- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT06692738
Een wereldwijde fase III-studie van rilvegostomig of pembrolizumab plus chemotherapie voor eerstelijnsbehandeling van gemetastaseerde plaveiselcel niet-kleincellige longkanker (NSCLC)
Een fase III, gerandomiseerde, dubbelblinde, multicentrische, mondiale studie van rilvegostomig of pembrolizumab in combinatie met op platina gebaseerde chemotherapie voor de eerstelijnsbehandeling van patiënten met gemetastaseerde plaveiselcel-niet-kleincellige longkanker waarvan de tumoren PD-L1 tot expressie brengen (ARTEMIDE -Long02)
The purpose of ARTEMIDE-Lung02 is to assess the efficacy and safety of rilvegostomig in combination with platinum-based chemotherapy for the first-line (1L) treatment of patients with locally advanced or metastatic squamous non-small cell lung cancer (mNSCLC) whose tumors express programmed death-ligand 1 (PD-L1).
Studie Overzicht
Toestand
Conditie
Gedetailleerde beschrijving
This is a Phase III, two-arm, randomized, double-blind, global, multicenter study assessing the efficacy and safety of rilvegostomig compared to pembrolizumab, both in combination with platinum-based doublet chemotherapy, as a first-line (1L) treatment for patients with squamous locally advanced or metastatic non-small cell lung cancer (mNSCLC) whose tumors express PD-L1 (tumor cells (TC) ≥ 1%).
Studietype
Inschrijving (Geschat)
Fase
- Fase 3
Contacten en locaties
Studiecontact
- Naam: AstraZeneca Clinical Study Information Center
- Telefoonnummer: 1-877-240-9479
- E-mail: information.center@astrazeneca.com
Studie Locaties
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Buenos Aires, Argentinië, C1431FWO
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CABA, Argentinië, 1425
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La Plata, Argentinië, 1900
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Pilar, Argentinië, B1629ODT
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Rosario, Argentinië, S2000DEJ
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Darlinghurst, Australië, 2010
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Hyde Park, Australië, 4812
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Southport, Australië, 4215
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Wollongong, Australië, 2500
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Brussels, België, 1160
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Charleroi, België, 6060
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Kortrijk, België, 8500
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Florianópolis, Brazilië, 88034-000
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Londrina, Brazilië, 86015-520
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Porto Alegre, Brazilië, 91350-200
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Salvador, Brazilië, 40050 410
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São Paulo, Brazilië, 01246-000
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São Paulo, Brazilië, 05652-900
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Taubaté, Brazilië, 12030-200
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Győr, Hongarije, 9024
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Székesfehérvár, Hongarije, 8000
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Delhi, Indië, 110029
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Gūrgaon, Indië, 122001
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Kolkata, Indië, 700054
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Mumbai, Indië, 400012
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New Delhi, Indië, 110075
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Florence, Italië, 50134
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Legnano, Italië, 20025
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Livorno, Italië, 57126
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Monza, Italië, 20900
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Padova, Italië, 35128
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Roma, Italië, 00168
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Fukuoka, Japan, 814-0180
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Kobe, Japan, 650-0017
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Kyoto, Japan, 612-8555
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Obihiro-shi, Japan, 080-0024
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Osaka, Japan, 541-8567
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Kentucky
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Lexington, Kentucky, Verenigde Staten, 40509
- Werving
- Research Site
-
Lexington, Kentucky, Verenigde Staten, 40536
- Ingetrokken
- Research Site
-
Louisville, Kentucky, Verenigde Staten, 40207
- Werving
- Research Site
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Louisville, Kentucky, Verenigde Staten, 40202
- Werving
- Research Site
-
-
Louisiana
-
Alexandria, Louisiana, Verenigde Staten, 71301
- Ingetrokken
- Research Site
-
Baton Rouge, Louisiana, Verenigde Staten, 70808
- Werving
- Research Site
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Covington, Louisiana, Verenigde Staten, 70433
- Ingetrokken
- Research Site
-
Shreveport, Louisiana, Verenigde Staten, 71105
- Werving
- Research Site
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Shreveport, Louisiana, Verenigde Staten, 71103
- Werving
- Research Site
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-
Maine
-
Scarborough, Maine, Verenigde Staten, 04074
- Werving
- Research Site
-
-
Maryland
-
Baltimore, Maryland, Verenigde Staten, 21202
- Voltooid
- Research Site
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Bethesda, Maryland, Verenigde Staten, 20817
- Werving
- Research Site
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Bethesda, Maryland, Verenigde Staten, 20889
- Nog niet aan het werven
- Research Site
-
-
Michigan
-
Detroit, Michigan, Verenigde Staten, 48202
- Werving
- Research Site
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Grand Rapids, Michigan, Verenigde Staten, 49503
- Werving
- Research Site
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Saginaw, Michigan, Verenigde Staten, 48602
- Nog niet aan het werven
- Research Site
-
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Minnesota
-
Duluth, Minnesota, Verenigde Staten, 55802
- Werving
- Research Site
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Rochester, Minnesota, Verenigde Staten, 55905
- Werving
- Research Site
-
-
Missouri
-
Bridgeton, Missouri, Verenigde Staten, 63044
- Werving
- Research Site
-
Columbia, Missouri, Verenigde Staten, 65212
- Ingetrokken
- Research Site
-
Kansas City, Missouri, Verenigde Staten, 64108
- Werving
- Research Site
-
-
Nebraska
-
Lincoln, Nebraska, Verenigde Staten, 68506
- Werving
- Research Site
-
-
New Jersey
-
Camden, New Jersey, Verenigde Staten, 08103
- Werving
- Research Site
-
-
New York
-
Buffalo, New York, Verenigde Staten, 14221
- Werving
- Research Site
-
East Syracuse, New York, Verenigde Staten, 13057
- Werving
- Research Site
-
Westbury, New York, Verenigde Staten, 11590
- Werving
- Research Site
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-
North Carolina
-
Wilson, North Carolina, Verenigde Staten, 27893
- Werving
- Research Site
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-
North Dakota
-
Grand Forks, North Dakota, Verenigde Staten, 58201
- Werving
- Research Site
-
-
Ohio
-
Cincinnati, Ohio, Verenigde Staten, 45267
- Werving
- Research Site
-
-
Oregon
-
Bend, Oregon, Verenigde Staten, 97701
- Ingetrokken
- Research Site
-
Medford, Oregon, Verenigde Staten, 97504
- Werving
- Research Site
-
Salem, Oregon, Verenigde Staten, 97301
- Werving
- Research Site
-
-
Pennsylvania
-
Hershey, Pennsylvania, Verenigde Staten, 17033
- Werving
- Research Site
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York, Pennsylvania, Verenigde Staten, 17403
- Werving
- Research Site
-
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South Dakota
-
Sioux Falls, South Dakota, Verenigde Staten, 57105
- Werving
- Research Site
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-
Tennessee
-
Chattanooga, Tennessee, Verenigde Staten, 37404
- Werving
- Research Site
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Nashville, Tennessee, Verenigde Staten, 37203
- Werving
- Research Site
-
-
Texas
-
Fort Worth, Texas, Verenigde Staten, 76104
- Werving
- Research Site
-
Houston, Texas, Verenigde Staten, 77090
- Voltooid
- Research Site
-
Kingwood, Texas, Verenigde Staten, 77339
- Werving
- Research Site
-
Lubbock, Texas, Verenigde Staten, 79410
- Werving
- Research Site
-
Round Rock, Texas, Verenigde Staten, 78665
- Werving
- Research Site
-
-
Virginia
-
Fairfax, Virginia, Verenigde Staten, 22031
- Werving
- Research Site
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Fredericksburg, Virginia, Verenigde Staten, 22408
- Werving
- Research Site
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Washington
-
Olympia, Washington, Verenigde Staten, 98506
- Werving
- Research Site
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Seattle, Washington, Verenigde Staten, 98101
- Werving
- Research Site
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Silverdale, Washington, Verenigde Staten, 98383
- Ingetrokken
- Research Site
-
Spokane, Washington, Verenigde Staten, 99208
- Werving
- Research Site
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Tacoma, Washington, Verenigde Staten, 98405
- Werving
- Research Site
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Wenatchee, Washington, Verenigde Staten, 98801
- Ingetrokken
- Research Site
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Can Tho, Vietnam, 900000
- Werving
- Research Site
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Hanoi, Vietnam, 100000
- Werving
- Research Site
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Ho Chi Minh City, Vietnam, 700000
- Werving
- Research Site
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Vinh, Vietnam, 460000
- Werving
- Research Site
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-
-
-
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Changwon-si, Zuid -Korea, 51353
- Werving
- Research Site
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Cheongju-si, Zuid -Korea, 28644
- Werving
- Research Site
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Incheon, Zuid -Korea, 21565
- Werving
- Research Site
-
JinJoo, Zuid -Korea, 52727
- Werving
- Research Site
-
Seoul, Zuid -Korea, 03080
- Werving
- Research Site
-
Seoul, Zuid -Korea, 06351
- Werving
- Research Site
-
Seoul, Zuid -Korea, 05505
- Werving
- Research Site
-
Seoul, Zuid -Korea, 03722
- Werving
- Research Site
-
Suwon, Zuid -Korea, 16247
- Werving
- Research Site
-
Suwon, Zuid -Korea, 16499
- Werving
- Research Site
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Histologically or cytologically documented squamous NSCLC.
- Stage III B/C or IV mNSCLC (based on the American Joint Committee on Cancer Edition 8) not amenable to curative treatment.
- Absence of documented tumor genomic mutation results from tests conducted as part of standard local practice in any actionable driver oncogenes for which there are locally approved and available targeted 1L therapies.
- Provision of acceptable tumor sample to confirm tumor PD-L1 expression TC ≥ 1%.
- At least one lesion not previously irradiated that qualifies as a RECIST 1.1 TL at baseline and can be accurately measured at baseline as ≥ 10 mm in the longest diameter (except lymph nodes, which must have short axis ≥ 15 mm) with CT or MRI and is suitable for accurate repeated measurements.
- Adequate organ and bone marrow function.
Exclusion Criteria:
- Presence of small cell and neuroendocrine histology components.
- Brain metastases unless asymptomatic, stable, and not requiring steroids or anticonvulsants for at least 7 days prior to randomization. A minimum of 2 weeks must have elapsed between the end of local therapy (brain radiotherapy or surgery) and randomization. Participants must have recovered from the acute toxic effect of radiotherapy (eg, dizziness and signs of increased intracranial pressure) or surgery prior to randomization.
- Any prior systemic, non-curative therapy received for NSCLC.
- Any prior treatment with an anti-PD-1 or anti-PD-L1 agent.
- Any prior exposure to an anti-TIGIT therapy or any other anticancer therapy targeting immune-regulatory receptors or mechanisms.
- History of another primary malignancy except for malignancy treated with curative intent with no known active disease ≥ 2 years before the first dose of study intervention and of low potential risk for recurrence.
- Active or prior documented autoimmune or inflammatory disorders requiring chronic systemic treatment with the use of disease-modifying agents or other immunosuppressive drugs.
- Active primary immunodeficiency/active infectious disease(s).
- Active tuberculosis infection.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Arm A
Rilvegostomig in combination with carboplatin and paclitaxel or nab-paclitaxel followed by rilvegostomig |
Administered intravenously (IV) on Day 1 of each 21-day cycle
Andere namen:
Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles |
|
Actieve vergelijker: Arm B
Pembrolizumab in combination with carboplatin and paclitaxel or nab-paclitaxel followed by pembrolizumab |
Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles Administered intravenously (IV) on Day 1 of each 21-day cycle
Andere namen:
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Overall survival (OS)
Tijdsspanne: Up to approximately 6 years
|
OS is defined as the time from randomization until the date of death due to any cause. |
Up to approximately 6 years
|
|
Progression-free survival (PFS)
Tijdsspanne: Up to approximately 6 years
|
PFS is defined as the time from randomization until radiological progression per Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1) or death due to any cause (in the absence of progression). |
Up to approximately 6 years
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Landmark overall survival (OS) rates
Tijdsspanne: Up to approximately 6 years
|
OS is defined as the time from randomization until the date of death due to any cause. |
Up to approximately 6 years
|
|
Landmark progression-free survival (PFS) rates
Tijdsspanne: Up to approximately 6 years
|
PFS is defined as the time from randomization until radiological progression per Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1) or death due to any cause (in the absence of progression). |
Up to approximately 6 years
|
|
Time to second progression or death (PFS2)
Tijdsspanne: Up to approximately 6 years
|
PFS2 is defined as the time from randomization until the earliest of the progression event (following the initial progression event), after the start of the first subsequent therapy, or death from any cause, whichever occurs first. The date of the second progression will be recorded by the investigator in the electronic Case Report Form (eCRF) and defined according to local standard clinical practice. |
Up to approximately 6 years
|
|
Overall response rate (ORR)
Tijdsspanne: Up to approximately 6 years
|
ORR is defined as the proportion of participants who have a confirmed complete response (CR) or confirmed partial response (PR), by using Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1). |
Up to approximately 6 years
|
|
Duration of response (DoR)
Tijdsspanne: Up to approximately 6 years
|
DoR is defined as the time from the date of first documented response until the date of documented progression using Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1) or death due to any cause (in the absence of progression). |
Up to approximately 6 years
|
|
Pharmacokinetic (PK) of rilvegostomig
Tijdsspanne: Up to approximately 6 years
|
Concentration of rilvegostomig in serum. |
Up to approximately 6 years
|
|
Immunogenicity of rilvegostomig
Tijdsspanne: Up to approximately 6 years
|
Presence of antidrug antibodies (ADAs), titer, and neutralizing antibodies for rilvegostomig. |
Up to approximately 6 years
|
|
Patient-reported physical functioning
Tijdsspanne: Up to approximately 6 years
|
Proportion of participants with maintained or improved physical functioning as measured by Patient-Reported Outcomes Measurement Information System Physical Function - Short Form 8c - 7 day (PROMIS PF-SF 8c - 7 day) at each time point. |
Up to approximately 6 years
|
|
Patient-reported global health status (GHS)/quality of life (QoL)
Tijdsspanne: Up to approximately 6 years
|
Time to deterioration (TTD) of GHS/QoL as measured by the European Organization for Research and Treatment of Cancer Item Library 172 (EORTC IL172). TTD is defined as time from randomization to the date of first deterioration. Deterioration is defined as a worsening change from baseline that reaches a clinically meaningful change threshold. |
Up to approximately 6 years
|
|
Patient-reported lung cancer symptoms of non-small cell lung cancer (NSCLC)
Tijdsspanne: Up to approximately 6 years
|
Time to deterioration (TTD) in pulmonary symptoms as measured by the Non-Small Cell Lung Cancer Symptom Assessment Questionnaire (NSCLC-SAQ). TTD is defined as time from randomization to the date of first deterioration. |
Up to approximately 6 years
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata per site
- Neoplasmata
- Ziekten van de luchtwegen
- Longziekten
- Neoplasmata van de luchtwegen
- Thoracale neoplasmata
- Longneoplasmata
- Carcinoom, bronchogeen
- Bronchiale neoplasmata
- Carcinoom, niet-kleincellige long
- Organische chemicaliën
- Koolwaterstoffen
- Cycloparaffins
- Koolwaterstoffen, alicyclisch
- Koolwaterstoffen, cyclisch
- Terpenen
- Coördinatiecomplexen
- Taxoids
- Cyclodecanes
- Diterpenen
- Carboplatine
- Paclitaxel
- pembrolizumab
- 130-nm albumine-gebonden Paclitaxel
Andere studie-ID-nummers
- D702BC00001
- 2024-514281-39-00 (Register-ID: CTIS (EU))
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca (AZ) group of companies sponsored clinical trials via the request portal Vivli.org. All requests will be evaluated as per the AZ disclosure commitment:
https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure. "Yes", indicates that AZ are accepting requests for Important Protocol Deviation (IPD), but this does not mean all requests will be approved.
IPD-tijdsbestek voor delen
AstraZeneca will meet or exceed data availability as per the commitments made to the European Federation of Pharmaceutical Industries and Associations (EFPIA)/Pharmaceutical Research and Manufacturers of America (PhRMA) Data-Sharing Principles. For details of our timelines, please refer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure
IPD-toegangscriteria voor delen
When a request has been approved AstraZeneca will provide access to the anonymized individual patient-level data via secure research environment Vivli.org. A Signed Data Usage Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .