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.
Real-World Clinical Experience of Patients With Metastatic Castration-Resistant Prostate Cancer Treated With Olaparib + Abiraterone (PROceed)
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
PROceed is a multisite, prospective, observational study that describes the real-world use and clinical experience of mCRPC patients treated with the combination of olaparib and abiraterone in the mCRPC setting. Clinical outcomes will be assessed in patients who are either NHA-naive or NHA-exposed prior to initiating olaparib + abiraterone treatment, respectively. Patient demographic and clinical characteristics, as well as treatment received prior and subsequent to olaparib + abiraterone, will also be described. The study plans to enroll patients for a maximum of 2 years and follow up patients from initiation of olaparib until 1 year post last patient in.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Wiek co najmniej 18 lat
- •Potwierdzony rozpoznaniem raka gruczołu krokowego (adenokarcinoma)
- •Zaawansowany rak prostaty oporny na leczenie hormonalne
- •Rozpoczęcie leczenia kombinacją olaparibu i abirateronu
- •Gotowość do podpisania zgody na uczestnictwo w badaniu
✗ Disqualifies
- •Uczestnictwo w innym badaniu klinicznym nad lekami na raka prostaty w ciągu ostatnich 30 dni przed rozpoczęciem olaparibu
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- September 16, 2026
- Sex
- Male only
Locations (36)
Research Site
Aschaffenburg, Germany
Research Site
Augsburg, Germany
Research Site
Bergisch Gladbach, Germany
Research Site
Berlin, Germany
Research Site
Bonn, Germany
Research Site
Cologne, Germany
Research Site
Dresden, Germany
Research Site
Duisburg, Germany
Research Site
Eisenach, Germany
Research Site
Eisleben Lutherstadt, Germany
Research Site
Frankfurt, Germany
Research Site
Greifswald, Germany
Research Site
Halle, Germany
Research Site
Hamburg, Germany
Research Site
Hanover, Germany
Research Site
Heidelberg, Germany
Research Site
Heinsberg, Germany
Research Site
Herzogenaurach, Germany
Research Site
Leipzig, Germany
Research Site
Lichtenfels, Germany
Research Site
Lübeck, Germany
Research Site
Lüneburg, Germany
Research Site
Magdeburg, Germany
Research Site
Marburg, Germany
Research Site
Mülheim, Germany
Research Site
Münster, Germany
Research Site
Nuremberg, Germany
Research Site
Rüsselsheim am Main, Germany
Research Site
Saalfeld, Germany
Research Site
Speyer, Germany
Research Site
Trier, Germany
Research Site
Tübingen, Germany
Research Site
Westerstede, Germany
Research Site
Wetzlar, Germany
Research Site
Winnenden, Germany
Research Site
Wuppertal, Germany
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/18/2026.
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