in combination with Izalontamab Brengitecan in participants with advanced or metastatic Non-small Cell Lung Cancer (NSCLC) with homozygous MTAP deletion or MTAP loss after progression on prior therapies.
About the trial
This is a pilot study to determine feasibility and safety of the combination of Dendritic Cell (DC1) vaccines and elacestrant in patients with hormone positive HER2 negative metastatic breast cancer.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Rak piersi z przerzutami, który reaguje na hormony (ER lub PR dodatni) i nie ma nadekspresji HER2.
- •Potwierdzona mutacja ESR1 w guzie lub we krwi.
- •Pacjentka była wcześniej leczona terapią hormonalną i lekiem z grupy inhibitorów CDK4/6 w leczeniu rozsianego raka.
- •Choroba jest widoczna na obrazach (na przykład na tomografii komputerowej lub rezonansie magnetycznym) i możliwa do zmierzenia lub oceny.
- •Ogólny stan zdrowia pacjentki pozwala na udział w badaniu (stan sprawności ECOG 0-2).
- •Pacjentka jest pełnoletnia (ukończone 18 lat).
- •Pacjentka rozumie zasady badania i zgadza się na udział.
- •Wystarczająca wydolność narządów (np. prawidłowa liczba białych krwinek, płytek krwi, wątroby i nerek).
✗ Disqualifies
- •Ciąża lub karmienie piersią.
- •Stosowanie niektórych innych leków przeciwnowotworowych lub terapeutycznych, które mogą wpływać na wyniki badania.
- •Aktywna lub niedawno przebyta choroba autoimmunologiczna, która wymaga leczenia.
- •Wcześniejsze leczenie leczeniem, które miało na celu aktywację układu odpornościowego w sposób, który mógłby zakłócić działanie szczepionki.
- •Ważne problemy kardiologiczne, które nie są pod kontrolą.
- •Znaczne problemy z wątrobą lub nerkami, które nie są ujęte w kryteriach włączenia.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- August 18, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (1)
Moffitt Cancer Center
Tampa, United States
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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