- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Classical conditioning.
Displaying page 1 of 1.
| EudraCT Number: 2015-004708-51 | Sponsor Protocol Number: ABR55478 | Start Date*: 2015-12-17 |
| Sponsor Name:LUMC, VRSP | ||
| Full Title: Facilitating Sexual Memory consolidation by a partial NMDA receptors agonist | ||
| Medical condition: Sexual arousal disorders | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000605-72 | Sponsor Protocol Number: CB+MSCforEB | Start Date*: 2014-02-06 |
| Sponsor Name:Universitair Medisch Centrum Utrecht | ||
| Full Title: Unrelated cord blood transplantation after reduced toxicity conditioning with mesenchymal stromal cell co-infusion in patients with severe epidermolysis bullosa | ||
| Medical condition: The source population consists of patients referred to or within the UMC Groningen because they have diagnosed clinically and genetically severe generalized RDEB. | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-000684-16 | Sponsor Protocol Number: 03MI10 | Start Date*: 2010-01-21 | |||||||||||
| Sponsor Name:Great Ormond Street Hospital NHS Trust / University College London - Institute of Child Health | |||||||||||||
| Full Title: Gene therapy for SCID-X1 using a self-inactivating (SIN) gammaretroviral vector. | |||||||||||||
| Medical condition: X-Linked severe combined Immunodeficiency (SCID-X1) | |||||||||||||
|
|||||||||||||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001509-42 | Sponsor Protocol Number: CA209-205 | Start Date*: 2014-07-11 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: Non-Comparative, Multi-Cohort, Single Arm, Open-Label, Phase 2 Study of Nivolumab (BMS-936558) in classical Hodgkin Lymphoma (cHL) Subjects | |||||||||||||
| Medical condition: Hodgkin Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) BE (Completed) DE (Completed) IT (Completed) NL (Completed) ES (Ongoing) CZ (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000356-18 | Sponsor Protocol Number: NL64877.041.18 | Start Date*: 2018-11-19 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University Medical Center utrecht | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Individualized dosing of fludarabine during innate allo SCT: A randomized phase II study (TARGET Study) | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: AML, MDS, ALL, CML, CLL, NHL, HL, or a myeloproliferative disease (MPD) | |||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
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
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| 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. | |
Query did not match any studies.