Study of Monoclonal Antibody Cocktail Being Tested for the Prevention of COVID-19

SARS-CoV-2 Clinical Trial

Official title:

A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety, Pharmacokinetics, and Immunogenicity of ADM03820 in Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04592549
• Other study ID #: ADM03820-001
• Status: Completed
• Phase: Phase 1
• Start date: December 4, 2020
• Est. completion date: October 6, 2023

Study information

• Verified date: November 2023
• Source: Ology Bioservices
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase 1, randomized, double-blind, placebo-controlled, dose escalation study to evaluate the safety, pharmacokinetics, and immunogenicity of ADM03820 administered as IM injections in healthy adults for the prevention of COVID-19.

Description:

The primary objective of this study is to assess the safety and tolerability of escalating IM doses of ADM03820 in healthy adults. Secondary objectives include assessing the pharmacokinetic characteristics and immunogenicity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: October 6, 2023
• Est. primary completion date: October 6, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Informed consent understood and signed

2. Healthy male or healthy, non-pregnant, non-lactating female

3. Willingness to comply and be available for all protocol procedures for the duration of the study

4. Between the ages of 18 and 55, inclusive on the day of dosing

5. Body Mass Index (BMI) of =18.5 and =35 kg/m2

6. Female subjects of childbearing potential must have a negative serum pregnancy test at screening and negative urine pregnancy test on Day 1 prior to dosing.

• Note: A woman is considered of childbearing potential unless post-menopausal (> or = 1 year without menses without other known or suspected cause and appropriately elevated FSH) or surgically sterilized via bilateral oophorectomy or hysterectomy

7. Females of childbearing potential and males agree to use acceptable contraception for the duration of the study

• Note: These include progestin implants, intrauterine devices (IUDs), surgical (hysterectomy or tubal ligation; vasectomy) or abstinence. Use of methods such as progestin injectables, combined oral hormonal contraceptives, condoms, and diaphragms will not be acceptable when used alone, but they could be considered, if used in combination with another method (for example, a female using combined oral contraceptives if her male partner is sterile, or if she and her non-sterile male partner use a double-barrier method), after consultation with the Ology Bioservices MM. All males will be required to use a barrier method (condoms) for the duration of the study

8. Screening laboratory tests are within normal ranges or outside the normal ranges and considered not clinically significant by the Principal Investigator

1. If urinalysis by dipstick is abnormal, a complete urinalysis with microscopic evaluation will be performed and the results will supersede the results of the dipstick for blood, glucose, and protein.

2. Menstruating females failing inclusion criteria due to a positive blood on urine test may be retested following cessation of menses.

3. Other laboratory values that are outside the range of eligibility but are thought to be due to an acute condition or collection or laboratory error may be repeated once.

9. The urine drug screen is negative

10. Breathalyzer test or blood/saliva alcohol test is negative and subject agrees to abstain from alcohol consumption for a period of 2 days prior to dosing and 2 days prior to any study visit.

11. Agree to minimize risk of SARS-CoV-2 infection.

Exclusion Criteria:

1. History of chronic medical condition that would either interfere with the accurate assessment of the objectives of the study or increase the risk profile of the subject.

2. Subjects with cardiovascular disease

3. Subjects with diabetes

4. Subjects with pulmonary diseases such as COPD or asthma

5. History of severe allergic reactions of any type to medications, bee stings, food, or environmental factors or hypersensitivity or reaction to immunoglobins.

6. A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 milliseconds)

7. Clinically significant abnormal electrocardiogram at screening.

• Note: Clinically significant abnormal ECG results include but not limited to:

complete left or right bundle branch block; other ventricular conduction block; 2nd degree or 3rd degree atrioventricular (AV) block; sustained ventricular arrhythmia; sustained atrial arrhythmia; two Premature Ventricular Contractions in a row; pattern of ST elevation felt consistent with cardiac ischemia; or any condition deemed clinically significant by a study investigator

• Incomplete right bundle branch block is not exclusionary if there are no abnormal ECG findings and there is no clinical history or evidence on physical examination to indicate cardiac disease.

8. Positive serology results for HIV, HBsAg, or HCV antibodies

9. Febrile illness with temperature =38°C within 7 days of dosing

10. Female subject who is pregnant or breastfeeding

11. Donated blood within 56 days of enrollment

12. Known allergic reactions to any of the study product components present in the formulation or in the processing, as listed in the Investigator Brochure

13. Treatment with another investigational drug within 28 days of dosing

14. Treatment with a monoclonal antibody within 3 months of enrollment

15. Positive serology results for SARS-CoV-2 antibodies (Not applicable for Cohort 5).

16. Positive results from a reverse transcriptase polymerase chain reaction (RT PCR) test for SARS CoV 2

17. Receipt of antibody (e.g. TIG, VZIG, IVIG, IM gamma globulin) or blood transfusion within 6 months or within 5 half-lives of the specific product given

18. Active drug or alcohol use disorder or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements

19. Use of H1 antihistamines or beta-blockers within 5 days of dosing

20. Use of any prohibited medication within 28 days prior to screening or planned use during the study period

• Note: Prohibited medications include immunosuppressives (except Nonsteroidal Anti-Inflammatory Drugs [NSAIDS]); immune modulators; oral corticosteroids (topical/intranasal steroids are acceptable); anti-neoplastic agents

21. Any specific condition that in the judgment of the investigator precludes participation because it could affect subject safety

22. Plans to enroll or is already enrolled in another clinical trial that could interfere with safety assessment of the investigational product at any time during the study period

• Note: Includes trials that have a study intervention such as a drug, biologic, or device

23. Is a study site employee or staff

• Note: Site employees or staff include the PIs and sub-investigators or staff who are supervised by the PI or Sub-Investigators

24. Received an approved COVID-19 vaccine (subjects can receive an approved COVID-19 vaccine after completing their Day 90 visit). For Cohort 5, subjects who received a COVID-19 vaccine within 14 days prior to enrollment are excluded.

Related Conditions & MeSH terms

• SARS-CoV-2

Intervention

Drug:
• ADM03820
ADM03820 is a 1:1 mixture of two human IgG1 non-competitive binding anti-SARS-CoV-2 antibodies

Other:
• Placebo
Placebo

Locations

Country	Name	City	State
United States	ICON Early Phase Services, LLC	San Antonio	Texas
United States	PMG Research of Winston-Salem, LLC	Winston-Salem	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Ology Bioservices	Enabling Biotechnologies (EB)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The number of participants with Serious Adverse Events following administration of ADM03820 to the final visit		540 days
Primary	The number of participants with AEs following administration of ADM03820 to the final visit		540 days
Primary	The number of participants with changes from baseline in physical examination, vital signs and clinical safety laboratory values following administration of ADM03820 to the final visit		540 days
Secondary	The assessment of Peak Plasma Concentration (Cmax) for total antibodies of ADM03820 as measured by enzyme-linked immunosorbent assay (ELISA) methods designed for total monoclonal antibody in the Drug Product (Cohorts 1-2).		365 days
Secondary	The assessment of Tmax for total antibodies of ADM03820 as measured by enzyme-linked immunosorbent assay (ELISA) methods designed for total monoclonal antibody in the Drug Product (Cohorts 1-2).		365 days
Secondary	The assessment of the Area under the plasma concentration (AUC(0-t)) for the total antibodies of ADM03820 as measured by enzyme-linked immunosorbent assay (ELISA) methods designed for total monoclonal antibody in the Drug Product (Cohorts 1-2).		365 days
Secondary	The assessment of Peak Plasma Concentration (Cmax) for each of the monoclonal antibodies of ADM03820 as measured by enzyme-linked immunosorbent assay (ELISA) methods designed for total monoclonal antibody in the Drug Product (Cohorts 3-5).		365 days
Secondary	The assessment of Tmax for each of the monoclonal antibodies of ADM03820 as measured by enzyme-linked immunosorbent assay (ELISA) methods designed for total monoclonal antibody in the Drug Product (Cohorts 3-5).		365 days
Secondary	The assessment of Area under the plasma concentration (AUC(0-t)) for each of the monoclonal antibodies of ADM03820 as measured by enzyme-linked immunosorbent assay (ELISA) methods designed for total monoclonal antibody in the Drug Product (Cohorts 3-5).		365 days
Secondary	To assess the anti-drug antibody levels		365 days
Secondary	The number of participants with SARS-CoV-2 RT-PCR positive symptomatic illness occurring after dosing		365 days
Secondary	The number of participants with SARS-CoV-2 RT-PCR positive severe or critical symptomatic illness occurring after dosing		365 days
Secondary	The number of participants with COVID-19 related Emergency Department visits occurring after dosing		365 days
Secondary	The assessment of Peak Plasma Concentrations (Cmax) for neutralizing antibody concentrations of ADM03820 as measured by microneutralization (MN) methods		180 days
Secondary	The assessment of Tmax for neutralizing antibody concentrations of ADM03820 as measured by microneutralization (MN) methods		180 days
Secondary	The assessment of Area under the plasma concentration (AUC(0-t)) for neutralizing antibody concentrations of ADM03820 as measured by microneutralization (MN) methods		180 days