A Double-Blind Placebo-Control Dose Escalating Study to Evaluate the Safety and Immunogenicity of dmLT by Oral, Sublingual and Intradermal Vaccination in Adults Residing in an Endemic Area

Immunisation Clinical Trial

Official title:

A Phase 1 Double-Blinded, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety and Immunogenicity of Double Mutant Heat-Labile Toxin LTR192G/L211A (dmLT) From Enterotoxigenic Escherichia Coli (ETEC) by Oral, Sublingual, or Intradermal Vaccination in Adults Residing in an Endemic Area

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03548064
• Other study ID #: 14-0031
• Secondary ID: HHSN272201300022
• Status: Terminated
• Phase: Phase 1
• Start date: March 10, 2019
• Est. completion date: December 31, 2020

Study information

• Verified date: December 14, 2017
• Source: National Institute of Allergy and Infectious Diseases (NIAID)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a trial to evaluate the safety and immunogenicity of double mutant heat-labile toxin LTR192G/L211A (dmLT) from Enterotoxigenic Escherichia coli (ETEC) by oral, sublingual, or intradermal vaccination in approximately 135 healthy adult volunteers, age 18-45 years. Study duration is approximately 2.5 years, with each participant duration for up to 9 months depending on the route of dmLT administered. There is no specific hypothesis being tested in this study. The primary objective of this study is to assess the reactogenicity, safety, and tolerability of dmLT when administered in three sequential doses, over a range of dosages by oral, sublingual, or intradermal routes.

Description:

This is a Phase 1 double-blinded, placebo-controlled, dose-escalation trial to evaluate the safety and immunogenicity of double mutant heat-labile toxin LTR192G/L211A (dmLT) from Enterotoxigenic Escherichia coli (ETEC) by oral, sublingual, or intradermal vaccination in approximately 135 healthy adult volunteers, age 18-45 years, who meet all the eligibility criteria and reside in Bangladesh. Study duration is approximately 2.5 years, with each participant duration for up to 9 months depending on the route of dmLT administered. The study population will be recruited from Mirpur, a community of Dhaka, Bangladesh, known as having a high rate of diarrheal, respiratory, and enteric disease. This clinical trial is designed to assess the safety, reactogenicity, tolerability, and immunogenicity of a range of dosages of dmLT administered by three different routes: oral, sublingual, or intradermal. The oral and sublingual routes of administration will evaluate dosages of 5, 25, and 50 micrograms of dmLT; the intradermal route of administration will evaluate dosages of 0.3, 1.0, and 2.0 micrograms of dmLT. Participants will receive a total of three sequential doses of dmLT; the oral and sublingual routes will be at days 1, 15, and 29 and the intradermal route will be at days 1, 22, and 43. There is no specific hypothesis being tested in this study. The primary objective of this study is to assess the reactogenicity, safety, and tolerability of dmLT when administered in three sequential doses, over a range of dosages by oral, sublingual, or intradermal routes. The secondary objectives of this study are: 1) to assess the long-term safety, from first vaccination through 6 months following the last dose of vaccine, 2) to evaluate the serum anti-dmLT IgG and IgA response, 3) to evaluate the IgG and IgA anti-dmLT Antibody Secreting Cell (ASC) response, 4) to evaluate the IgG and IgA anti-dmLT Antibodies in Lymphocyte Supernatant (ALS) response, 5) to evaluate the total fecal IgA and fecal anti-dmLT IgA response, and 6) to evaluate the total salivary IgA and the saliva-derived anti-dmLT IgA response.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 75
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Male or female age 18-45 years old, inclusive.

2. Provides written informed consent before initiation of any study procedures.

3. Healthy as judged by the site investigators and determined by medical history, medication history, and physical examination.

4. Capable of understanding, consenting, and complying with all the study visits and procedures.

5. Body Mass Index of no less than 18.5.

6. Agrees not to participate in another clinical trial during the study period.

7. Agrees to complete all study visits and procedures.

8. Agrees not to donate blood to a blood bank for 12 months after receiving the last vaccine.

Exclusion Criteria:

1. Women who are pregnant or lactating or have a positive urine pregnancy test at screening or on the day of vaccinations. Note: all women presenting for screening will have urine pregnancy testing. "Females of childbearing potential must agree to use an efficacious hormonal or barrier method of birth control from screening and through 28 days post last dose of vaccine. Abstinence is also acceptable."

2. Presence or history of a chronic medical condition* that would, in the opinion of the investigator, render vaccination unsafe or interfere with the evaluation of the vaccine. *Note: this may include, but is not limited to: significant renal disease, unstable or progressive neurological disorders, diabetes, heart disease, asthma, lung disease, liver disease, organ transplant recipients and cancer.

3. Presence of a significant dermatologic condition*, or tattoo(s), scarring or significant skin damage at the vaccination site that would impede evaluation of local reactogenicity. *Note: this may include severe eczema, psoriasis or history of keloid formation. Participants with history of squamous cell or basal cell skin cancer that has been surgically excised and considered cured may be enrolled in the study if the skin cancer site is healed and is not at proposed vaccine administration site.

4. Any developmental abnormality of the palate.

5. Participants diagnosed with autoimmune disorders, chronic inflammatory disorders or neurological disorders with a potential autoimmune correlation.

6. Use of long-term (> / = 2 weeks) oral steroids, intranasal or topical prednisone (or equivalent), parenteral steroids, or high-dose inhaled steroids (> 800 microgram/day of beclomethasone dipropionate or equivalent) within the preceding 6 months.

7. Has major psychiatric illness* during last 12 months that in the investigator's opinion would preclude participation. *Note: Participants taking antipsychotic or antimanic drugs should not be enrolled. These include: aripiprazole, clozapine, ziprasidone, haloperidol, molindone, lamotrigine, gabapentin, topiramate, loxapine, thioridazine, thiothixene, pimozide, fluphenazine, risperidone, mesoridazine, quetiapine, trifluoperazine, chlorprothixene, chlorpromazine, perphenazine, olanzapine, carbamazepine, divalproex sodium, lithium carbonate, or lithium citrate. Participants taking a single antidepressant drug and are stable without de-compensating symptoms in the preceding 3 months can be enrolled in the study.

8. Use of prescription or over-the-counter (OTC) anti-inflammatory medications* 48 hours prior to receiving the investigational product. *Note: This includes naproxen, aspirin, ibuprofen, and other non-steroidal anti-inflammatory drugs.

9. Gastrointestinal symptoms* in the past 24 hours or abdominal pain lasting for more than 2 weeks in the past 6 months. *Note: this may include, but is not limited to: abdominal pain or cramps, loss of appetite, nausea, general ill-feeling or vomiting.

10. Moderate or severe diarrheal illness* during the 6 weeks prior to enrollment. *Note: Moderate or severe diarrheal illness is defined by the passage of > / = 4 unformed or loose stools (mix of liquid and solid components) in a 24 hour period

11. History of chronic gastrointestinal illness*. *Note: this includes severe dyspepsia or gastroesophageal reflux disease, constipation, irritable bowel syndrome (IBS), hemorrhoids, diverticular disease, colitis, colon polyps, colon cancer, and inflammatory bowel disease. Mild or moderate heartburn or epigastric pain occurring no more than three times per week is permitted.

12. Regular use (weekly or more often) of laxatives, anti-diarrheal, anti-constipation, or antacid therapy.

13. History of major gastrointestinal surgery, excluding uncomplicated appendectomy or cholecystectomy.

14. History of systemic antimicrobial treatment (i.e., topical treatments are not an exclusion) during the week prior to any administration of dmLT.

15. Acute febrile illness (body temperature > / = 38 degrees Celsius) during the week prior to enrollment.

16. Abnormal screening laboratories. Note: screening labs include white blood cell count (WBC), absolute neutrophil count (ANC), hemoglobin (Hg), platelet count, serum creatinine, serum albumin, alanine aminotransferase (ALT, also known as SGPT), and serologic testing for Hepatitis B virus surface antigen (HBsAg) and Hepatitis C virus (HCV) antibody. Abnormal vital signs.

17. Isolation of specific bacteria* from screening stool cultures. *Note: bacteria include ETEC, Vibrio cholerae, and Shigella spp. Salmonella and Campylobacter will not be evaluated as part this criterion.

18. Received an inactivated licensed vaccine within 2 weeks of enrollment or live licensed vaccine within 4 weeks of enrollment.

19. Received a cholera (licensed or experimental) vaccine, E. coli vaccine, or Shigella vaccine in the last 3 years.

20. History of receiving immune globulin or other blood product within the 3 months before enrollment in this study.

21. Currently enrolled in another study, involving an experimental agent. Participants involved in observational studies or surveys remain eligible.

22. Any condition that would, in the opinion of the Site Investigator, place the participant at an unacceptable risk of injury or render the participant unable to meet the requirements of the protocol.

23. Known allergies to study compound or components of the study vaccine.

24. Donating blood in the 8 weeks prior to study entry.

Related Conditions & MeSH terms

• Escherichia coli Infections
• Gastroenteritis
• Gastroenteritis Escherichia Coli
• Immunisation

Intervention

Other:
• Placebo
Placebo
• Placebo
Placebo
• Placebo
Placebo

Biological:
• Recombinant Double Mutant Heat-Labile Toxin LT(R192G/L211A) (dmLT) Oral enterotoxigenic Escherichia coli (ETEC) Vaccine
LT(R192G/L211A), or dmLT is a derivative of wild-type enterotoxigenic Escherichia coli heat-labile enterotoxin that has been genetically modified by replacing the arginine at amino acid position 192 with glycine and the leucine at amino acid position 211 with alanine. These two amino acid substitutions take place in proteolytic cleavage sites which are critical for activation of the secreted toxin molecules.
• Recombinant Double Mutant Heat-Labile Toxin LT(R192G/L211A) (dmLT) Oral enterotoxigenic Escherichia coli (ETEC) Vaccine
LT(R192G/L211A), or dmLT is a derivative of wild-type enterotoxigenic Escherichia coli heat-labile enterotoxin that has been genetically modified by replacing the arginine at amino acid position 192 with glycine and the leucine at amino acid position 211 with alanine. These two amino acid substitutions take place in proteolytic cleavage sites which are critical for activation of the secreted toxin molecules.
• Recombinant Double Mutant Heat-Labile Toxin LT(R192G/L211A) (dmLT) Oral enterotoxigenic Escherichia coli (ETEC) Vaccine
LT(R192G/L211A), or dmLT is a derivative of wild-type enterotoxigenic Escherichia coli heat-labile enterotoxin that has been genetically modified by replacing the arginine at amino acid position 192 with glycine and the leucine at amino acid position 211 with alanine. These two amino acid substitutions take place in proteolytic cleavage sites which are critical for activation of the secreted toxin molecules.

Locations

Country	Name	City	State
Bangladesh	International Center for Diarrheal Disease Research Bangladesh - Infectious Diseases Division - Mucosal Immunology and Vaccinology Unit	Dhaka

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

Bangladesh, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants in the Oral Arms With Solicited Local Reactogenicity Events Post Each Dose	Solicited adverse events were collected post-vaccination and for 7 days after. Local events for the oral route include irritation of the oral cavity or tongue, diarrhea, nausea, vomiting, and abdominal discomfort.	Day 1 through Day 8 (post dose 1), Day 15 through Day 22 (post dose 2), Day 29 through Day 36 (post dose 3)
Primary	Number of Participants in the Sublingual Arms With Solicited Local Reactogenicity Events Post Each Dose	Solicited adverse events were collected post-vaccination and for 7 days after. Local events for the sublingual route include irritation of the oral cavity or tongue, facial nerve disturbance, diarrhea, nausea, vomiting, or abdominal discomfort.	Day 1 through Day 8 (post dose 1), Day 15 through Day 22 (post dose 2), Day 29 through Day 36 (post dose 3)
Primary	Number of Participants in the Intradermal Arms With Solicited Local Reactogenicity Events Post Each Dose	Solicited adverse events were collected post-vaccination and for 7 days after. Local events for the intradermal route include injection site pain, redness, swelling, bruising, itching, hypo/hyper pigmentation and induration, vesicles, or hardened mass.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 8 (post dose 1), Day 22 through Day 29 (post dose 2)
Primary	Number of Participants in the Oral and Sublingual Arms With Solicited Systemic Reactogenicity Events Post Each Dose	Solicited adverse events were collected post-vaccination and for 7 days after. Systemic events for the oral and sublingual routes include fever, feverishness, fatigue, malaise, myalgia, or headache.	Day 1 through Day 8 (post dose 1), Day 15 through Day 22 (post dose 2), Day 29 through Day 36 (post dose 3)
Primary	Number of Participants in the Intradermal Arms With Solicited Systemic Reactogenicity Events Post Each Dose	Solicited adverse events were collected post-vaccination and for 7 days after. Systemic events for the intradermal route include fever, feverishness, fatigue, malaise, myalgia, headache, diarrhea, nausea, vomiting, or abdominal discomfort.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 8 (post dose 1), Day 22 through Day 29 (post dose 2)
Primary	Number of Participants Who Withdrew From the Study	Participants could voluntarily withdraw their consent for study participation for any reason at any time. Primary reason for withdrawal was recorded and early termination visits were attempted.	Day 1 through Day 209 (Day 223 for Intradermal cohorts)
Primary	Number of Participants Who Discontinued Study Vaccination	Participants who received the first vaccination could choose to discontinue receipt of study vaccine for any reason and could choose to remain in the study (i.e., not withdraw from study). In addition, a participant could be discontinued from receipt of the second or third vaccination. Discontinuation from vaccination did not mean automatic withdrawal from the study, and participants were monitored for safety and immunogenicity if the participant consented.	Day 1 through Day 29 (Day 43 for Intradermal cohorts)
Primary	Number of Vaccine-related Unsolicited Adverse Events From First Dose Through 28 Days After Last Dose	Adverse events were defined as any untoward medical occurrence in a participant administered a pharmaceutical product regardless of its causal relationship to the study treatment.	Day 1 through Day 57 (Day 71 for Intradermal cohorts)
Secondary	Number of Vaccine-related Serious Adverse Events From Post Dose 1 Through 6 Months After Last Dose	Serious Adverse Events (SAE) were defined as an adverse event which resulted in death, was life threatening, resulted in an inpatient hospitalization, prolongation of an existing hospitalization, led to persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, or led to a congenital anomaly/birth defect. Important medical events that may not result in death, be life-threatening, or require hospitalizations were considered serious when, based upon appropriate medical judgment, they jeopardize the participant and may require medical or surgical intervention to prevent one of the outcomes listed in this definition.	Day 1 through Day 209 (Day 223 for Intradermal cohorts)
Secondary	Percentage of Participants With a >= 4-fold Rise in dmLT-specific Serum IgA Titers Over Baseline Measured by ELISA	Blood was collected for the IgA and IgG assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with a >= 4-fold rise in dmLT-specific serum IgA and IgG titers over baseline was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 8 through Day 114
Secondary	Percentage of Participants With a >= 4-fold Rise in dmLT-specific Serum IgG Titers Over Baseline Measured by ELISA	Blood was collected for the IgG and IgA assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with a >= 4-fold rise in dmLT-specific serum IgG and IgA titers over baseline was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 8 through Day 114
Secondary	Percentage of Participants With >= 8 dmLT-specific IgA ASC / 10^6 PBMC as Measured by ELISpot	PBMCs were collected for the IgA and IgG assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with >= 8 dmLT-specific IgA and IgG ASC / 10^6 PBMC was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 36
Secondary	Percentage of Participants With >= 8 dmLT-specific IgG ASC / 10^6 PBMC as Measured by ELISpot	PBMCs were collected for the IgA and IgG assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with >= 8 dmLT-specific IgA and IgG ASC / 10^6 PBMC was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 36
Secondary	Percentage of Participants With >= 2-fold Rise in ALS Anti-dmLT-specific IgA Titers Over Baseline Measured by ELISA	Blood was collected for the IgA and IgG assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with a >= 2-fold rise in ALS anti-dmLT-specific IgG and IgA titers over baseline was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 36
Secondary	Percentage of Participants With >= 2-fold Rise in ALS Anti-dmLT-specific IgG Titers Over Baseline Measured by ELISA	Blood was collected for the IgA and IgG assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with a >= 2-fold rise in ALS anti-dmLT-specific IgG and IgA titers over baseline was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 36
Secondary	Percentage of Participants With >= 4-fold Rise Over Baseline in dmLT-specific Fecal IgA Titers Measured by ELISA	Stool was collected for the IgA assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with a >= 4-fold rise over baseline in dmLT-specific fecal IgA titers was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 57
Secondary	Percentage of Participants With >= 4-fold Rise Over Baseline in dmLT-specific Salivary IgA Titers Measured by ELISA	Saliva was collected for the IgA assay which was conducted with dmLT as the antigen. Each sample was tested per the laboratory's standard operating procedure. The percentage of participants with a >= 4-fold rise over baseline in dmLT-specific salivary IgA titers was calculated for each study arm from the available results at any time post-first study vaccination.; Study halted on Day 43 due to COVID-19 pandemic and the intradermal group did not receive the final dose.	Day 1 through Day 57