- Trials with a EudraCT protocol (128)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
128 result(s) found for: Peptides.
Displaying page 1 of 7.
EudraCT Number: 2010-023757-11 | Sponsor Protocol Number: myDC/pDCinstageIIImelanoma | Start Date*: 2014-11-06 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Myeloid and plasmacytoid blood dendritic cells for immunotherapy of stage III melanoma patients scheduled for radical lymph node dissection | ||
Medical condition: melanoma patients with regional lymph node metastases (stage III) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003025-18 | Sponsor Protocol Number: VAPER | Start Date*: 2015-05-08 |
Sponsor Name:King's College London [...] | ||
Full Title: In Vivo Generation of Optimal Tumour Antigen-specific Anticancer Immune Responses, by Vaccination with Human Telomerase Reverse Transcriptase (hTERT) Peptides, in Combination with Specific Adjuvant... | ||
Medical condition: Advanced malignancies | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006369-10 | Sponsor Protocol Number: BTT-gpASIT003 | Start Date*: 2009-01-22 |
Sponsor Name:BioTech Tools S.A. | ||
Full Title: Preliminary assessment of the clinical tolerability, safety and immunogenicity of three different doses of grass pollen-derived peptides for oral use in antigen-specific immunotherapy of seasonal a... | ||
Medical condition: seasonal allergic rhinoconjunctivitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002373-35 | Sponsor Protocol Number: T153/2016 | Start Date*: 2016-07-04 |
Sponsor Name: | ||
Full Title: The Effects of Dietary Peptides on Human Brown Adipose Tissue | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000228-14 | Sponsor Protocol Number: LUC 05-003 | Start Date*: 2006-02-21 |
Sponsor Name:Cliniques Universitaires Saint-Luc | ||
Full Title: Immunization of disease-free melanoma patients with different HLA-A2 peptides. | ||
Medical condition: We want to vaccine HLA-A2 patients who had a cutaneous melanoma at the following AJCC stage T3b-T4 N0 M0, Tx N1-3 M0, Tx Nx M0. Disease-free after surgery. With no previous immunizations with the s... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002531-29 | Sponsor Protocol Number: NaturalDCformCRPC | Start Date*: 2014-10-30 |
Sponsor Name:Radboud University Medical Centre Nijmegen | ||
Full Title: A randomized phase IIa study: natural dendritic cells for immunotherapy of chemo-naive metastatic castration-resistant prostate cancer patients | ||
Medical condition: Asymptomatic or minimally symptomatic, chemo-naive mCRPC patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005322-19 | Sponsor Protocol Number: MIND-DC | Start Date*: 2016-01-21 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: A randomized, double-blind, placebo-controlled phase III study to evaluate active immunization in adjuvant therapy of patients with stage IIIB and IIIC melanoma with natural dendritic cells pulsed ... | ||
Medical condition: melanoma patients with regional lymph node metastases (stage III) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002109-22 | Sponsor Protocol Number: 02/05/Hü | Start Date*: 2005-12-01 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Comparative Effects of Telmisartan and Candesartan on glucose metabolism in patients with chronic heart failure | ||
Medical condition: both investigated drugs are well established in the treatment of heart failure or hypertension respectively. As the investigateed Patients have this conditions according to the inclusion criteria, ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004467-31 | Sponsor Protocol Number: DECENDO | Start Date*: 2019-04-05 |
Sponsor Name: | ||
Full Title: An exploratory study: Dendritic cells for immunotherapy of metastatic endometrial cancer patients | ||
Medical condition: metastatic endometrial cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004325-16 | Sponsor Protocol Number: RC31/16/8407 | Start Date*: 2016-12-22 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: Long term evaluation of infants aged from 3 to 4 years old included in the OTBB2 study (repeated administrations of oxytocin in infants with PWS aged from 0 to 6 months) and comparison with not tre... | ||
Medical condition: Prader Willi Syndrom | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017798-39 | Sponsor Protocol Number: PROVAX study | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: An open label, Phase II study of vaccination with Survivin peptides emulsified in Montanide ISA 51VG after IMP 321 injection in prostate carcinoma patients with biochemical failure (PROVAX study) | |||||||||||||
Medical condition: Prostate cancer, biochemical failure after all potentially curative standard local therapies (radiotherapy, brachytherapy and surgery) or biochemical progression while patients have castrated level... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005230-37 | Sponsor Protocol Number: HPV01/01 | Start Date*: 2008-04-02 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Randomised Controlled Study on the Effects of Imiquimod, a TLR 7 Activating Agent, on the HPV16-Specific Immune Response Following HPV16 E6/E7 Synthetic Long Peptides Vaccination in Women with HPV1... | |||||||||||||
Medical condition: Adult female patients, with histological evidence of Vulvar intraepithelial neoplasia (VIN) grade III lesions of the squamous cell type, positive for HPV (Human Papilloma Virus)16. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001374-60 | Sponsor Protocol Number: MOB-02 | Start Date*: 2022-07-21 |
Sponsor Name:BCN Peptides | ||
Full Title: A randomized, double blinded, placebo controlled clinical trial to evaluate the antipruritic efficacy of the topical application of PARENTIDE cream in histamine-induced itch in healthy volunteers | ||
Medical condition: Treatment of pruritus or uticaria | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001745-42 | Sponsor Protocol Number: 3045 | Start Date*: 2005-12-06 |
Sponsor Name:University of Liverpool and Royal Liverpool University Hospital | ||
Full Title: BCR-ABL Peptide Vaccination in Normal Subjects.An investigation in normal subjects with HLA-A3 and HLA-B8, as an extension of an identical study in patients with Chronic Myeloid Leukaemia. | ||
Medical condition: Healthy Subjects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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: 2019-001434-34 | Sponsor Protocol Number: MPN19H2 | Start Date*: 2019-07-04 | |||||||||||||||||||||
Sponsor Name:Department of haematology, Zealand university hospital | |||||||||||||||||||||||
Full Title: Dual Vaccine Trial in Myeloproliferative Neoplasms | |||||||||||||||||||||||
Medical condition: Myeloproliferative Neoplasms | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002411-26 | Sponsor Protocol Number: UV1/hTERT-2012-P | Start Date*: 2013-03-18 | ||||||||||||||||
Sponsor Name:Oslo University Hospital | ||||||||||||||||||
Full Title: A PHASE I/IIA STUDY OF UV1 VACCINATION IN PATIENTS WITH HORMONE-SENSITIVE METASTATIC PROSTATE CANCER. | ||||||||||||||||||
Medical condition: Patients with advanced oligometastatic prostate cancer (PCa) without lung and/or liver metastases who are eligible to Complete Androgen Blockade therapy (GnRH-agonist combined with anti-androgen). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: NO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004686-15 | Sponsor Protocol Number: LUD 03-007 | Start Date*: 2005-08-04 |
Sponsor Name:Ludwig Institute For Cancer Research | ||
Full Title: Phase I/II study of immunization with multiple peptides mixed with the immunological adjuvant CpG 7909 in HLA-A2 patients with metastatic melanoma ... | ||
Medical condition: HLA-A2 patients with metastatic melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000765-12 | Sponsor Protocol Number: MICORYX | Start Date*: 2011-08-22 | |||||||||||
Sponsor Name:Oryx GmbH & Co. KG | |||||||||||||
Full Title: Phase I/IIa study of immunization with frameshift peptides administered with Montanide ISA-51 VG in patients with advanced MSI-H colorectal cancer | |||||||||||||
Medical condition: advanced MSI-H colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007734-19 | Sponsor Protocol Number: P53SLP01/01 | Start Date*: 2008-07-03 | |||||||||||
Sponsor Name:University Medical Center Groningen, UMCG-Department of Gynaecologic Oncology | |||||||||||||
Full Title: p53 synthetic long peptides vaccine with cyclophosphamide for ovarian cancer, a phase II trial. | |||||||||||||
Medical condition: This is an uncontrolled, mono-centre, phase II single dose trial for patients with ovarian cancer, who have a rising serum tumor marker CA-125 after previous treatment (surgery and platinum based c... | |||||||||||||
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Population Age: | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
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