The study is for patients with advanced melanoma who are eligible for standard therapy with Pembrolizumab.
Phase 1/1b/2 Study of Oral PMD-026 in Patients With 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 purpose of this study is to test the safety and tolerability of PMD-026 in patients with metastatic breast cancer. PMD-026 is a targeted oral agent designed to kill tumor cells in metastatic breast cancer.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Rak piersi z przerzutami, który nie reaguje na leczenie celowane w konkretne zmiany genetyczne (RSK2-dodatni).
- •Rak piersi z grupy hormonozależnych, ale negatywnych dla HER2.
- •Rak piersi, w którym nie stwierdzono specyficznej mutacji genetycznej (ESR1 wild type).
- •Choroba zaawansowana lub z przerzutami, której nie można leczyć operacyjnie ani radioterapią w celu całkowitego wyleczenia.
- •Pacjentka musi być odpowiednim kandydatem do hormonoterapii.
- •Wcześniejsze leczenie hormonoterapią raka piersi z przerzutami lub nawrót po leczeniu uzupełniającym.
- •Przynajmniej jedna widoczna zmiana nowotworowa na badaniach obrazowych.
- •Progresja choroby lub brak poprawy po leczeniu inhibitorem CDK4/6 w połączeniu z hormonoterapią.
✗ Disqualifies
- •Wcześniejsze leczenie chemioterapią.
- •Obecność specyficznych mutacji genetycznych (ESR1 mutations).
- •Zbyt krótki czas od zakończenia wcześniejszego leczenia eksperymentalnego.
- •Stan zagrażający życiu z powodu zmian w narządach wewnętrznych.
- •Przerzuty do mózgu, chyba że są odpowiednio leczone i pacjentka jest stabilna neurologicznie.
- •Wcześniejsze problemy z płynem mózgowo-rdzeniowym (leptomeningeal metastases).
- •Aktywne infekcje wymagające leczenia ogólnoustrojowego.
- •Znana infekcja wirusem zapalenia wątroby typu B lub C.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- July 16, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (10)
Banner MD Anderson Cancer Center
Gilbert, United States
City of Hope
Duarte, United States
City of Hope Orange County, Lennar
Irvine, United States
University of California, Los Angeles (UCLA)
Los Angeles, United States
Moffitt Cancer Center
Tampa, United States
City of Hope Chicago
Zion, United States
Massachusetts General Hospital Cancer Center
Boston, United States
Profound Research
Farmington Hills, United States
Ohio State University
Columbus, United States
South Texas Accelerated Research Therapeutics
San Antonio, United States
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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