- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Budding yeast.
Displaying page 1 of 1.
| EudraCT Number: 2018-001269-18 | Sponsor Protocol Number: VMT-VT-1161-CL-011 | Start Date*: 2019-03-13 | |||||||||||
| Sponsor Name:Mycovia Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of VT-1161 Oral Capsules in the Treatment of Subjects with Recurrent Vulvovaginal Candidiasis | |||||||||||||
| Medical condition: Recurrent Vulvovaginal Candidiasis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: BG (Completed) PL (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001270-26 | Sponsor Protocol Number: VMT-VT-1161-CL-012 | Start Date*: 2018-12-12 | |||||||||||
| Sponsor Name:Mycovia Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of VT-1161 Oral Capsules in the Treatment of Subjects with Recurrent Vulvovaginal Candidiasis | |||||||||||||
| Medical condition: Recurrent Vulvovaginal Candidiasis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) BE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007659-15 | Sponsor Protocol Number: NC-07-03 | Start Date*: 2008-04-22 | ||||||||||||||||||||||||||
| Sponsor Name:Lumavita AG | ||||||||||||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase II Study to Investigate the Efficacy, Safety, and Tolerability of 3 doses of SPK 0602 (pentamycin) Vaginal Tablets vs Placebo (veh... | ||||||||||||||||||||||||||||
| Medical condition: Symptomatic Vaginitis due to Bacterial Vaginosis, Candidiasis or Trichomoniasis | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: EE (Completed) DE (Completed) HU (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2019-002600-40 | Sponsor Protocol Number: SCY-078-304 | Start Date*: 2020-01-17 | |||||||||||
| Sponsor Name:SCYNEXIS, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral Ibrexafungerp (SCY-078) Compared to Placebo in Subjects with Recurrent Vulvova... | |||||||||||||
| Medical condition: Recurrent Vulvovaginal Candidiasis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004492-12 | Sponsor Protocol Number: SCY-078-306 | Start Date*: 2019-06-05 | |||||||||||
| Sponsor Name:SCYNEXIS, Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral Ibrexafungerp (SCY-078) vs. Placebo in Subjects with Acute Vulvovaginal Candid... | |||||||||||||
| Medical condition: Acute Vulvovaginal Candidiasis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003147-22 | Sponsor Protocol Number: GLBR-101-2011 | Start Date*: 2011-12-02 | |||||||||||
| Sponsor Name:Glenmark Farmaceutica LTDA | |||||||||||||
| Full Title: A Multicenter, Open-Label, Comparator-Controlled, Parallel Group, Phase 3 Study to Assess the Efficacy and Safety of Clotrimazole/Clindamycin (200 mg/100 mg FDC) Ovules Compared with Metronidazole ... | |||||||||||||
| Medical condition: vaginitis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016655-21 | Sponsor Protocol Number: P-090756-01 | Start Date*: 2010-04-30 | |||||||||||
| Sponsor Name:Ferrer Internacional, S.A | |||||||||||||
| Full Title: A Multi-Centre, Randomized, Placebo-controlled, Parallel-Group, Double-Blinded Study to Compare the Therapeutic Efficacy, Safety and Tolerability of 3 Single Vaginal Doses of Arasertaconazole Nitra... | |||||||||||||
| Medical condition: Vulvovaginal Candidiasis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) FR (Completed) LT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001201-75 | Sponsor Protocol Number: FHP-2021-2-26 | Start Date*: 2021-09-13 |
| Sponsor Name:Female Healthcare Purna | ||
| Full Title: A Phase 2, Randomized, Double-Blind, Active-Controlled Study to Evaluate the Efficacy and Safety of Miconazole Nitrate 2% + Domiphen Bromide Vaginal cream in the Treatment of Subjects with Acute Vu... | ||
| Medical condition: acute vulvovaginal candidiasis | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000925-27 | Sponsor Protocol Number: ProF-001_Phase_IIb/III | Start Date*: 2019-08-27 | |||||||||||
| Sponsor Name:Profem GmbH | |||||||||||||
| Full Title: A phase IIb/III, parallel-arm, randomized, active-controlled, double-blind, double-dummy, study in patients with recurrent vulvovaginal candidiasis to compare the clinical efficacy, safety and tole... | |||||||||||||
| Medical condition: recurrent vulvovaginal candidiasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: AT (Completed) SK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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