Optimal Human Dose for GII.2 Norovirus (Snow Mountain) Challenge Studies

Gastroenteritis Norovirus Clinical Trial

Official title:

Phase I Study to Determine the Optimal Human Dose for GII.2 Norovirus (Snow Mountain) Challenge Studies

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02473224
• Other study ID #: 12-0034
• Status: Completed
• Phase: Phase 1
• Start date: October 28, 2015
• Est. completion date: November 27, 2018

Study information

• Verified date: June 15, 2018
• 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 phase I, randomized, double blind, as well as partially blinded (for Cohort 4), placebo-controlled safety, illness, and infection study of a new experimental human challenge stock of the Norovirus genogroup II, genotype 2 (GII.2) isolate designated Snow Mountain virus (SMV). The study duration is 24 - 36 months. The primary objectives are to: 1) evaluate the safety and reactogenicity of the GII.2 Snow Mountain norovirus challenge stock and 2) determine a safe and optimal challenge dose of GII.2 Snow Mountain norovirus to achieve illness in a high proportion (= / > 75%) of subjects.

Description:

This is a phase I, randomized, double blind, as well as partially blinded (for Cohort 4), placebo-controlled safety, illness, and infection study of a new experimental human challenge stock of the Norovirus genogroup II, genotype 2 (GII.2) isolate designated Snow Mountain virus (SMV), administered to healthy adults 18-49 years of age. Groups of 11 subjects each will be admitted to the inpatient hospital research unit, challenged with live SMV or placebo by oral administration, and remain in isolation in the unit for at least 4 days following challenge. The study duration is 24 - 36 months. Subjects will be followed post-challenge for safety, reactogenicity, and illness (primary objectives), and secondary or exploratory objectives including infection and immune responses. There will be multiple clinical assessments and collection of blood, emesis, saliva, and stool specimens. The primary objectives are to: 1) evaluate the safety and reactogenicity of the GII.2 Snow Mountain norovirus challenge stock and 2) determine a safe and optimal challenge dose of GII.2 Snow Mountain norovirus to achieve illness in a high proportion (= / > 75%) of subjects. The secondary objectives are to: 1) determine the rate of infection in study participants after norovirus GII.2 challenge, 2) determine the quantity and duration of virus shedding in stool by RT-qPCR, 3) estimate the median time to cessation of shedding, 4) determine the modified Vesikari score as a measure of gastroenteritis severity, 5) determine GII.2 Snow Mountain norovirus-specific Immunoglobulin titers by ELISA before and after the challenge, 6) determine the effect of pre-existing GII.2 Snow Mountain norovirus-specific immunoglobulin in serum and saliva on the rate of infection, 7) determine total and GII.2 Snow Mountain norovirus-specific IgA- and IgG-Secreting Cells in circulation by ELISpot assay, 8) once the optimal challenge dose is determined in secretor positive subjects: investigate the safety and illness rate using that dose of the GII.2 challenge stock in secretor negative subjects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: November 27, 2018
• Est. primary completion date: November 27, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 49 Years

Eligibility

Inclusion Criteria:

1. Subject able to provide written informed consent

2. Male or non-pregnant females between the ages of 18 and 49 years, inclusive

3. Women of childbearing potential must be practicing abstinence or using an acceptable method of birth control for at least 30 days prior to enrollment through day 45 after receipt of the challenge virus. Male subjects must agree not to father a child prior to day 45 after receipt of the challenge virus

• A woman is considered of childbearing potential unless post-menopausal (absence of menses for > /= 1 year) or surgically sterilized (tubal ligation, bilateral oophorectomy or hysterectomy)

• Acceptable contraception methods for women include but are not limited to: sexual abstinence from intercourse with men, monogamous relationship with vasectomized partner who has been vasectomized for 6 months or more prior to the subject enrolling in the study, barrier methods such as condoms or diaphragms with spermicide or foam, effective devices (IUDs, NuvaRing) or licensed hormonal products such as implants, injectables or oral contraceptives

4. For women of childbearing potential, must have a negative serum or urine pregnancy test at screening and negative urine pregnancy test within 24 hours prior to challenge

5. Are in good general health, as determined by the study investigator within 60 days of challenge

6. Demonstrate knowledge and comprehension of the study by scoring >/= 70 percent on a quiz of the study protocol and policies

7. Willing and able to participate in all study visits, including an inpatient stay of at least 96 hours

8. Demonstrated to be H type I secretor positive for HBGA binding by assay of saliva (this applies to all cohorts except the SN cohort, which will include secretor negative subjects only)

Exclusion Criteria:

1. Have household contact with or have daily contact with children under 2 years of age or persons older than 70 years of age

2. Have expected occupational or social contact with immunocompromised individuals in the 8 weeks after challenge, including persons with HIV infection or active cancer, children <2 years of age, pregnant women or persons who are immunosuppressed (e.g. history of stem cell or organ transplantation). Individuals who provide any child day care services (in-home or non-residential facility) are also excluded

3. Are healthcare workers with patient contact in the 8 weeks after challenge

4. Are food service workers expected to prepare/handle food in the 8 weeks after challenge

5. Plan to be living in a confined environment (e.g. ship, camp, or dormitory) within 8 weeks after receiving the challenge strain

6. For females, are pregnant or plan to become pregnant at any time between the Screening Visit through 45 days after receipt of the challenge virus

7. Are breastfeeding or plan to breastfeed at any given time throughout the study

8. Have a history of gastroenteritis in the 4 weeks prior to challenge or any history of chronic or recurrent diarrhea or vomiting

9. Have a history of malabsorption or maldigestion disorder (e.g. celiac sprue), major gastrointestinal (GI) surgery, irritable bowel syndrome or any other chronic GI disorders that would interfere with the study, including chronic constipation or increased stool frequency

10. Have moderate or severe illness and/or an oral temperature >/=100.4 degrees F and/or diarrhea or vomiting within seven days prior to challenge

11. Have a pulse rate less than 55 beats per minute (bpm) or greater than 100 bpm. If heart rate is <55 bpm and the investigator determines that this is not clinically significant (e.g., athletes) and heart rate increases > 55 bpm on moderate exercise (two flights of stairs), subject will not be excluded

12. Have a systolic blood pressure less than 90 mmHg or greater than 140 mmHg on two separate measurements (screening and pre-challenge)

13. Have a diastolic blood pressure less than 50 mmHg or greater than 90 mmHg on two separate measurements (screening and pre-challenge)

14. Have long-term use (> /= 2 weeks) of high-dose oral (>/= 20 mg per day prednisone or equivalent) or parenteral glucocorticoids, or high-dose inhaled steroids for greater than 7 days in the last 6 months

15. Have an autoimmune, inflammatory, vasculitic or rheumatic disease, including but not limited to systemic lupus erythematosus, polymyalgia rheumatic, rheumatoid arthritis or scleroderma

16. Have HIV, hepatitis B, hepatitis C infection or untreated latent syphilis

17. Have a seizure disorder

18. Have an active malignancy, history of malignancy (excluding nonmelanotic skin cancer in remission without treatment for more than 5 years) or current use of immunosuppressive or cytotoxic therapy

19. Have positive fecal culture for E. coli O157:H7, Salmonella, Campylobacter, Yersinia, or Shigella, evidence of norovirus in the stool by RT-qPCR or pathogenic ova and parasites detected on microscopic examination at screening

20. Have abnormal screening laboratory test results per laboratory reported normal values for white blood cells (WBCs), hemoglobin (Hgb), platelets, absolute neutrophil count (ANC), elevated total bilirubin, potassium, sodium and hemoglobin A1c (HbA1c) and urine protein

21. Have a serum creatinine greater than 1.1 x ULN

22. Have an ALT (SGPT) greater than 1.1 x ULN

23. Have a chronic condition that the study physician feels would pose a threat to participating subjects, including, but not limited to solid organ or stem cell transplantation, diabetes, clinically significant history of immunosuppressive illness, gall bladder disease, heart disease, lung disease, pancreatic disease, renal disease or neurological disease 24. Have abnormal findings on screening electrocardiogram deemed clinically significant by study physician

25. Have ongoing drug abuse/dependence (including alcohol), or a history of these issues within 5 years of enrollment 26. Have a positive urine test for opiates 27. Have any medical, psychiatric, occupational, or behavioral problems that make it unlikely for the subject to comply with the protocol as determined by the investigator 28. Are unwilling to comply with study procedures including abstaining from smoking for the duration of the inpatient portion of the study 29. Have participated in a previous NoV challenge study or NoV vaccine study 30. Have received experimental products within 30 days before study entry or plan to receive experimental products at any time during the study 31. Plans to enroll in another clinical trial that could interfere with safety assessment of the investigational product at any time during the study period, including study interventions such as drugs, biologics or devices 32. Plan to donate blood during the course of the study

33. Have received a live vaccine within 30 days before study entry or plan to receive a live vaccine prior to Day 30 of the study 34. Have received an inactivated vaccine within 14 days before study entry or plan to receive an inactivated vaccine prior to Day 14 of the study 35. Have received parenteral immunoglobulin or blood products within 3 months of the study start, or plan to receive parenteral immunoglobulin or blood products within 3 months after receiving the study agent 36. Use of antibiotics within 7 days prior to entry into the inpatient facility 37. Use of any H2 receptor antagonists (e.g., Tagamet, Zantac, and Pepcid), proton pump inhibitors (e.g., Prilosec, Protonix, and Prevacid), or prescription acid suppression medication or over-the-counter (OTC) antacids in the 72 hours prior to NoV challenge 38. Use of prescription and OTC medications containing acetaminophen, aspirin, ibuprofen, and other non-steroidal anti-inflammatory drugs within 48 hours prior to NoV challenge 39. Regular use of laxatives or anti-motility agents 40. Have a history of allergy to sodium bicarbonate 40. Have a history of allergy to sodium bicarbonate

Related Conditions & MeSH terms

• Gastroenteritis
• Gastroenteritis Norovirus

Intervention

Biological:
• Norovirus GII.2 Challenge
GII.2 Snow Mountain Norovirus Filtrate. Cohort 1: 1.2x10^4 Genome Equivalent Copies (GEC) oral dose on Day 1. Cohort 2: either 1.2 x 10^2 GEC or 1.2 x10^6 GEC oral dose on Day 1, depending on the results of prior Cohort 1. Cohort 3: either 1GEC, 1.2 x 10^1 GEC, 1.2 x 10^2 GEC, 1.2 x 10^3 GEC, 1.2 x 10^5 GEC, or 1.2 x 10^6 GEC, or 1.2 GEC x 10^7 oral dose on Day 1, depending on the percentage of subjects with illness from Cohorts 1 and 2. Cohort 4: optimal dose of GEC as determined by the results of cohorts 1-3

Other:
• Placebo
Placebo: 80 ml of sterile water for oral administration

Locations

Country	Name	City	State
United States	Emory Vaccine Center - The Hope Clinic	Decatur	Georgia

Sponsors (1)

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

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Infectious Dose-50 based on infection rate after challenge with various doses		Day 2 to Day 5
Primary	Number of serious adverse events related to virus challenge		Day 1 to Day 180
Primary	Number of subjects experiencing any mild reactogenicity outcomes		Day 1 to Day 10
Primary	Number of subjects experiencing any moderate reactogenicity outcomes		Day 1 to Day 10
Primary	Number of subjects experiencing any severe reactogenicity outcomes		Day 1 to Day 10
Primary	Number of subjects experiencing Grade 3 adverse events		Day 1 to Day 30
Primary	Proportion of subjects with GII.2 Snow Mountain norovirus-associated illness following GII.2 challenge		Day 1 to Day 5
Secondary	Duration of diarrhea related to the challenge strain		Day 1 to Day 5
Secondary	Duration of virus shedding in PCR-positive stool for each challenge dose		Day -60 to Day 75
Secondary	Duration of vomiting related to the challenge strain		Day 1 to Day 5
Secondary	Levels of pre-existing serum blockage IgG prior to challenge		Inpatient Admission
Secondary	Levels of pre-existing serum IgA prior to challenge		Inpatient Admission
Secondary	Levels of pre-existing serum IgG prior to challenge		Inpatient Admission
Secondary	Levels of pre-existing serum salivary IgA prior to challenge		Inpatient Admission
Secondary	Magnitude of virus shedding in PCR-positive stools, reported as GEC/ml		Day -60 to Day 75
Secondary	Proportion of subjects excreting challenge virus in stool		Day 1 to Day 30
Secondary	Proportion of subjects showing a >/= 4 fold rise in virus-specific serum IgG		Day 1 to Day 30
Secondary	Proportion of subjects with =/> 4 fold rise in virus-specific salivary IgA		Day 1 to Day 45
Secondary	Proportion of subjects with =/> 4 fold rise in virus-specific serum blockage IgG		Day 1 to Day 45
Secondary	Proportion of subjects with =/> 4 fold rise in virus-specific serum IgG		Day 1 to Day 45
Secondary	Proportion of subjects with >/= 4 fold rise in virus-specific serum IgA		Day 1 to Day 45
Secondary	Proportion of subjects with norovirus specific IgA-ASC/10^6 PBMC (freshly isolated PBMCs)		Day 1 to Day 45
Secondary	Proportion of subjects with norovirus specific IgG-ASC/10^6 PBMC (freshly isolated PBMCs)		Day 1 to Day 45
Secondary	Severity of diarrhea related to the challenge strain, determined using the Vesikari Score		Day 1 to Day 5
Secondary	Severity of vomiting related to the challenge strain, determined using the Vesikari Score		Day 1 to Day 5