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).
A Study of Lorlatinib in Combination With Ramucirumab in People With Lung 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 is open to adults with extensive-stage small cell lung cancer. The purpose of this study is to find out how well people with this type of cancer tolerate taking study medicines called obrixtamig and pumitamig. Another purpose is to check whether the combination study treatment can make tumours shrink. Obrixtamig and pumitamig are being developed to help the immune system fight cancer. Participants are put into 2 groups. One group gets obrixtamig and pumitamig. The other group gets obrixtamig and pumitamig with standard chemotherapy (carboplatin and etoposide). All study treatments are given as infusions into a vein. This study does not have a fixed duration. Participants can receive obrixtamig and pumitamig for up to 2 years if they benefit from treatment and can tolerate it. Participants visit the study site regularly, with some overnight stays required. During this time, doctors regularly check for health problems that could be caused by the study treatment. They also monitor the size of the tumour(s) and take laboratory tests.
The study is for patients with advanced melanoma who are eligible for standard therapy with Pembrolizumab.
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.
About the trial
This study will test the safety of the combination of ramucirumab and lorlatinib. The researchers will test one or two different doses of lorlatinib in combination with ramucirumab to find the drug combination dose that causes few or mild side effects in participants. Once the researchers find this dose, they can test it in future participants to see if it is effective in treating their metastatic ALK-rearranged NSCLC. The researchers are also looking to see whether there are specific genes or DNA sequences associated with a response to treatment with lorlatinib and ramucirumab.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Wiek powyżej 18 lat
- •Zaawansowany lub nawracający rak płuca (nie drobnokomórkowy) potwierdzony biopsją
- •Obecność mutacji ALK wykryta w badaniu genetycznym
- •Ogólny stan zdrowia pozwalający na uczestnictwo w badaniu (skala wydolności ≥70%)
- •Prawidłowa funkcja narządów (wątroba, nerki, krew)
- •Brak aktywnego krwawienia i brak wysokiego ryzyka krwawienia
- •Wyzdrowiał z działań niepożądanych poprzednich terapii
- •Dla części pacjentów: brak wcześniejszego leczenia tego zaawansowanego raka (wcześniejsze chemioterapia dopuszczalna)
✗ Disqualifies
- •Pacjenci przyjmujący określone leki antykoagulacyjne mogą być wykluczeni w zależności od stabilności dawki
- •Pacjenci w drugiej grupie muszą wykazać brak odpowiedzi lub tolerancji na wcześniejsze leki ALK
Simplified criteria — AI translation
Trial details
- Minimum age
- 19 Years
- Last updated (source)
- August 13, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (6)
Memorial Sloan Kettering Monmouth (All Protocol Activities)
Middletown, United States
Memorial Sloan Kettering Bergen (All Protocol Activities)
Montvale, United States
Memorial Sloan Kettering Cancer Center Suffolk - Commack (All Protocol Activities)
Commack, United States
Memorial Sloan Kettering West Harrison (All Protocol Activities)
Harrison, United States
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, United States
Memorial Sloan Kettering Nassau (All Protocol Activities)
Rockville Centre, United States
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/11/2026.
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