- Trials with a EudraCT protocol (479)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
479 result(s) found for: Carcinoma in Situ.
Displaying page 16 of 24.
EudraCT Number: 2007-001152-39 | Sponsor Protocol Number: SSG XX | Start Date*: 2024-05-21 |
Sponsor Name:Scandinavian Sarcoma Group | ||
Full Title: SSGXX A Scandinavian Sarcoma Group treatment protocol for adult patients with non-metastatic high-risk soft tissue sarcoma of the extremities and trunk wall | ||
Medical condition: SSG XX is a phase II trial for high-risk soft tissue sarcoma(STS) of the extremities and trunk wall. Prognostic markers are used to identify high-risk tumors. SSG XX will evaluate chemo-and radioth... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005081-17 | Sponsor Protocol Number: ARV-471-BC-201 | Start Date*: 2023-01-20 | ||||||||||||||||
Sponsor Name:Arvinas Estrogen Receptor, Inc. (Arvinas) | ||||||||||||||||||
Full Title: An Open-Label, Randomized, Non-Comparative Phase 2 Study of ARV-471 or Anastrozole in Post-Menopausal Women With ER+/HER2– Breast Cancer in the Neoadjuvant Setting | ||||||||||||||||||
Medical condition: Post-menopausal women with ER+ HER2– breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002190-21 | Sponsor Protocol Number: MAR-BAS-18-005 | Start Date*: 2020-07-08 | |||||||||||||||||||||
Sponsor Name:Fondazione per la Medicina Personalizzata | |||||||||||||||||||||||
Full Title: The ROME trial from histology to target: the road to personalize target therapy and immunotherapy | |||||||||||||||||||||||
Medical condition: Patients with progressive disease (recurrent and/or metastatic) of breast cancer, metastatic gastro-intestinal tumors, non small cell lung cancer (NSCLC) or others. Patients should have completed a... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004024-37 | Sponsor Protocol Number: A6181109 | Start Date*: 2007-07-05 | |||||||||||
Sponsor Name:Pfizer Inc. - 235 East 42nd Street - New York - 10017 | |||||||||||||
Full Title: SUNITINIB TREATMENT OF RENAL ADJUVANT CANCER (S-TRAC): A RANDOMIZED DOUBLE-BLIND PHASE 3 STUDY OF ADJUVANT SUNITINIB VS. PLACEBO IN SUBJECTS WITH HIGH RISK RCC | |||||||||||||
Medical condition: Adjuvant treatment of subjects with “high risk” Renal Cell Carcinoma (RCC) following nephrectomy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) CZ (Completed) DE (Completed) GR (Completed) AT (Completed) IT (Completed) IE (Completed) SE (Completed) PL (Completed) SK (Completed) DK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003874-29 | Sponsor Protocol Number: E-3810-II-02 | Start Date*: 2014-01-20 | |||||||||||
Sponsor Name:EOS S.p.A. | |||||||||||||
Full Title: A single arm, open-label, phase II study to assess the efficacy of the dual VEGFR-FGFR tyrosine kinase inhibitor, lucitanib, given orally as a single agent to patients with FGFR1-driven lung cancer | |||||||||||||
Medical condition: FGFR1-amplified squamous non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005328-17 | Sponsor Protocol Number: MO28048 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A phase III prospective, two-cohort non-randomised, multi-centre, multinational, open label study to assess the safety of assisted- and self-administered subcutaneous trastuzumab as therapy in pati... | |||||||||||||
Medical condition: HER2-positive primary breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) CZ (Completed) DE (Completed) ES (Completed) FR (Completed) HU (Completed) PT (Completed) GB (Completed) NO (Completed) IT (Completed) GR (Completed) LT (Completed) PL (Completed) SI (Completed) SK (Completed) FI (Completed) BG (Completed) NL (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000824-21 | Sponsor Protocol Number: IJB-NERABRAIN-ODN-007 | Start Date*: 2021-10-05 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: An open label phase II study to evaluate neratinib for treatment and prevention of subsequent CNS event(s) in patients with brain metastasis of advanced HER2 positive breast cancer | |||||||||||||
Medical condition: HER2 positive breast cancer patients with brain metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002437-21 | Sponsor Protocol Number: GEICAM/2014-12 | Start Date*: 2015-11-09 | |||||||||||
Sponsor Name:GEICAM (Spanish Breast Cancer Research Group Foundation) | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, multicentre, phase II study to compare the efficacy and tolerability of fulvestrant (FaslodexTM) 500mg with placebo and fulvestrant (FaslodexTM) 500mg in... | |||||||||||||
Medical condition: Postmenopausal women presenting with HR-positive/HER2-negative metastatic breast cancer who have received at least 5 years of endocrine therapy in the adjuvant setting as treatment for early diseas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) IE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004472-30 | Sponsor Protocol Number: MITO23 | Start Date*: 2015-12-02 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Randomized phase III trial on Trabectedin (ET-743) vs clinician’s choice chemotherapy in recurrent ovarian, primary peritoneal or fallopian tube cancers of BRCA mutated or BRCAness phenotype patients | |||||||||||||
Medical condition: recurrent ovarian, primary peritoneal or fallopian tube cancers of BRCA mutated or BRCAness phenotype patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003112-31 | Sponsor Protocol Number: LP0041-63 | Start Date*: 2013-07-13 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Risk of Squamous Cell Carcinoma on Skin Areas Treated with Ingenol Mebutate Gel, 0.015% and Imiquimod Cream, 5% | |||||||||||||
Medical condition: Actinic keratosis on the face and scalp | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000654-23 | Sponsor Protocol Number: EORTC 18032 | Start Date*: 2004-12-09 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: Extended schedule, escalated dose Temozolomide versus Dacarbazine in Stage IV Metastatic Melanoma: A Randomized Phase III Study of the EORTC Melanoma Group | |||||||||||||
Medical condition: Stage IV Metastatic Melanoma: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006363-24 | Sponsor Protocol Number: TTD-06-04 | Start Date*: 2007-04-20 | |||||||||||
Sponsor Name:Grupo de Tratamiento de los Tumores Digestivos (TTD) | |||||||||||||
Full Title: An Phase 2 Clinical Trial of Panitumumab in Conbination vith Irinotecan chemotherapy as 2nd line Therapy in subjects with Metastatic Colorectal Cancer. Ensayo Clínico fase II de Panitumumab combin... | |||||||||||||
Medical condition: Cáncer colorectal metastásico. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002760-16 | Sponsor Protocol Number: 04/QO603/42 HEXVIX | Start Date*: 2005-01-12 | |||||||||||
Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | |||||||||||||
Full Title: A randomised Study of “bluelight” hexyl amino levulinic acid (HAL) photodynamic assisted resection of bladder tumours versus conventional “white light” transurethral resection of newly diagnosed bl... | |||||||||||||
Medical condition: Superficial Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004505-29 | Sponsor Protocol Number: 2676 | Start Date*: 2008-05-15 | |||||||||||
Sponsor Name:Royal Marsden NHS Trust | |||||||||||||
Full Title: Phase II clinical trial of capecitabine and oxaliplatin plus bevacizumab as neoadjuvant treatment for patients with previously untreated unresectable liver-only metastases from colorectal cancer | |||||||||||||
Medical condition: Metastatic colorectal adenocarcinoma with metastases involving the liver only | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010975-26 | Sponsor Protocol Number: ACROSS-08-01 | Start Date*: 2009-07-16 |
Sponsor Name:Associació Catalana per a la Recerca Oncológica i les seves implicacions Sanitáries i Socials | ||
Full Title: Estudio clínico abierto de fase II de panitumumab en combinación con quimioterapia FOLFIRI como tratamiento de segunda línea en sujetos con cáncer colorrectal metastásico que expresa KRAS no mutado... | ||
Medical condition: Cáncer colorrectal metastásico que expresa KRAS no mutado | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001036-22 | Sponsor Protocol Number: SOLTI-1114 | Start Date*: 2013-10-15 | |||||||||||
Sponsor Name:SOLTI | |||||||||||||
Full Title: PAM50 HER2-enriched phenotype as a predictor of early response to neoadjuvant lapatinib plus trastuzumab in Stage I to IIIA HER2-positive breast cancer | |||||||||||||
Medical condition: Untreated invasive breast carcinoma eligible for primary definitive surgery (Stage I-IIIA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001181-36 | Sponsor Protocol Number: SOLTI-2103 | Start Date*: 2022-11-21 |
Sponsor Name:SOLTI | ||
Full Title: A phase 2 trial of neoadjuVAnt muLti-agENt chemotherapy or patritumab deruxtecan (HER3-DXd; HER3-DXd) with or without endocrINE therapy for high-risk HR+/HER2- breast cancer – VALENTINE trial | ||
Medical condition: treatment naïve patients with HR+/HER2-negative high-risk early breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000432-10 | Sponsor Protocol Number: 26866138MMY2084 | Start Date*: 2013-05-23 |
Sponsor Name:DUTCH BELGIAN COOPERATIVE GROUP FOR HEMATOLOGY ONCOLOGY - HOVON | ||
Full Title: A PHASE II MULTI-CENTRE, RANDOMIZED, OPEN LABEL STUDY OF PROLONGED THERAPY WITH SUBCUTANEOUS BORTEZOMIB TWICE MONTHLY ASSOCIATED WITH DEXAMETHASONE, IN RELAPSED AND REFRACTORY MULTIPLE MYELOMA PAT... | ||
Medical condition: Patients with Multiple Myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001503-20 | Sponsor Protocol Number: MedOPP150(ATRACTIB) | Start Date*: 2021-07-30 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
Full Title: PHASE II CLINICAL TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF FIRST LINE ATEZOLIZUMAB IN COMBINATION WITH PACLITAXEL AND BEVACIZUMAB (AVASTIN®) IN PATIENTS WITH ADVANCED OR METASTATIC TRIPLE-NEGAT... | |||||||||||||
Medical condition: Advanced or metastatic triple-negative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004651-23 | Sponsor Protocol Number: IJB-SYNERGY-012017 | Start Date*: 2018-10-16 | |||||||||||||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||||||||||||
Full Title: A Phase I/II Study of Paclitaxel plus Carboplatin and Durvalumab (MEDI4736) with or without Oleclumab (MEDI9447) for Previously Untreated Locally Recurrent Inoperable or Metastatic Triple-negative ... | |||||||||||||||||||||||
Medical condition: Previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer (TNBC) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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