Otes is indicated to reduce the incidence of recurrent vulvovaginal candidiasis (RVVC) in females with a history of RVVC who are not of reproductive potential. If specimens for fungal culture are obtained prior to therapy, antifungal therapy may be instituted before the results of the cultures are known. However, once these results become available, antifungal therapy should be adjusted accordingly.
Oteseconazole is an antifungal drug. Oteseconazole exposure-response relationships and the time course of pharmacodynamic response are unknown. Oteseconazole is an azole metalloenzyme inhibitor targeting the fungal sterol, 14α demethylase (CYP51), an enzyme that catalyzes an early step in the biosynthetic pathway of ergosterol, a sterol required for fungal cell membrane formation and integrity. Inhibition of CYP51 results in the accumulation of 14-methylated sterols, some of which are toxic to fungi. Through the inclusion of a tetrazole metal-binding group, oteseconazole has a lower affinity for human CYP enzymes.
There are two recommended Oteseconazole dosage regimens: For the Oteseconazole-only dosage regimen: On Day 1 : Administer Oteseconazole 600 mg (as a single dose), then On Day 2 : Administer Oteseconazole 450 mg (as a single dose), then Beginning on Day 14 : Administer Oteseconazole 150 mg once a week (every 7 days) for 11 weeks (Weeks 2 through 12). For the Fluconazole/Oteseconazole dosage regimen, prescribe Fluconazole and: On Day 1, Day 4, and Day 7 : Administer fluconazole 150 mg orally, then On Days 14 through 20 : Administer Oteseconazole 150 mg once daily for 7 days, then Beginning on Day 28 : Administer Oteseconazole 150 mg once a week (every 7 days) for 11 weeks (Weeks 4 through 14). Administer Oteseconazole orally with food. Swallow the capsules whole. Do not chew, crush, dissolve, or open the capsules.
Always consult a registered doctor before taking any medicine. This information is for general knowledge only.
The most frequently reported adverse reactions (incidence >2%) were headache and nausea.
Oteseconazole is contraindicated in: Females of reproductive potential Pregnant and lactating women Patients with known hypersensitivity to oteseconazole
BCRP (Breast Cancer Resistance Protein) Substrates: Concomitant use of Otes with BCRP substrates may increase the exposure of drugs that are BCRP substrates, which may increase the risk of adverse reactions associated with these drugs. Use the lowest possible starting dose of the BCRP substrate or consider reducing the dose of the substrate drugs and monitor for adverse reactions.
Embryo-Fetal Toxicity : Otes is contraindicated in females of reproductive potential, and in pregnant and lactating women. Based on animal studies, Otes may cause fetal harm. The drug exposure window of approximately 690 days (based on 5 times the half-life of Otes) precludes adequate mitigation of the embryo-fetal toxicity risks. Ocular abnormalities were observed in the offspring of pregnant rats dosed at 7.5-mg/kg/day during organogenesis through lactation in pre and postnatal developmental studies. The observed ocular abnormalities included cataracts, opacities, exophthalmos/buphthalmos, optic nerve/retinal atrophy, lens degeneration and hemorrhage. Ocular abnormalities occurred at doses about 3.5 times the steady state clinical exposure seen with patients being treated for RVVC. Advise patients that Otes is contraindicated in females of reproductive potential, and in pregnant and lactating women because of potential risks to a fetus or breastfed infan.