The purpose of this study is to compare the efficacy of zipalertinib versus placebo in participants with early stage resected non-small cell lung cancer (NSCLC) harboring uncommon epidermal growth factor receptor mutation (EGFRmt).
Nowe leczenie raka piersi potrójnie ujemnego - połączenie trzech leków
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.
The overall aim of this project is to help improve the Health Related Quality of Life (HRQOL) of metastatic breast cancer (MBC) patients. There is currently an urgent and unmet need for specific tools to aid in the evaluation of HRQOL in MBC and this project aims to address these needs by developing a comprehensive EORTC questionnaire for assessing the HRQOL of this group. The new module will be used in conjunction with EORTC QLQ-C30 and will provide better measurement of the quality of life issues experienced by women with MBC. Interviews will be conducted with patients from several centres across Europe, guiding the development process in a patient centred way.
This is a Phase III, multicenter, randomized, open-label, global study designed to evaluate the efficacy and safety of inavolisib plus fulvestrant compared with alpelisib plus fulvestrant in patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2) -negative, PIK3CA-mutated, locally advanced (LA) or metastatic breast cancer (mBC), who progressed during or after cyclin dependent kinase 4/6i (CDK4/6i)-based therapy. Enrollment for the main study is now complete.
The main purpose of this study is to evaluate the efficacy of divarasib compared with investigator's choice of immunotherapy (pembrolizumab or nivolumab) or observation in participants with resected Kirsten rat sarcoma viral oncogene homolog glycine 12 to cysteine (KRAS G12C)-positive Stage II-IIIB NSCLC, regardless of tumor programmed death-ligand 1 (PD-L1) status, who have not achieved pathologic complete response (pCR) following neoadjuvant chemoimmunotherapy.
About the trial
Badanie testuje nowy lek (Trilaciclib) podawany razem z immunoterapią i chemioterapią. Trilaciclib ma chronić zdrowe komórki krwi przed szkodą chemioterapii. Uczestniczy 50 pacjentów z nowo rozpoznanym rakiem piersi potrójnie ujemnym. Leczenie podawane przed operacją.
Who can (and can't) join
✓ Qualifies
- •Pełne zrozumienie badania i dobrowolny udział ze signed zgodą na uczestnictwo
- •Wiek od 18 do 75 lat
- •Nowo zdiagnozowany rak piersi (typ TNBC) w określonym stadium zaawansowania
- •Planowane leczenie przed operacją (chemioterapia neoadiuwantna)
- •Obecne mierzalne zmiany nowotworowe o odpowiedniej wielkości
- •Brak wcześniejszego leczenia przeciwnowotworowego
- •Dobry stan ogólny (skala ECOG 0-1)
- •Prawidłowe funkcje narządów wewnętrznych (wyniki badań krwi i biocheicznych w normie)
✗ Disqualifies
- •Rak piersi z dodatnim wynikiem receptorów hormonalnych lub HER2
- •Przerzuty nowotworu potwierdzone badaniami obrazowymi
- •Inne raki poza rakiem piersi w przeszłości lub aktualnie
- •Aktywna choroba autoimmunologiczna lub jej historia
- •Stosowanie leków immunosupresyjnych lub hormonów w dużych dawkach
- •Nawrót choroby po operacji lub wcześniejsze leczenie przeciwnowotworowe
- •Znana alergia na składniki badanego leku
- •Poważne problemy sercowe lub niewydolność serca
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Maximum age
- 75 Years
- Last updated (source)
- May 2, 2025
- Sex
- No restrictions
Therapies / drugs in trial
Locations (1)
National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
Beijing, China
Trial contact
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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