- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Levonorgestrel releasing intrauterine system.
Displaying page 1 of 3.
EudraCT Number: 2010-020922-16 | Sponsor Protocol Number: BAY 86-5028/15105 | Start Date*: 2011-03-01 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: International, prospective, double-blind, 3-arm comparative, randomized, placebo controlled phase IV study on the effect of counseling and either tranexamic acid or mefenamic acid or placebo, on th... | |||||||||||||
Medical condition: Management of bleeding/spotting in women using the levonorgestrel-releasing intrauterine system (Mirena) for contraception. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002291-42 | Sponsor Protocol Number: 308901 | Start Date*: 2005-03-17 | |||||||||||
Sponsor Name:Schering AG | |||||||||||||
Full Title: Multi-center, open, randomized, dose finding phase II study to investigate for a maximum of three years ultra low dose levonorgestrel contraceptive intrauterine systems (LCS) releasing in vitro 12 ... | |||||||||||||
Medical condition: Contraception | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) HU (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001552-37 | Sponsor Protocol Number: RG07-066(FormerlyHTA02/06/02) | Start Date*: 2008-07-25 |
Sponsor Name:University of Birmingham | ||
Full Title: Effectiveness and Cost-effectiveness of Levonorgestrel containing Intrauterine system in Primary care against Standard Treatment for menorrhagia | ||
Medical condition: Menorrhagia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002350-22 | Sponsor Protocol Number: LR-201 | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:Chemo Research S.L. | |||||||||||||
Full Title: Multi-center, phase 2, open-label, randomized clinical trial to evaluate the inhibition of ovulation of 3 dosing strengths of levonorgestrel (LNG) vaginal delivery system (VDS), releasing during 28... | |||||||||||||
Medical condition: Women´s healthcare (Contraception, inhibition of ovulation) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001984-21 | Sponsor Protocol Number: 3/013/13 | Start Date*: 2013-09-11 | |||||||||||
Sponsor Name:University of Aberdeen & NHS Grampian | |||||||||||||
Full Title: PRE-EMPT: Preventing Recurrence of Endometriosis by Means of long acting Protestogen Therapy | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004956-23 | Sponsor Protocol Number: IIBSP-DIU-2015-85 | Start Date*: 2016-02-25 |
Sponsor Name:Institut de Recerca HSCSP | ||
Full Title: COLIBRI STUDY, Cooper and Levonorgestrel Intrauterine Device (IUD) Barcelona Research Initiative. A randomized controlled trial to compare the menstrual bleeding profile among cooper and 13,5mg lev... | ||
Medical condition: Contraception | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003980-74 | Sponsor Protocol Number: BAY1007626/15731 | Start Date*: 2015-06-17 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: Multi-center, randomized, comparator-controlled, single-blind, parallel-group study to investigate the pharmacodynamics, pharmacokinetics and safety of an intrauterine system releasing BAY 1007626,... | |||||||||||||
Medical condition: Contraception | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) GB (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000612-17 | Sponsor Protocol Number: HyperplasiLNG | Start Date*: Information not available in EudraCT |
Sponsor Name:University Hospital of North Norway | ||
Full Title: Significance of intrauterine progestogen therapy in endometrial proliferative conditions | ||
Medical condition: Endometrial cancer has presently become the most frequent gynaecologic malinancy in the Western World and the incidence is still increasing. In Norway a 50% increase in occurence has been observed ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003367-19 | Sponsor Protocol Number: NUC-5/PSC | Start Date*: 2017-09-28 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase III study comparing norursodeoxycholic acid capsules with placebo in the treatment of primary sclerosing cholangitis | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) is a slowly progressing chronic cholestatic liver disease of assumed autoimmune, but finally unidentified etiology, characterized by a chronic inflammatory and ... | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) GB (GB - no longer in EU/EEA) HU (Trial now transitioned) LT (Completed) FI (Trial now transitioned) CZ (Prematurely Ended) BE (Completed) DK (Trial now transitioned) NL (Trial now transitioned) FR (Trial now transitioned) SE (Completed) NO (Trial now transitioned) PL (Trial now transitioned) IE (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010824-25 | Sponsor Protocol Number: DSHNHL 2008-R6 | Start Date*: 2010-04-12 |
Sponsor Name:GMIHO Gesellschaft für Medizinische Innovation-Hämatologie und Onkologie mbH | ||
Full Title: Open-label, Multicenter Phase I/II Study: Salvage Therapy of Progressive and Relapsed Aggressive Non-Hodgkin-Lymphoma by Combination of Lenalidomide (Revlimid®) with Rituximab, Dexamethason, High-d... | ||
Medical condition: Patients with relapsed or primary progressive aggressive non-Hodgkin's lymphoma. These lymphomas comprise: 1. Follicular lymphoma grade III (FL III°) 2. Diffuse large B cell lymphoma (DLBCL), all v... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-000167-69 | Sponsor Protocol Number: AIC649-02-II-01 | Start Date*: 2021-06-30 | |||||||||||
Sponsor Name:AiCuris Anti-Infective Cures AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled trial to evaluate the efficacy and safety of AIC649 in the treatment of otherwise healthy subjects with asymptomatic or mildly symptomatic SARS-CoV-2 ... | |||||||||||||
Medical condition: asymptomatic or mildly symptomatic SARS-CoV-2 infection | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007246-60 | Sponsor Protocol Number: NLG-MCL4(LENA-BERIT) | Start Date*: 2009-06-23 | |||||||||||||||||||||
Sponsor Name:Nordic Lymphoma Group | |||||||||||||||||||||||
Full Title: Lenalidomide, bendamustine and rituximab as first-line therapy for patients >65 years with mantle cell lymphoma | |||||||||||||||||||||||
Medical condition: Mantle cell lymphoma | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) FI (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000087-15 | Sponsor Protocol Number: CRd | Start Date*: 2012-03-30 |
Sponsor Name:FONDAZIONE NEOPLASIE SANGUE ONLUS | ||
Full Title: A PHASE II, MULTI-CENTER, OPEN LABEL STUDY OF CYCLOPHOSPHAMIDE IN MULTIPLE MYELOMA PATIENTS WITH BIOCHEMICAL PROGRESSION DURING LENALIDOMIDE-DEXAMETHASONE TREATMENT FOR RELAPSED/REFRACTORY MULTIPLE... | ||
Medical condition: RELAPSED/REFRACTORY MULTIPLE MYELOMA PATIENTS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013423-31 | Sponsor Protocol Number: TEXO0309 | Start Date*: 2010-01-21 | ||||||||||||||||
Sponsor Name:Medizinische Universität Innsbruck, Universitätsklinik für Innere Medizin I | ||||||||||||||||||
Full Title: Phase I/II study of lenalidomide and Cetuximab in patients with advanced solid tumors | ||||||||||||||||||
Medical condition: Advanced solid tumors | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001296-20 | Sponsor Protocol Number: MITOCET | Start Date*: 2013-12-20 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Randomized Phase IV Trial to Compare Cetuximab with Concomitant Radiation Therapy with Concomitant Mitomycin-C and 5-FU with Radiation Therapy for Locally Advanced Squamous Cell Carcinomas of The H... | ||
Medical condition: Locally advanced squamous cell carcinomas of head and neck | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-010947-15 | Sponsor Protocol Number: LENALIDOMIDE-MALT | Start Date*: 2010-02-25 |
Sponsor Name:MUW, Klinik für Innere Med. I, Onkologie | ||
Full Title: PHASE II TRIAL OF LENALIDOMIDE (REVLIMID®) IN PATIENTS WITH LYMPHOMA OF THE MUCOSA ASSOCIATED LYMPHOID TISSUE (MALT) | ||
Medical condition: MALT Lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003115-21 | Sponsor Protocol Number: 2018/2798 | Start Date*: 2019-02-19 | |||||||||||||||||||||||||||||||
Sponsor Name:Gustave Roussy | |||||||||||||||||||||||||||||||||
Full Title: A phase II whole exoMe sequencing-bAsed baskeT trIal for combination therapy with durvaLumab (anti-PDL1) (MEDI4736) anD tremelimumAb (anti-CTLA4) in patients with metastatic solid tumors | |||||||||||||||||||||||||||||||||
Medical condition: Metastatic colorectal adenocarcinoma (without microsatellite instability (not MSI)), triple negative breast cancer, prostate adenocarcinoma, stomach and esophageal gastric junction adenocarcinoma a... | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005818-10 | Sponsor Protocol Number: AGMT_MALT-2 | Start Date*: 2012-05-02 | |||||||||||
Sponsor Name:Arbeitsgemeinschaft medikamentöse Tumortherapie gemeinnützige GmbH | |||||||||||||
Full Title: PHASE II TRIAL OF RITUXIMAB (MABTHERA®) PLUS LENALIDOMIDE (REVLIMID®) IN PATIENTS WITH LYMPHOMA OF THE MUCOSA ASSOCIATED LYMPHOID TISSUE (MALT) | |||||||||||||
Medical condition: Lymphoma of the Mucosa-Associated Lymphoid Tissue (MALT) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002768-32 | Sponsor Protocol Number: MM03 | Start Date*: 2009-06-08 | |||||||||||
Sponsor Name:Freistaat Bayern | |||||||||||||
Full Title: A prospective phase I/II, one-arm, one-stage multi-center, open label study of lenalidomide in combination with pioglitazone, dexamethasone and metronomic low-dose chemotherapy with treosulfan in p... | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000682-32 | Sponsor Protocol Number: PAUF-I | Start Date*: 2022-02-16 |
Sponsor Name:Prestige Biopharma Limited | ||
Full Title: A First in human, Phase 1/2a, Multicentre, Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of PBP1510 in Patients with Advanced/Metastatic Pancreatic Cancer | ||
Medical condition: Advanced and/or metastatic pancreatic adenocarcinoma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
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

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. |
