Last reviewed · How we verify
Fluconazole and Secnidazole
Fluconazole and secnidazole is a combination antifungal and antiprotozoal agent that inhibits fungal ergosterol synthesis and disrupts protozoal DNA, respectively.
Fluconazole and secnidazole is a combination antifungal and antiprotozoal agent that inhibits fungal ergosterol synthesis and disrupts protozoal DNA, respectively. Used for Vulvovaginal candidiasis with concurrent trichomoniasis or bacterial vaginosis.
At a glance
| Generic name | Fluconazole and Secnidazole |
|---|---|
| Sponsor | Universidad Nacional de Colombia |
| Drug class | Antifungal/antiprotozoal combination |
| Target | Fungal CYP51 (lanosterol 14α-demethylase); protozoal DNA |
| Modality | Small molecule |
| Therapeutic area | Infectious Disease |
| Phase | Phase 3 |
Mechanism of action
Fluconazole is an azole antifungal that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane. Secnidazole is a nitroimidazole antiprotozoal that generates reactive intermediates that damage protozoal DNA and cellular structures. Together, they provide broad-spectrum coverage against fungal and protozoal infections.
Approved indications
- Vulvovaginal candidiasis with concurrent trichomoniasis or bacterial vaginosis
Common side effects
- Headache
- Nausea
- Abdominal pain
- Vulvovaginal irritation
- Metallic taste
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Fluconazole and Secnidazole CI brief — competitive landscape report
- Fluconazole and Secnidazole updates RSS · CI watch RSS
- Universidad Nacional de Colombia portfolio CI