
SCYNEXIS, Inc.
SCYXHealthcare|Medical - Pharmaceuticals|US
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Clinical Trials (18)
| Trial | Conditions | Phase | Status | Enrollment | Design | Drug |
|---|---|---|---|---|---|---|
| NCT05399641 Ibrexafungerp for the Treatment of Complicated Vulvovaginal Candidiasis | Vulvovaginal Candidiasis | P3 | Completed | 150 | RCT, Open-label | Ibrexafungerp |
| NCT03734991 Efficacy and Safety of Oral Ibrexafungerp (SCY-078) vs. Placebo in Subjects With Acute Vulvovaginal Candidiasis (VANISH 303) | Candida Vulvovaginitis | P3 | Completed | 376 | RCT, Double-blind | Ibrexafungerp, Placebo |
| NCT04029116 Phase 3 Study of Oral Ibrexafungerp (SCY-078) Vs. Placebo in Subjects With Recurrent Vulvovaginal Candidiasis (VVC) | Recurrent Vulvovaginal Candidiasis | P3 | Completed | 440 | RCT, Double-blind | Fluconazole Tablet, IBREXAFUNGERP, Placebo oral tablet |
| NCT05178862 A Phase 3, Randomized, Double-blind Study for Patients With Invasive Candidiasis Treated With IV Echinocandin Followed by Either Oral Ibrexafungerp or Oral Fluconazole | Candidiasis, Invasive, Candidemia | P3 | Terminated | 68 | RCT, Double-blind | SCY-078, Fluconazole, Echinocandin |
| NCT03987620 Efficacy and Safety of Oral Ibrexafungerp (SCY-078) vs. Placebo in Subjects With Acute Vulvovaginal Candidiasis | Candida Vulvovaginitis | P3 | Completed | 455 | RCT, Double-blind | Ibrexafungerp, Placebo |
| NCT03059992 Study to Evaluate the Efficacy and Safety of Ibrexafungerp in Patients With Fungal Diseases That Are Refractory to or Intolerant of Standard Antifungal Treatment | Invasive Candidiasis, Mucocutaneous Candidiasis | P3 | Completed | 233 | Open-label | Ibrexafungerp |
| NCT03363841 Open-Label Study to Evaluate the Efficacy and Safety of Oral Ibrexafungerp (SCY-078) in Patients With Candidiasis Caused by Candida Auris (CARES) | Candidiasis, Invasive, Candidemia | P3 | Completed | 30 | Open-label | SCY-078 |
| NCT02679456 Safety and Efficacy of Oral Ibrexafungerp (SCY-078) vs. Oral Fluconazole in Subjects With Vulvovaginal Candidiasis | Vulvovaginal Candidiasis | P2 | Completed | 96 | RCT, Single-blind | SCY-078, Fluconazole |
| NCT03672292 Evaluate Safety and Efficacy of the Coadministration of Ibrexafungerp With Voriconazole in Patients With Invasive Pulmonary Aspergillosis | Invasive Pulmonary Aspergillosis | P2 | Terminated | 22 | RCT, Double-blind | SCY-078, Voriconazole |
| NCT01265511 Study of SCY-635, Pegasys and Copegus in Hepatitis C | Hepatitis C Infection | P2 | Completed | 10 | RCT, Double-blind | Placebo, SCY-635, Pegasys, Copegus |
| NCT03253094 Dose-Finding Study of Oral Ibrexafungep (SCY-078) vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis | Candida Vulvovaginitis | P2 | Completed | 186 | RCT, Double-blind | Fluconazole, SCY-078 |
| NCT02244606 Oral Ibrexafungerp (SCY-078) vs Standard-of-Care Following IV Echinocandin in the Treatment of Invasive Candidiasis | Mycoses, Candidiasis, Invasive | P2 | Completed | 27 | RCT, Open-label | SCY-078, Fluconazole, Micafungin |
| NCT06954493 Pharmacokinetic Study in Healthy Lactating Women Exposed to Ibrexafungerp | Vulvovaginal Candidiasis, Candida Infection | P1 | Completed | 5 | Open-label | Ibrexafungerp |
| NCT04092751 Study to Evaluate the Effect of SCY-078 (Ibrexafungerp) on the PK of Pravastatin in Healthy Subjects | Pharmacokinetics | P1 | Completed | 28 | RCT, Open-label | PRA, SCY-078 plus PRA |
| NCT01290965 Safety, PK and Efficacy of 15 Days of SCY-635 Treatment in Hepatitis C Patients | Chronic Hepatitis C | P1 | Completed | 57 | RCT, Double-blind | Placebo, SCY-635 |
| NCT04092725 Study to Evaluate the Effect of SCY-078 on the PK of Dabigatran in Healthy Subjects | Pharmacokinetics | P1 | Completed | 36 | RCT, Open-label | DAB, SCY-078 plus DAB |
| NCT04307082 ADME Study of [14C]-Ibrexafungerp in Healthy Male Subjects | Fungal Infection | P1 | Completed | 6 | Open-label | [14C]-Ibrexafungerp |
| NCT05668429 ADME Study of [14^C]-Ibrexafungerp in Healthy Male Subjects | Fungal Disease | P1 | Completed | 6 | Open-label | Ibrexafungerp |