Introduction
Vulvovaginal candidiasis (VVC) is a common fungal infection caused by
Candida species and is a source of significant morbidity in women from all social classes. [
1,
2]. About 75% of women will experience at least one episode of VVC, and 40 ~ 45% will experience multiple VVC episodes [
1,
3]. The most common causative pathogen is
C. albicans, and
C. glabrata accounts for the most non-
albicans Candida (NAC) [
2]. Currently, azole antifungals are still preferable as the first-line therapy for VVC, including oral and topical formulations. Nevertheless, long-term use of azole antifungals and abuse of over-the-counter antifungals reduced fluconazole sensitivity among
Candida species and increased drug resistance, especially for vaginal
C. albicans isolates in China [
4‐
7]. And there are limited options for VVC patients with azole non-susceptible
Candida infection or with azole intolerance. Hence, new treatment approaches and agents possessing both broad-spectrum fungicidal activity and favorable safety profile, are urgently needed.
HS-10366 (generic name: ibrexafungerp) is a first-in-class, orally active, semisynthetic, triterpenoid derivative that blocks the synthesis of the fungal cell wall polymer β-(1,3)-
d-glucan, which has broad-spectrum anti-
Candida fungicidal activity, especially against echinocandin- and azole-resistant
Candida species[
8,
9]. The efficacy and safety of ibrexafungerp for treating VVC have been evaluated in two multicenter, global, randomized, double-blind, placebo-controlled phase III clinical trials in US and Bulgaria (VANISH 303, conducted in US, NCT03734991; VANISH 306, conducted in US and Bulgaria, NCT03987620). Both of trials demonstrated the superiority of ibrexafungerp over placebo in clinical cure, mycological eradication and overall success. Furthermore, ibrexafungerp was safe and generally well tolerated in VVC woman [
10,
11].
Based on positive results of the VANISH 303/306 studies, ibrexafungerp received its first approval on 1 Jun 2021 in the US for the treatment of VVC in adult and post-menarchal pediatric females. The recommended dosage of ibrexafungerp is 300 mg twice daily for 1 day [
12]. Furthermore, it was approved in the US for the prevention of recurrent vulvovaginal candidiasis (RVVC) in Nov 2022 based on another pivotal phase III clinical trial (CANDLE, NCT04029116) [
12]. Ibrexafungerp is the only oral antifungal US FDA-approved treatment for VVC and reduction of RVVC.
Our study adopted a similar study design and the same dosage regimen as VANISH 303/306 study, which firstly intended to explore the efficacy and safety of ibrexafungerp in China’s VVC patients.
Methods
Study design and participants
This was a multicenter, randomized, double-blinded, placebo-controlled study. It aimed to assess the efficacy and safety of oral ibrexafungerp vs placebo among Chinese female patients with VVC. The pivotal study (Registry number: CTR20220918) was conducted at 31 tertiary hospitals in China (Appendix
1).
Female patients aged 18–64 (inclusive) were eligible if they were generally healthy and had a diagnosis of symptomatic VVC fulfilling the following criteria: (1) presenting at least two symptoms and/or signs that matched the vulvovaginal signs and symptoms (VSS) score (Supplementary Table 1) ≥ 2; (2) a microscopic result indicating positive Candida (showing hyphae/pseudohyphae/budding yeast); (3) vaginal pH ≤ 4.5 (considered as normal pH). Patients were excluded if they were pregnant, or concomitant with uncontrolled diabetes (HbA1c > 9%), other vaginal infections, or immunosuppression. A full version of the eligibility criteria is displayed in Appendix 2.
Eligible patients were randomly assigned in a 2:1 ratio to receive ibrexafungerp 300 mg (two 150-mg tablets) or matching placebo BID for 1 day. At randomization, patients were stratified by the diagnosis of diabetes mellitus (yes/no). A centralized, interactive response system was adopted for the randomization procedure. All patients, site staff and sponsor personnel were blinded to treatment assignment, except for a sponsor representative responsible for drug distribution. Placebo tablets were made indistinguishable from ibrexafungerp tablets.
The study was conducted under the guiding principles of the Declaration of Helsinki, Good Clinical Practice, and the current International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use Guidelines. Written informed consent was obtained from all participants before the initiation of any study procedure.
Study assessments
The study consisted of screening (day − 2 ~ − 1), baseline (day 1), test-of-cure (TOC, day 11 ± 3), and follow-up (FU, day 25 ± 4) visits. Screening and baseline visits may occur on the same day. Rating of each vulvovaginal symptom (itching, pain) of VSS score was recorded by the subject in a diary from day 1 to the TOC visit, and the procedure was done under the supervision of the investigator at screening, TOC and FU visits. Each vulvovaginal sign (congestion/edema, scratches/rhagades/erosions, secretion volume) of the VSS score was rated by the investigator based on physical examinations at screening and TOC visits, and at FU visit only when the patient was symptomatic. VSS score was calculated at each visit.
Mycological evaluation for vulvovaginal samples included fungal cultures, vaginal pH test, and microscopic examination. Vaginal pH test and microscopic examination should be performed at the local labs of study centers at screening, and at TOC and FU visits when the patient was symptomatic. Fungal cultures and susceptibility tests should be performed at central laboratories at screening and TOC visits, and at FU visit if symptomatic. Susceptibility tests were performed under Clinical and Laboratory Standards Institute (CLSI) M59 and M60 guidelines [
13,
14].
The patient could return to study centers for rescue therapy if she experienced persistence, worsening, or recurrence of symptoms ideally 48–72 h after first dose of the study drug. If rescue antifungal therapy was administered before or at TOC visit, the patient would be considered a failure for the efficacy endpoints evaluated at TOC visit due to lack of efficacy. Clinical and mycological assessments should be conducted at the discretion of investigators before the prescription of rescue antifungal agents (e.g., fluconazole).
Endpoints
The primary efficacy endpoint was the proportion of patients who reached clinical cure (VSS score = 0) at TOC visit. Main secondary efficacy endpoints included the proportion of patients with mycological eradication, overall response (achieving both clinical cure and mycological eradication), and clinical improvement at TOC visit, as well as vulvovaginal symptom resolution at FU visit. The definition of efficacy outcomes above was summarized in Supplementary Table 2. Safety endpoints focused on the incidence of treatment-emergent adverse events (TEAE), treatment-related treatment-emergent adverse events (TRAE), serious adverse events (SAE), and TEAE leading to study discontinuation.
Given an increasing emergence of NAC species and fluconazole-resistant C. albicans, post-hoc analyses for efficacy endpoints were conducted in patients infected by fluconazole susceptible and non-susceptible C. albicans and other Candida species.
Statistical analyses
All analyses were performed using SAS software (version 9.4; SAS Institute Inc., Cary, NC, USA). A sample size of 258 was calculated to provide about 90% power to detect a difference between Ibrexafungerp and placebo based on Pearson’s Chi-squared test with a type I error of 5%, an assumed clinical cure rate of 56.9% for ibrexafungerp and 35.7% for placebo, and a 2:1 randomization ratio. With an estimated 30% of patients without mycological culture-confirmed infection at baseline, a sample size of 369 (Ibrexafungerp, n = 246; placebo, n = 123) was planned to be randomized. Diagnosis of diabetes mellitus was used as a stratification factor during randomization.
Categorical variables were summarized by counts and percentages. Means (± SD) were used to descriptively summarize continuous variables. A 2-sided alpha of 0.05 was used for all hypothesis tests. Safety analyses were conducted for the safety set, which included randomized patients who received ≥ 1 dose of study drug. Cochran–Mantel–Haenszel test adjusted for diagnosis of diabetes mellitus was used for efficacy analyses primarily based on the modified intent-to-treat (mITT) population, which consisted of patients in the safety population who had a positive culture for Candida species at baseline. Patients who received rescue antifungal treatment on or before a specific visit and patients who were missing categorical response data at specific visit were considered to be non-responders. Three sensitivity analyses were also performed: Strategy 1 performed multiple imputation (MI) for 100 times in patients lacking clinical cure data at TOC visit due to COVID-19; Strategy 2 performed Copy Reference MI for 100 times in patients lacking clinical cure data at TOC visit; Strategy 3 only included patients with collected clinical cure response data or those who received rescue antifungal treatment before or at TOC visit (considered as failure). Details of the three strategies are described in Supplementary Table 3. Subgroup analyses were performed for BMI category at screening (< 28, ≥ 28 kg/m2), diagnosis of diabetes mellitus, severity of infection at baseline (mild to moderate, severe), and Candida species at screening.
Role of the funding source
The study was sponsored by Jiangsu Hansoh Pharmaceutical Group Co. Ltd (China). The sponsor was involved in study design, study monitoring, data collection, data analysis and interpretation, reporting of the study, and authorization of study results for publication.
Discussion
This was the first clinical trial to evaluate the efficacy and safety of ibrexafungerp in Chinese VVC patients. Our study demonstrated that ibrexafungerp was efficacious and well tolerated in Chinese VVC patients under the conditions of this study. The clinical cure (absence of vulvovaginal symptoms and signs) rates with ibrexafungerp vs. placebo in our study (51.0% vs. 25.6%, respectively) were similar to that of VANISH 303 study (50.5% vs. 28.6%) as well as US patients in VANISH 306 study (54.5% vs. 27.8%) [
10,
11]. In the present study, ibrexafungerp demonstrated reproducible statistical superiority over placebo for VVC treatment in Chinese patients, in consistency with the result of similarly designed VANISH 303/306 study.
Our study revealed the sustained efficacy of ibrexafungerp. In the ibrexafungerp group, 80.3% of patients who achieved clinical cure at TOC visit (day 11 ± 3) remained asymptomatic at FU visit (day 25 ± 4). Whereas, several published studies showed that fluconazole under various regimens reported an 11%-20% decrease in sustained response from day 7–14 to day 28–35[
15‐
17]. It may be attributed to the fungicidal activity of ibrexafungerp in comparison to the fungistatic activity of fluconazole [
18,
19]. Therefore, it indicated that ibrexafungerp was superior to fluconazole in sustained therapeutic effect.
Based on the susceptibility tests for fluconazole against
Candida species obtained at screening, our study also explored the efficacy of ibrexafungerp in both patients with fluconazole-susceptible and patients with non-susceptible
C. albicans. In the ibrexafungerp group, it was observed a similar clinical cure rate between patients with fluconazole-susceptible and non-susceptible
C. albicans (55.8% vs. 52.1%). Moreover, in the ibrexafungerp group, patients infected with fluconazole susceptible and non-susceptible
C. albicans both had a high-mycological eradication rate (77.0% and 75%). The clinical benefits of ibrexafungerp for patients with fluconazole non-susceptible
C. albicans were consistent with a preclinical study. In the preclinical study, MIC of the
Candida isolates against ibrexafungerp was determined per broth microdilution method published by CLSI. A total of 178
Candida were tested, including 44
Candida isolates with known genotypic (
FKS1 or
FKS2 mutations), phenotypic, or clinical resistance to echinocandins. Ibrexafungerp MICs were low (≤ 0.5 μg/ml) for azole-resistant
C. albicans,
C. parapsilosis, and
C. tropicalis isolates, which demonstrated in vitro fungicidal activity of ibrexafungerp against azole-resistant
Candida species [
20]. Nowadays, fluconazole-resistant
C. albicans has been a growing and perplexing problem for treating VVC. One up-to-date literature published in 2022 collected 2000
Candida isolates from VVC patients in 23 hospitals to explore the sensitivity of
Candida species to common antifungals in China. The result showed that the resistance rate for vulvovaginal
C. albicans was significantly higher than that of non-
C. albicans (73.41% [715/974] vs. 50.88% [115/226],
P < 0.001). [
6]. Based on the positive results of our study, ibrexafungerp would probably be an alternative option for treatment of patients with fluconazole non-susceptible
C. albicans in China.
Among patients with NAC in the ibrexafungerp group, the clinical cure rate was 43.6%, while the mycological eradication rate was just 12.8% at TOC visit. Of these, 67.6% of patients with positive culture for NAC were asymptomatic. The inconsistency between clinical cure and mycological eradication rate may be explained by the
Candida colonization in vagina. A previous study of Kennedy et al. showed that at least 50% of women with positive cultures for NAC might be minimally symptomatic or had no symptoms, while 80–85% of patients with positive cultures for
C. albicans would be likely to have symptoms [
21], which was consistent with our study. Moreover, clinical practice guidelines recommended that asymptomatic patients with mere mycological persistence required no further therapy [
3,
22].
According to pharmaceutical industry guidance issued by the Food and Drug Administration in 2019, our study chose placebo rather than fluconazole as a comparator using a superiority design and adopted clinical cure (i.e., the complete resolution of signs and symptoms of VVC without need for further antifungal treatment before or at TOC visit) as the primary endpoint. Nevertheless, the efficacy of single-dose fluconazole and single-day ibrexafungerp was compared in a US phase II study (DOVE), in which the clinical cure rate in ibrexafungerp group was similar with that of fluconazole group on day 10 (51.9% vs. 58.3%) but higher than that of fluconazole group on day 25 (70.4% vs. 50.0%)[
23]. Moreover, a randomized, double-blind phase III trial of a new antifungal agent in China adopted the same definition of clinical cure (VSS score = 0) and mITT population. The study found that in the fluconazole group, the percentage of subjects reaching clinical cure on day 14 in the mITT population and subgroup of
C. albicans was 50.31% and 53.72%, respectively, which is similar to those of ibrexafungerp in our study (51.0% for mITT population; 55.8% for a subgroup of
C. albicans on day 11 ± 3) [
24].
Ibrexafungerp was well tolerable in China’s VVC patients when administered as a 300 mg oral tablet BID for 1 day. Although, a higher percentage of patients receiving ibrexafungerp (54.1%) experienced at least one TRAE compared with those receiving placebo (17.1%), most TRAEs were mild to moderate and recovered without any intervention. Consistent with VANISH 303/306 study, the most common TRAEs were gastrointestinal disorders. The incidence of gastrointestinal disorders in Chinese patients was similar to that of U.S. patients in VANISH 303/306 study (50.8% vs. 42.9%). Chinese patients experienced a higher incidence of diarrhea than U.S. patients (43.0% vs. 23.9%), but fewer nausea and abdominal pain (9.0% each) than US patients (16.8% and 14.8%, respectively) [
25]. It was speculated that the differences in dietary habits between Chinese and US patients contributed to the various gastrointestinal reactions. All three clinical trials demonstrated the good safety of ibrexafungerp.
While, some limitations existed in our study the clinical efficacy of ibrexafungerp in obese or diabetic patients could not be determined in the subgroup analyses due to the small sample size. Therefore, future research on ibrexafungerp was warranted, especially its effectiveness in specific patients.