- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Sargramostim (GM-CSF).
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EudraCT Number: 2006-002211-26 | Sponsor Protocol Number: PX115.1.1-201 | Start Date*: 2006-09-10 | |||||||||||
Sponsor Name:Pharmexa A/S | |||||||||||||
Full Title: “Heptovax” - Ensayo de fase II, abierto, para evaluar la seguridad y la eficacia de GV1001 para el carcinoma hepatocelular avanzado. (CHC). | |||||||||||||
Medical condition: Carcinoma hepatocelular avanzado | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005910-17 | Sponsor Protocol Number: KKSH176 | Start Date*: 2021-06-01 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | |||||||||||||
Full Title: Phase 2 multicenter study investigating the tolerability and efficacy of UV1 vaccine in patients with recurrent or metastatic PD-L1 positive (CPS≥1) head and neck squamous cell carcinoma planned fo... | |||||||||||||
Medical condition: Recurrent or metastatic Head and Neck Squamous Cell Carcinoma (HNSCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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 (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005281-29 | Sponsor Protocol Number: IVAC-ALL-1 | Start Date*: 2016-06-07 | ||||||||||||||||
Sponsor Name:University Hospital Tuebingen | ||||||||||||||||||
Full Title: Prospective phase I/II study: Patient-individualized peptide vaccination based on whole exome sequencing with adjuvant GM-CSF in children with relapsed acute lymphoblastic leukemia | ||||||||||||||||||
Medical condition: Relapsed acute lymphatic leukemia | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006302-13 | Sponsor Protocol Number: CT-BI Vacc-4x 2007/1 | Start Date*: 2008-06-04 | |||||||||||
Sponsor Name:Bionor Immuno AS | |||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Multicenter, Immunogenicity Study of Vacc-4x Versus Placebo in Patients Infected with HIV-1 Who Have Maintained an Adequate Response to ART | |||||||||||||
Medical condition: HIV positive subjects who have been clinically stable on antiretroviral therapy for the last six months with a viral load less than 50 copies/mL for the last six months and a CD4 cell count => 400 ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001852-20 | Sponsor Protocol Number: UV1/hTERT-2012-L | Start Date*: 2013-01-17 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: A PHASE I/IIa STUDY OF UV1 VACCINATION IN PATIENTS WITH NON-SMALL CELL LUNG CANCER | |||||||||||||
Medical condition: Patient with metastatic Non Small Cell Lung Cancer (NSCLC) stage IV. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005219-98 | Sponsor Protocol Number: PH3-01 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Galena Biopharma, Inc | |||||||||||||
Full Title: Prevention of Recurrence in Early-Stage, Node-Positive Breast Cancer with Low to Intermediate HER2 Expression with NeuVax™ Treatment (PRESENT) | |||||||||||||
Medical condition: Operable early-stage, node-positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) HU (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001256-22 | Sponsor Protocol Number: GL0817-01 | Start Date*: 2017-01-31 | |||||||||||
Sponsor Name:Gliknik Inc | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Determine the Safety and Efficacy of GL-0817 (with Cyclophosphamide) for the Prevention of Recurrence in HLA-A2+ Patients wi... | |||||||||||||
Medical condition: Prevention of Recurrence in HLA-A2+ Patients with High-Risk Squamous Cell Carcinoma of the Oral Cavity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022459-45 | Sponsor Protocol Number: IMA901-301 | Start Date*: 2010-12-15 | ||||||||||||||||
Sponsor Name:immatics biotechnologies GmbH | ||||||||||||||||||
Full Title: A randomized, controlled Phase III study investigating IMA901 multipeptide cancer vaccine in patients receiving sunitinib as first-line therapy for advanced/metastatic renal cell carcinoma | ||||||||||||||||||
Medical condition: The study population consists of HLA-A*02-positive metastatic and/or locally advanced RCC patients with histology of the clear-cell type who are aged 18 years or older and have a favorable or inter... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) HU (Completed) GB (Completed) NL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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