A Clinical Trial in Healthy Volunteers to Study the Safety, Tolerability, and Immune Responses After Vaccination With an Investigational Vaccine Designed to Prevent Genital Herpes Lesions

Genital Herpes Simplex Type 2 Clinical Trial

Official title:

Phase I, Randomized, Observer-blinded, Placebo-controlled, 2-part, Dose Escalation and Expanded Safety Evaluation Trial to Evaluate the Safety, Tolerability, and Immunogenicity of an Investigational Prophylactic Vaccine for the Prevention of Genital Lesions Caused by Herpes Simplex Virus (HSV)-2 and Potentially HSV-1

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05432583
• Other study ID #: BNT163-01
• Status: Recruiting
• Phase: Phase 1
• Start date: December 8, 2022
• Est. completion date: December 2025

Study information

• Verified date: April 2024
• Source: BioNTech SE
• Contact: BioNTech clinical trials patient information
• Phone: +49 6131 9084
• Email: patients[@]biontech.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This exploratory trial will have two parts. Part A is a dose escalation part and Part B is an expanded safety and dose evaluation part.

Part A will focus on the safety evaluations, but vaccine-induced immune responses (specifically neutralizing antibodies) will also be analyzed to assess if there is a dose-response. Part B of the trial will expand the safety characterization for two dose levels of BNT163 selected based on Part A data and also enable a more comprehensive assessment of the impact of pre-existing immunity to Herpes Simplex Virus (HSV)-1 and -2 on the safety and BNT163-induced immune responses than could be assessed in Part A.

Description:

In Part A, participants will be randomized 5:1 to BNT163:placebo. In part B, participants will be randomized 1:1 to either of the two selected dose levels based on data from Part A. Participants will receive three intramuscular doses of a fixed dose level of the BNT163 vaccine (Part A and B) or placebo (Part A only).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 248
• Est. completion date: December 2025
• Est. primary completion date: December 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Have given informed consent by signing and dating the informed consent form (ICF) before initiation of any trial-specific procedures.

• Are aged 18 to 55 years, have a body mass index over 18.5 kg/m^2 and under 35 kg/m^2 and weigh at least 50 kg at Visit 0.

• Are willing and able to comply with scheduled visits, treatment schedule, laboratory tests, and other requirements of the trial. This includes that they are able to understand and follow trial-related instructions.

• Are overall healthy in the clinical judgment of the investigator based on medical history, physical examination, 12-lead electrocardiogram (ECG), vital signs, and screening laboratory tests (blood clinical laboratory) at Visit 0.

• Negative human immunodeficiency virus (HIV)-1 and HIV-2 blood test at Visit 0.

• Negative Hepatitis B surface antigen at Visit 0.

• Negative anti-Hepatitis C virus (anti-HCV) antibodies, or undetectable HCV viral load if the anti-HCV is positive at Visit 0.

• Negative syphilis test at Visit 0.

• Volunteers of childbearing potential (VOCBP): negative serum beta human chorionic gonadotropin (ß-HCG) pregnancy test at Visit 0 and negative urine pregnancy test prior to each investigational medicinal product (IMP) administration and at the end of the trial. Volunteers born female that are postmenopausal (verified by follicle stimulating hormone [FSH] level) or permanently sterilized will not be considered VOBCP.

• VOCBP who agree to practice a highly effective form of contraception and to require their male partners to use condoms coated with a spermicidal agent, starting at Visit 0 and continuously until 60 days after receiving the last trial treatment.

• VOCBP who agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during trial, starting at Visit 0 and continuously until 60 days after receiving the last trial treatment.

• Men who are sexually active with a VOCBP and have not had a vasectomy who agree to use condoms coated with a spermicidal agent and to practice a highly effective form of contraception with their partners of childbearing potential during the trial, starting at Visit 0 and continuously until 90 days after receiving the last trial treatment.

• Men who are willing to refrain from sperm donation, starting at Visit 0 and continuously until 90 days after receiving the last trial treatment.

Exclusion Criteria:

• Breastfeeding or intending to become pregnant within the projected duration of the trial starting with Visit 0 until 60 days after receiving the last trial treatment or intending to father children within the projected duration of the trial starting with Visit 0 until 90 days after receiving the last trial treatment.

• Current or history of symptomatic genital herpes infections. Volunteers with oral herpes or herpetic whitlow will not be excluded.

• Current or history of any form of ocular HSV infection or HSV-related central nervous system disease or complication.

• History of any serious adverse reactions to vaccines or to vaccine components such as lipids, and including history of anaphylaxis and related symptoms such as hives, respiratory difficulty, angioedema, and/or abdominal pain.

• Current or history of the following medical conditions:

• Uncontrolled or moderate or severe respiratory diseases (e.g., asthma, chronic obstructive pulmonary disease); symptoms of asthma severity as defined in the most recent National Asthma Education and Prevention Program Expert Panel report;

• History of thyroidectomy, or thyroid disease requiring medication during the last 12 months;

• History of diabetes mellitus type 1 or type 2, including cases controlled with diet alone (Not excluded: history of isolated gestational diabetes);

• Hypertension (elevated blood pressure or hypertension during screening or previously that is not well controlled only [consistently =140 mm Hg systolic and =90 mm Hg diastolic, with or without medication, with only isolated, brief instances of higher readings, which must be =150 mm Hg systolic and =90 mm Hg diastolic at enrollment] or if systolic blood pressure =150 mm Hg at enrollment or diastolic blood pressure =100 mm Hg confirmed by two measurements prior to enrollment);

• Malignancy within 5 years of Visit 0, excluding localized basal or squamous cell cancer;

• Current or history of cardiovascular diseases, e.g., myocardial infarction, congestive heart failure, cardiomyopathy, or clinically significant arrhythmias, myocarditis, or pericarditis;

• Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions);

• Seizure disorder: History of seizure(s) within past 3 years. Also exclude if volunteer has used medications in order to prevent or treat seizure(s) at any time within the past 3 years.

• History of psychiatric illness, including alcohol abuse or drug addiction within 1 year before Visit 0, or a history (within the past 5 years) of substance abuse or known medical, psychological, or social conditions which, in the opinion of the investigator, could compromise their wellbeing if they participate as participants in the trial, or that could prevent, limit, or confound the protocol specified assessments.

• Any of the following associated with immune dysregulation:

• Primary immunodeficiencies.

• History of solid organ or bone marrow transplantation.

• Asplenia: any condition resulting in the absence of a functional spleen.

• Currently existing or history of autoimmune disease including and not limited to thyroid autoimmune disease, multiple sclerosis, psoriasis, etc.

• Use of any non-trial IMP within 28 days before Dose 1 in this trial (Visit 1) or planned receipt continuously until Visit 12 in this trial, or participation in the active treatment phase of another interventional clinical trial.

• Previous vaccination with an investigational herpes virus vaccine at any time.

• Any non-trial vaccination within 28 days before Dose 1 and continuously until 28 days after receiving Dose 3.

o Note: Licensed inactivated and mRNA vaccines (e.g., seasonal influenza and COVID-19 vaccines) are allowed to be given at least 14 days before or 14 days after each IMP administration. Licensed live attenuated vaccines (e.g., influenza vaccines) are allowed at least 28 days before or 28 days after any IMP administration.

• Received allergy treatment with antigen injections within 28 days before first IMP administration or that are scheduled within 14 days after Visit 1.

• Received blood/plasma products or immunoglobulin within 120 days before Visit 1 or planned administration starting at Visit 0 until completion of Visit 12.

• Received chronic suppressive antiviral therapy for treatment of recurrent HSV-1 and/or HSV-2 genital herpes infections (i.e., oral acyclovir, oral valacyclovir, oral famciclovir, and/or intravenous ganciclovir) from 1 year prior to Visit 0 until completion of Visit 12.

• Any existing condition which may affect vaccine injection and/or assessment of local reactions assessment at the injection site, e.g., tattoos, severe scars.

• Vulnerable individuals as per International Council for Harmonisation (of Technical Requirements for Pharmaceuticals for Human Use) (ICH) E6 definition, i.e., are individuals whose willingness to volunteer in a clinical trial may be 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.

• Any screening hematology and/or blood chemistry laboratory value that meets the definition of a Grade =2 abnormality at Visit 0. For laboratory values for which toxicity grading guidance is not available, or for Grade =1 abnormalities, participant eligibility will be determined at the discretion of the investigator.

• Part B only: Applicable HSV serology stratum is already full or the HSV serostatus is reported as indeterminate.

Related Conditions & MeSH terms

• Genital Herpes Simplex Type 2
• Herpes Genitalis
• Herpes Simplex

Intervention

Biological:
• BNT163
Anti-viral ribonucleic acid (RNA) vaccine for active immunization against HSV-2 administered as intramuscular injection

Other:
• Placebo
Placebo

Locations

Country	Name	City	State
United States	Great Lakes Clinical Trials - Flourish Research	Chicago	Illinois
United States	CTI Clinical Research Center	Cincinnati	Ohio
United States	Hospital of the University of Pennsylvania	Philadelphia	Pennsylvania
United States	Accellacare Raleigh Medical Group	Raleigh	North Carolina
United States	Alliance for Multispecialty Research, LLC	Tempe	Arizona
United States	Accellacare PMG Research Wilmington LLC	Wilmington	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
BioNTech SE

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of solicited local reactions at the injection site (pain, erythema/redness, induration/swelling) recorded up to 7 days after each dose	For each dose level (DL) per BNT163 dosing schedule and for the combined placebo group	Up to 7 days after each dose
Primary	Frequency of solicited systemic reactions (vomiting, diarrhea, headache, fatigue/tiredness, myalgia, arthralgia, chills, and fever) recorded up to 7 days after each dose	For each DL per BNT163 dosing schedule and for the combined placebo group	Up to 7 days after each dose
Primary	Percentage of participants with at least one unsolicited adverse event (AE) occurring up to 28 days after each dose	For each DL per BNT163 dosing schedule and for the combined placebo group	From Day 1 up to Day 197
Primary	Percentage of participants in each cohort with at least one serious adverse event, or adverse event of special interest, or medically attended adverse event occurring up to 24 weeks post-Dose 3	For each DL per BNT163 dosing schedule and for the combined placebo group	From Day 1 up to Day 337
Primary	Number of unsolicited AEs occurring up to 28 days after each dose	For each DL per BNT163 dosing schedule and for the combined placebo group	From Day 1 up to Day 197
Primary	Percentage of unsolicited AEs occurring up to 28 days after each dose	For each DL per BNT163 dosing schedule and for the combined placebo group	From Day 1 up to Day 197
Secondary	Geometric mean titer (GMT) at each time point	HSV-2 glycoproteins (g)C2, gD2, and gE2 binding antibody titers enzyme-linked immunosorbent assay (ELISA). HSV-2 neutralizing antibody titers.; For each DL per BNT163 dosing schedule	From Day 1 up to Day 337
Secondary	Geometric mean fold (GMF) change from baseline of neutralizing and binding antibody titers to each time point after vaccination	HSV-2 gC2, gD2, and gE2 binding antibody titers enzyme-linked immunosorbent assay (ELISA). HSV-2 neutralizing antibody titers.; For each DL per BNT163 dosing schedule	From Day 1 up to Day 337
Secondary	Percentage of participants with seroconversion defined as a minimum of 4-fold increase from baseline of neutralizing and binding antibody titers to each subsequent time point after vaccination	For each DL per BNT163 dosing schedule	From Day 1 up to Day 337