Study of Datopotamab Deruxtecan, Durvalumab, and Carboplatin for Advanced Non-Small Cell Lung Cancer in Patients Without Actionable Genomic Alterations

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What is this study about?

This clinical trial is focused on studying treatments for Non-Small Cell Lung Cancer (NSCLC), a common type of lung cancer. The study will compare two different treatment combinations. One group will receive a combination of Datopotamab Deruxtecan (also known as DS-1062a), Durvalumab (also known as MEDI4736), and Carboplatin. The other group will receive Pembrolizumab along with a type of chemotherapy that includes platinum-based drugs. The purpose of the study is to see which combination works better for patients with advanced NSCLC that does not have certain genetic changes known as actionable genomic alterations.

Participants in the study will be randomly assigned to one of the two treatment groups. The treatments will be given through an intravenous infusion, which means the medication is delivered directly into the bloodstream through a vein. The study will monitor how long patients live without their cancer getting worse, as well as their overall survival. The study will also look at how well the cancer responds to the treatment and how long any positive effects last.

The study aims to provide important information about the effectiveness of these treatment combinations for patients with advanced NSCLC. By comparing these treatments, researchers hope to find the best option for managing this type of lung cancer. The study will continue for several years to gather enough data to make informed conclusions about the treatments’ benefits and safety.

1 joining the study

Upon joining the study, eligibility is confirmed based on specific criteria such as age, type of lung cancer, and overall health status.

Participants must have non-small cell lung cancer (NSCLC) that is advanced or metastatic and lacks certain genetic mutations.

2 randomization

Participants are randomly assigned to one of two treatment groups.

One group receives datopotamab deruxtecan in combination with durvalumab and carboplatin, while the other group receives pembrolizumab with platinum-based chemotherapy.

3 treatment administration

Treatment is administered through intravenous infusion, which means the medication is given directly into a vein.

The specific dosage and frequency depend on the treatment group and the individual treatment plan.

4 monitoring and assessments

Regular monitoring is conducted to assess the response to treatment and any side effects.

Assessments include imaging tests to evaluate cancer progression and routine blood tests to check overall health.

5 follow-up

Participants continue to be monitored for progression-free survival, which is the time during and after treatment that the cancer does not get worse.

Overall survival is also tracked, which is the time from the start of the study until death from any cause.

6 end of study

The study is estimated to conclude in February 2027.

Final assessments are conducted to gather data on the effectiveness and safety of the treatments.

Who Can Join the Study?

  • Participants must be 18 years or older at the time of screening.
  • Must have Non-Small Cell Lung Cancer (NSCLC) that is either locally advanced or has spread to other parts of the body (metastatic). The cancer should not be treatable with surgery or a combination of chemotherapy and radiation.
  • The cancer should not have certain genetic changes, such as EGFR, ALK, ROS1, NTRK, BRAF, RET, MET, or other specific genes that have approved treatments. Testing for these changes is not needed for certain types of lung cancer, with some exceptions.
  • Must have an ECOG Performance Status of 0 or 1, which means the participant is fully active or has some symptoms but can still carry out light work.
  • Must provide a sample of the tumor tissue from a previous biopsy or surgery.
  • Must have enough healthy bone marrow and properly working organs, as shown by tests done within 7 days before joining the study.

Who Cannot Join the Study?

  • Patients who have a different type of cancer other than Non-Small Cell Lung Cancer (NSCLC).
  • Patients who do not have the TROP2 biomarker in their cancer. A biomarker is a substance in the body that can indicate the presence of a disease.
  • Patients who have already received treatment for their lung cancer.
  • Patients who are not in the age range specified for the study.
  • Patients who are not able to follow the study procedures or attend the required visits.
  • Patients who have other serious health conditions that might interfere with the study.
  • Patients who are pregnant or breastfeeding.
  • Patients who are participating in another clinical trial at the same time.
  • Patients who have had an allergic reaction to any of the study drugs or similar drugs in the past.
  • Patients who have an active infection that requires treatment.
  • Patients who have a history of certain heart problems.
  • Patients who have a history of certain lung problems not related to cancer.
  • Patients who have a history of certain immune system problems.
  • Patients who have a history of drug or alcohol abuse.
  • Patients who have received a live vaccine within a certain time before starting the study.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Centre Hospitalier Universitaire Rouen Rouen France
Karolinska University Hospital Solna Sweden
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Hopital Beaujon Clichy France
Katholisches Klinikum Koblenz Montabaur gGmbH Koblenz Germany
Ospedale P. Pederzoli Casa Di Cura Privata S.p.A. Peschiera Del Garda Italy
Staedtisches Krankenhaus Kiel GmbH Kiel Germany
Centre De Cancerologue Du Grand Montpellier Montpellier France
Complejo Hospitalario Universitario Insular Materno Infantil Las Palmas De Gran Canaria Spain
Mazowiecki Szpital Wojewodzki Im. Sw. Jana Pawła II W Siedlcach Sp. z o.o. Siedlce Poland
Romed Klinikum Rosenheim Rosenheim Germany
Azienda Ospedaliera Papardo Messina Italy
Metropolitan Hospital Athens Greece
Ljzgv Glhsrsz Hkmbjlyn Og Azqbaj Athens Greece
Vrloua dbf Rzbhr Uwsxvurjkw Hnugcjqi Sevilla Spain
Rnybbs Snpzi Shiqlj Upmtueduxnwdiuhlzwq Lund Sweden
Uveuxxt Uiqxoasyzt Haqjoufz Uppsala Sweden
Mjsntsk Uukwyzzoij Ok Gvwr Graz Austria
Cwbsjj Hmoqhplzsps Rjmzhnul Uauxosuxiooyz Dx Tdzzx Tours France
Khavrjhb Kfjhhe Gytf Kassel Germany
Aitjnj Mchagek Cutmau Sbyr Thessaloniki Greece
Cpeazx Hesvlucudzg Uwkjwslzwjuqh Dq Nvmld Nimes France
Avbicgniy Kdbzua Gcgiltz Gmkw Gauting Germany
Hzlbxvma Uvhjdnvwlqtuf 1v Dy Oxiocnq Madrid Spain
Hyvvawdi Uletmzdvvdcyf Mczxflp Dk Vsuglcowla Santander Spain
Knpwcgikgii Nayg Kyjfun Fiosysoeyat Vienna Austria
Jslceual Wzdillh Kzymvqfe Msawqs Minden Germany
Hwxnozsc Cxgssfz Upqwigqfnpsde Lquxzf Bbydz Zaragoza Spain
Hzlqahja Udenzcwrbeiswe Syyyrbjxwk &pywwwp Hvwopoq df Hrqpquwbxfy STRASBOURG, Alsace France
Izidtgbu Ojwstghbpf Vtsudh Padua Italy
Uwsjlzscmm Mmijcwyzklce Htllxxqh Fvr Aryiyu Thqjrhxkv Sjmpvnlq Odp Sofia Bulgaria
Osubbct Gpua Guetersloh Germany
Hpl Sgazye Ajbi Toulon France
Tyqlt Vrlgxeort Bjqlxwi Jumfn Kutvps Szekszard Hungary
Wovxpervzyoztokpivn Cdvakzl Clkust Ppxe W Otfvqhvta Olsztyn Poland
Ozuzsjid Oyaytlvuay Iqilhuv Budapest Hungary
Spdonh Voxiowgup Kvgnfi Mbu Olaunl Kycqoi Kaposvar Hungary
Myeczb Gogltihwenkx Gyongyos Hungary
Lvy Fhysmewrj Icvvch E aw Lht Rvmeaqer Rankweil Austria
Motbauf Cobdnn Nycnqqcu Ckiwqsrh Epbf Sofia Bulgaria
Lbz Hmkltftz Ntitryqdcu Villefranche sur Saône France
Aqrgjgg Oejtvjucvckqbjwkzfhjpumxo Sca Lqddz Girsmap Orbassano Italy
Aivcjclazy Muqlnvy Hvjispcd Lecco Italy
Hzsiujpt Ugzdrgeclljib Lqcoy Aoebrvz Lugo Spain
Gghlqd Ukkfyjrjrp Fndlxikmd Frankfurt Germany
Soyauugizeftgr Cgkqdrx Onfxqnobd Smqtiyxfqyl Pvqmuhdap Zqkvwj Ozouyk Zbonjdrebp W Kzzzadir Kielce Poland
Thjgttcojuccbxzuh Tjykuapcialbn Torokbalint Hungary
Svu Llrvdylpxrqo Hsrbdelo Scuu Thessaloniki Greece
Wdngwaxdyrhsz Cyqgkuo Pqjclpycfeso I Tzpcqfphjyczpwb Ivl Etjoikw I Jdbzdqt Zxvnacdjp Poznan Poland
Kcyzukb Nrubphvlpptznmipdxr Srq z odxn Radom Poland
Ulqldamhms Oc Pvmj Pecs Hungary
Kuarowcj Wkktydiad Muipz gyfvj Wuerzburg Germany
Aljxhef Okqbldonyqw Utzvcncsqldmx Pmaxi Parma Italy
Cccnpde Owkzquyik Ivv Pphur Fqjdvryjqv Lwzllqfyurr W Brpjonrnde Bydgoszcz Poland
Gnjhqk Hklizzxhejf Uygeymunbohql Pfwxd Prfrikuahdw Ea Nsylcutrggic Paris France
Rdoytt Osvmfdjmkbdelm Linkoping Sweden
Knimjshc Mluyn Hdgk Gllf Mndijhuqplbdeoyy Moenchengladbach Germany
Zycqxgbehyqbb Bsl Bkzet Geie Bad Berka Germany
Vipfmdmz Nrxzuook fqif Gjdvghmmle Gffn Berlin Germany
Mtrc Stekc Mfglzm Esh Varna Bulgaria
Hzicxr Kimuujgs Ertw voj Bmbrktr Glff Berlin Germany
Dvdkklqakuxy Cdgpkmy Ohxohhmxe Pmwapvxalkmq I Hactmfrjqsk Wroclaw Poland
Jwrovhphktjeleifauil Vjgvrupml Hnkselr Gfhy Kkozbqbukrircdjmgtomi Szolnok Hungary
Scrgwxd Rdzswrgo Idl Da Jegfel Rykebz W Rkjspkove Raciborz Poland
Radoycucqu Siucgpt Szqztdrytnrbzuc Irv Dce Wjcvynieph Bywwfsjowwkh Grudziadz Poland
Meisehviesqcr Viuuuml Gxe Velbert Germany
Hgwua Dzozly Hbggmufc Cfangd Athens Greece
Cgnsvti Papluolmygow I Tcmwutceprrwlsp W Bfuvpvd Wilkowice Poland
Wnypltsjyd Smfqcwm Iwu Sticrjz Prh W Pxfqwyeqz Przemysl Poland
Rpksln Gzeaqyvgki Gavle Sweden
Htwzrshrkbncsxos Hhtyckg Hamburg Germany

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

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
13.01.2023
Bulgaria Bulgaria
Not recruiting
13.01.2023
France France
Not recruiting
13.01.2023
Germany Germany
Not recruiting
13.01.2023
Greece Greece
Not recruiting
13.01.2023
Hungary Hungary
Not recruiting
13.01.2023
Italy Italy
Not recruiting
13.01.2023
Poland Poland
Not recruiting
13.01.2023
Spain Spain
Not recruiting
13.01.2023
Sweden Sweden
Not recruiting
13.01.2023

Trial locations

Datopotamab Deruxtecan (Dato-DXd) is an experimental medication being studied for its potential to treat certain types of lung cancer. It is designed to target and deliver chemotherapy directly to cancer cells, which may help to reduce the growth of tumors.

Durvalumab is a type of immunotherapy that helps the body’s immune system recognize and attack cancer cells. It is used in combination with other treatments to enhance the body’s natural defenses against cancer.

Carboplatin is a chemotherapy drug that works by interfering with the DNA of cancer cells, preventing them from growing and dividing. It is commonly used to treat various types of cancer, including lung cancer.

Pembrolizumab is another form of immunotherapy that boosts the immune system’s ability to fight cancer. It is often used in combination with other treatments to improve outcomes for patients with advanced cancer.

Platinum-based Chemotherapy refers to a group of chemotherapy drugs that contain platinum, which are used to damage the DNA of cancer cells and stop them from multiplying. These drugs are often used in combination with other treatments to enhance their effectiveness against cancer.

Non-Small Cell Lung Cancer (NSCLC) – This is a type of lung cancer that includes several subtypes such as adenocarcinoma, squamous cell carcinoma, and large cell carcinoma. It is the most common type of lung cancer, accounting for about 85% of all cases. NSCLC typically grows and spreads more slowly than small cell lung cancer. The disease often begins in the cells lining the air passages and can spread to other parts of the body. Symptoms may include a persistent cough, chest pain, and shortness of breath. As the disease progresses, it may lead to more severe respiratory issues and other systemic symptoms.

Trial ID:
2023-505993-14-00
Protocol code:
D926NC00001
Trial Phase:
Therapeutic confirmatory (Phase III)

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