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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT05298254
Registration number
NCT05298254
Ethics application status
Date submitted
4/03/2022
Date registered
28/03/2022
Date last updated
26/04/2024
Titles & IDs
Public title
A Study on the Reactogenicity, Safety, Immune Response, and Efficacy of a Targeted Immunotherapy Against HSV in Healthy Participants Aged 18-40 Years or in Participants Aged 18-60 Years With Recurrent Genital Herpes
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Scientific title
A Phase I/II, Observer-blind, Randomised, Placebo-controlled, Multi-country Study to Evaluate Reactogenicity, Safety, Immune Response, and Efficacy of an HSV-targeted Immunotherapy in Healthy Participants Aged 18-40 Years or in Participants Aged 18-60 Years With Recurrent Genital Herpes
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Secondary ID [1]
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2021-003586-35
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Secondary ID [2]
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215336
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Herpes Simplex
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Condition category
Condition code
Infection
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Other infectious diseases
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Skin
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Other skin conditions
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Infection
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Sexually transmitted infections
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Renal and Urogenital
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Other renal and urogenital disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Other interventions - Non-adjuvanted HSV formulation 1
Other interventions - Non-adjuvanted HSV formulation 2
Other interventions - Non-adjuvanted HSV formulation 3
Other interventions - HSV formulation 1 with adjuvant 1
Other interventions - HSV formulation 2 with adjuvant 1
Other interventions - HSV formulation 3 with adjuvant 1
Other interventions - HSV formulation 1 with adjuvant 2
Other interventions - HSV formulation 2 with adjuvant 2
Other interventions - HSV formulation 3 with adjuvant 2
Treatment: Drugs - Placebo
Other interventions - HSVTI_F1
Other interventions - HSVTI_F2
Experimental: Non-adjuvanted HSV formulation 1 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the non-adjuvanted HSV formulation 1 vaccine, one at Day 1 and one at Day 29.
Experimental: Non-adjuvanted HSV formulation 2 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the non-adjuvanted HSV formulation 2 vaccine, one at Day 1 and one at Day 29.
Experimental: Non-adjuvanted HSV formulation 3 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the non-adjuvanted HSV formulation 3 vaccine, one at Day 1 and one at Day 29.
Experimental: HSV formulation 1 with adjuvant 1 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the HSV formulation 1 with adjuvant 1 vaccine, one at Day 1 and one at Day 29.
Experimental: HSV formulation 2 with adjuvant 1 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the HSV formulation 2 with adjuvant 1 vaccine, one at Day 1 and one at Day 29.
Experimental: HSV formulation 3 with adjuvant 1 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the HSV formulation 3 with adjuvant 1 vaccine, one at Day 1 and one at Day 29.
Experimental: HSV formulation 1 with adjuvant 2 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the HSV formulation 1 with adjuvant 2 vaccine, one at Day 1 and one at Day 29.
Experimental: HSV formulation 2 with adjuvant 2 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the HSV formulation 2 with adjuvant 2 vaccine, one at Day 1 and one at Day 29.
Experimental: HSV formulation 3 with adjuvant 2 - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of the HSV formulation 3 with adjuvant 2 vaccine, one at Day 1 and one at Day 29.
Placebo Comparator: Placebo - Part I Group - Participants enrolled in Part I of the study who receive 2 doses of Placebo, one at Day 1 and one at Day 29.
Experimental: HSVTI formulation (F) 1 - Part II Group - Participants enrolled in Part II of the study who receive 2 doses of the formulation of the HSVTI_F1 selected from Part I of the study, one at Day 1 and one at Day 29.
Experimental: HSVTI_F2 - Part II Group - Participants enrolled in Part II of the study who receive 2 doses of the HSVTI_F2 selected from Part I of the study, one at Day 1 and one at Day 29.
Placebo Comparator: Placebo - Part II Group - Participants enrolled in Part II of the study who receive 2 doses of Placebo, one at Day 1 and one at Day 29.
Other interventions: Non-adjuvanted HSV formulation 1
Two doses of the non-adjuvanted HSV formulation 1 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: Non-adjuvanted HSV formulation 2
Two doses of the non-adjuvanted HSV formulation 2 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: Non-adjuvanted HSV formulation 3
Two doses of the non-adjuvanted HSV formulation 3 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: HSV formulation 1 with adjuvant 1
Two doses of the HSV formulation 1 with adjuvant 1 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: HSV formulation 2 with adjuvant 1
Two doses of the HSV formulation 2 with adjuvant 1 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: HSV formulation 3 with adjuvant 1
Two doses of the HSV formulation 3 with adjuvant 1 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: HSV formulation 1 with adjuvant 2
Two doses of the HSV formulation 1 with adjuvant 2 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: HSV formulation 2 with adjuvant 2
Two doses of the HSV formulation 2 with adjuvant 2 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Other interventions: HSV formulation 3 with adjuvant 2
Two doses of the HSV formulation 3 with adjuvant 2 vaccine administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I of the study.
Treatment: Drugs: Placebo
Two doses of Placebo administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part I and Part II of the study.
Other interventions: HSVTI_F1
Two doses of the formulation of the HSVTI_F1 selected from Part I of the study administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part II of the study.
Other interventions: HSVTI_F2
Two doses of the formulation of the HSVTI_F2 selected from Part I of the study administered intramuscularly in the deltoid region of the non-dominant arm, one each at Day 1 and Day 29, during Part II of the study.
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Intervention code [1]
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Other interventions
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Intervention code [2]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Percentage of participants reporting each solicited administration site event
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Assessment method [1]
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The solicited administration site events are pain, redness and swelling.
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Timepoint [1]
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Within 7 days after the first study intervention dose (administered at Day 1)
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Primary outcome [2]
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Percentage of participants reporting each solicited administration site event
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Assessment method [2]
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The solicited administration site events are pain, redness and swelling.
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Timepoint [2]
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Within 7 days after the second study intervention dose (administered at Day 29)
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Primary outcome [3]
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Percentage of participants reporting each solicited systemic event
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Assessment method [3]
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The solicited systemic events are fever, fatigue, headache, myalgia and arthralgia. The preferred location for measuring temperature is the oral cavity. Fever is defined as temperature equal to or above (=) 38.0 degree Celsius (°C)/ 100.4 degree Fahrenheit (°F), regardless the location of measurement.
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Timepoint [3]
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Within 7 days after the first study intervention dose (administered at Day 1)
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Primary outcome [4]
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Percentage of participants reporting each solicited systemic event
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Assessment method [4]
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The solicited systemic events are fever, fatigue, headache, myalgia and arthralgia. The preferred location for measuring temperature is the oral cavity. Fever is defined as temperature equal to or above (=) 38.0 degree Celsius (°C)/ 100.4 degree Fahrenheit (°F), regardless the location of measurement.
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Timepoint [4]
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Within 7 days after the second study intervention dose (administered at Day 29)
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Primary outcome [5]
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Percentage of participants reporting unsolicited adverse events (AEs)
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Assessment method [5]
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An unsolicited AE is any AE reported in addition to those solicited during the clinical study. Also, any 'solicited' symptom with onset outside the specified period of follow-up for solicited symptoms (7 days after each dose) is reported as an unsolicited AE.
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Timepoint [5]
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Within 28 days after the first study intervention dose (administered at Day 1)
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Primary outcome [6]
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Percentage of participants reporting unsolicited adverse events (AEs)
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Assessment method [6]
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An unsolicited AE is any AE reported in addition to those solicited during the clinical study. Also, any 'solicited' symptom with onset outside the specified period of follow-up for solicited symptoms (7 days after each dose) is reported as an unsolicited AE.
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Timepoint [6]
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Within 28 days after the second study intervention dose (administered at Day 29)
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Primary outcome [7]
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Percentage of participants reporting medically attended events (MAEs)
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Assessment method [7]
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An MAE is an unsolicited AE for which the participants received medical attention defined as any symptoms or illnesses requiring hospitalization, or an emergency room visit, or visit to/by healthcare professionals.
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Timepoint [7]
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From Dose 1 (Day 1) up 12 months after last study intervention administration (Day 394)
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Primary outcome [8]
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Percentage of participants reporting any serious adverse events (SAEs)
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Assessment method [8]
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An SAE is any untoward medical occurrence that results in death, is life-threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect in the offspring of a study participant or results in abnormal pregnancy outcomes.
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Timepoint [8]
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From Dose 1 (Day 1) up to 12 months after last study intervention administration (Day 394)
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Primary outcome [9]
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Percentage of participants reporting any potential immune-mediated disease (pIMDs) (classified as newly diagnosed or exacerbation of pre-existing events)
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Assessment method [9]
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PIMDs are a subset of adverse events of special interest (AESIs) that include autoimmune diseases and other inflammatory and/or neurologic disorders of interest which may or may not have an autoimmune aetiology.
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Timepoint [9]
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From Dose 1 (Day 1) up to 12 months after last study intervention administration (Day 394)
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Primary outcome [10]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at pre-study intervention administration (Day 1) in Part I of the study
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Assessment method [10]
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Clinically significant haematological and biochemical abnormal laboratory findings are those which are not associated with an underlying disease, unless judged by the investigator to be more severe than expected for the participant's condition.
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Timepoint [10]
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At pre-study intervention administration (Day 1)
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Primary outcome [11]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 8 in Part I of the study
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Assessment method [11]
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Timepoint [11]
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At Day 8
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Primary outcome [12]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 29 in Part I of the study
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Assessment method [12]
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0
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Timepoint [12]
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At Day 29
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Primary outcome [13]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 36 in Part I of the study
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Assessment method [13]
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Timepoint [13]
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At Day 36
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Primary outcome [14]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 64 in Part I of the study
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Assessment method [14]
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Timepoint [14]
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At Day 64
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Primary outcome [15]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at pre-study intervention administration (Day 1) in Part II of the study
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Assessment method [15]
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Timepoint [15]
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At pre-study intervention administration (Day 1)
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Primary outcome [16]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 8 in Part II of the study
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Assessment method [16]
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Timepoint [16]
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At Day 8
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Primary outcome [17]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 29 in part II of the study
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Assessment method [17]
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Timepoint [17]
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At Day 29
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Primary outcome [18]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 36 in Part II of the study
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Assessment method [18]
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Timepoint [18]
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At Day 36
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Primary outcome [19]
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Percentage of participants reporting any haematological and biochemical laboratory abnormalities at Day 57 in Part II of the study
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Assessment method [19]
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Timepoint [19]
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At Day 57
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Primary outcome [20]
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Time-to-first confirmed HSV-2 RGH episode in Part II of the study
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Assessment method [20]
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A suspected RGH episode will be classified as confirmed HSV-2 RGH episode if at least one of the lesional or anogenital swabs taken during the concerned episode is positive for HSV-2 as measured by PCR.
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Timepoint [20]
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14 days post-Dose 2 (Day 43) to Day 759
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Secondary outcome [1]
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Number of confirmed HSV-2 RGH episodes in Part II of the study
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Assessment method [1]
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A suspected RGH episode will be classified as confirmed HSV-2 RGH episode if at least one of the lesional or anogenital swabs taken during the concerned episode is positive for HSV-2 as measured by PCR.
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Timepoint [1]
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14 days post-Dose 2 (Day 43) to Day 759
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Secondary outcome [2]
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Percentage of participants free from confirmed HSV-2 RGH episode in Part II of the study
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Assessment method [2]
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A suspected RGH episode will be classified as confirmed HSV-2 RGH episode if at least one of the lesional or anogenital swabs taken during the concerned episode is positive for HSV-2 as measured by PCR.
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Timepoint [2]
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At 6, 12, 18 and 24 months after the last study intervention administration (Day 29)
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Secondary outcome [3]
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Herpes Symptoms Checklist (HSC) total score during each confirmed HSV-2 RGH episode in Part II of the study
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Assessment method [3]
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During genital herpes recurrences, participants are asked to complete the HSC, a 13-item checklist of herpes symptoms, where respondents record the severity of symptoms on a 4-point scale where 0 indicates no symptom and a higher point for more symptoms and severity. Total scores range from 0 (no symptom) to 39 (severe symptoms). At the onset of the genital herpes recurrence, this questionnaire is to be completed once daily, until no lesions or symptoms are present.
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Timepoint [3]
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14 days post-Dose 2 (Day 43) to Day 759
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Secondary outcome [4]
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Number of days with RGH-associated symptoms during each confirmed HSV-2 RGH episode in Part II of the study
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Assessment method [4]
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Duration in days (i.e., number of days with RGH-associated symptoms) of each genital herpes recurrence is displayed by arm group.
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Timepoint [4]
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14 days post-Dose 2 (Day 43) to Day 759
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Secondary outcome [5]
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Number of days with confirmed HSV-2 genital herpes lesions in Part II of the study
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Assessment method [5]
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Number of days on which lesions (swelling, blisters, sores, or crusts) are reported by the participant in the anogenital area during confirmed RGH episodes divided by the number of days of follow-up.
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Timepoint [5]
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14 days post-Dose 2 (Day 43) to Day 759
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Secondary outcome [6]
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HSV-2 shedding rate reduction from baseline to 6 weeks post-Dose 2 (Day 71) in Part II of the study
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Assessment method [6]
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The HSV-2 shedding rate reduction is calculated as 1- (the HSV-2 shedding rate one month post-Dose 2 divided by the baseline HSV-2 shedding rate)*100.
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Timepoint [6]
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At 6 weeks post-Dose 2 (Day 71) compared to baseline (Day -28 to Day -1)
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Secondary outcome [7]
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HSV-2 shedding rate reduction from baseline to 6 months post-Dose 2 (Day 209) in Part II of the study
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Assessment method [7]
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The HSV-2 shedding rate reduction is calculated as 1 - (the HSV-2 shedding rate 6 months post-Dose 2 divided by the baseline HSV-2 shedding rate)*100.
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Timepoint [7]
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At 6 months post-Dose 2 (Day 209) compared to baseline (Day -28 to Day -1)
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Secondary outcome [8]
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HSV-2 shedding rate reduction from baseline to 12 months post-Dose 2 (Day 394) in Part II of the study
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Assessment method [8]
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The HSV-2 shedding rate reduction is calculated as 1 - (the HSV-2 shedding rate 12 months post-Dose 2 divided by the baseline HSV-2 shedding rate)*100.
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Timepoint [8]
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At 12 months post-Dose 2 (Day 394) compared to baseline (Day -28 to Day -1)
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Secondary outcome [9]
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HSV-2 shedding rate reduction from baseline to 24 months post-Dose 2 (Day 759) in Part II of the study
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Assessment method [9]
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The HSV-2 shedding rate reduction is calculated as 1 - (the HSV-2 shedding rate 24 months post-Dose 2 divided by the baseline HSV-2 shedding rate)*100.
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Timepoint [9]
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At 24 months post-Dose 2 (Day 759) compared to baseline (Day -28 to Day -1)
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Secondary outcome [10]
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Number of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [10]
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Number of HSV-2 shedding episodes during the 28-day swabbing period.
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Timepoint [10]
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Day -28 to Day -1
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Secondary outcome [11]
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Number of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [11]
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Number of HSV-2 shedding episodes during the 28-day swabbing period.
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Timepoint [11]
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Day 43 to Day 70
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Secondary outcome [12]
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Number of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [12]
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Number of HSV-2 shedding episodes during the 28-day swabbing period.
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Timepoint [12]
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Day 181 to Day 208
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Secondary outcome [13]
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0
Number of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [13]
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Number of HSV-2 shedding episodes during the 28-day swabbing period.
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Timepoint [13]
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Day 366 to Day 393
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Secondary outcome [14]
0
0
Number of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [14]
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0
Number of HSV-2 shedding episodes during the 28-day swabbing period.
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Timepoint [14]
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Day 731 to Day 758
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Secondary outcome [15]
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Duration of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [15]
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Number of days of a HSV-2 shedding episode.
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Timepoint [15]
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Day -28 to Day -1
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Secondary outcome [16]
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Duration of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [16]
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Number of days of a HSV-2 shedding episode.
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Timepoint [16]
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Day 43 to Day 70
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Secondary outcome [17]
0
0
Duration of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [17]
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Number of days of a HSV-2 shedding episode.
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Timepoint [17]
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Day 181 to Day 208
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Secondary outcome [18]
0
0
Duration of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [18]
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0
Number of days of a HSV-2 shedding episode.
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Timepoint [18]
0
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Day 366 to Day 393
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Secondary outcome [19]
0
0
Duration of HSV-2 DNA shedding episodes in Part II of the study
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Assessment method [19]
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Number of days of a HSV-2 shedding episode.
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Timepoint [19]
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Day 731 to Day 758
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Secondary outcome [20]
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0
Anti-HSVTI antibody geometric mean concentrations (GMCs) in Part I of the study
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Assessment method [20]
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0
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Timepoint [20]
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At pre-study intervention administration (Day 1), Day 29, Day 64, Day 209 and Day 394
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Secondary outcome [21]
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Anti-HSVTI antibody geometric mean concentrations (GMCs) in Part II of the study
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Assessment method [21]
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0
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Timepoint [21]
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At pre-study intervention administration (Day 1), Day 29, Day 57, Day 209 and Day 394, Day 574, and Day 759
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Secondary outcome [22]
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Percentage of seropositive participants for anti-HSVTI antibodies in Part I of the study
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Assessment method [22]
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0
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Timepoint [22]
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At pre-study intervention administration (Day 1), Day 29, Day 64, Day 209 and Day 394
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Secondary outcome [23]
0
0
Percentage of seropositive participants for anti-HSVTI antibodies in Part II of the study
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Assessment method [23]
0
0
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Timepoint [23]
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At pre-study intervention administration (Day 1), Day 29, Day 57, Day 209 and Day 394, Day 574, and Day 759
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Secondary outcome [24]
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0
Geometric mean of HSVTI-specific Cluster of Differentiation (CD)4+ T-cells frequency expressing at least two activation markers and including at least one cytokine in Part I of the study
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Assessment method [24]
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0
Query!
Timepoint [24]
0
0
At pre-study intervention administration (Day 1), Day 29, Day 64, Day 209 and Day 394
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Secondary outcome [25]
0
0
Geometric mean of HSVTI-specific CD4+ T-cells frequency expressing at least 2 activation markers and including at least 1 cytokine in Part II of the study
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Assessment method [25]
0
0
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Timepoint [25]
0
0
At pre-study intervention administration (Day 1), Day 29, Day 57, Day 209 and Day 394, Day 574, and Day 759
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Secondary outcome [26]
0
0
Geometric mean of HSVTI-specific CD8+ T-cells frequency expressing at least two activation markers and including at least one cytokine in Part I of the study
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Assessment method [26]
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0
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Timepoint [26]
0
0
At pre-study intervention administration (Day 1), Day 29, Day 64, Day 209 and Day 394
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Secondary outcome [27]
0
0
Geometric mean of HSVTI-specific CD8+ T-cells frequency expressing at least 2 activation markers and including at least 1 cytokine in Part II of the study
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Assessment method [27]
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0
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Timepoint [27]
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At pre-study intervention administration (Day 1), Day 29, Day 57, Day 209 and Day 394, Day 574, and Day 759
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Secondary outcome [28]
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Percentage of participants with a fatal SAE, SAE related to study intervention and potential immune-mediated disease (pIMDs) related to study intervention in Part II of the study
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Assessment method [28]
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A SAE related to study intervention is an SAE judged by the investigator as related to the study intervention. A fatal SAE is any untoward medical occurrence that results in death.
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Timepoint [28]
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From Dose 1 (Day 1) up to study end (Day 759)
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Eligibility
Key inclusion criteria
- • Participants, who, in the opinion of the investigator, can and will comply with the
requirements of the Protocol.
- Written informed consent obtained from the participant prior to performance of any
study-specific procedure.
- Women of non-childbearing potential can be enrolled in the study.
- Women of childbearing potential can be enrolled in the study, if the participant:
- Has practiced highly effective contraception for one month prior to study
intervention administration, and,
- Has a negative pregnancy test result at the Screening visit and on the day of
each study intervention administration, and,
- For PART I: Has agreed to continue highly effective contraception until the end
of the study.
- For PART II: Has agreed to continue highly effective contraception until 3 months
after last study intervention administration.
- Seronegative for human immunodeficiency virus (HIV), as determined by laboratory
screening tests. Participants documented to be seropositive to HIV will not be
eligible for study participation.
- Only for PART I: Healthy participants as established by medical history and physical
examination, at the discretion of the investigator, before entering into the study.
- Only for PART I: Man or woman aged 18 to 40 years, included, at the time of the first
study intervention administration.
- Only for PART I: Seronegative for HSV-2 as determined by Western blot performed at the
Screening visit.
- Only for PART II: Participants with recurrent genital herpes and with no significant
health problems as established by medical history and physical examination, at the
discretion of the investigator, before entering the study.
- Diagnosis of genital herpes for at least one year before the Screening visit.
- History of self-reported or documented recurrent lesional genital herpes
frequency of at least 3 and no more than 9 reported clinical recurrences in the
12 months preceding the screening visit, or, if still on suppressive therapy
within 3 months before the Screening visit, prior to initiation of suppressive
therapy.
- Only for PART II: Man or woman aged 18 to 60 years, included, at the time of the first
study intervention administration.
- Only for PART II: Seropositive for HSV-2 as determined by serological testingperformed
at the Screening visit, or having documented laboratory-confirmed HSV 2 genital herpes
(i.e., HSV-2 DNA positive by a molecular technique such as polymerase chain reaction
[PCR], or HSV-2 seropositive by a type-specific serology assay such as Western Blot or
other immunoassay).Only for PART II (shedding sub-cohort): Participants agreeing to
collect 2 swabs per day from anogenital area for the full duration of the 5 swabbing
periods planned in the study.
- Only for PART II (shedding sub-cohort) after baseline completion: Participants having
collected at least 45 out of 56 anogenital swabs during the baseline period.
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Minimum age
18
Years
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Maximum age
60
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Medical Conditions
- Acute or chronic clinically significant pulmonary, cardiovascular, hepatic, endocrine,
or renal functional abnormality, as determined by physical examination or laboratory
screening tests.
- Any other clinical condition that, in the opinion of the investigator, might pose
additional risk to the participant due to participation in the study or that would
interfere with the efficacy and immunogenicity assessments planned in this study.
- History of any reaction or hypersensitivity likely to be exacerbated by any component
of the study intervention.
- Any confirmed or suspected immunosuppressive or immunodeficient condition, based on
medical history and physical examination.
- Hypersensitivity to latex.
- Recurrent history or uncontrolled neurological disorders or seizures.
- Haematological and/or biochemical parameters outside the normal laboratory ranges at
the Screening visit, unless the laboratory abnormalities are considered not clinically
significant by the investigator.
- Body mass index =<18 kg/m^2 or >=35 kg/m^2.
- Past or current Guillain-Barré syndrome.
- History of any form of ocular HSV infection, HSV-related erythema multiforme, or
HSV-related neurological complications.
Prior/Concomitant Therapy
- Use of any investigational or non-registered product other than the study intervention
during the period beginning as of the Screening visit, or planned use during the study
period.
- Planned administration/administration of a vaccine not foreseen by the Protocol in the
period starting 15 days before each dose and ending 15 days after each dose of study
intervention administration.
- Administration or planned administration of long-acting immune-modifying drugs at any
time during the study period.
- Administration of immunoglobulins and/or any blood products or plasma derivatives
during the period starting 3 months before the first dose of study intervention or
planned administration during the study period.
- Chronic administration of immunosuppressants or other immune-modifying drugs during
the period starting 3 months prior to the first study intervention dose. For
corticosteroids, this will mean prednisone equivalent >= 20 mg/day, or equivalent.
Inhaled, intra articular and topical steroids are allowed.
- Prior receipt of another vaccine containing HSV antigens.
- Only for PART II: Planned use of suppressive anti-HSV therapy from the Screening visit
until the end of the study.
- Only for PART II: Planned use of tenofovir therapy, or other medication known to
affect HSV shedding or genital lesions from the Screening visit until the end of the
study. Only for PART II: Planned use of topical antiviral medication in the anogenital
region from the Screening visit until the end of the study.
- Only for PART II: Planned use of any episodic antiviral medications during the 5
swabbing periods (including the baseline period) (only for the shedding sub-cohort).
Prior/Concurrent Clinical Study Experience
• Concurrently participating in another clinical study, at any time during the study
period, in which the participant has been or will be exposed to an investigational or a
non-investigational intervention.
Other Exclusions
- Pregnant or lactating women.
- Woman planning to become pregnant or planning to discontinue contraceptive precautions
in the period starting from the Screening visit up to 3 months post-last dose of study
intervention.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 1/Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
7/03/2022
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
5/07/2026
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Actual
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Sample size
Target
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Accrual to date
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Final
342
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
0
0
GSK Investigational Site - Darlinghurst, Sydney
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Recruitment hospital [2]
0
0
GSK Investigational Site - Sydney
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Recruitment postcode(s) [1]
0
0
2010 - Darlinghurst, Sydney
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Recruitment postcode(s) [2]
0
0
2010 - Sydney
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Recruitment outside Australia
Country [1]
0
0
United States of America
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State/province [1]
0
0
Arizona
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Country [2]
0
0
United States of America
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State/province [2]
0
0
Florida
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Country [3]
0
0
United States of America
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State/province [3]
0
0
Kansas
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Country [4]
0
0
United States of America
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State/province [4]
0
0
Missouri
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Country [5]
0
0
United States of America
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State/province [5]
0
0
New York
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Country [6]
0
0
United States of America
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State/province [6]
0
0
Virginia
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Country [7]
0
0
United States of America
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State/province [7]
0
0
Washington
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Country [8]
0
0
Belgium
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State/province [8]
0
0
Antwerpen
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Country [9]
0
0
Belgium
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State/province [9]
0
0
Brussels
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Country [10]
0
0
Belgium
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State/province [10]
0
0
Edegem
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Country [11]
0
0
Belgium
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State/province [11]
0
0
Gent
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Country [12]
0
0
Canada
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State/province [12]
0
0
Quebec
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Country [13]
0
0
Estonia
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State/province [13]
0
0
Tartu
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Country [14]
0
0
Germany
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State/province [14]
0
0
Hessen
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Country [15]
0
0
Germany
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State/province [15]
0
0
Nordrhein-Westfalen
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Country [16]
0
0
Germany
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State/province [16]
0
0
Berlin
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Country [17]
0
0
Germany
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State/province [17]
0
0
Hamburg
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Country [18]
0
0
Spain
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State/province [18]
0
0
Madrid
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Country [19]
0
0
Spain
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State/province [19]
0
0
Barcelona
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Country [20]
0
0
Spain
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State/province [20]
0
0
Marbella
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Country [21]
0
0
United Kingdom
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State/province [21]
0
0
East Sussex
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Country [22]
0
0
United Kingdom
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State/province [22]
0
0
Liverpool
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Country [23]
0
0
United Kingdom
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State/province [23]
0
0
London
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Country [24]
0
0
United Kingdom
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State/province [24]
0
0
Southampton
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
GlaxoSmithKline
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this first-time-in-human (FTiH) study is to evaluate the reactogenicity,
safety, immune response, and efficacy of an investigational herpes simplex virus
(HSV)-targeted immunotherapy (TI). The study will be conducted in 2 parts: Part I assessing
different formulations of the Herpes Simplex Virus-targeted immunotherapy (HSVTI) in healthy
participants aged 18-40 years; Part II assessing the 2 formulations of the HSVTI in
participants aged 18-60 years with recurrent genital herpes.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT05298254
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
0
0
GSK Clinical Trials
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Address
0
0
GlaxoSmithKline
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Country
0
0
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Phone
0
0
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Fax
0
0
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Email
0
0
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Contact person for public queries
Name
0
0
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Address
0
0
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Country
0
0
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Phone
0
0
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Fax
0
0
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Email
0
0
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT05298254
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