A First-in-human Safety Trial of BNT331 Administered as Single Ascending Doses in Healthy Women and as Multiple Ascending Doses in Women Diagnosed With Bacterial Vaginosis

Inclusion Criteria (applicable to all participants unless otherwise specified):

• Had given written informed consent by signing and dating the informed consent form (ICF) before initiation of any study-specific procedures.
• Participant reported assigned female sex at birth, at least 18 years of age and pre-menopausal, as determined by the investigator.
• Not menstruating or having vaginal bleeding:
• Part A: At Visit 0 and not expected to menstruate during Visit 1 and until Visit 3.
• Part B only: At Visit 0 and Visit 1 and not expected to menstruate within the next 6 days after Visit 1, until the Early Response Visit (Visit 2).
• Part A only: Were healthy according to screening procedures. Part B only: Participants suffering from BV but who were otherwise healthy in the clinical judgement of the investigator.
• Note: Participants with pre-existing stable disease (e.g., obesity, hypertension, etc.), defined as disease not requiring significant change in therapy or hospitalization for worsening disease during the 90 days before Visit 0, were included.
• Part A only: Should not have any clinical signs of BV as assessed by the absence of all Amsel's criteria and a normal Nugent score at screening, or other vaginal symptoms, including symptomatic vulvo-vaginal candidiasis (VVC) or infection with sexually transmitted infection (STI) pathogens including Chlamydia trachomatis, Trichomonas vaginalis, or Neisseria gonorrhoeae.
• Able to participate in the study as an outpatient, to attend all required visits, and to comply with all study requirements.
• Women of childbearing potential must have a negative highly sensitive urine pregnancy test result prior to study treatment initiation.
• The participant must have been on the same form of highly effective contraception for at least 3 months prior to dosing (Visit 1) and must agree to keep this method until:
• Part A: 60 days after Follow-up Visit (Visit 3)
• Part B: at least 60 days after Test of Cure (ToC) Visit (Visit 3).
• Women of childbearing potential who agree not to donate or cryopreserve eggs (ova, oocytes) for the purposes of assisted reproduction during study:
• Part A: Within 3 months prior to dosing (Visit 1) and continuously until 60 days after Follow-up Visit (Visit 3)
• Part B: Starting at Visit 0 and continuously until the Late Follow-up Visit (Visit 5).
• Agree to abstain from vaginal intercourse:
• Part A: From 72 hours prior to dosing until the Follow-up Visit (Visit 3)
• Part B: For the duration of treatment (~5 days) and until ToC Visit (Visit 3).
• Agree to not use any vaginal products, e.g., creams, gels, foams, sponges, douches, and tampons (except during menstruation):
• Part A: From 72 hours prior to dosing until the Follow-up Visit (Visit 3)
• Part B: Until ToC Visit (Visit 3).
• Part B only: Have a clinical diagnosis of BV, defined as having all the following Amsel's criteria (4/4):

1. Off-white (milky or gray), thin, homogeneous vaginal discharge.
2. Vaginal pH >4.5.
3. Presence of clue cells ≥20% of the total epithelial cells/high power field on microscopic examination of the vaginal saline wet mount.
4. A positive 10% potassium hydroxide (KOH) Whiff test.

• Part B only: Have a sample collected within 72 h prior to first dose for a Gram stain slide to assess Nugent score by the central laboratory.

Exclusion Criteria (applicable to all participants unless otherwise specified):

• Pregnant, lactating, or planning to become pregnant during their study participation and for at least:
• Part A: 60 days after Follow-up Visit (Visit 3)
• Part B: 60 days after ToC Visit (Visit 3).
• Had genital lesions, including active herpes simplex virus or syphilitic lesions, or other vaginal or vulvar conditions.
• Part A only: Had active STI.
• Had received antifungal or antimicrobial therapy (in Part A, systemic or topical; in Part B, systemic or vaginal) within 14 days prior to the Visit 1.
• Were using a Copper intrauterine device, or any vaginal hormonal products (including NuvaRing®) as a form of contraception.
• Had a history of drug or alcohol abuse within the past 12 months, as determined by the investigator.
• Had participated in any investigational study within 30 days before the Visit 1 or is currently participating or plans to participate in any investigational, or observational study.
• Had any history of allergies, hypersensitivities, or intolerance to the study treatments including any excipients thereof.
• Had any history of an abnormal Pap smear which required cervical biopsy and/or cervical cauterization within 6 months of Visit 1.
• Malignancy within 5 years of screening, including but not limited to cervical carcinoma and carcinomas of the vagina and vulva.
• Had any condition including psychiatric illnesses that could interfere with their ability to understand or comply with the requirements of the study as determined by the investigator.
• Vulnerable individuals, i.e., were individuals whose willingness to participate in a clinical study was unduly influenced by the expectation, whether justified or not, of benefits associated with participation, or of a retaliatory response from senior members of a hierarchy in case of refusal to participate. This includes all sponsor, study site, or third party (e.g., Clinical Research Organization, vendor) personnel directly involved in the conduct of the study and their family members or dependents, as well as all study site personnel otherwise supervised by the investigator.
• Part B only: Currently suspected clinically (or confirmed diagnostically) of having alternative causes of vaginal disease symptoms including symptomatic VVC or infection with STI including Chlamydia trachomatis, Trichomonas vaginalis, or Neisseria gonorrhoeae.