- Trials with a EudraCT protocol (197)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
197 result(s) found for: Fertility.
Displaying page 7 of 10.
| EudraCT Number: 2018-000125-30 | Sponsor Protocol Number: PT2977-202 | Start Date*: 2018-05-25 | |||||||||||
| Sponsor Name:Peloton Therapeutics, Inc. | |||||||||||||
| Full Title: An Open-Label Phase 2 Study to Evaluate PT2977 for the Treatment of von Hippel-Lindau Disease-Associated Renal Cell Carcinoma | |||||||||||||
| Medical condition: Von Hippel-Lindau Disease-Associated Renal Cell Carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002803-37 | Sponsor Protocol Number: XC001-1001 | Start Date*: 2022-01-20 | |||||||||||
| Sponsor Name:XyloCor Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase 1/2 Trial of Direct Administration of AdVEGF-All6A+, a Replication Deficient Adenovirus Vector Expressing a cDNA/Genomic Hybrid of Human Vascular Endothelial Growth Factor, to the Ischemic ... | |||||||||||||
| Medical condition: Angina Pectoris Secondary | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020559-29 | Sponsor Protocol Number: IVF-03-01-052 | Start Date*: 2010-09-23 | ||||||||||||||||
| Sponsor Name:Pantec Biosolutions AG | ||||||||||||||||||
| Full Title: Proof of concept study to investigate the efficacy, safety and tolerability as well as the pharmacokinetics and pharmacodynamics of a newly developed patch containing follicle-stimulating hormone a... | ||||||||||||||||||
| Medical condition: Healthy female oocyte donors of normal body weight (body mass index within 18 to 29 kg/m2), age from 20 to 30 years (inclusive), ultrasound of ovaries, normal endocrine status, non-smoker | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: CZ (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-008299-14 | Sponsor Protocol Number: IGG-MOMA- 002 | Start Date*: 2009-01-01 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Hypogonadotropic hypogonadism in male newborn | |||||||||||||
| Medical condition: MICROPENIS DUE TO HYPOGONADOTROPIC HYPOGONADISM | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005452-24 | Sponsor Protocol Number: KvL | Start Date*: 2008-10-30 | |||||||||||
| Sponsor Name:Fertilitetsklinikken, Afsnit 455, Gynækologisk-Obstetrisk Afdeling, Hvidovre Hospital | |||||||||||||
| Full Title: Kort versus lang reagensglasbehandling. En prospektiv, konsekutiv og randomiseret sammenlignende undersøgelse. | |||||||||||||
| Medical condition: Infertility | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002562-19 | Sponsor Protocol Number: LIGHT | Start Date*: 2006-04-21 | |||||||||||
| Sponsor Name:Dipartimento di Neuroscienze Oftalmologia e Genetica DINOG - Universita di Genova | |||||||||||||
| Full Title: Immunoablation with Cyclophosphamide at high dosage and Rabbit antithymoglobulin followed by autologous hematopoietic stem cell transplantation in severe multiple sclerosis | |||||||||||||
| Medical condition: VERIFICARE Patients with multiple sclerosis, age between 18 and 50 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017854-11 | Sponsor Protocol Number: FIBHGM-ECNC004-2010(FEBRES-09) | Start Date*: 2010-06-22 | ||||||||||||||||
| Sponsor Name:Fundación para la Investigación Biomédica del Hospital Gregorio Marañón | ||||||||||||||||||
| Full Title: Efecto de la dosis de FSH recombinante en el resultado de la estimulación ovárica para fecundación in vitro en pacientes con baja reserva ovárica. Estudio aleatorizado y abierto de no inferioridad.... | ||||||||||||||||||
| Medical condition: Hiperestimulación ovárica controlada para inducir el desarrollo de folículos múltiples en programas de reproducción asistida | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-002482-19 | Sponsor Protocol Number: 13EU/FSH01 | Start Date*: 2013-12-12 | |||||||||||
| Sponsor Name:IBSA Institut Biochimique S.A. | |||||||||||||
| Full Title: Randomised clinical trial comparing highly purified FSH formulation (Fostimon®) and recombinant FSH (Gonal-F®) in GnRH-antagonist controlled ovarian hyperstimulation cycles. | |||||||||||||
| Medical condition: female infertility | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) GB (Completed) ES (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003120-17 | Sponsor Protocol Number: PDY16963 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Genzyme Corporation | |||||||||||||
| Full Title: A 3-part study to evaluate the efficacy and safety of venglustat in combination with Cerezyme in adult and pediatric patients with Gaucher disease Type 3 (GD3) with open-label long-term treatment | |||||||||||||
| Medical condition: Gaucher disease type 3 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) DE (Prematurely Ended) HU (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000633-36 | Sponsor Protocol Number: 000009 | Start Date*: 2011-08-09 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: A randomised, controlled, assessor-blind, parallel groups, multinational, multicentre trial assessing the dose-response relationship of FE 999049 in controlled ovarian stimulation in women undergoi... | |||||||||||||
| Medical condition: Infertility | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) BE (Completed) CZ (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002856-26 | Sponsor Protocol Number: ADO-EP02(ML29328) | Start Date*: 2016-12-19 | |||||||||||
| Sponsor Name:SRH Wald-Klinikum Gera GmbH | |||||||||||||
| Full Title: A PHASE II, SINGLE-ARMED, MULTICENTER TRIAL OF NEOADJUVANT VISMODEGIB IN PATIENTS WITH LARGE AND/OR RECURRENT RESECTABLE BASAL CELL CARCINOMA | |||||||||||||
| Medical condition: Patients with large and/or recurrent resectable basal cell carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005326-29 | Sponsor Protocol Number: IBCSG_41-13 | Start Date*: 2013-11-11 |
| Sponsor Name:International Breast Cancer Study Group (IBCSG) | ||
| Full Title: A randomized phase II trial evaluating the endocrine activity and efficacy of neoadjuvant degarelix versus triptorelin in premenopausal patients receiving letrozole for locally advanced endocrine r... | ||
| Medical condition: Premenopausal patients with histologically confirmed locally advanced breast cancer and with primary tumor of ER+/PgR+ and HER2 negative or not amplified. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003796-58 | Sponsor Protocol Number: NAC-GED-0507-ACN-02-17 | Start Date*: 2017-12-13 | |||||||||||
| Sponsor Name:PPM SERVICES S.A. | |||||||||||||
| Full Title: AN OPEN LABEL CLINICAL STUDY TO EVALUATE THE LONG-TERM DERMAL SAFETY PROFILE OF 12-WEEKS TOPICAL ADMINISTRATION OF N-ACETYL-GED-0507-34-LEVO GEL 5% IN PATIENTS WITH FACIAL ACNE | |||||||||||||
| Medical condition: FACIAL ACNE | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001656-35 | Sponsor Protocol Number: LIFE-02-MF | Start Date*: 2019-01-10 | |||||||||||
| Sponsor Name:Dept.Dermotology , Aarhus University | |||||||||||||
| Full Title: Metabolic imaging of patients with mycosis fungoides using hyperpolarized 13C-Pyruvate magnetic resonance imaging – A feasibility study | |||||||||||||
| Medical condition: mycosis fungiodes | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001830-32 | Sponsor Protocol Number: RC31/17/0448 | Start Date*: 2019-12-18 |
| Sponsor Name:University Hospital Toulouse | ||
| Full Title: Phase III Trial to assess impact of ultra-long versus long down-regulation protocol on IVF/ICSI outcomes in infertile women presenting with adenomyosis. | ||
| Medical condition: Infertilty in women with adenomyosis. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-004916-21 | Sponsor Protocol Number: EROS | Start Date*: 2019-07-02 | |||||||||||
| Sponsor Name:Karolinska Institute | |||||||||||||
| Full Title: Early intervention and recovery of sexual function in men and women after treatment of rectal cancer–a randomized controlled study with tadalafil compared to standard care | |||||||||||||
| Medical condition: sexual/ erectile function in women and men after treatment for rectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004214-35 | Sponsor Protocol Number: P170706J | Start Date*: 2021-03-18 | |||||||||||
| Sponsor Name:Assistance Publique Hôpitaux de Paris | |||||||||||||
| Full Title: Amélioration des taux de Naissance après ICSI, par le cpFT. Etude multicentrique prospective randomisée. « FERTICSI ». | |||||||||||||
| Medical condition: infertility | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-003108-15 | Sponsor Protocol Number: UC-GIG-2003 | Start Date*: 2022-11-04 | |||||||||||
| Sponsor Name:UNICANCER | |||||||||||||
| Full Title: A multicentric national phase II trial assessing TIslelizumab in monotherapy for patients with Hepatocellular Carcinoma Child-Pugh B and ALBI grade 1 or 2 liver function Score | |||||||||||||
| Medical condition: Hepatocellular Carcinoma (HCC), Child-Pugh B, ALBI grade 1 or 2 liver function | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001527-39 | Sponsor Protocol Number: SGN22E-002 | Start Date*: 2021-02-16 | ||||||||||||||||||||||||||
| Sponsor Name:Seagen Inc. | ||||||||||||||||||||||||||||
| Full Title: A study of enfortumab vedotin (ASG-22CE) as monotherapy or in combination with other anticancer therapies for the treatment of urothelial cancer | ||||||||||||||||||||||||||||
| Medical condition: Urothelial cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
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