- Trials with a EudraCT protocol (287)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
287 result(s) found for: Neuropathic pain.
Displaying page 15 of 15.
| EudraCT Number: 2015-004851-28 | Sponsor Protocol Number: EVG001BC | Start Date*: 2016-12-07 |
| Sponsor Name:Evgen Pharma PLC | ||
| Full Title: A Multicentre Phase 2 Study of SFX-01 Treatment and Evaluation in Patients with Estrogen Receptor (ER) Positive and Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer... | ||
| Medical condition: Estrogen Receptor (ER) Positive and Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer Progressing on either an Aromatase Inhibitor (AI) or Tamoxifen or Fulvestrant | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) ES (Completed) FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-015811-42 | Sponsor Protocol Number: GZGD03109 | Start Date*: 2010-12-20 | |||||||||||
| Sponsor Name:Genzyme Europe B.V. | |||||||||||||
| Full Title: A Phase 3, Randomized, Multi-Center, Multi-National, Double-Blind Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Once Daily versus Twice Daily Dosing of Genz-112638 in Patients wit... | |||||||||||||
| Medical condition: Gaucher Disease Type I | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) PT (Completed) AT (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-006319-69 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-10-25 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Pedro Villarejo Campos(Hospital Universitario Ciudad Real) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Closed abdomen hyperthermic intraperitoneal chemotherapy with paclitaxel for advanced epithelial ovarian cancer | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: ovarian cancer (II,III,IV FIGO staging and tumoral recurrence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2022-001542-38 | Sponsor Protocol Number: ANVS-22001 | Start Date*: 2023-01-09 |
| Sponsor Name:Annovis Bio, Inc. | ||
| Full Title: A 6-month prospective, randomized, double-blind, placebo-controlled clinical trial investigating the efficacy, safety, and tolerability of two different doses of buntanetap or placebo in patients w... | ||
| Medical condition: Parkinson’s disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) HU (Completed) IT (Completed) PL (Completed) ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005223-28 | Sponsor Protocol Number: GZGD02607 | Start Date*: 2009-11-04 | |||||||||||
| Sponsor Name:Genzyme Europe B.V. | |||||||||||||
| Full Title: A Phase 3, Randomized, Multi-Center, Multi-National, Open-Label, Active Comparator Study to Evaluate the Efficacy and Safety of Genz-112638 in Patients with Gaucher Disease Type 1 who have Reached ... | |||||||||||||
| Medical condition: Gaucher Disease type I | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) GB (Completed) FR (Completed) DE (Completed) ES (Completed) CZ (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000196-24 | Sponsor Protocol Number: 402-C-1504 | Start Date*: 2016-07-04 |
| Sponsor Name:Reata Pharmaceuticals, Inc. | ||
| Full Title: A STUDY OF THE EFFICACY AND SAFETY OF BARDOXOLONE METHYL IN PATIENTS WITH CONNECTIVE TISSUE DISEASE-ASSOCIATED PULMONARY ARTERIAL HYPERTENSION | ||
| Medical condition: Connective Tissue Disease-Associated Pulmonary Arterial Hypertension (WHO Group I CTD-PAH) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) DE (Prematurely Ended) BE (Completed) NL (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000585-30 | Sponsor Protocol Number: I16016 | Start Date*: 2017-12-13 | ||||||||||||||||
| Sponsor Name:CHU de Limoges | ||||||||||||||||||
| Full Title: Pilot study, single-blind, candesartan versus usual care of peripheral neuropathy development induced by vincristine (PNIV) in patients treated for lymphoma B. | ||||||||||||||||||
| Medical condition: peripheral neuropathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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