- Trials with a EudraCT protocol (2,303)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
2,303 result(s) found for: Oophorectomy.
Displaying page 4 of 116.
EudraCT Number: 2007-005744-24 | Sponsor Protocol Number: DM-99-07 | Start Date*: 2008-02-11 |
Sponsor Name:DiaMedica Inc. | ||
Full Title: A phase IIa, placebo controlled, randomized, cross-over study to evaluate the effects of DM-99 on a meal tolerance test in subjects with type 2 diabetes mellitus | ||
Medical condition: Cukrzyca | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002124-21 | Sponsor Protocol Number: GINECO-EN105b | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:ARCAGY-GINECO | |||||||||||||
Full Title: Randomized phase III trial in MMR deficient endometrial cancer patients comparing chemotherapy alone versus Dostarlimab in first line advanced/metastatic setting: DOMENICA STUDY (GINECO-EN105b/ENGO... | |||||||||||||
Medical condition: Endometrial cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004682-39 | Sponsor Protocol Number: KFJ-2020-02_NORMOSANG | Start Date*: 2020-11-16 |
Sponsor Name:Thomayerova nemocnice | ||
Full Title: Pilot, open-label, monocentric study evaluating safety and clinical effect of application of NORMOSANG® in patients with COVID-19 disease | ||
Medical condition: Patients with COVID -19 disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005071-17 | Sponsor Protocol Number: 15-50615 | Start Date*: 2006-11-06 | |||||||||||
Sponsor Name:Hormos Medical Ltd | |||||||||||||
Full Title: Preliminary efficacy of OphenaTM (ospemifene) in the treatment of vasomotor symptoms associated with the menopause: a 6-week, randomized, double-blind, placebo-controlled, parallel-group study | |||||||||||||
Medical condition: Postmenopausal symptoms (hot flashes) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004874-42 | Sponsor Protocol Number: TRAFO001 | Start Date*: 2009-02-06 | |||||||||||
Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||
Full Title: Evaluation of predictive Factors for the Effectivity of Aromatase Inhibitor Therapy - Offene, prospektive, multizentrische Phase IV-Studie zur Untersuchung des Einflusses von pharmakogenetischen M... | |||||||||||||
Medical condition: The study examines the influence of pharmacogenetic markers on the efficacy and side effects in postmenopausal, steroid hormone positive breast cancer patients, who are treated with Letrozol. The p... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001684-34 | Sponsor Protocol Number: HUM05/086 | Start Date*: 2006-06-21 |
Sponsor Name:Knud Kragballe, Dermatological Department, Århus Sygehus (Hospital) | ||
Full Title: Adalimumab clinical trial in plaque psoriasis – effect on expression of TNF-a and MAP-kinases in psoriatic skin – ACTION An open-label trial investigating adalimumab (HUMIRA) 80 mg s.c. at week 0 ... | ||
Medical condition: Patients with psoriasis vulgaris (plaque psoriasis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005297-48 | Sponsor Protocol Number: HUM 06-0023 | Start Date*: 2007-03-20 | |||||||||||
Sponsor Name:University of Copenhagen, Roskilde, Department of Dermatology | |||||||||||||
Full Title: Adalimumab s.c. for the treatment of patients with hidradenitis suppurativa – clinical efficacy, safety and tolerability - SOPHISTICATE | |||||||||||||
Medical condition: Patients with hidradenitis suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019821-32 | Sponsor Protocol Number: 20090508 | Start Date*: 2010-11-04 | |||||||||||
Sponsor Name:Amgen Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind Trial of Weekly Paclitaxel Plus AMG 386 or Placebo in Women With Recurrent Partially Platinum Sensitive or Resistant Epithelial Ovarian, Primary Peritoneal or Fa... | |||||||||||||
Medical condition: Recurrent partially platinum sensitive or resistant epithelial ovarian, primary peritoneal or fallopian tube cancers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) PT (Completed) CZ (Prematurely Ended) SI (Completed) GR (Completed) SE (Completed) LV (Completed) EE (Completed) IT (Completed) BG (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001715-79 | Sponsor Protocol Number: BL-8040.SCM.301 | Start Date*: 2019-05-14 | |||||||||||
Sponsor Name:BioLineRx Ltd. | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blinded, Placebo-Controlled, Multi-Centre Study Evaluating the Safety, Tolerability and Efficacy of Combination Treatment of BL-8040 and G-CSF as compared to Placebo... | |||||||||||||
Medical condition: Hematopoietic Stem Cell mobilization in Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) CZ (Prematurely Ended) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001272-29 | Sponsor Protocol Number: BCX7353-203 | Start Date*: 2016-07-26 | |||||||||||
Sponsor Name:BioCryst Pharmaceuticals Inc | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, dose-ranging, parallel-group study to evaluate the efficacy, safety, tolerability, pharmacokinetics and pharmacodynamics of BCX7353 as a preventative... | |||||||||||||
Medical condition: Hereditary Angioedema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) HU (Completed) ES (Completed) AT (Completed) DK (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004835-56 | Sponsor Protocol Number: GEMCAD-1703 | Start Date*: 2019-08-13 | |||||||||||
Sponsor Name:Grupo español mutidisciplinar en cáncer digestivo (GEMCAD) | |||||||||||||
Full Title: Phase II study of Durvalumab (MEDI4736) plus Total Neoadjuvant Therapy (TNT) in locally advanced rectal cancer | |||||||||||||
Medical condition: Locally advanced rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002632-21 | Sponsor Protocol Number: VRA107438 | Start Date*: 2006-11-13 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled, single dose, two-period crossover study to investigate the therapeutic potential of the TRPV1 antagonist SB-705498 in treatment of subjects with rect... | |||||||||||||
Medical condition: Rectal Hyperalgesia (in patients with irritable bowel syndrome and feacal urgency) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003935-12 | Sponsor Protocol Number: ATRiUM | Start Date*: 2019-06-13 | ||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | ||||||||||||||||||
Full Title: ATRiUM: A phase 1 trial to assess the safety, tolerability, pharmacokinetics and preliminary antitumor activity of ascending doses of combined therapy with ATR inhibitor AZD6738 and gemcitabine, Us... | ||||||||||||||||||
Medical condition: Locally advanced or metastatic solid tumour. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000809-39 | Sponsor Protocol Number: AA-HPP-405 | Start Date*: 2016-02-04 | |||||||||||
Sponsor Name:Alexion Pharma International Sàrl | |||||||||||||
Full Title: An Open-label, Multicenter, Expanded Access Program for Asfotase Alfa (human recombinant tissue-nonspecific alkaline phosphatase fusion protein) Treatment for Patients with Infantile- or Juvenile-o... | |||||||||||||
Medical condition: Hypophosphatasia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004548-30 | Sponsor Protocol Number: D7917C00225 (1839IL/0225) | Start Date*: 2005-11-23 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II randomised, double-blind, stratified, multi-centre trial comparing the Nolvadex 20 mg and placebo combination to the Nolvadex 20 mg and ZD1839 (IRESSA™) 250 mg combination in patients wi... | ||
Medical condition: Female patients aged ³18 years, pre/post menopausal with ER and/or PR positive metastatic adenocarcinoma of the breast determined by each laboratory in each centre. Patients will be stratified int... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001660-29 | Sponsor Protocol Number: FAB18 | Start Date*: 2019-01-16 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: FAB: Functional Analysis of BRCAness | |||||||||||||
Medical condition: Recurrent epithelial ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001804-39 | Sponsor Protocol Number: GLLC-EARLY | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Fundación PETHEMA | |||||||||||||
Full Title: Phase III Randomized Study to Investigate the Use of Acalabrutinib in the Treatment of Patients With Early Stage CLL With High Risk of Early Disease Progression | |||||||||||||
Medical condition: Early Stage CLL With High Risk of Early Disease Progression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003688-73 | Sponsor Protocol Number: D9170C00001 | Start Date*: 2019-09-10 | ||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||
Full Title: A Phase I/IIa, Open-Label Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of Ascending Doses of AZD7648 Monotherapy or in Combination with either Cytotoxic Chemo... | ||||||||||||||||||
Medical condition: Advanced Malignancies | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003420-46 | Sponsor Protocol Number: MYL-1410A-3001 | Start Date*: 2015-07-22 | |||||||||||
Sponsor Name:Mylan GmbH (Mylan) | |||||||||||||
Full Title: Multicenter, Double-Blind, Randomized, 2-Arm, Parallel-Group, Equivalence Study Evaluating Efficacy and Safety Similarity of Mylan Adalimumab (MYL-1401A) Compared With Humira® in Subjects With Mode... | |||||||||||||
Medical condition: Chronic Plaque-Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) EE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003896-20 | Sponsor Protocol Number: 3667 | Start Date*: 2013-02-14 |
Sponsor Name:The Royal Marsden NHS Foundation Trust [...] | ||
Full Title: TAX-TORC: A Phase I multi-centre trial of the combination of AZD2014 (dual TORC1 and TORC2 inhibitor) and weekly paclitaxel in patients with solid tumours | ||
Medical condition: Solid tumours | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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