The study is for patients with advanced melanoma who are eligible for standard therapy with Pembrolizumab.
A Trial of HRS-1358 Tablets in Metastatic or Local Advanced 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 study is being conducted to evaluate the safety and tolerability of HRS-1358 monotherapy or combination with Dalpiciclib Isethionate Tablets in patients with metastatic or locally advanced breast cancer in order to estimate the Dose-Limiting Toxicity (DLT), Maximum Tolerated Dose (MTD) and select the Recommended Phase 2 Dose (RP2D).
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Rak piersi w zaawansowanym stadium lub z przerzutami, potwierdzony badaniami.
- •Kobiety po menopauzie lub kobiety w wieku przed/okołomenopauzalnym, które stosują leczenie hamujące funkcje jajników.
- •Przynajmniej jedna linia leczenia hormonalnego w stadium zaawansowanym lub z przerzutami.
- •Ogólny stan zdrowia pozwalający na codzienne funkcjonowanie (punktacja 0-1 w skali ECOG).
- •Odpowiednie wyniki badań krwi i narządów wskazujące na dobrą funkcję organizmu.
- •Zdolność do zrozumienia badania i dobrowolna zgoda na udział poprzez podpisanie formularza świadomej zgody.
✗ Disqualifies
- •Jeśli lekarze uznają, że pacjent nie jest odpowiedni do leczenia hormonalnego.
- •Aktywne przerzuty do mózgu, które nie są pod kontrolą lub powodują objawy.
- •Wcześniejsze poważne choroby serca lub naczyń mózgowych.
- •Stan zdrowia lub inne czynniki, które mogą wpływać na wchłanianie lub metabolizm leków.
- •Aktywne choroby autoimmunologiczne, historia niedoborów odporności (w tym pozytywny wynik testu na HIV).
- •Przyjmowanie podobnych leków w przeszłości.
- •Znana alergia na składniki leku HRS-1358.
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Maximum age
- 75 Years
- Last updated (source)
- March 17, 2025
- Sex
- Female only
Therapies / drugs in trial
Locations (1)
Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Beijing, China
Trial contact
Xia Zhang
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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