- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Langerhans cell sarcoma.
Displaying page 1 of 1.
EudraCT Number: 2020-005051-20 | Sponsor Protocol Number: HISTIOGEN | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Institute of Mother and Child | ||||||||||||||||||||||||||||
Full Title: Determination Of Molecular Status And Benefit Of Use Fludeoxyglucose (18F-FDG) In PET/CT imagining In Juvenile Patients With Histiocytosis | ||||||||||||||||||||||||||||
Medical condition: histiocytic cell proliferation | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005052-37 | Sponsor Protocol Number: BRAVO | Start Date*: 2021-04-01 | ||||||||||||||||||||||||||
Sponsor Name:Institute of Mother and Child | ||||||||||||||||||||||||||||
Full Title: Optymalizacja czasu leczenia i dawkowania wemurafenibu u małoletnich pacjentów z opornymi na konwencjonalną terapię rozrostami z komórek histiocytarnych z obecnością mutacji w genie BRAF. | ||||||||||||||||||||||||||||
Medical condition: histiocytic cell proliferation | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005053-25 | Sponsor Protocol Number: TRAM | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Institute of Mother and Child | ||||||||||||||||||||||||||||
Full Title: Optimalization Of The Time And Dosage Of Trametinib In BRAF Negative Juvenile Patients With Refractory Histiocytosis Or After Failure Of Vemurafenib Treatment. | ||||||||||||||||||||||||||||
Medical condition: histiocytic cell proliferation | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: PL (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000425-45 | Sponsor Protocol Number: | Start Date*: 2012-07-03 | |||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||
Full Title: Effects of morning vs evening dosing on the pharmacokinetics and pharmacodynamics of sunitinib. | |||||||||||||||||||||||
Medical condition: Renal Cell Cancer, GIST, pancreatic neuroendocrine tumor | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000461-23 | Sponsor Protocol Number: CA209-627 | Start Date*: 2017-03-07 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: An Open-label Phase 2 Multi-cohort Trial of Nivolumab in Advanced or Metastatic Malignancies | ||||||||||||||||||
Medical condition: Advanced/Metastatic malignancies | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
