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BREXAFEMME, available as an oral tablet, contains ibrexafungerp citrate, a triterpenoid antifungal agent.
Ibrexafungerp is designated chemically as (1S,4aR,6aS,7R,8R,10aR,10bR,12aR,14R,15R)-15[(2R)-2-amino-2,3,3-trimethylbutoxy]-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-14[5-(pyridine-4-yl)-1H-1,2,4-triazol-1-yl]-1,6,6a,7,8,9,10,10a,10b,11,12,12a-dodecahydro-2H,4H1,4a-propanophenanthro[1,2-c]pyran-7-carboxylic acid compound with 2-hydroxypropane-1,2,3tricarboxylic acid (1:1) with an empirical formula of C44H67N5O4 • C6H8O7 and a molecular weight of 922.18 grams per mole. The chemical structure is:
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BREXAFEMME tablet for oral administration is a purple, oval, biconvex shaped, film-coated tablet containing 189.5 mg of ibrexafungerp citrate equivalent to 150 mg of ibrexafungerp. In addition to the active ingredient, the tablet formulation contains butylated hydroxyanisole, colloidal silicon dioxide, crospovidone, magnesium stearate, mannitol, and microcrystalline cellulose. The tablet film-coating contains FD&C Blue #2, FD&C Red #40, hydroxypropyl cellulose, hydroxypropylmethyl cellulose 2910, talc and titanium dioxide.
BREXAFEMME® is indicated in adult and post-menarchal pediatric females for:
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.
The recommended dosage of BREXAFEMME in adult and post-menarchal pediatric females is 300 mg (two 150 mg tablets) administered approximately 12 hours apart (e.g., in the morning and in the evening) for one day, for a total daily dosage of 600 mg (four 150 mg tablets).
The recommended dosage of BREXAFEMME to prevent recurrences is 300 mg (two 150 mg tablets) administered approximately 12 hours apart (e.g., in the morning and in the evening) for one day, for a total daily dosage of 600 mg (four 150 mg tablets) monthly for six months.
BREXAFEMME may be taken with or without food.
With concomitant use of a strong CYP3A inhibitor, administer BREXAFEMME 150 mg approximately 12 hours apart (e.g., in the morning and in the evening) for one day. No dosage adjustment is warranted in patients with concomitant use of a weak or moderate CYP3A inhibitor [see DRUG INTERACTIONS and CLINICAL PHARMACOLOGY].
For females of reproductive potential, verify that the patient is not pregnant prior to initiating treatment with BREXAFEMME. Reassessment of pregnancy status prior to each dose is recommended when BREXAFEMME is used monthly for 6 months for reduction in the incidence of RVVC [see CONTRAINDICATIONS, WARNING AND PRECAUTIONS and Use In Specific Populations].
BREXAFEMME tablets are purple, oval, biconvex shaped tablets debossed with 150 on one side and SCYX on the other side containing 150 mg of ibrexafungerp.
BREXAFEMME (ibrexafungerp tablets) are purple, oval, biconvex shaped tablets debossed with 150 on one side and SCYX on the other side. Each tablet contains 150 mg ibrexafungerp (equivalent to 189.5 mg of ibrexafungerp citrate).
Tablets are packaged in polyvinyl/polyvinylidene chloride child-resistant blister packs, four (4) tablets per pack. (NDC 75788-115-04)
Store BREXAFEMME tablets at 20°C to 25°C (68°F to 77°F). Brief exposure to 15°C to 30°C (59°F to 86°F) permitted (see USP Controlled Room Temperature).
Manufactured for: SCYNEXIS, Inc., Jersey City, New Jersey, 07302 ©2021 SCYNEXIS, Inc. Revised: Nov 2022
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
A total of 545 patients were exposed to BREXAFEMME in two clinical trials of post-menarchal females with VVC (Trial 1 and Trial 2). The patients were treated with BREXAFEMME 300 mg (two 150 mg tablets) twice a day, 12 hours apart, for one day. The patients were 18 to 76 years of age (mean 34 years); 69% were White and 28% were Black or African American; 18% were of Hispanic or Latina ethnicity.
The most frequently reported adverse reactions are presented in Table 1.
There were no serious adverse reactions and 2 out of 545 (0.4%) patients discontinued treatment with BREXAFEMME due to vomiting (1 patient) and dizziness (1 patient).
Table 1. Adverse Reactions with Rates ≥2% in BREXAFEMME-Treated Patients with VVC in Trials 1 and 2
| Adverse Reaction | BREXAFEMME N = 545 n (%) |
Placebo N = 275 n (%) |
| Diarrhea | 91 (16.7%) | 9 (3.3%) |
| Nausea | 65 (11.9%) | 11 (4.0%) |
| Abdominal pain1 | 62 (11.4%) | 14 (5.1%) |
| Dizziness2 | 18 (3.3%) | 7 (2.5%) |
| Vomiting | 11 (2.0%) | 2 (0.7%) |
| 1 Includes abdominal pain, abdominal pain upper, abdominal pain lower, and abdominal discomfort 2 Includes dizziness and postural dizziness |
||
The following adverse reactions occurred in < 2% of patients receiving BREXAFEMME in Trial 1 and Trial 2: dysmenorrhea, flatulence, back pain, elevated transaminases, vaginal bleeding, rash/hypersensitivity reaction.
A total of 130 patients were exposed to BREXAFEMME in a clinical trial of post-menarchal females with RVVC (Trial 3). The patients were treated with BREXAFEMME 300 mg (two 150 mg tablets) twice a day, 12 hours apart, for one day, monthly for six consecutive months. The patients were 18 to 65 years of age (mean 34 years), of which, 59% of patients were between 18 to 35 years, and 41% between 36 to 65 years. Ninety two percent (92%) were White, 7% were Black or African American, and 1% were Asian. Nine percent (9%) of patients were of Hispanic or Latina ethnicity.
The most frequently reported adverse reactions are presented in Table 2.
There were no serious adverse reactions and no patients discontinued treatment with BREXAFEMME due to adverse reaction.
Table 2. Adverse Reactions with Rates ≥2% in BREXAFEMME-Treated Patients with RVVC in Trial 3
| Adverse Reaction1 | BREXAFEMME N = 130 n (%) |
Placebo N = 130 n (%) |
| Headache | 23 (17.6) | 10 (7.6) |
| Abdominal pain2 | 13 (10.0) | 9 (6.9) |
| Diarrhea | 10 (7.7) | 5 (3.8) |
| Nausea | 7 (5.4) | 5 (3.8) |
| Urinary tract infection | 5 (3.8) | 1 (0.8) |
| Fatigue | 4 (3.1) | 0 |
| 1 A single patient may have had multiple instances of adverse reactions. Only one episode of adverse reaction is counted per patient. 2 Includes abdominal pain, abdominal pain upper, abdominal pain lower, and abdominal discomfort |
||
Ibrexafungerp is a substrate of CYP3A4. Drugs that inhibit or induce CYP3A may alter the plasma concentrations of ibrexafungerp and affect the safety and efficacy of BREXAFEMME [see CLINICAL PHARMACOLOGY]
Table 3 Effect of Coadministered Drugs on Ibrexafungerp Pharmacokinetics:
| Concomitant Drugs | Effect on Ibrexafungerp Concentration | Recommendation |
| Strong CYP3A inhibitors: | Significantly increased | Reduce the BREXAFEMME dosage [see DOSAGE AND ADMINISTRATION] |
| (e.g., ketoconazole, itraconazole) | ||
| Strong and Moderate CYP3A inducers: | Not studied in vivo or in vitro, but likely to result in significant reduction | Avoid concomitant administration |
| (e.g., rifampin, carbamazepine, phenytoin, St. John’s wort, long acting barbiturates, bosentan, efavirenz, or etravirine) |
Ibrexafungerp is an inhibitor of CYP3A4, P-gp and OATP1B3 transporter [(see CLINICAL PHARMACOLOGY]. However, given the short treatment duration for VVC, the effect of BREXAFEMME on the pharmacokinetics of substrates of CYP3A4, P-gp and OATP1B3 transporters is not considered to be clinically significant.
Included as part of the "PRECAUTIONS" Section
Based on findings from animal studies, BREXAFEMME use is contraindicated in pregnancy because it may cause fetal harm. In animal reproduction studies, ibrexafungerp administered orally to pregnant rabbits during organogenesis was associated with fetal malformations including absent forelimb(s), absent hindpaw, absent ear pinna, and thoracogastroschisis at dose exposures greater or equal to approximately 5 times the human exposure at the recommended human dose (RHD).
For females of reproductive potential, verify that the patient is not pregnant prior to initiating treatment with BREXAFEMME. Reassessment of pregnancy status prior to each dose is recommended when BREXAFEMME is used monthly for 6 months for reduction in the incidence of RVVC. Advise females of reproductive potential to use effective contraception during treatment of VVC and throughout the 6-month treatment period for reduction in the incidence of RVVC with BREXAFEMME and, for 4 days after the last dose [see Use In Specific Populations].
Advise the patient to read the FDA approved patient labeling (Medication Guide)
For treatment of VVC, inform the patient that each BREXAFEMME dose consists of two tablets. A total treatment course for VVC is two doses taken approximately 12 hours apart and consists of a total of four tablets.
For reduction in the incidence of RVVC, inform the patients that the total treatment course is for six months. Each dose consists of two tablets taken approximately 12 hours apart for a total daily dosage of four tablets, taken monthly for six months.
If the first two tablets are taken in the morning, the second two tablets should be taken that same day in the evening. If the first two tablets are taken in the afternoon or evening, the second two tablets should be taken the following morning.
Inform the patient that BREXAFEMME can be taken with or without food [see DOSAGE AND ADMINISTRATION].
Advise the patient to inform their health care provider if they are taking any other medications as certain medications can increase or decrease blood concentrations of BREXAFEMME or BREXAFEMME may increase or decrease blood concentrations of certain medications [see DOSAGE AND ADMINISTRATION].
Two-year carcinogenicity studies of ibrexafungerp have not been performed.
No mutagenic or clastogenic effects were detected in an in vitro bacterial reverse mutation assay, an in vitro chromosomal aberration assay, and an in vivo bone marrow micronucleus assay in rats.
In a male and female fertility study in rats, ibrexafungerp was administered to male rats by oral gavage in doses of 10, 20, 40, and 80 mg/kg/day for 28 days before mating and throughout mating and to female rats for 15 days before mating, during mating, and until gestation day (GD) 6. Ibrexafungerp did not impair fertility in either sex at any dose up to the highest dose of 80 mg/kg/day (approximately 10 times the RHD based on AUC comparison).
Based on findings from animal studies, BREXAFEMME use is contraindicated in pregnancy because it may cause fetal harm. In pregnant rabbits, oral ibrexafungerp administered during organogenesis was associated with fetal malformations including absent forelimb(s), absent hindpaw, absent ear pinna, and thoracogastroschisis at dose exposures greater or equal to approximately 5 times the human exposure at the RHD. Oral ibrexafungerp administered to pregnant rats during organogenesis was not associated with fetal toxicity or increased fetal malformations at a dose exposure approximately 5 times the human exposure at the RHD (see Data). Available data on BREXAFEMME use in pregnant women are insufficient to draw conclusions about any drug-associated risks of major birth defects, miscarriage, or other adverse maternal or fetal outcomes.
There is a pregnancy safety study for BREXAFEMME. If BREXAFEMME is inadvertently administered during pregnancy or if pregnancy is detected within 4 days after a patient receives BREXAFEMME, pregnant women exposed to BREXAFEMME and healthcare providers should report pregnancies to SCYNEXIS, Inc. at 1-888-982-SCYX (7299).
Animal Data
In a rat embryo-fetal study, ibrexafungerp was administered to pregnant rats by oral gavage from gestation days (GDs) 6 through 17 at doses of 10, 20, 35, and 50 mg/kg/day. No fetal malformations or changes in embryo-fetal survival or fetal body weights occurred with any of the doses of ibrexafungerp up to the high-dose of 50 mg/kg/day (approximately 5 times the RHD based on plasma AUC comparison).
In an embryo-fetal study in rabbits, ibrexafungerp was administered by oral gavage at doses of 10, 25, and 50 mg/kg/day from GD 7 through GD 19. In the mid-dose group administered 25 mg/kg/day (approximately 5 times the RHD based on AUC comparison), fetal malformations, including absent ear pinna, craniorachischisis, thoracogastroschisis, trunk kyphosis, absent forelimbs, absent forepaws, and absent hindpaw occurred in a single fetus. Malformations including absent hindpaw and anencephaly occurred with an increased litter incidence in the high-dose group of 50 mg/kg/day (approximately 13 times the RHD based on AUC comparison), and other malformations occurred in single fetuses and litters including absent ear pinna, thoracogastroschisis, absent forelimb, and absent thyroid gland. No changes in embryo-fetal survival or fetal body weights were observed with any of the ibrexafungerp doses, and fetal malformations were not observed with the 10 mg/kg/day dose of ibrexafungerp (approximately 2 times the RHD based on AUC comparison).
In a pre-postnatal study in rats, ibrexafungerp was administered by oral gavage from GD 6 through the lactation period until lactation day 20 in maternal doses of 10, 20, 35, and 50 mg/kg/day. No maternal toxicity or adverse effects on the survival, growth, behavior, or reproduction of first-generation offspring occurred with any of the ibrexafungerp doses up to the high dose of 50 mg/kg/day (approximately 5 times the RHD based on AUC comparison).
There are no data on the presence of ibrexafungerp in either human or animal milk, the effects on the breast-fed infant, or the effects on milk production.
The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for BREXAFEMME and any potential adverse effects on the breastfed child from BREXAFEMME or from the underlying maternal condition.
Based on animal data, BREXAFEMME may cause fetal harm when administered to a pregnant female [see Pregnancy ].
For females of reproductive potential, verify that the patient is not pregnant prior to initiating treatment with BREXAFEMME. Reassessment of pregnancy status prior to each dose is recommended when BREXAFEMME is used monthly for 6 months for reduction in the incidence of RVVC. [see DOSAGE AND ADMINISTRATION, CONTRAINDICATIONS and Pregnancy ].
Females
For treatment of VVC, advise females of reproductive potential to use effective contraception during treatment with BREXAFEMME and for 4 days after the last dose.
For reduction in the incidence of RVVC, advise females of reproductive potential to use effective contraception throughout the 6-month treatment period with BREXAFEMME and, for 4 days after the last dose.
The safety and effectiveness of BREXAFEMME for treatment of VVC have been established in post-menarchal pediatric females. BREXAFEMME is also indicated for the reduction in the incidence of RVVC [see INDICATIONS]. Use of BREXAFEMME in postmenarchal pediatric patients is supported by evidence from adequate and well-controlled studies of BREXAFEMME in adult non-pregnant women with additional pharmacokinetic and safety data from post-menarchal pediatric females [see ADVERSE REACTIONS, CLINICAL PHARMACOLOGY, and Clinical Studies].
The safety and effectiveness of BREXAFEMME have not been established in pre-menarchal pediatric females.
Clinical studies with ibrexafungerp did not include sufficient numbers of subjects aged 65 and older to determine whether they respond differently from younger subjects. No clinically meaningful differences in the pharmacokinetics of ibrexafungerp were observed in geriatric patients compared to younger adults [see CLINICAL PHARMACOLOGY].
No dosage adjustment of BREXAFEMME is recommended in patients with mild hepatic impairment (Child-Pugh Class A) or moderate hepatic impairment (Child-Pugh Class B).
Administration of BREXAFEMME in patients with severe hepatic impairment (Child-Pugh Class C) has not been studied [see CLINICAL PHARMACOLOGY].
There is no experience with overdosage of BREXAFEMME.
There is no specific antidote for ibrexafungerp. Treatment should be supportive with appropriate monitoring.
BREXAFEMME is contraindicated in:
Ibrexafungerp is a triterpenoid antifungal drug [see Microbiology].
Ibrexafungerp exposure-response relationships and the time course of pharmacodynamic response are unknown.
At a concentration of 5 times or greater than that achieved after a single day 300 mg twice daily dose, ibrexafungerp does not prolong the QTc interval to any clinically relevant extent.
In healthy subjects, ibrexafungerp area under the curve (AUC) and maximal concentration (Cmax) increased approximately dose-proportionally following single dose administration from 10 to 1600 mg (0.02 to 2.67 times the approved recommended daily dose) and multiple-dose administration from 300-800 mg (0.50 to 1.33 times the approved recommended daily dose).
Based on a population pharmacokinetic analysis in patients with VVC, the model predicts that 300 mg twice a day for 2 doses achieves a mean (%CV) AUC0-24 exposure of 6832 (15%) ng•hr/mL and Cmax of 435 (15%) ng/mL under fasted conditions and a mean AUC0-24 exposure of 9867 (15%) ng•h/mL and Cmax of 629 (15%) ng/mL under fed conditions.
After oral administration of BREXAFEMME in healthy volunteers, ibrexafungerp generally reaches maximum plasma concentrations 4 to 6 hours after single and multiple dosing.
Effect of Food
Following administration of BREXAFEMME to healthy volunteers, the ibrexafungerp Cmax increased 32% and the AUC increased 38% with a high fat meal (800-1000 calories; 50% fat), compared to fasted conditions. This exposure change is not considered clinically significant [see DOSAGE AND ADMINISTRATION].
The mean steady state volume of distribution (Vss) of ibrexafungerp is approximately 600 L. Ibrexafungerp is highly protein bound (greater than 99%), predominantly to albumin. Animal studies demonstrate a 9-fold higher exposure in vaginal tissue than in blood.
Ibrexafungerp is eliminated mainly via metabolism and biliary excretion. The elimination halflife is approximately 20 hours.
Metabolism
In vitro studies show that ibrexafungerp undergoes hydroxylation by CYP3A4, followed by glucuronidation and sulfation of a hydroxylated inactive metabolite.
Excretion
Following oral administration of radio-labeled ibrexafungerp to healthy volunteers, a mean of 90% of the radioactive dose (51% as unchanged ibrexafungerp) was recovered in feces and 1% was recovered in urine.
The pharmacokinetics of ibrexafungerp were not altered in post-menarchal pediatric females (ages 13 to 17 years) or in geriatric patients (ages 65 to 76 years).
The pharmacokinetics of ibrexafungerp were not altered in subjects with mild (Child-Pugh Class A) to moderate (Child-Pugh Class B) hepatic impairment when the total AUC estimates were compared to healthy subjects.
The impact of severe hepatic impairment (Child-Pugh Class C) on the pharmacokinetics of ibrexafungerp is unknown.
Ibrexafungerp is a substrate of CYP3A4 and P-gp. In vitro, ibrexafungerp is an inhibitor of CYP2C8, CYP3A4, P-gp transporter, and OATP1B3 transporter. Ibrexafungerp is not an inducer of CYP3A4.
The effect of coadministration of drugs on the pharmacokinetics of ibrexafungerp and the effect of ibrexafungerp on the pharmacokinetics of coadministered drugs were studied in healthy subjects.
Strong CYP3A4 Inhibitor
Ketoconazole (400 mg once daily for 15 days), a strong CYP3A4 and P-gp inhibitor, increased the ibrexafungerp AUC by 5.8-fold and Cmax by 2.5-fold [see DRUG INTERACTIONS].
Moderate CYP3A4 Inhibitor
Diltiazem (240 mg once daily for 15 days) increased the ibrexafungerp AUC by 2.5-fold and Cmax by 2.2-fold. This exposure change is not considered clinically significant at the approved recommended dosage for VVC.
Proton Pump Inhibitor
Pantoprazole (40 mg once daily for 5 days) decreased ibrexafungerp AUC by approximately 25% and Cmax by 22%. This exposure change is not considered clinically significant at the approved recommended dosage for VVC.
The effects of ibrexafungerp on substrates of CYP2C8, CYP3A4, P-gp, and OATP1B3 transporters were evaluated in studies that included loading doses of ibrexafungerp of 1250 to 1500 mg (2.1 to 2.5 times the approved recommended daily dose) for two days followed by 750 mg (1.25 times the approved recommended daily dose) once daily for 3-7 days.
CYP2C8 substrates
Ibrexafungerp did not increase the AUC0-inf or Cmax of rosiglitazone, a moderate sensitive CYP2C8 substrate.
CYP3A4 substrates
Ibrexafungerp resulted in 1.4-fold increase in the AUC0-inf and no effect on the Cmax of the sensitive CYP3A4 and P-gp substrate tacrolimus.
P-gp substrates
Ibrexafungerp resulted in a 1.4-fold increase in the AUC0-48 and a 1.25-fold increase in the Cmax of the P-gp substrate dabigatran.
OATP1B3 transporters
Ibrexafungerp resulted in a 2.8-fold increase in the AUC0-24 and a 3.5- fold increase in the Cmax of the OATP1B3 transporter substrate pravastatin.
Ibrexafungerp, a triterpenoid antifungal agent, inhibits glucan synthase, an enzyme involved in the formation of 1,3-β-D-glucan, an essential component of the fungal cell wall.
Ibrexafungerp has concentration-dependent fungicidal activity against Candida species as measured by time kill studies. Ibrexafungerp retains in vitro antifungal activity when tested at pH 4.5 (the normal vaginal pH).
The potential for resistance to ibrexafungerp has been evaluated in vitro and is associated with mutations of the fks-2 gene; the clinical relevance of these findings is unknown. Ibrexafungerp retains activity against most fluconazole resistant Candida spp. No resistance development was observed after monthly BREXAFEMME dosing in patients with RVVC.
In vitro studies have not demonstrated antagonism between ibrexafungerp and azoles or echinocandins.
Ibrexafungerp has been shown to be active against most isolates of the following microorganism both in vitro and in clinical infections [see INDICATIONS]:
Candida albicans
The following in vitro data are available, but their clinical significance is unknown.
Ibrexafungerp has in vitro activity against most isolates of the following microorganisms:
Candida auris
Candida dubliniensis
Candida glabrata
Candida guilliermondii
Candida keyfr
Candida krusei
Candida lusitaniae
Candida parapsilosis
Candida tropicalis
Daily administration of oral ibrexafungerp for 26 weeks in rats, at the highest dose of 80 mg/kg/day (approximately 10 times the RHD based on AUC comparison), was associated with marked, but reversible, phospholipidosis and foamy histiocytes in alveolar tissue in the lung and labored breathing, marked irritation and metaplasia in gastric mucosa, and peripheral nerve degeneration accompanied by hind-limb paralysis.
Two randomized placebo-controlled clinical trials (Trial 1, NCT03734991 and Trial 2, NCT03987620) with a similar design were conducted to evaluate the safety and efficacy of a single day of BREXAFEMME 600 mg (two 150 mg tablets per dose, administered 12 hours apart) for the treatment of VVC. Non-pregnant post-menarchal females with a diagnosis of VVC were eligible. A diagnosis of VVC was defined as (a) minimum composite vulvovaginal signs and symptoms (VSS) score of ≥4 with at least two signs or symptoms having a score of 2 (moderate) or greater; (b) positive microscopic examination with 10% KOH in a vaginal sample revealing yeast forms (hyphae/pseudohyphae) or budding yeasts, and (c) normal vaginal pH (≤4.5). The total composite VSS score was based on the vulvovaginal signs (erythema, edema, excoriation) and vulvovaginal symptoms (itching, burning, or irritation) where each was scored as 0= absent, 1= mild, 2= moderate, or 3= severe. Study visits included the test of cure (TOC, Day 8 to 14) visit and a follow-up (Day 21 to 29) visit. The modified intent to treat (MITT) population included randomized subjects with a baseline culture positive for Candida species who took at least 1 dose of study medication.
Trial 1 was conducted in the United States. The MITT population consisted of 190 patients treated with BREXAFEMME and 100 patients treated with placebo. The average age was 34 years (range 17-67 years), with 91% less than 50 years. Fifty-four percent (54%) were White and 40% were Black or African American, 26% were of Hispanic or Latino ethnicity. The average BMI was 30 and 9% had a history of diabetes. The median VSS score at baseline was 9 (range 4- 18). The majority (92%) of the subjects were culture-positive with C. albicans.
Trial 2 was conducted in the United States (39%) and Bulgaria (61%). The MITT population consisted of 189 patients treated with BREXAFEMME and 89 patients treated with placebo. The average age was 34 years (range 18-65 years), with 92% less than 50 years. Eighty-one percent (81%) were White and 19% were Black or African American, 10% were of Hispanic or Latino ethnicity. The average BMI was 26 and 5% had a history of diabetes. The median VSS score at baseline was 10 (range 4-18). The majority (89%) of the subjects were culture-positive with C. albicans.
Efficacy was assessed by clinical outcome at the TOC visit. A complete clinical response was defined as the complete resolution of signs and symptoms (VSS score of 0). Additional endpoints included a negative culture for Candida spp. at the TOC visit, and clinical outcome at the follow-up visit.
Statistically significantly greater percentages of patients experienced a complete clinical response at TOC, negative culture at TOC, and complete clinical response at follow-up with treatment with BREXAFEMME compared to placebo. The results for the clinical and mycological responses are presented in Table 4.
Table 4. Clinical and Mycological Response in Post-menarchal Females with VVC in Trials 1 and 2, MITT Population
| Trial 1 | Trial 2 | |||
| BREXAFEMME N = 190 n (%) |
Placebo N = 100 n (%) |
BREXAFEMME N = 189 n (%) |
Placebo N = 89 n (%) |
|
| Complete Clinical Response at TOC1 | 95 (50.0) | 28 (28.0) | 120 (63.5) | 40 (44.9) |
| Difference (95% CI) P-value |
22.0 (10.2, 32.8) 0.001 |
18.6 (6.0, 30.6) 0.009 |
||
| Negative Culture at TOC | 94 (49.5) | 19 (19.0) | 111 (58.7) | 26 (29.2) |
| Difference (95% CI) P-value |
30.5 (19.4, 40.3) < 0.001 |
29.5 (17.2, 40.6) < 0.001 |
||
| Complete Clinical Response at follow-up2 | 113 (59.5) | 44 (44.0) | 137 (72.5) | 44 (49.4) |
| Difference (95% CI) P-value |
15.5 (3.4, 27.1) 0.007 |
23.1 (10.8, 35.0) 0.006 |
||
| 1Absence of signs and symptoms (VSS Score of 0) without need for additional antifungal therapy or topical drug therapy for the treatment of vulvovaginal symptoms at test of cure (TOC) visit. 2Absence of signs and symptoms (VSS Score of 0) without need for further antifungal treatment or topical drug therapy for the treatment of vulvovaginal symptoms prior to follow-up visit. |
||||
A randomized placebo-controlled clinical trial (Trial 3, NCT04029116) was conducted to evaluate the safety and efficacy of BREXAFEMME 300 mg (two 150 mg tablets) administered approximately 12 hours apart (e.g., in the morning and in the evening) for one day, for a total daily dosage of 600 mg (four 150 mg tablets) administered once monthly for six months. Trial 3 was conducted in the United States (33%), Bulgaria (28%), Poland (12%), and Russia (28%). Non-pregnant post-menarchal females presenting with a symptomatic VVC episode and a history of recurrent VVC (at least 3 episodes of VVC in the previous 12 months) were eligible. The symptomatic episode at Screening was treated with 3 doses of fluconazole 150 mg 3 days apart.
To be randomized, patients had to have a culture-confirmed VVC episode at Screening and had to achieve significant resolution of their vulvovaginal signs and symptoms (defined as a total composite score ≤ 2 on the VSS Scale) after fluconazole treatment. Patients were randomized at a 1:1 ratio to receive double-blind BREXAFEMME or placebo administered as a single-day treatment repeated every 4 weeks for a total of 6 single-day treatments. Study visits included the test of cure (TOC) at Week 24 (4 weeks after the last dose) and a follow-up visit at Week 36.
The intent to treat (ITT) population was all randomized patients.
The ITT population consisted of 130 patients treated with BREXAFEMME and 130 patients treated with placebo. The average age was 34 years (range 18-65 years) with 95% less than 50 years. Ninety percent (90%) of patients were White, 8% were Black or African American, and 2% were Asian and other race. Eight percent (8%) of patients were of Hispanic or Latino ethnicity. The average BMI of the patient population was 25 and 16.5% were obese (BMI >30).
Efficacy was assessed as the percentage of patients with Clinical Success, defined as subjects with No Culture Proven, Presumed or Suspected Recurrence of VVC requiring antifungal therapy up to TOC at Week 24. Clinical Success was also assessed at the Week 36 Follow-up visit.
Statistically significantly greater percentages of patients experienced Clinical Success at TOC compared to placebo. The clinical success rate at TOC was lower for patients in the United States when compared to patients outside the United States (ex-US) for both BREXAFEMME and placebo groups. In both regions, the BREXAFEMME group had a higher clinical success rate compared to placebo (US: 33% vs 23% and ex-US: 81% vs 68% in BREXAFEMME vs placebo arms, respectively) and the difference between the treatment groups was consistent [US: 10.1% (-9.0, 29.1) and ex-US: 12.9% (0.04, 25.7)]. Clinical Success at Week 36 was also greater for BREXAFEMME compared to placebo. The results for clinical success and reasons for clinical failure are presented in Table 5.
Table 5. Clinical and Mycological Response in Post-menarchal Females with RVVC in Trial 3, ITT Population
| Trial 3 | |||
| BREXAFEMME N = 130 n (%) |
Placebo N = 130 n (%) |
Difference (95% CI) P-value |
|
| Clinical success at TOC (Week 24) | 85 (65.4) | 69 (53.1) | 12.7 (2.2, 23.1) 0.020 |
| Reasons For Clinical Failure at TOC | |||
| Mycologically Proven Recurrence | 30 (23.1) | 47 (36.2) | |
| Presumed Recurrence | 7 (5.4) | 3 (2.3) | |
| Suspected Recurrence | 2 (1.5) | 4 (3.1) | |
| Imputed Recurrence1 | 6 (4.6) | 7 (5.4) | |
| Clinical success at Week 36 Follow Up Visit | 75 (57.7) | 60 (46.2) | 11.9 (1.1, 22.6) 0.034 |
| Reasons For Clinical Failure at Week-36 | |||
| Follow-up Visit | |||
| Mycologically Proven Recurrence | 37 (28.5) | 51 (39.2) | |
| Presumed Recurrence | 8 (6.2) | 5 (3.8) | |
| Suspected Recurrence | 4 (3.1) | 5 (3.8) | |
| Imputed Recurrence1 | 6 (4.6) | 9 (6.9) | |
| Abbreviations: CI = confidence interval; TOC = test of cure. 1Imputed recurrences are subjects whose clinical outcome cannot be determined due to early termination or missing critical efficacy assessment at TOC. |
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BREXAFEMME®
(brex a fem)
(ibrexafungerp tablets) for oral use
What is the most important information I should know about BREXAFEMME?
BREXAFEMME may cause serious side effects, including:
What is BREXAFEMME?
Do not take BREXAFEMME if you:
Before you take BREXAFEMME, tell your healthcare provider about all of your medical conditions, including if you:
BREXAFEMME may affect the way other medicines work, and other medicines may affect how BREXAFEMME works.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
How should I take BREXAFEMME?
What are the possible side effects of BREXAFEMME?
The most common side effects of BREXAFEMME include headache, loose stools, nausea, stomach pain, dizziness, and vomiting.
These are not all the possible side effects of BREXAFEMME.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
How should I store BREXAFEMME?
Keep BREXAFEMME and all medicines out of reach of children.
General information about the safe and effective use of BREXAFEMME.
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use BREXAFEMME for a condition for which it was not prescribed. Do not give BREXAFEMME to other people even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about BREXAFEMME that is written for health professionals.
What are the ingredients in BREXAFEMME?
Active ingredient: ibrexafungerp
Inactive ingredients:
Tablet core: butylated hydroxyanisole, colloidal silicon dioxide, crospovidone, magnesium stearate, mannitol, and microcrystalline cellulose. Tablet film coating: FD&C Blue #2, FD&C Red #40, hydroxypropyl cellulose, hydroxypropylmethyl cellulose 2910, talc and titanium dioxide.
This Patient Information has been approved by the U.S. Food and Drug Administration
