The study is for patients with advanced melanoma who are eligible for standard therapy with Pembrolizumab.
PAveMenT: Palbociclib and Avelumab in Metastatic AR+ Triple Negative 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
This clinical study is aiming to determine the safest doses and schedule for the combination of two drugs named palbociclib and avelumab. The study will also be investigating how effective the combination is for a subgroup of breast cancer patients whose cancer expresses the androgen receptor (AR) but not the oestrogen (hormone) or HER2 receptors. Palbociclib is a drug used in routine care for hormone-receptor (HR) positive and HER2 negative advanced breast cancer, the most common subtype of breast cancer. It is possible that the combination of palbociclib and avelumab will be a more effective cancer treatment than each drug separately, but this is unknown and this study is needed to establish the best dosage and schedule of each drug as well as how effective the combination is.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Pacjenci z nawrotowym, nieoperacyjnym zaawansowanym rakiem piersi lub rakiem z przerzutami
- •Wcześniej leczeni chemioterapią (1-2 linie); pacjenci z rakiem ER+ muszą mieć wcześniejszą hormonoterapię; pacjenci z rakiem HER2+ muszą mieć wcześniejszą terapię skierowaną na HER2
- •Mierzalne zmiany nowotworowe
- •Prawidłowe wyniki badań krwi i biochimicznych (badania w ciągu tygodnia przed rozpoczęciem)
- •Kobiety w wieku rozrodczym muszą mieć negatywny test ciąży; muszą stosować skuteczną antykoncepcję przez 2 tygodnie przed leczeniem, podczas leczenia i 1 miesiąc po zakończeniu
- •Wiek 18 lat lub więcej
- •Dobry lub bardzo dobry stan ogólny (WHO 0-1)
- •Spodziewana długość życia co najmniej 3 miesiące
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- August 21, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (9)
The Christie NHS Foundation Trust
Manchester, United Kingdom
Addenbrooke's Hospital Cambridge University Hospitals NHS Foundation Trust
Cambridge, United Kingdom
Beatson West of Scotland Cancer Centre
Glasgow, United Kingdom
Hope Clinical Trials Cancer Centre
Leicester, United Kingdom
Barts Cancer Institute
London, United Kingdom
Royal Marsden NHS Foundation Trust
London, United Kingdom
University College London Hospitals NHS Foundation Trust
London, United Kingdom
Nottingham University Hospital
Nottingham, United Kingdom
Weston Park Hospital
Sheffield, United Kingdom
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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