- Trials with a EudraCT protocol (360)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
360 result(s) found for: oncology and PET.
Displaying page 1 of 18.
EudraCT Number: 2019-003713-33 | Sponsor Protocol Number: 70903 | Start Date*: 2020-03-02 | |||||||||||
Sponsor Name:Princess Máxima Center for pediatric oncology | |||||||||||||
Full Title: Diagnostic accuracy of neuroblastoma patient imaging with [18F]-mFBG PET-CT compared to [123]I-mIBG scanning | |||||||||||||
Medical condition: Neuroblastoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006570-23 | Sponsor Protocol Number: FAPI-POLMONE-2021 | Start Date*: 2022-03-17 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: The Role Of The New Promising Oncological Pet/Ct Tracer [68Ga] Ga-Fapi For Staging Lung Cancer: A Preliminary Study | |||||||||||||
Medical condition: suspected / newly diagnosed lung cancer in staging, patients already on a conventional staging diagnostic path (including FDG-PET / standard CT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000398-64 | Sponsor Protocol Number: VHIO18001 | Start Date*: 2018-06-18 | |||||||||||
Sponsor Name:Vall d' Hebron Institute of Oncology (VHIO) | |||||||||||||
Full Title: Patterns of uptake of 18F-FDG and 68Ga-DOTA PET in advanced neuroendoctrine tumors | |||||||||||||
Medical condition: Gastroenteropancreatic neuroendocrine tumor disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001219-26 | Sponsor Protocol Number: N20PIP | Start Date*: 2021-02-11 |
Sponsor Name:tichting Het Nederlands Kanker Instituut_Antoni van Leeuwenhoek | ||
Full Title: Prostatic Artery Injection vs Intra-Venous Injection of 18F-DCFPyL to evaluate treatment strategy in Prostate Cancer | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003981-42 | Sponsor Protocol Number: 2012.2708 | Start Date*: 2014-10-20 |
Sponsor Name:University Medical Center Groningen [...] | ||
Full Title: Estrogen receptor and androgen receptor imaging in metastatic breast cancer patients | ||
Medical condition: Estrogen receptor positive metastatic breast cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004425-13 | Sponsor Protocol Number: PP01 | Start Date*: 2016-01-22 | |||||||||||
Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
Full Title: Prospective evaluation of 68-Ga-PSMA-PET and early PSA kinetics during salvage radiotherapy for personalizing the management of men with relapse of prostate cancer after radical prostatectomy. | |||||||||||||
Medical condition: Patients with prostate cancer, with a PSA recurrence of ˃ 0.2 ng/ml after prostatectomy, and who are going to receive radiotherapy to the prostate bed. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001811-16 | Sponsor Protocol Number: PS21GAP | Start Date*: 2022-12-19 | |||||||||||
Sponsor Name:Princess Maxima Center for pediatric oncology | |||||||||||||
Full Title: 68Ga-SATO in pediatric neuroblastoma patient; exploratory, safety, non-randomized, open label, comparative study | |||||||||||||
Medical condition: Neuroblastoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002013-35 | Sponsor Protocol Number: FORESIGHT | Start Date*: 2018-10-19 |
Sponsor Name:VU University Medical Center | ||
Full Title: FES (16α-[18F]-fluoro-17β-estradiol)-PET: Towards a new standard to stage clinical stage II/III and recurrent, estrogen receptor positive (ER+) breast cancer? Pilot study to compare [18F]FES-PET an... | ||
Medical condition: Breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000148-23 | Sponsor Protocol Number: FAPI-PET-Trial | Start Date*: 2021-06-30 |
Sponsor Name:University Hospital Essen | ||
Full Title: 68Ga-FAPI-46 PET for imaging of FAP expressing cancer: A single-center prospective interventional single-arm clinical Trial | ||
Medical condition: Patients receiving 68Ga-FAPI-46 PET both at initial diagnosis and restaging before treatment decisions | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005786-60 | Sponsor Protocol Number: FET-PET-2010 | Start Date*: Information not available in EudraCT |
Sponsor Name:Charité Universitaetsmedizin Berlin | ||
Full Title: A prospective, multicentre trial on the value of 18F-FET PET in the post-therapeutic evaluation of childhood brain tumours | ||
Medical condition: Children and adolescents with a primary brain tumour after first line therapy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-002676-27 | Sponsor Protocol Number: MedOPP096-MO39229 | Start Date*: 2017-05-25 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MedSIR) | |||||||||||||
Full Title: Chemotherapy-free trastuzumab and pertuzumab in HER2-positive breast cancer: FDG-PET response-adapted strategy. The PHERGain study | |||||||||||||
Medical condition: HER2-positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Completed) FR (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000744-10 | Sponsor Protocol Number: P.64Cu.003.01 | Start Date*: 2019-06-28 | |||||||||||
Sponsor Name:A.C.O.M. -ADVANCED CENTER ONCOLOGY MACERATA -S.R.L. | |||||||||||||
Full Title: Higher diagnostic accuracy of 64Cu PET/CT compared to standard 18F-choline PET/CT in the detection rate of metastasis from prostate cancer. Phase III multicenter, sponsored, interventional "open-la... | |||||||||||||
Medical condition: Prostate cancer at risk of developing metastatic lesions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000625-37 | Sponsor Protocol Number: BED-004 | Start Date*: 2015-08-28 | |||||||||||
Sponsor Name:Blue Earth Diagnostics Limited | |||||||||||||
Full Title: A phase 3, open-label study to assess the clinical utility of fluciclovine (18F) PET/CT in patients with prostate cancer with biochemical recurrence after radical treatment | |||||||||||||
Medical condition: Prostate cancer with biochemical recurrence after radical treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005192-39 | Sponsor Protocol Number: 202100663 | Start Date*: 2022-04-11 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Programmed death ligand 1 (PD-L1) PET imaging in patients with (Diffuse) Large B-cell lymphoma who are treated with CD19-directed CAR T-cell therapy | ||
Medical condition: Patients with relapsed/refractory large B-cell lymphoma (LBCL) after two or more lines of therapy who fulfill the eligibility criteria for CD19-directed CAR T-cell therapy according the Immune Effe... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004974-27 | Sponsor Protocol Number: BP28015 | Start Date*: 2012-03-26 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: 89Zr-RO5323441 PET imaging in patients with recurrent glioblastoma treated with bevacizumab | |||||||||||||
Medical condition: Recurrent malignant glioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002957-46 | Sponsor Protocol Number: 56021927PCR3015 | Start Date*: 2020-05-13 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Controlled, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Adding Apalutamide to Radiotherapy and LHRH Agonist in High-Risk Patients with Hormone-Sensitive Pr... | |||||||||||||
Medical condition: High risk recurrent prostate cancer previously treated with radical prostatectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Trial now transitioned) CZ (Trial now transitioned) DK (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) PT (Trial now transitioned) BE (Trial now transitioned) SK (Trial now transitioned) IT (Trial now transitioned) HU (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001429-25 | Sponsor Protocol Number: 2011.0704 | Start Date*: 2011-08-23 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Feasibility Study: FES-PET to determine ER-expression in epithelial ovarian cancer | ||
Medical condition: epithelial ovarian cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003959-16 | Sponsor Protocol Number: CAAA405A12301 | Start Date*: 2021-04-27 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: Phase III study for evaluation of the diagnostic performance of [18F]CTT1057 PET imaging in patients with prostate cancer with rising PSA levels [biochemical recurrence (BCR)] (GuidePath) | |||||||||||||
Medical condition: Prostate cancer with rising PSA levels [biochemical recurrence (BCR)] | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002480-15 | Sponsor Protocol Number: M14REP | Start Date*: 2014-10-15 | ||||||||||||||||
Sponsor Name:The Dutch Working Group on Immunotherapy of Oncology (WIN-O) | ||||||||||||||||||
Full Title: A Phase II, Open-Label, Multicenter Study of Vemurafenib plus Cobimetinib (GDC-0973) in Unresectable Stage IIIc or Metastatic Melanoma; Response Monitoring and Resistance Prediction with Positron E... | ||||||||||||||||||
Medical condition: BRAFV600-mutation positive patients with unresectable stage IIIc or IV melanoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005610-33 | Sponsor Protocol Number: IAB-CD8-203 | Start Date*: 2022-02-09 | |||||||||||
Sponsor Name:ImaginAb, Inc. | |||||||||||||
Full Title: iPREDICT Trial: A Phase IIB, Open Label, Study of 89Zr-Df-Crefmirlimab PET/CT in Subjects with Selected Advanced or Metastatic Malignancies including Melanoma, Merkel Cell, Renal Cell and Non-Small... | |||||||||||||
Medical condition: To predict if patients with selected advanced or metastatic malignancies including Melanoma, Merkel Cell, Renal Cell and Non-Small Cell Lung Cancers, will respond to standard-of-care Immunotherapy ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
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