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Uno studio globale su Volrustomig (MEDI5752) per partecipanti con carcinoma a cellule squamose della testa e del collo localmente avanzato non resecato dopo chemioradioterapia concomitante definitiva (eVOLVE-HNSCC)

29 settembre 2026 aggiornato da: AstraZeneca

Uno studio globale di Fase III, randomizzato, in aperto, multicentrico su Volrustomig (MEDI5752) come terapia sequenziale rispetto all'osservazione in partecipanti con carcinoma a cellule squamose della testa e del collo localmente avanzato non resecato, che non hanno progredito dopo chemioradioterapia concomitante definitiva (eVOLVE- HNSCC)

The main purpose of this study is to assess the efficacy and safety of volrustomig compared to observation in participants with unresected locally advanced head and neck squamous cell carcinoma (LA-HNSCC) who have not progressed after receiving definitive concurrent chemoradiotherapy (cCRT).

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

1145

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

      • Graz, Austria, 8036
        • Reclutamento
        • Research Site
      • Innsbruck, Austria, 6020
        • Reclutamento
        • Research Site
      • Linz, Austria, 4010
        • Reclutamento
        • Research Site
      • Salzburg, Austria, 5020
        • Reclutamento
        • Research Site
      • Vienna, Austria, 1080
        • Reclutamento
        • Research Site
      • Charleroi, Belgio, 6060
        • Reclutamento
        • Research Site
      • Edegem, Belgio, 2650
        • Reclutamento
        • Research Site
      • Jette, Belgio, 1090
        • Reclutamento
        • Research Site
      • La Louvière, Belgio, 7100
        • Reclutamento
        • Research Site
      • Namur, Belgio, 5000
        • Reclutamento
        • Research Site
      • Barretos, Brasile, 14784-400
        • Reclutamento
        • Research Site
      • Florianópolis, Brasile, 88034-000
        • Reclutamento
        • Research Site
      • Fortaleza, Brasile, 60336-045
        • Reclutamento
        • Research Site
      • Ijuí, Brasile, 98700-000
        • Reclutamento
        • Research Site
      • Ipatinga, Brasile, 35162-189
        • Reclutamento
        • Research Site
      • Londrina, Brasile, 86015-520
        • Reclutamento
        • Research Site
      • Natal, Brasile, 59075-740
        • Reclutamento
        • Research Site
      • Porto Alegre, Brasile, 91350200
        • Reclutamento
        • Research Site
      • Ribeirão Preto, Brasile, 14051-140
        • Sospeso
        • Research Site
      • Rio de Janeiro, Brasile, 20231-050
        • Sospeso
        • Research Site
      • São Paulo, Brasile, 04538-132
        • Reclutamento
        • Research Site
      • São Paulo, Brasile, 01509-900
        • Reclutamento
        • Research Site
      • Teresina, Brasile, 64049-200
        • Reclutamento
        • Research Site
      • Regina, Canada, S4T 7T1
        • Ritirato
        • Research Site
    • Alberta
      • Calgary, Alberta, Canada, T2N 5G2
        • Reclutamento
        • Research Site
      • Edmonton, Alberta, Canada, T6G 1Z2
        • Reclutamento
        • Research Site
    • British Columbia
      • Kelowna, British Columbia, Canada, V1Y 5L3
        • Reclutamento
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    • Ontario
      • Kingston, Ontario, Canada, K7L 2V7
        • Reclutamento
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      • London, Ontario, Canada, N6A 5W9
        • Reclutamento
        • Research Site
      • Toronto, Ontario, Canada, M4N 3M5
        • Reclutamento
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    • Quebec
      • Chicoutimi, Quebec, Canada, G7H 5H6
        • Non ancora reclutamento
        • Research Site
      • Montreal, Quebec, Canada, H4A 3J1
        • Reclutamento
        • Research Site
      • Montreal, Quebec, Canada, H3T 1E2
        • Terminato
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      • Montreal, Quebec, Canada, H2X 0C1
        • Completato
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      • Beijing, Cina, 100210
        • Reclutamento
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      • Beijing, Cina, 100142
        • Reclutamento
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      • Bengbu, Cina, 233004
        • Ritirato
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      • Changchun, Cina, 130000
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      • Changsha, Cina, 410008
        • Reclutamento
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      • Changsha, Cina, 410013
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      • Chengdu, Cina, 610000
        • Reclutamento
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      • Chengdu, Cina, 610072
        • Reclutamento
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      • Chengdu, Cina, 610042
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      • Chongqing, Cina, 400016
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      • Chongqing, Cina, 400030
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      • Dongwan, Cina, 523058
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      • Fuzhou, Cina, 350014
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      • Guangzhou, Cina, 510080
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      • Guangzhou, Cina, 510060
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      • Guangzhou, Cina, 510095
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      • Guangzhou, Cina, 510700
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      • Guiyang, Cina, 550002
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      • Hangzhou, Cina, 310022
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      • Harbin, Cina, 150049
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      • Hefei, Cina, 230001
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      • Huizhou, Cina, 516001
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      • Jinan, Cina, 250117
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      • Kunming, Cina, 650118
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      • Lanzhou, Cina, 730000
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      • Nanchang, Cina, 330029
        • Reclutamento
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      • Nanning, Cina, 530021
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      • Shanghai, Cina, 20032
        • Reclutamento
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      • Shenyang, Cina, 110004
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      • Shijiazhuang, Cina, 050000
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        • Research Site
      • Tianjin, Cina, 300060
        • Reclutamento
        • Research Site
      • Tianjin, Cina, 300060
        • Ritirato
        • Research Site
      • Wuhan, Cina, 430030
        • Reclutamento
        • Research Site
      • Wuhan, Cina, 430060
        • Reclutamento
        • Research Site
      • Wuxi, Cina, 214122
        • Ritirato
        • Research Site
      • Xi'an, Cina, 710061
        • Reclutamento
        • Research Site
      • Xiamen, Cina, 361003
        • Ritirato
        • Research Site
      • Zhengzhou, Cina, 450008
        • Reclutamento
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      • Zhuhai, Cina, 519000
        • Reclutamento
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      • Ürümqi, Cina, 830000
        • Ritirato
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      • Goyang-si, Corea del Sud, 410-769
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      • Gyeonggi-do, Corea del Sud, 13620
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      • Incheon, Corea del Sud, 21565
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      • Seoul, Corea del Sud, 06351
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      • Seoul, Corea del Sud, 5505
        • Reclutamento
        • Research Site
      • Seoul, Corea del Sud, 3722
        • Reclutamento
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      • Suwon, Corea del Sud, 16247
        • Reclutamento
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      • Cebu City, Filippine, 6000
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      • General Santos, Filippine, 9500
        • Non ancora reclutamento
        • Research Site
      • Iloilo City, Filippine, 5000
        • Reclutamento
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      • Pasig, Filippine, 1605
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      • Quezon City, Filippine, 1112
        • Ritirato
        • Research Site
      • West San Juan City, Filippine, 1502
        • Ritirato
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      • Avignon, Francia, 84918
        • Reclutamento
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      • Bordeaux, Francia, 33075
        • Reclutamento
        • Research Site
      • Le Mans, Francia, 72000
        • Reclutamento
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      • Lyon, Francia, 69373
        • Reclutamento
        • Research Site
      • Nice, Francia, 06100
        • Reclutamento
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      • Saint-Herblain, Francia, 44805
        • Reclutamento
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      • Toulouse, Francia, 31059
        • Reclutamento
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      • Villejuif, Francia, 94805
        • Reclutamento
        • Research Site
      • Berlin, Germania, 12200
        • Reclutamento
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      • Erlangen, Germania, 91054
        • Reclutamento
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      • Essen, Germania, 45122
        • Reclutamento
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      • Freiburg im Breisgau, Germania, 79106
        • Reclutamento
        • Research Site
      • Greifswald, Germania, 17475
        • Reclutamento
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      • Hamburg, Germania, 20246
        • Reclutamento
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      • Hanover, Germania, 30625
        • Reclutamento
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      • Leipzig, Germania, 04103
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      • Lübeck, Germania, 23538
        • Reclutamento
        • Research Site
      • München, Germania, 81675
        • Reclutamento
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      • Rostock, Germania, 18059
        • Reclutamento
        • Research Site
      • Tübingen, Germania, 72076
        • Reclutamento
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      • Ulm, Germania, 89075
        • Reclutamento
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      • Würzburg, Germania, 97070
        • Reclutamento
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      • Bunkyō City, Giappone, 113-8431
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      • Chiba, Giappone, 260-8717
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      • Chiba, Giappone, 260-8677
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      • Chūōku, Giappone, 104-0045
        • Reclutamento
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      • Fukuoka, Giappone, 811-1395
        • Reclutamento
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      • Hidaka-shi, Giappone, 350-1298
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      • Hiroshima, Giappone, 734-8551
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      • Kashiwa, Giappone, 277-8577
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      • Kobe, Giappone, 650-0017
        • Reclutamento
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      • Kyoto, Giappone, 606-8507
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      • Kōtoku, Giappone, 135-8550
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      • Nagoya, Giappone, 464-8681
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      • Nagoya, Giappone, 466-8560
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      • Niigata, Giappone, 951-8520
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      • Okayama, Giappone, 700-8558
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      • Osaka, Giappone, 541-8567
        • Reclutamento
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      • Osakasayama-shi, Giappone, 589-8511
        • Reclutamento
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      • Sagamihara-shi, Giappone, 252-0375
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      • Sapporo, Giappone, 060-8638
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      • Sendai, Giappone, 980-8574
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      • Shinjuku-ku, Giappone, 160-0023
        • Reclutamento
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      • Shiwa-gun, Giappone, 028-3695
        • Reclutamento
        • Research Site
      • Sunto-gun, Giappone, 411-8777
        • Reclutamento
        • Research Site
      • Yokohama, Giappone, 241-8515
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        • Research Site
      • Yokohama, Giappone, 236-0004
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      • Bengaluru, India, 560027
        • Reclutamento
        • Research Site
      • Hyderabad, India, 500032
        • Reclutamento
        • Research Site
      • Jaipur, India, 302022
        • Ritirato
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      • Kanpur, India, 208005
        • Reclutamento
        • Research Site
      • Kochi, India, 682027
        • Attivo, non reclutante
        • Research Site
      • Kolkata, India, 700099
        • Reclutamento
        • Research Site
      • Lucknow, India, 226003
        • Ritirato
        • Research Site
      • Madurai, India, 625107
        • Reclutamento
        • Research Site
      • Mohali, India, 160055
        • Ritirato
        • Research Site
      • Nashik, India, 422002
        • Reclutamento
        • Research Site
      • New Delhi, India, 110076
        • Reclutamento
        • Research Site
      • Thiruvananthapuram, India, 695011
        • Reclutamento
        • Research Site
      • Vadodara, India, 391760
        • Reclutamento
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      • Varanasi, India, 221005
        • Reclutamento
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      • Aviano, Italia, 33081
        • Reclutamento
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      • Florence, Italia, 50139
        • Reclutamento
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      • Milan, Italia, 20133
        • Reclutamento
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      • Modena, Italia, 41124
        • Reclutamento
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      • Naples, Italia, 80131
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      • Padova, Italia, 35128
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      • Pavia, Italia, 27100
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      • Rozzano, Italia, 20089
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      • George Town, Malaysia, 10450
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      • Johor Bahru, Malaysia, 81100
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      • Siedlce, Polonia, 08-110
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      • Tomaszów Mazowiecki, Polonia, 97-200
        • Ritirato
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      • Warsaw, Polonia, 02-781
        • Reclutamento
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      • San Juan, Porto Rico, 00927
        • Completato
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      • Aberdeen, Regno Unito, AB25 2ZN
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      • Sutton, Regno Unito, SM2 5PT
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      • Taunton, Regno Unito, TA1 5DA
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      • Badalona, Spagna, 08916
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      • Barcelona, Spagna, 08035
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      • Jaén, Spagna, 23007
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      • Madrid, Spagna, 28007
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    • Arkansas
      • Springdale, Arkansas, Stati Uniti, 72762
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      • Fountain Valley, California, Stati Uniti, 92708
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    • Utah
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    • Virginia
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      • Spokane, Washington, Stati Uniti, 99204
        • Ritirato
        • Research Site
      • Tacoma, Washington, Stati Uniti, 98405
        • Ritirato
        • Research Site
      • Tacoma, Washington, Stati Uniti, 98415
        • Attivo, non reclutante
        • Research Site
      • Bangkok, Tailandia, 10300
        • Reclutamento
        • Research Site
      • Bangkok, Tailandia, 10400
        • Reclutamento
        • Research Site
      • Bangkok, Tailandia, 10700
        • Reclutamento
        • Research Site
      • Chaing Mai, Tailandia, 50200
        • Reclutamento
        • Research Site
      • Hat Yai, Tailandia, 90110
        • Reclutamento
        • Research Site
      • Khon Kaen, Tailandia, 40002
        • Ritirato
        • Research Site
      • Lampang, Tailandia, 52000
        • Reclutamento
        • Research Site
      • Muang, Tailandia, 22000
        • Reclutamento
        • Research Site
      • Mueang, Tailandia, 20000
        • Reclutamento
        • Research Site
      • Changhua, Taiwan, 500
        • Reclutamento
        • Research Site
      • Kaohsiung City, Taiwan, 80756
        • Reclutamento
        • Research Site
      • Kaohsiung City, Taiwan, 833401
        • Reclutamento
        • Research Site
      • Taichung, Taiwan, 40705
        • Reclutamento
        • Research Site
      • Taichung, Taiwan, 404
        • Reclutamento
        • Research Site
      • Taipei, Taiwan, 10002
        • Reclutamento
        • Research Site
      • Taipei, Taiwan, 11217
        • Reclutamento
        • Research Site
      • Taoyuan, Taiwan, 333
        • Reclutamento
        • Research Site
      • Ankara, Turchia (Türkiye), 06230
        • Reclutamento
        • Research Site
      • Ankara, Turchia (Türkiye), 6200
        • Reclutamento
        • Research Site
      • Antalya, Turchia (Türkiye), 07059
        • Reclutamento
        • Research Site
      • Cordaleo, Turchia (Türkiye), 35575
        • Reclutamento
        • Research Site
      • Eskişehir, Turchia (Türkiye), 26040
        • Reclutamento
        • Research Site
      • Istanbul, Turchia (Türkiye), 34722
        • Ritirato
        • Research Site
      • Yenimahalle, Turchia (Türkiye), 06170
        • Reclutamento
        • Research Site
      • Budapest, Ungheria, 1083
        • Reclutamento
        • Research Site
      • Budapest, Ungheria, 1122
        • Reclutamento
        • Research Site
      • Budapest, Ungheria, 1062
        • Reclutamento
        • Research Site
      • Budapest, Ungheria, 1145
        • Reclutamento
        • Research Site
      • Gyula, Ungheria, 5700
        • Reclutamento
        • Research Site
      • Győr, Ungheria, 9024
        • Reclutamento
        • Research Site
      • Kecskemét, Ungheria, 6000
        • Reclutamento
        • Research Site
      • Miskolc, Ungheria, 3526
        • Reclutamento
        • Research Site
      • Nyíregyháza, Ungheria, 4400
        • Reclutamento
        • Research Site
      • Pécs, Ungheria, 7624
        • Reclutamento
        • Research Site
      • Szekszárd, Ungheria, 7100
        • Reclutamento
        • Research Site
      • Da Nang, Vietnam, 550000
        • Reclutamento
        • Research Site
      • Hanoi, Vietnam, 100000
        • Reclutamento
        • Research Site
      • Ho Chi Minh City, Vietnam, 700000
        • Reclutamento
        • Research Site
      • Huế, Vietnam, 530000
        • Reclutamento
        • Research Site
      • Hà Nội, Vietnam, 100000
        • Reclutamento
        • Research Site
      • Vinh, Vietnam, 460000
        • Reclutamento
        • Research Site

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 130 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • Histologically or cytologically documented locally advanced squamous cell carcinoma of the oropharynx, hypopharynx, oral cavity, or larynx with no evidence of metastatic disease (i.e. M0).
  • Confirmed unresected Stage III, Stage IVA or IVB according to the eighth edition of the American Joint Committee on Cancer (AJCC) staging manual (tumor, node, metastasis (TNM) staging system).
  • Participants will have completed definitive concurrent chemoradiotherapy (cCRT) with curative intent prior to randomization.

Exclusion Criteria:

  • Histologically/cytologically confirmed head and neck cancer of any other primary anatomic location in the head and neck not specified in the inclusion criteria including participants with squamous cell carcinoma of unknown primary or non-squamous histologies (eg, nasopharynx or salivary gland). Participants with >1 primary tumors are not eligible for the study.

  • Participants with any of the following:

    1. LA-HNSCC that was resected before definitive cCRT
    2. LA-HNSCC that was treated and is recurrent at the time of screening
  • Participants who have received radiotherapy (RT) alone as definitive local therapy for LA-HNSCC.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Study Arm

Participants in this arm will receive volrustomig.

volrustomig

Altri nomi:
  • MEDI5752
Nessun intervento: Observation Arm

Patients in this arm will undergo observation.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression-Free Survival (PFS) in participants with unresected LA-HNSCC with PD-L1 expressing tumors
Lasso di tempo: Up to approximately 8 years

PFS is defined as time from randomization until first objective radiological progression per RECIST 1.1 as assessed by Blinded Independent Central Review (BICR), or death due to any cause (in the absence of progression).

The analysis will include all randomized participants with PD-L1 expressing tumors.

Up to approximately 8 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression-Free Survival (PFS) in the unresected LA-HNSCC intent-to-treat (ITT) population
Lasso di tempo: Up to approximately 8 years

PFS is defined as time from randomization until first objective radiological progression per RECIST 1.1 as assessed by BICR, or death due to any cause (in the absence of progression).

The analysis will include all randomized participants.

Up to approximately 8 years
Landmark Progression-Free Survival (PFS) Rates
Lasso di tempo: Up to approximately 8 years

PFS is defined as time from randomization until first objective radiological progression per RECIST 1.1 as assessed by BICR, or death due to any cause (in the absence of progression).

These analyses will include participants with PD-L1 expressing tumors and all randomized participants.

Up to approximately 8 years
Overall Survival (OS) in participants with unresected LA-HNSCC with PD-L1 expressing tumors
Lasso di tempo: Up to approximately 8 years

Overall survival (OS) is defined as the time from randomization until the date of death due to any cause.

The analysis will include all randomized participants with PD-L1 expressing tumors.

Up to approximately 8 years
Landmark Overall Survival (OS) Rates
Lasso di tempo: Up to approximately 8 years

OS is defined as the time from randomization until the date of death due to any cause.

These analyses will include participants with PD-L1 expressing tumors as randomized and all randomized participants.

Up to approximately 8 years
Overall Survival (OS) in the unresected LA-HNSCC ITT population
Lasso di tempo: Up to approximately 8 years

OS is defined as the time from randomization until the date of death due to any cause.

The analysis will include all randomized participants.

Up to approximately 8 years
Progression Free Survival 2 (PFS2)
Lasso di tempo: Up to approximately 8 years

PFS2 is defined as the time from randomization until the earliest of the progression event (following the initial investigator-assessed progression), 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 eCRF and defined according to local standard clinical practice.

These analyses will include participants with PD-L1 expressing tumors as randomized and all randomized participants.

Up to approximately 8 years
Presence of Anti-Drug-Antibodies (ADAs) against volrustomig in serum
Lasso di tempo: Up to approximately 8 years

To investigate the immunogenicity of volrustomig.

Up to approximately 8 years
Participant-reported physical functioning
Lasso di tempo: Up to approximately 8 years

Change from baseline of physical functioning as measured by scores on the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form v.20 - Physical Function 8c are reported on a T score metric (mean = 50 and SD = 10), with higher scores reflecting better physical functioning.

The analysis will include all randomized participants.

Up to approximately 8 years
Participant-reported global health status (GHS)/quality of life (QoL)
Lasso di tempo: Up to approximately 8 years

Change from baseline of Global Health Status/Quality of Life subscale scores as measured by the European Organization for Research and Treatment of Cancer (EORTC) Item Library 172 are transformed to a 0-100 range; a higher score represents higher quality of life.

The analysis will include all randomized participants.

Up to approximately 8 years
Percentage of participants with Adverse Events
Lasso di tempo: Up to approximately 8 years

Adverse Events as assessed by Common Terminology Criteria for Adverse Events (CTCAE).

Up to approximately 8 years
Area under the curve (AUC)
Lasso di tempo: Up to approximately 8 years

The concentration of Volrustomig in serum will be determined. Area under the curve is the integral of the concentration-time curve. The AUC reflects the actual body exposure to drug after administration. The AUC is dependent on the rate of elimination of the drug from the body and the dose administered.

Up to approximately 8 years
Maximum plasma concentration of the drug (Cmax)
Lasso di tempo: Up to approximately 8 years

The concentration of Volrustomig in serum will be determined (Cmax will be derived).

Up to approximately 8 years
The time taken to reach the maximum concentration (Tmax)
Lasso di tempo: Up to approximately 8 years

The concentration of Volrustomig in serum will be determined (Tmax will be derived).

Up to approximately 8 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Cattedra di studio: Robert Haddad, MD, Dana Farber Cancer Institute Massachusetts, USA
  • Cattedra di studio: Lisa Licitra, MD, Fondazione IRCCS Istituto Nazionale dei Tumori and University of Milan Milan, Italy

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

14 dicembre 2023

Completamento primario (Stimato)

17 aprile 2030

Completamento dello studio (Stimato)

28 febbraio 2031

Date di iscrizione allo studio

Primo inviato

3 novembre 2023

Primo inviato che soddisfa i criteri di controllo qualità

10 novembre 2023

Primo Inserito (Effettivo)

13 novembre 2023

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • D798EC00001

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal.

All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure

Periodo di condivisione IPD

AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles.

For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure

Criteri di accesso alla condivisione IPD

When a request has been approved AstraZeneca will provide access to the deidentified individual patient-level data in an approved sponsored tool .

Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.

Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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