- Trials with a EudraCT protocol (1,056)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
1,056 result(s) found for: Malignant Solid Tumor.
Displaying page 1 of 53.
EudraCT Number: 2021-004395-34 | Sponsor Protocol Number: C4221026 | Start Date*: 2022-04-25 | ||||||||||||||||||||||||||
Sponsor Name:Pfizer Inc. | ||||||||||||||||||||||||||||
Full Title: ENCORAFENIB/BINIMETINIB MASTER PROTOCOL: AN OPEN-LABEL CONTINUATION STUDY FOR PARTICIPANTS CONTINUING FROM ENCORAFENIB/BINIMETINIB CLINICAL STUDIES | ||||||||||||||||||||||||||||
Medical condition: solid tumors | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) BE (Trial now transitioned) SK (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) PT (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005190-36 | Sponsor Protocol Number: 20050252 | Start Date*: 2015-01-22 | ||||||||||||||||||||||||||
Sponsor Name:Amgen Inc | ||||||||||||||||||||||||||||
Full Title: A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of Panitumumab in Children with Solid Tumors | ||||||||||||||||||||||||||||
Medical condition: Solid Tumours | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005605-27 | Sponsor Protocol Number: TNG908-C101 | Start Date*: 2022-09-07 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Tango Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Phase 1: • Locally advanced or metastatic MTAP-deleted solid tumors (with the exception of gliomas) Phase 2: • Arm 1: Locally advanced or metastatic MTAP-deleted squamous and nonsquamous NSCLC ... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001403-33 | Sponsor Protocol Number: TCTLR-101 | Start Date*: 2023-06-06 | ||||||||||||||||||||||||||
Sponsor Name:Ascendis Pharma Oncology Division A/S | ||||||||||||||||||||||||||||
Full Title: Phase 1/2, Open-label, Dose Escalation and Dose Expansion Study of TransCon TLR7/8 Agonist Alone or in Combination with Pembrolizumab in Participants with Locally Advanced or Metastatic Solid Tumor... | ||||||||||||||||||||||||||||
Medical condition: Locally advanced or metastatic solid tumor malignancies | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) HU (Prematurely Ended) NL (Trial now transitioned) PL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001596-14 | Sponsor Protocol Number: TYR300-101 | Start Date*: 2023-06-26 | |||||||||||||||||||||||||||||||
Sponsor Name:Tyra Biosciences, Inc. | |||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Open-label Phase 1/2 Study of TYRA 300 in Advanced Urothelial Carcinoma and Other Solid Tumors with Activating FGFR3 Gene Alterations (SURF 301) | |||||||||||||||||||||||||||||||||
Medical condition: Advanced Urothelial Carcinoma and Other Solid Tumors with Activating FGFR3 Gene Alterations | |||||||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000509-29 | Sponsor Protocol Number: GCT1042-02 | Start Date*: 2022-11-04 | ||||||||||||||||
Sponsor Name:Genmab A/S | ||||||||||||||||||
Full Title: A Phase 1/2, Randomized, Open-Label Trial to Evaluate the Safety and Clinical Activity of Immunoradiotherapy Combinations as a Treatment Option for Subjects With Metastatic Solid Tumors | ||||||||||||||||||
Medical condition: Metastatic Solid Malignant tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000157-27 | Sponsor Protocol Number: INCB86550-203 | Start Date*: 2020-08-25 | ||||||||||||||||
Sponsor Name:Incyte Corporation | ||||||||||||||||||
Full Title: A Phase 2 Study of INCB086550 (Oral PD-L1 Inhibitor) in Participants Who Are Immune Checkpoint Inhibitor–Naïve With Selected Solid Tumors | ||||||||||||||||||
Medical condition: Immune Checkpoint Inhibitor–Naïve Selected Solid Tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001155-39 | Sponsor Protocol Number: D8480C00016 | Start Date*: 2012-03-09 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: Phase I trial of AZD2171, an orally bioavailable antiangiogenic agent, in children and adolescents with refactory or recurrent solid tumours or acute myelogenous leukemia | |||||||||||||
Medical condition: Refractory or recurrent solid tumours or acute myelogenous leukemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003998-26 | Sponsor Protocol Number: GCT1044-01 | Start Date*: 2020-05-16 | |||||||||||
Sponsor Name:Genmab A/S | |||||||||||||
Full Title: First-in-human, open-label, dose-escalation trial with expansion cohorts to evaluate safety of GEN1044 in subjects with malignant solid tumors | |||||||||||||
Medical condition: Malignant Solid Tumors, per protocol GCT1044-01 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002009-31 | Sponsor Protocol Number: MO25757 | Start Date*: 2012-03-23 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A single arm open label multicentre extension study of bevacizumab in patients with solid tumours on study treatment with bevacizumab at the end of a F. Hoffmann-La Roche and/or Genentech sponsored... | ||||||||||||||||||
Medical condition: Solid tumours | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) GB (Completed) ES (Completed) SK (Completed) NL (Completed) FR (Completed) IT (Prematurely Ended) DE (Completed) EE (Completed) HU (Completed) LV (Prematurely Ended) AT (Completed) GR (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024237-23 | Sponsor Protocol Number: CDI-CS-001 | Start Date*: 2011-05-06 | |||||||||||
Sponsor Name:Basilea Pharmaceutica International Ltd. | |||||||||||||
Full Title: An Open-Label Phase I/IIa Study of Intravenous BAL101553 in Adult Patients with Advanced Solid Tumors | |||||||||||||
Medical condition: Advanced or recurrent solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002184-42 | Sponsor Protocol Number: TED12689 | Start Date*: 2016-02-19 | ||||||||||||||||
Sponsor Name:Sanofi-aventis | ||||||||||||||||||
Full Title: A Phase 1-2 Dose Finding, Safety and Efficacy Study of Cabazitaxel in Pediatric Patients with Refractory Solid Tumors Including Tumors of the Central Nervous System | ||||||||||||||||||
Medical condition: Cancer | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005939-28 | Sponsor Protocol Number: BO21495 | Start Date*: 2008-04-29 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: Estudio de fase I/II multicéntrico, abierto, de escalada de dosis, para evaluar la seguridad, farmacocinética y actividad de RO5083945, un anticuerpo glico-modificado anti-EGFR, en pacientes con tu... | ||||||||||||||||||
Medical condition: Parte I: Tumores sólidos malignos metastáticos y/o localmente avanzados que expresan el receptor del factor de crecimiento endotelial (EGFR) Parte II: Cáncer colorrectal metastático o localmente a... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000729-55 | Sponsor Protocol Number: 8669-056 | Start Date*: 2011-12-15 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase I Study of Ridaforolimus in Paediatric Patients with Advanced Solid Tumours | |||||||||||||
Medical condition: advanced solid tumours including lymphoma and tumours of the central nervous system | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003912-11 | Sponsor Protocol Number: Sym015-01 | Start Date*: 2017-03-10 | |||||||||||
Sponsor Name:Symphogen A/S | |||||||||||||
Full Title: An Open-label, Multicenter Phase 1a/2a Trial Investigating the Safety, Tolerability and Antitumor Activity of Multiple Doses of Sym015, a Monoclonal Antibody Mixture Targeting MET, in Patients with... | |||||||||||||
Medical condition: Advanced Solid Tumor Malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006246-33 | Sponsor Protocol Number: LTS12674 | Start Date*: 2012-06-28 | |||||||||||
Sponsor Name:Sanofi-aventis recherche et développement | |||||||||||||
Full Title: International, Multi-Center, Open-label, Treatment Extension Study of Iniparib as Monotherapy or in Combination Chemotherapeutic Regimens in Cancer Patients Who Have Derived Clinical Benefit From I... | |||||||||||||
Medical condition: Solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003385-84 | Sponsor Protocol Number: GO40782(RXDX-101-02) | Start Date*: 2016-03-15 | ||||||||||||||||
Sponsor Name:F. Hoffman-La Roche Ltf | ||||||||||||||||||
Full Title: AN OPEN-LABEL, MULTICENTER, GLOBAL PHASE 2 BASKET STUDY OF ENTRECTINIB FOR THE TREATMENT OF PATIENTS WITH LOCALLY ADVANCED OR METASTATIC SOLID TUMORS THAT HARBOR NTRK1/2/3, ROS1, OR ALK GENE REARRA... | ||||||||||||||||||
Medical condition: Locally Advanced or Metastatic Solid Tumors that Harbor NTRK1/2/3, ROS1, or ALK Gene Rearrangements | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) DE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005100-34 | Sponsor Protocol Number: VX13-970-002 | Start Date*: 2014-04-16 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: An Open-Label Study of the Safety, Tolerability, and Pharmacokinetic / Pharmacodynamic Profile of VX-970 as a Single Agent in Combination With Carboplatin in Subjects With Advanced Solid Tumors | |||||||||||||
Medical condition: Cancer (malignant solid tumors) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005646-15 | Sponsor Protocol Number: 21-BI-1607-01 | Start Date*: 2022-07-06 | ||||||||||||||||||||||||||
Sponsor Name:BioInvent International AB | ||||||||||||||||||||||||||||
Full Title: Phase 1/2a Open-label Clinical Trial of BI-1607, an Fc-Engineered Monoclonal Antibody to CD32b (FcγRIIB), in Combination with Trastuzumab in Subjects with HER2-positive Advanced Solid Tumors - CONT... | ||||||||||||||||||||||||||||
Medical condition: HER2-positive locally Advanced unresectable or metastatic solid tumors in Phase 1 HER2+ breast cancer and subjects with HER2+ metastatic gastric or gastroesophageal junction adenocarcinoma in Pha... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001394-16 | Sponsor Protocol Number: GCT1029-01 | Start Date*: 2018-03-29 | |||||||||||
Sponsor Name:Genmab B.V. | |||||||||||||
Full Title: First-in-human, open-label, dose-escalation trial with expansion cohorts to evaluate safety of GEN1029 in patients with malignant solid tumors | |||||||||||||
Medical condition: Malignant solid tumors: Patients with advanced and/or metastatic colorectal cancer (CRC), non-small cell lung cancer (NSCLC), triple negative breast cancer (TNBC), renal cell carcinoma (RCC), gastr... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
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