Study of Niraparib and Pembrolizumab for Patients with Advanced Non-Small Cell Lung Cancer

3 1 1

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). The study is investigating the effectiveness of a combination of two treatments: Niraparib and Pembrolizumab. Niraparib is a medication that is taken orally in tablet form, while Pembrolizumab is given as an infusion, which means it is administered directly into the bloodstream through a vein. The trial will compare the effects of these medications against a placebo, which is a substance with no active drug, to see if the combination can help maintain the stability of the disease or improve the response after initial chemotherapy treatment.

The purpose of the study is to determine if the combination of Niraparib and Pembrolizumab can help patients live longer without the disease getting worse, and to see if it can improve overall survival compared to the placebo. Participants in the study will have already received a first-line treatment with platinum-based chemotherapy and Pembrolizumab, and their disease should have either remained stable or shown improvement. The study will involve regular monitoring and assessments to track the progress of the disease and the effects of the treatment.

Throughout the study, participants will receive either the combination of Niraparib and Pembrolizumab or a placebo with Pembrolizumab. The trial is designed to be double-blind, meaning neither the participants nor the researchers will know who is receiving the actual medication or the placebo. This helps ensure that the results are unbiased. The study will continue for a set period, during which participants will be closely monitored for any changes in their condition and any side effects they may experience. The ultimate goal is to find a more effective maintenance therapy for patients with advanced or metastatic NSCLC.

1 joining the study

Upon joining the study, eligibility is confirmed based on specific criteria, including age, health status, and ability to take oral medication.

Participants must have completed a certain number of chemotherapy cycles and show stable or improved disease status.

2 treatment phase

Participants receive a combination of medications as maintenance therapy. This includes pembrolizumab, administered as an infusion, and either niraparib or a placebo, taken orally.

The dosage for pembrolizumab is 25 mg/mL, and it is given as a solution for infusion. The specific dosage and frequency for niraparib or placebo are determined by the study protocol.

3 monitoring and assessments

Regular assessments are conducted to monitor the progression of the disease and overall health. This includes imaging tests and evaluations based on specific criteria.

Participants are observed for any side effects or adverse reactions to the medications.

4 end of treatment

The treatment phase continues until the study’s end date or until specific criteria for discontinuation are met.

Participants may continue to be monitored for a period after the treatment phase to assess long-term effects and overall survival.

Who Can Join the Study?

  • Participants must be at least 18 years old. In Korea, participants must be at least 19 years old.
  • Participants who had side effects from their initial treatment must have recovered to a certain level of health, and there should be no severe ongoing side effects.
  • Participants must be able to swallow and keep the study medication in their system.
  • Female participants must not be pregnant or breastfeeding. They must either not be of childbearing potential or use a highly effective birth control method. They must also have a negative pregnancy test before starting the study.
  • Male participants must agree not to donate sperm and either abstain from sexual activity or use a condom during the study and for 90 days after the last dose.
  • Participants must understand the study procedures and agree to participate by signing a consent form.
  • Participants must have a confirmed diagnosis of Non-Small Cell Lung Cancer (NSCLC) without specific genetic changes that can be targeted by approved treatments.
  • Participants must have advanced or metastatic NSCLC, meaning the cancer has spread and cannot be treated with standard chemotherapy and radiation.
  • Participants must have completed 4 to 6 cycles of initial chemotherapy with pembrolizumab, a type of cancer treatment.
  • Participants must have stable disease, partial response, or complete response to their cancer treatment as assessed by their doctor.
  • Participants must have an ECOG performance status of 0 or 1, which means they are fully active or have some symptoms but can carry out light work.
  • Participants must have a life expectancy of at least 12 weeks.
  • Participants must have adequate organ and bone marrow function, which includes specific levels of blood cells and liver function.
  • Participants must provide a sample of their tumor tissue, preferably collected after being diagnosed with advanced or metastatic NSCLC and before starting initial treatment.

Who Cannot Join the Study?

  • Patients with other types of cancer besides Non-Small Cell Lung Cancer cannot participate. This means if you have a different kind of cancer, you are not eligible.
  • Patients who are not within the specified age range for the study cannot participate. The study is looking for people in certain age groups.
  • Patients who are part of a vulnerable population, which means people who might need special protection or care, are not eligible for this study.
  • Patients who do not meet the specific health requirements set by the study cannot participate. This means if your health condition does not match what the study needs, you cannot join.

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
Ospedale San Raffaele S.r.l. Milan Italy
Karolinska University Hospital Solna Sweden
Centre Hospitalier Universitaire De Nantes Nantes France
Hospital General Universitario Gregorio Maranon Madrid Spain
Hopital Beaujon Clichy France
Metropolitan General Hospital/Healthcare Facilities Operation And Management Single Member S.A Cholargos Greece
St. Antonius Ziekenhuis Nieuwegein The Netherlands
Centro Di Riferimento Oncologico Di Aviano Aviano Italy
Complejo Hospitalario Universitario Insular Materno Infantil Las Palmas De Gran Canaria Spain
LungenClinic Grosshansdorf GmbH Grosshansdorf Germany
Complex Oncology Center Ruse EOOD Ruse Bulgaria
Metropolitan Hospital Athens Greece
Gokcgqz Uhixhhvssd Hiwsppcd Ow Lseytyc Larissa Greece
Lnejn Gqndjow Hcplplip Ok Alcbsj Athens Greece
Hwhttidm Vqhv dsainwzx Barcelona Spain
Hwltrpxk Uqetxappulnrx dv A Cuhqyn A Coruna Galicia Spain
Fjzrgrtqio Ioaqx Ca Gagqsz Oxiuauml Mlavfhbo Plznfdarwbz Milan Italy
Anstlxxxf Htgbsfnt Athens Greece
Aouwxtbx Uyayeouwut Heqkntxz Lorenskog Norway
Upjkwih Uawkavdynt Hmduuyti Uppsala Sweden
Hpzdlugx Cztczl Dq Bltddroby Barcelona Spain
Gxqzmft Uqgopmpadi Hnvpwwlf Oz Pjnpos Patras Greece
Akngav Makehcv Ctkgrt Suku Thessaloniki Greece
Kfxwfbnw dmi Uzlsjiovaxml Mdnspwdc Aqr Munich Germany
Cfyvfs Hjtmlxndrdy Uhfaevyrtrcoe Dn Rezljb Rennes France
Tsxxaxolkyef Hgovuahqal gbncq Heidelberg Germany
Uciuuaiqkm Oe Aehkdns Edegem Belgium
Ubezfjbnfwgfjfiayxkal Elveu Ays Essen Germany
Atqfdpakt Kotrnc Gwckfsz Gcwm Gauting Germany
Htnkjyvr Ubenlclzeazlv Pjheyv Ds Hcvzvj Dq Mksjykxaxmt Majadahonda Spain
Hzjgjmzh Ugvrbewhfixot 1a Dz Ohogddx Madrid Spain
Hduixkxn Ujnjfyagptgzz Mvwojrc Dp Vyigufxrwg Santander Spain
Ilimnpvz Clrali Dpbzoizfbbhqtcviw L'hospitalet De Llobregat Spain
Fimqneuwq Pttj Lh Ilngbvxcwnmhw Bcmhxysdz Dxn Haovtuan Ukseggrsfckae Le Pem Madrid Spain
Iyrnbfxo Tmjqgn Bkuu Gptideal Punyl Iv Bari Italy
Gnaqox Nzclldhmqf Tmhoyndbdvwna Gtieuv Pmfandsoqedy Thessaloniki Greece
Hwmnzxfu Cmnxyxu Uryblqixzztie Lmjqhk Btkkl Zaragoza Spain
Uhestqpprm Gpwyvuh Hqkdfhau Oz Holfryrtg Heraklion Greece
Fvpkgkskea Ibjkj Sku Gxzlnst Dwq Tynsxyn Monza Italy
Mvuteoo Sjpzwtnf Tbntbw Enschede The Netherlands
Fbbmersjdu Iaasxrerhu Iavzsvfw Nyitbldfcol Bwriw Milan Italy
Ubfaqaatkc Grqdjrh Hfsxonfs Axalhlp Govkvgd Hrefkdkj Ov Wgfx Asaoch H Aqpp Vtqevvl Chaidari Greece
Aluundn Oiuywadpvxg Uhzxtqqkcvdsg Pwlhmr Pisa Italy
Ijqyykvm Dm Cezktuktkopf Scsllkkthp Endhfi STRASBOURG, Alsace France
Amcnggx Uvws 9 Ssadafnow Legnago Italy
Chclny Hqhtrapedtb Iutfrrwhmdwms Tudomk / Ly Scrmwynnoxcrq Toulon France
Cpcrajt Dp Oppzewbvb Sp Ncmldjps Ssdlnr Craiova Romania
Azwufcf Okhuzdoioejrdewxmzbhthmel Pidtehflhrk Gy Rtdrwoavrikj Mdmwe Da Cqnficf Catania Italy
Wslqtjqtwhqjvciducq Ctmfhfn Cpekab Pjby W Otpoinimm Olsztyn Poland
Mytcsh Cqfdxi Cwrqgd Henysgqf Oj Pxquokn Piraeus Greece
Oeqhntuk Ocpqmpcavf Ixvlofw Budapest Hungary
Typlunclvc Cckopb Hlbqnmjc Thessaloniki Greece
Mowhyh Gqgqrjjlwvxc Gyongyos Hungary
Mmnw Sapdkap Lzsp Sofia Bulgaria
Ucvrlngfnwdth Sbuvwmc Kvcdbbpsm W Bvvofgiigqg Bialystok Poland
Vgdaet Vcnjm Hq Drammen Norway
Aymeywu Oiuuzltigsilxltfsjdxsvswv Spm Lktqa Gpsizss Orbassano Italy
Mfdospn Mkamibg Ccmlcb Amersfoort The Netherlands
Ocsamhx Sfjhbd Timisoara Romania
Mpbxlkna Kpggvd gglxo Munich Germany
Lcnhuvzsmiyp Hvkeo Dbbkaosbn Gtannhkzoefeagrqukftirlhrdpbs Gqoy Hemer Germany
Tgonnbijybvxmuidz Toqmncusrjmwt Torokbalint Hungary
Ntstohyfkwv Cdqwjh Isfwixysb Amsterdam The Netherlands
Rmhmqj Bhheg Gnbkzvwywhuc fqhn mrqjnhawzcxy Fmcojmoio mkd Stuttgart Germany
Iszns Kcarkdwdj Svpjvuntf Zwolle The Netherlands
Kryxfppj Ryjrkh Hhejhkhh Gmqi Hanover Germany
Jbtoai Buycz Zzfuxmagjm Sdplyrksd S-Hertogenbosch The Netherlands
Brqsifgtq Stvi Thessaloniki Greece
Epimososqh Gikprlo Cqkkeg Oy Tnuewxletinl Thessaloniki Greece
Kjqvuuvbknvvdyqwx Vgkrevwqe Segzp Brfqmgq Kvfbii Tatabanya Hungary
Mhkgselvvzvh Kdfxnzvznsh Hlgmvrpfcfor gyvvl Halle (Saale) Germany
Eolexvnjcckb Lvceumcqnzcb Bcjcrc Ktseimjcwlvjuqcpflw gbonk Berlin Germany
Abgr Swi Gednqwqf Mnnrkcs Adjaecyk Avellino Italy
Mcimnxyanokz Hbbhdhal Fnh Ajgmbu Ttpdgyiwqsaok Htagkymh Lhjr Panagyurishte Bulgaria
Mpkvolihondbu Hxnvpgld fcb Ahnryz Trmjezvdd Hihvj agr Bdvli Ela Pleven Bulgaria
Mrxnyufkicgznprky Hijbemdz Fqt Ayromh Tvckblsnc Phjd Hzxtzkjg Lond Branipole Bulgaria
Mhmyitjilyvqc Vtdspxo Ghm Velbert Germany
Hvpqf Dwnven Hnqxnnnn Cbkkjl Athens Greece
Oikahrcj Tmhnpidcgqupn Gclzqkw Clmicn Oa Plercs Sdpt Patras Greece
Rwsrfm Gtesqgotav Gavle Sweden
Hsmehrvmfoexwqee Httkkte Hamburg Germany

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
29.01.2021
Bulgaria Bulgaria
Not recruiting
29.01.2021
France France
Not recruiting
29.01.2021
Germany Germany
Not recruiting
29.01.2021
Greece Greece
Not recruiting
29.01.2021
Hungary Hungary
Not recruiting
29.01.2021
Ireland Ireland
Not recruiting
29.01.2021
Italy Italy
Not recruiting
29.01.2021
Norway Norway
Not recruiting
29.01.2021
Poland Poland
Not recruiting
29.01.2021
Romania Romania
Not recruiting
29.01.2021
Spain Spain
Not recruiting
29.01.2021
Sweden Sweden
Not recruiting
29.01.2021
The Netherlands The Netherlands
Not recruiting
29.01.2021

Trial locations

Niraparib is a medication used in this trial as part of a maintenance therapy. It is designed to help keep the cancer from growing or spreading after initial treatment. Niraparib works by interfering with the cancer cells’ ability to repair their DNA, which can lead to the death of these cells.

Pembrolizumab is an immunotherapy drug used in this trial. It helps the body’s immune system recognize and attack cancer cells. Pembrolizumab works by blocking a specific protein on the surface of immune cells, which can enhance the immune response against cancer cells.

Non-Small Cell Lung Cancer – 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. The disease typically begins in the cells lining the lungs and can spread to other parts of the body. As it progresses, it may cause symptoms like persistent cough, chest pain, and shortness of breath. The progression of the disease can vary, with some tumors growing slowly and others more rapidly. Early detection is crucial for managing the disease effectively.

Trial ID:
2023-508443-40-00
Protocol code:
213400
NCT ID:
NCT04475939
Trial Phase:
Therapeutic confirmatory (Phase III)

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