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Safety and Immunogenicity of a Chlamydia Vaccine CTH522 (CHLM-02)

Primary Purpose

Trachoma

Status

Completed

Phase

Phase 1

Locations

United Kingdom

Study Type

Interventional

Intervention

CTH522-CAF01 IM

CTH522-CAF09b IM

CTH522 ID

CTH522 TO

Placebo (Saline)

About this trial

This is an interventional prevention trial for Trachoma focused on measuring CTH522, Chlamydia, C. Trachomatis

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

IC1: Healthy males and females between 18-45 years old on the day of the first vaccination IC2: Has been properly informed about the trial and signed the consent form IC3: Is willing and likely to comply with trial procedures IC4: Is prepared to grant authorised persons access to his/her trial-related medical record IC5: Is willing to use acceptable contraceptive measures during the trial (two weeks before and two weeks after the trial). Heterosexually active female capable of becoming pregnant must agree to use hormonal contraception, intrauterine device, intrauterine hormonereleasing system, or to complete abstinence from at least two weeks before the first vaccination until at least two weeks after the last. Complete abstinence (defined as refraining from heterosexual intercourse) must be in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g. calendar, ovulation, symptothermal, post-ovulation methods), withdrawal and progestogen-only oral hormonal contraception where inhibition of ovulation is not the primary mode of action are not acceptable methods of contraception

Exclusion criteria:

EX1: Is positive for C. trachomatis via urine PCR or has a known history of C. trachomatis EX2: Is positive for gonorrhoea via urine PCR test, or HIV, hepatitis B/C, syphilis via blood tests EX3: Has a significant active disease such as cardiac, liver, immunological, neurological, psychiatric or clinically significant abnormality of haematological or biochemical parameters EX4: Has BMI ≥ 35 kg/m2 EX5: Is currently participating in another clinical trial with an investigational or noninvestigational drug or device, or was treated with an investigational drug within 28 days before the first vaccination EX6: Has received, or plans to receive, any immunisation within 14 days of the start of the trial or during the trial immunisations EX7: Is currently receiving treatment with systemic immunosuppressive agents. Topical steroids are allowed unless applied to the IM or ID injection site EX8: Has a condition which in the opinion of the investigator is not suitable for participation in the trial EX9: Is known or confirmed to have an allergy to any of the vaccine constituents EX10: Is unable to refrain from the use of contact lenses. Contact lenses should be avoided two days before TO administration and for seven days later (longer if any ongoing local eye AE) EX11: Has any evident ocular disease upon ophthalmoscopic exam at screening or any medical history of ocular disease that, in the opinion of the investigator, may impact the subject's participation in the trial EX12: Is pregnant (positive pregnancy test) or breastfeeding or not willing to use contraception during the trial EX13: Has confirmed a history of pelvic inflammatory disease or significant gynaecological diseases

Sites / Locations

NIHR Imperial Center for Translational and Experimental Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Placebo Comparator

Arm Label

Cohort A - 85µg CTH522-CAF01

Cohort B - 85µg CTH522-CAF01+ TO CTH522

Cohort C - 85µg CTH522-CAF01+ID CTH522

Cohort D - 15µg CTH522-CAF01

Cohort E - 85µg CTH522-CAF09b

Cohort F - Placebo

Arm Description

Cohorts A will receive three IM vaccination of 85µg CTH522-CAF01. This cohort is divided into two groups: A1 will receive placebo at DAY 28 + Day 112 + Day 140, while A2 will receives placebo at Day 28 + Day 112, but non-adjuvanted TO CTH522 boost at Day 140.

Cohort B will receive three IM vaccination of 85 µg CTH522-CAF01. This cohort is divided into two groups: B1 will receive TO vaccination of the non-adjuvanted CTH522 at Day 28 + Day 112 and TO placebo at Day 140, while B2 will receive the same for Day 28 + Day 112, but non-adjuvanted TO CTH522 boost at Day 140. The two additional doses TO CTH522 (12µg) is administered in each eye. The rationale for this cohort is to investigate the impact of simultaneous TO administration of the antigen on the immunogenicity results obtained.

Cohort C will receive three IM vaccination of 85 µg CTH522-CAF01. This cohort is divided into two groups: C1 will receive ID vaccination of the non-adjuvanted CTH522 at Day 28 + Day 12 and TO placebo at Day 140, while C2 will receive the same for Day 28 + Day 112, but TO CTH522 boost at Day 140. The two additional doses of non-adjuvanted CTH522 (24µg) is administered ID. The rationale for this cohort is to investigate the impact of simultaneous ID administration of the antigen on the immunogenicity results obtained.

Cohort D is the same as cohort A except that the dose for CTH522-CAF01 is 15µg.

Cohort E is the same as cohort A except that the adjuvant is CAF09b and not CAF01. The rationale for the A, D and E cohorts is to investigate the impact of the CTH522 dose and adjuvant on the immunogenicity results.

Cohort F will receive only placebo in form of 0.9% NaCl saline.

Outcomes

Primary Outcome Measures

Local injection reactions

Local injection site reactions after intramuscular and intradermal vaccination

Local ocular reactions

Local ocular reactions after topical ocular vaccination

Systemic reactions

Systemic reactions after vaccinations

Secondary Outcome Measures

Secondary - immunogenicity

Seroconversion for anti-CTH522 IgG at any time points after vaccinations of CTH522

Full Information

NCT ID

NCT03926728

First Posted

April 15, 2019

Last Updated

May 4, 2022

Sponsor

Statens Serum Institut

Collaborators

Imperial College London

1. Study Identification

Unique Protocol Identification Number

NCT03926728

Brief Title

Safety and Immunogenicity of a Chlamydia Vaccine CTH522

Acronym

CHLM-02

Official Title

A Phase I, Double-blind, Parallel, Randomised and Placebo-controlled Trial Investigating the Safety and Immunogenicity of a Chlamydia Vaccine, CTH522, in Healthy Adults

Study Type

Interventional

2. Study Status

Record Verification Date

May 2022

Overall Recruitment Status

Completed

Study Start Date

February 17, 2020 (Actual)

Primary Completion Date

February 22, 2022 (Actual)

Study Completion Date

February 22, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Statens Serum Institut

Collaborators

Imperial College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

The present trial is a phase I, double-blind, parallel, randomised, and placebo-controlled trial of a chlamydia vaccine CTH522. Sixty-six subjects will be randomly assigned into six cohorts and are to receive four vaccination, in total of 12 trial visits. Cohorts A-D investigates CTH522-CAF01 administered IM in two doses (85 µg and 15 µg). Cohort E investigate CTH522-CAF09b also administered IM in one dose (85 µg). Cohort E is the placebo group. All subjects will receive a TO administration as a boost at Day 140 (4th vaccination). The TO boost will be non-adjuvanted CTH522 (12µg in each eye) or placebo. Nine subjects in each of cohorts A-E will receive the active boost (i.e. CTH522), three subjects will receive the placebo.

Detailed Description

This trial is a phase I, double-blind, parallel, randomised, and placebo-controlled trial of the chlamydia vaccine CTH522 in healthy adults. It is planned to randomly assign 66 subjects into six cohorts. Cohorts A-D investigate CTH522-CAF01 administered IM in two doses (85 μg and 15 μg). Cohort E investigates CTH522-CAF09b administered IM in one dose (85 μg). Cohort F is the placebo group. The enrolled subjects will complete 12 trial visits. All subjects in the active groups (cohort A-E) will receive three IM injections of the adjuvanted CTH522 and some (cohort B and C) will receive the non-adjuvanted CTH522 via the TO or ID route (given at the same time as the 2nd and 3rd IM vaccinations). All active groups will receive TO administration as a boost at Day 140 of either the non-adjuvanted CTH522 (12 μg in each eye) or placebo. Cohort A will receive three IM vaccination of 85μg CTH522-CAF01. This cohort is divided into two groups: A1 will receive ID placebo at Day 28 + Day 112, and TO placebo at Day 140, while A2 will receive TO placebo at Day 28 + Day 112, and non-adjuvanted TO CTH522 boost at Day 140. Cohort B will receive three IM vaccinations of 85 μg CTH522-CAF01. This cohort is divided into two groups: B1 will receive TO vaccination of the non-adjuvanted CTH522 at Day 28 and 112 and TO placebo at Day 140, while B2 will receive the same for Day 28 and 112, but non-adjuvanted TO CTH522 boost at Day 140. The two additional TO doses of CTH522 (12 μg in each eye) are administered in each eye. The rationale for this schedule is to investigate the impact of simultaneous TO administration of the antigen on the immunogenicity results. Cohort C will receive three IM vaccinations of 85 μg CTH522-CAF01. This cohort is divided into two groups: C1 will receive ID vaccination of the non-adjuvanted 24 μg CTH522 at Day 28 and 112 and TO placebo at Day 140, while C2 will receive the same for Day 28 and 112, but TO 12 μg CTH522 boost in each eye at Day 140. The rationale for this schedule is to investigate the impact of simultaneous ID administration of the antigen on the immunogenicity results. Cohort D will receive three IM vaccinations of 15 μg CTH522-CAF01. The rationale for the A and D cohorts is to investigate the impact of the two IM CTH522 doses on the immunogenicity results. Cohort E will receive three IM vaccinations of 85 μg CTH522-CAF09b. The rationale for the A and E cohorts is to investigate the impact of the adjuvant on the immunogenicity results. Cohort F will receive only placebo in the form of 0.9% NaCl saline (IM, ID and TO).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Trachoma

Keywords

CTH522, Chlamydia, C. Trachomatis

7. Study Design

Primary Purpose

Prevention

Study Phase

Phase 1

Interventional Study Model

Parallel Assignment

Masking

ParticipantCare ProviderInvestigatorOutcomes Assessor

Allocation

Randomized

Enrollment

65 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Cohort A - 85µg CTH522-CAF01

Arm Type

Experimental

Arm Description

Arm Title

Cohort B - 85µg CTH522-CAF01+ TO CTH522

Arm Type

Experimental

Arm Description

Arm Title

Cohort C - 85µg CTH522-CAF01+ID CTH522

Arm Type

Experimental

Arm Description

Arm Title

Cohort D - 15µg CTH522-CAF01

Arm Type

Experimental

Arm Description

Cohort D is the same as cohort A except that the dose for CTH522-CAF01 is 15µg.

Arm Title

Cohort E - 85µg CTH522-CAF09b

Arm Type

Experimental

Arm Description

Arm Title

Cohort F - Placebo

Arm Type

Placebo Comparator

Arm Description

Cohort F will receive only placebo in form of 0.9% NaCl saline.

Intervention Type

Biological

Intervention Name(s)

CTH522-CAF01 IM

Intervention Description

On-site reconstitution of IMPs is performed by mixing 85 microgram CTH522 with CAF01. The preferred for IM is in the non-dominant deltoid muscle. IM injection will be performed with a 1-2 ml polypropylene Luer-Lok™ syringe via 23-25-gauge needle. The identity of the injected trial vaccine will be known to the clinical site staff dispensing and/or injecting the trial vaccine to the subject and by the unblinded trial monitor. The identity of the trial vaccine administered will remain unknown to the subject during the trial.

Intervention Type

Biological

Intervention Name(s)

CTH522-CAF09b IM

Intervention Description

On-site reconstitution of IMPs is performed by mixing 85 microgram CTH522 with CAF09b. The preferred for IM is in the non-dominant deltoid muscle. IM injection will be performed with a 1-2 ml polypropylene Luer-Lok™ syringe via 23-25-gauge needle. The identity of the injected trial vaccine will be known to the clinical site staff dispensing and/or injecting the trial vaccine to the subject and by the unblinded trial monitor. The identity of the trial vaccine administered will remain unknown to the subject during the trial.

Intervention Type

Biological

Intervention Name(s)

CTH522 ID

Intervention Description

24 microgram CTH522 given ID is in the non-dominant deltoid muscle. ID with a 1 ml syringe via a 26-28 gauge needle using a NanoPass device or similar. The identity of the injected trial vaccine will be known to the clinical site staff dispensing and/or injecting the trial vaccine to the subject and by the unblinded trial monitor. The identity of the trial vaccine administered will remain unknown to the subject during the trial.

Intervention Type

Biological

Intervention Name(s)

CTH522 TO

Intervention Description

24 microgram CTH522 (12 microgram in each eye) TO administrations will be performed using a Gilson positive displacement pipette. The identity of vaccine will be known to the clinical site staff dispensing/administrating the trial vaccine to the subject and by the unblinded trial monitor. The identity of the trial vaccine administered will remain unknown to the subject during the trial.

Intervention Type

Biological

Intervention Name(s)

Placebo (Saline)

Intervention Description

Placebo only given as IM, ID and TO

Primary Outcome Measure Information:

Title

Local injection reactions

Description

Local injection site reactions after intramuscular and intradermal vaccination

Time Frame

Visit 2 (Day 0) to Visit 12 (Day 238)

Title

Local ocular reactions

Description

Local ocular reactions after topical ocular vaccination

Time Frame

Visit 2 (Day 0) to Visit 12 (Day 238)

Title

Systemic reactions

Description

Systemic reactions after vaccinations

Time Frame

Visit 2 (Day 0) to Visit 12 (Day 238)

Secondary Outcome Measure Information:

Title

Secondary - immunogenicity

Description

Seroconversion for anti-CTH522 IgG at any time points after vaccinations of CTH522

Time Frame

Visit 2 (Day 0) to Visit 12 (Day 238); except for Visit 10 (Day 143)

Other Pre-specified Outcome Measures:

Title

Exploratory - immunogenicity

Description

Systemic and ocular antibodies: cell-mediated immune response, antibody responses measured by T- and B-cell Elispot, serum neutralising antibodies against serovars D-G. Isolation and characterisation of CTH522-antigen-specific memory B-cells in the systemic compartments (dependent on the elicited specific memory T- and B-cell numbers)

Time Frame

Visit 2 (Day 0) to Visit 12 (Day 238); except for Visit 3 (Day 14) for ocular strip

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Maximum Age & Unit of Time

45 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: IC1: Healthy males and females between 18-45 years old on the day of the first vaccination IC2: Has been properly informed about the trial and signed the consent form IC3: Is willing and likely to comply with trial procedures IC4: Is prepared to grant authorised persons access to his/her trial-related medical record IC5: Is willing to use acceptable contraceptive measures during the trial (two weeks before and two weeks after the trial). Heterosexually active female capable of becoming pregnant must agree to use hormonal contraception, intrauterine device, intrauterine hormonereleasing system, or to complete abstinence from at least two weeks before the first vaccination until at least two weeks after the last. Complete abstinence (defined as refraining from heterosexual intercourse) must be in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g. calendar, ovulation, symptothermal, post-ovulation methods), withdrawal and progestogen-only oral hormonal contraception where inhibition of ovulation is not the primary mode of action are not acceptable methods of contraception Exclusion criteria: EX1: Is positive for C. trachomatis via urine PCR or has a known history of C. trachomatis EX2: Is positive for gonorrhoea via urine PCR test, or HIV, hepatitis B/C, syphilis via blood tests EX3: Has a significant active disease such as cardiac, liver, immunological, neurological, psychiatric or clinically significant abnormality of haematological or biochemical parameters EX4: Has BMI ≥ 35 kg/m2 EX5: Is currently participating in another clinical trial with an investigational or noninvestigational drug or device, or was treated with an investigational drug within 28 days before the first vaccination EX6: Has received, or plans to receive, any immunisation within 14 days of the start of the trial or during the trial immunisations EX7: Is currently receiving treatment with systemic immunosuppressive agents. Topical steroids are allowed unless applied to the IM or ID injection site EX8: Has a condition which in the opinion of the investigator is not suitable for participation in the trial EX9: Is known or confirmed to have an allergy to any of the vaccine constituents EX10: Is unable to refrain from the use of contact lenses. Contact lenses should be avoided two days before TO administration and for seven days later (longer if any ongoing local eye AE) EX11: Has any evident ocular disease upon ophthalmoscopic exam at screening or any medical history of ocular disease that, in the opinion of the investigator, may impact the subject's participation in the trial EX12: Is pregnant (positive pregnancy test) or breastfeeding or not willing to use contraception during the trial EX13: Has confirmed a history of pelvic inflammatory disease or significant gynaecological diseases

Overall Study Officials: