Study on Datopotamab Deruxtecan and Osimertinib for Patients with Advanced Non-Small Cell Lung Cancer After Osimertinib Treatment

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What is this study about?

This clinical trial is focused on studying a type of lung cancer known as non-small cell lung cancer (NSCLC), specifically in patients whose cancer has progressed after treatment with a medication called osimertinib. The study aims to evaluate the effectiveness and safety of a new treatment called Datopotamab deruxtecan, both on its own and in combination with osimertinib, compared to traditional chemotherapy treatments. Chemotherapy in this study includes drugs like carboplatin, pemetrexed, and cisplatin, which are commonly used to treat cancer by killing or stopping the growth of cancer cells.

Participants in the study will be randomly assigned to receive either Datopotamab deruxtecan alone, Datopotamab deruxtecan with osimertinib, or a combination of the chemotherapy drugs. The study will monitor how long patients live without their cancer getting worse, which is known as progression-free survival. It will also look at overall survival, which is the length of time patients live after starting the study, regardless of whether their cancer progresses. The study will also assess how the treatments affect symptoms and quality of life.

The trial is designed to provide important information about whether Datopotamab deruxtecan, alone or with osimertinib, is more effective than the standard chemotherapy options for patients with advanced NSCLC. This information could help improve treatment options for people with this type of lung cancer in the future.

1 joining the study

Upon joining the study, participants will be randomly assigned to one of the treatment groups. This means that the treatment you receive will be determined by chance, like flipping a coin. This process ensures that the study results are fair and reliable.

2 treatment with Dato-DXd

If assigned to the Dato-DXd group, you will receive an intravenous infusion of Datopotamab deruxtecan. This is a medication given directly into your vein through a needle. The frequency and duration of this treatment will be explained by the study team.

3 treatment with Dato-DXd and Osimertinib

If assigned to the combination group, you will receive both Datopotamab deruxtecan through an intravenous infusion and Osimertinib in the form of oral tablets. The tablets are taken by mouth, and the study team will provide instructions on how often and how long to take them.

4 treatment with platinum-based chemotherapy

If assigned to the chemotherapy group, you will receive a combination of Carboplatin or Cisplatin and Pemetrexed. These medications are administered through intravenous infusion. The study team will inform you about the schedule and duration of these treatments.

5 monitoring and follow-up

Throughout the study, regular monitoring will be conducted to assess your health and the effects of the treatment. This includes physical exams, blood tests, and imaging studies. The study team will provide details on the frequency and type of monitoring required.

6 completion of the study

At the end of the study, a final assessment will be conducted to evaluate your overall health and the outcomes of the treatment. The study team will discuss the results with you and provide any necessary follow-up care or recommendations.

Who Can Join the Study?

  • Must have a confirmed diagnosis of non-squamous non-small cell lung cancer (NSCLC).
  • Must have documented information about specific EGFR mutations (changes in the epidermal growth factor receptor gene) that are known to respond to certain treatments.
  • Must have shown disease progression outside the brain after previous treatment with osimertinib (a type of cancer medication) as the most recent treatment.
  • Must have had two or fewer previous treatments with EGFR tyrosine kinase inhibitors (TKIs), with osimertinib being the only allowed third-generation EGFR TKI.
  • Must have at least one tumor that has not been treated with radiation and can be accurately measured at the start of the study.
  • Must have a performance status of 0 or 1, which means being fully active or restricted in physically strenuous activity but able to carry out light work.
  • Must have adequate bone marrow reserve and organ function within 7 days before starting the study.
  • Both male and female participants are eligible.

Who Cannot Join the Study?

  • Patients with a type of lung cancer that is not non-squamous non-small cell lung cancer (NSCLC) cannot participate.
  • Patients who are not within the specified age range for the study cannot participate.
  • Patients who are part of a vulnerable population, which means they might need special protection or care, cannot participate.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Institut Gustave Roussy Villejuif France
Hopital Cardiologique Lille France
Hospital Universitario Y Politecnico La Fe Valencia Spain
IRCCS Humanitas Research Hospital Rozzano Italy
Centre Hospitalier Universitaire De Bordeaux Bordeaux France
Oncopole Claudius Regaud Toulouse France
Katholieke Universiteit te Leuven Leuven Belgium
Hospital Universitario De Navarra Pamplona Spain
Haemato-Onkologie Hamburg – Prof. Laack und Partner Hamburg Germany

Other Sites

Site Name City Country Status
Istituto Oncologico Veneto Padua Italy
Klinikum Nuernberg Nürnberg Germany
Asklepios Kliniken Hamburg GmbH Hamburg Germany
Franziskus Hospital Harderberg Georgsmarienhütte Germany
Pius-Hospital Oldenburg Oldenburg In Holstein Germany
Warminsko-Mazurskie Centrum Chorob Pluc W Olsztynie Olsztyn Poland
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Universitair Ziekenhuis Gent Gent Belgium
Vivantes Netzwerk fuer Gesundheit GmbH Berlin Germany
Hospital Universitario Puerta De Hierro De Majadahonda Majadahonda Spain
Hospital Del Mar Barcelona Spain
Hospital Santa Maria Della Misericordia Perugia Italy
Algemeen Ziekenhuis Delta Roeselare Belgium
Az Maria Middelares Gent Gent Belgium
HELIOS Klinikum Emil von Behring GmbH Berlin Germany
Istituto Tumori Bari Giovanni Paolo II Bari Italy
Geniko Nosokomeio Thessalonikis George Papanikolaou Thessaloniki Greece
Grand Hopital De Charleroi Charleroi Belgium
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur Namur Belgium
Humanitas Istituto Clinico Catanese S.p.A. Misterbianco Italy
Fondazione IRCCS San Gerardo Dei Tintori Monza Italy
Hospital Clinico Universitario De Valladolid Valladolid Spain
Instytut Msf Sp. z o.o. Lodz Poland
LungenClinic Grosshansdorf GmbH Grosshansdorf Germany
Henry Dunant Hospital Center Athens Greece
Hospital Quironsalud Malaga Malaga Spain
SLK-Kliniken Heilbronn GmbH Heilbronn Germany
Centre Hospitalier D Avignon Avignon France
Pratia Hematologia Sp. z o.o. Katowice Poland
General Hospital Of Thessaloniki Papageorgiou Thessaloniki Greece
Azienda Ospedaliero-Universitaria San Luigi Gonzaga Orbassano Italy
Universita’ Degli Studi Di Verona Verona Italy
Hospital Universitario De Cruces Barakaldo Spain
University Clinical Hospital Virgen De La Arrixaca Murcia Spain
Universidade De Santiago De Compostela Santiago De Compostela Spain
Jessa Ziekenhuis Hasselt Belgium
Hospital Universitario Virgen De Valme Sevilla Spain
Pratia S.A. Skorzewo Poland
Justus-Liebig-Universitaet Giessen Giessen Germany
Centre Hospitalier Universitaire De Nantes Nantes France
St. Luke’s Hospital S.A. Thessaloniki Greece
Wielkopolskie Centrum Pulmonologii I Torakochirurgii Im. Eugenii I Janusza Zeylandow Poznan Poland
CHU Helora La Louviere Belgium
Hopital Beaujon Clichy France
Vrije Universiteit Brussel Jette Belgium
Servei De Salut De Les Illes Balears Palma Spain
Centre Francois Baclesse Caen France
Direction Centrale Du Service De Sante Des Armees Toulon France
Metropolitan Hospital Athens Greece
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Agcesyf Oijoxqzkjyi Uyviiyryaoypb Pjvrr Parma Italy
Uihkduowogioermhlknie Egggy Aij Essen Germany
Ilxovy Iozvxepo Frfrduwoidhpa Oqvipaqzhlv Rome Italy
Hihhwuzb Uyjznebevmirf Mxncaaf Do Vcppncgvya Santander Spain
Iesygbpz Clcsfk Dkoxqresvfhqgdrug L'hospitalet De Llobregat Spain
Lmdvc Gcaocax Hcnqciyj Oj Afblrn Athens Greece
Celwvt Hcbnbiusysc Rsaanffr Unwibwnexbqzc Do Tppig Tours France
Ammyhc Mvkkmeh Cntpyr Spdr Thessaloniki Greece
Hwrzevwc Dt Lp Sqtii Cyzr I Syri Pyf Barcelona Spain
Udxgzskeha Ot Ahzrbpr Edegem Belgium
Golrjl Hsahtehgatv Urfnvihojiaky Pagqh Plsapznkzvi Ej Njhlilgqgngx Paris France
Cekmgo Hofhupjisov Rdmbulsh Dsubkikgxtwtsx Angers France
Fekbfbauf Pyxx La Ieidjnuzancgs Bjrtdigul Dev Hcrjxeou Ugbkvcoxqjhxt Lu Pvx Madrid Spain
Hnjigmac Urfvldtyirfco dm A Cinklk A Coruna Galicia Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Belgium Belgium
Recruiting
19.12.2024
France France
Recruiting
19.12.2024
Germany Germany
Recruiting
19.12.2024
Greece Greece
Recruiting
19.12.2024
Italy Italy
Recruiting
19.12.2024
Poland Poland
Recruiting
19.12.2024
Spain Spain
Recruiting
19.12.2024

Trial locations

Dato-DXd is a medication being studied for its potential to treat a type of lung cancer known as non-small cell lung cancer. This medication is designed to target and deliver a powerful anti-cancer drug directly to the cancer cells, which may help to stop the cancer from growing and spreading. In this trial, researchers are testing whether Dato-DXd can work better than standard chemotherapy treatments.

Osimertinib is a medication that is already used to treat certain types of lung cancer, particularly those with specific genetic mutations. It works by blocking the signals that tell cancer cells to grow. In this study, osimertinib is being combined with Dato-DXd to see if the combination can be more effective than chemotherapy in treating lung cancer that has progressed after previous treatment with osimertinib alone.

Platinum-based Doublet Chemotherapy is a standard treatment for lung cancer that uses two chemotherapy drugs together. These drugs work by killing cancer cells or stopping them from dividing. In this trial, the effectiveness of platinum-based doublet chemotherapy is being compared to the new treatment options involving Dato-DXd, with or without osimertinib, to see which approach is more effective in controlling the cancer.

Non-squamous non-small cell lung cancer (NSCLC) – Non-squamous non-small cell lung cancer is a type of lung cancer that originates in the epithelial cells of the lung, which are not of the squamous type. It is characterized by the uncontrolled growth of abnormal cells in the lung tissues, leading to the formation of tumors. As the disease progresses, these tumors can grow larger and may spread to other parts of the body, a process known as metastasis. The progression of the disease can lead to symptoms such as persistent cough, chest pain, and difficulty breathing. Over time, the cancer can invade nearby tissues and organs, further complicating the condition. The rate of progression can vary significantly among individuals, influenced by factors such as genetic mutations and overall health.

Trial ID:
2024-511362-37-00
Protocol code:
D516KC00001
NCT ID:
NCT06417814
Trial Phase:
Therapeutic confirmatory (Phase III)

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