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Safety, Tolerability, and Pharmacokinetics of SAB-301 in Healthy Adults

A Phase 1, Randomized Double-Blind, Placebo-Controlled, Single Ascending Dose Safety, Tolerability, and Pharmacokinetics Study of SAB-301 in Healthy Adults

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02788188
Enrollment
38
Registered
2016-06-02
Start date
2016-05-28
Completion date
2018-04-30
Last updated
2018-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Middle East Respiratory Syndrome Coronavirus

Keywords

First in Human, Middle East Respiratory Syndrome (MERS), Tc Bovine-Derived, Transchromosomic Cattle

Brief summary

Background: Middle East Respiratory Syndrome (MERS) is a newly discovered contagious and sometimes fatal respiratory virus. People often get MERS through close contact with an infected person. Scientists are worried that MERS may spread and cause more infections. There are no vaccines or treatments for MERS right now. Researchers think a new therapy called SAB-301 may be able to help. Antibodies are proteins the body makes to attack viruses. SAB-301 is made of antibodies made in cows to fight MERS. The antibodies are collected from plasma, the liquid part of cow blood. Objective: To evaluate the safety and tolerability of SAB-301 in healthy adults. Eligibility: Healthy people ages 18 60 who: Do not have chronic medical problems Do not take any medications (exceptions are acetaminophen, ibuprofen, vitamins, seasonal allergy meds and oral contraception) Do not have allergies to beef products Agree to use two forms of contraception while on study (both men and women) Design: Participants will be screened with: Medical history Physical examination Blood and urine tests Participants will have a return visit. They will have a physical exam and blood tests. They will be randomly assigned to receive either SAB-301 or a placebo which is given by infusion through an arm vein over 1 3 hours. They will be monitored at the clinic for 6 hours after the infusion. They will have additional blood draws. Participants will have 2-hour visits 1, 3, 7, 21, 42, and 90 days after the infusion. At each visit they will be evaluated and have blood and urine tests.

Detailed description

The administration of convalescent plasma or hyperimmune immunoglobulin is often used for treatment of emerging infectious diseases. However, production of large quantities of anti-pathogen human plasma and/or immunoglobulin with high affinity and avidity antibodies currently requires donations by convalescent humans, a process that can limit availability for a number of reasons. One novel alternative source is transchromosomic (Tc) cattle that produce fully human polyclonal IgG (hIgG) de novo and mount a robust antibody immune response after vaccination. This study will evaluate the safety, tolerability, and immunogenicity of SAB-301, a fully human polyclonal anti-MERS IgG collected from transchromosomic cattle. Beginning with a low single-dose, subjects are randomized to receive either SAB-301 or a normal saline control, and evaluated on Study Days 1, 3, 7, 21, 42, and 90. The safety and tolerability is evaluated using symptoms, clinical laboratory tests, pharmacokinetics, and immunogenicity assays. Utilizing a series of stopping rules and a medical monitor, the dose will be escalated as safety and tolerability are established.

Interventions

BIOLOGICALSAB-301

SAB-301 is a purified human immune globulin G (hIgG) polyclonal antibody designed to specifically bind to the MERS-CoV spike (S) protein, a component of the virion membrane that is responsible for binding of the virus to the host cell. The hIgG is purified from the plasma of immunized transchromosomic (Tc) bovines that were immunized with a recombinant spike protein produced in insect cells. SAB-301 is purified hIgG in a sterile liquid formulated in 10 mM glutamic acid monosodium salt, 262 mM D-sorbitol, 0.05 mg/mL Tween 80, pH 5.5. The drug product will be administered intravenously and will be diluted in saline per the clinical protocol.

OTHERNormal (9%) Saline

Normal (0.9%) saline in approximately the same volume as each cohort in the experimental drug arm.

Sponsors

Naval Medical Research Center
CollaboratorFED
SAb Biotherapeutics, Inc.
CollaboratorINDUSTRY
National Institute of Allergy and Infectious Diseases (NIAID)
Lead SponsorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* INCLUSION CRITERIA: 1. Age greater than or equal to 18 years and less than or equal to 60 years 2. Body mass index (BMI) of 19-32 kg/m(2) 3. Estimated glomerular filtration rate greater than or equal to 70 mL/min at screening, calculated using the CKD-EPI formula 4. Subjects must agree to: * Not take any prescription or OTC medications with the exception of acetaminophen, ibuprofen, vitamins, seasonal allergy medications, and/or contraceptive medications for a period 7 days prior to study drug administration (i.e., Day 0) 5\. One of the following in order to avoid pregnancy: * Females who are able to become pregnant (i.e., are not postmenopausal, have not undergone surgical sterilization, and are sexually active with men) must agree to use at least 2 effective forms of contraception from the date of the subject s signing of the informed consent form through 60 days after the last dose of study drug. At least one of the methods of contraception should be a barrier method. * Males who have not undergone surgical sterilization and are sexually active with women must agree to use condoms plus have a partner use at least one additional effective form of contraception from the date of the subject s signing of the informed consent form through 60 days after the last dose of study drug.

Exclusion criteria

1. Any history of allergy, anaphylaxis, or severe reaction to beef products (including milk and gelatin) 2. Any history of allergy, anaphylaxis, or severe reaction to IGIV or human blood products 3. Any chronic medical problem that requires daily oral medications (except Tylenol, ibuprofen, oral contraceptives, vitamins, and seasonal allergy medications). 4. History of cardiovascular disease, cardiomyopathy, heart failure, or unexplained syncope 5. Subjects that have had confirmed MERS 6. Women who are breast-feeding 7. Positive urine or serum pregnancy test 8. Abnormal chemistry panel -defined as any clinically significant baseline Grade 1 or greater toxicity, or any Grade 3 or greater toxicity (regardless of clinical significance) by the toxicity table --evaluating only sodium (Na), potassium (K), serum bicarbonate (total CO2), blood urea nitrogen (BUN), creatinine, glucose, asp (ALT), aspartate aminotransferase (AST), total bilirubin, lactate dehydrogenase (LDH), and estimated glomerular filtration rate (GFR) by the CKD-EPI equation. 9. Abnormal complete blood count (CBC) -defined as any clinically significant baseline Grade 1 or greater toxicity, or any Grade 3 or greater toxicity (regardless of clinical significance) by the toxicity table--evaluating only the WBC (to include absolute neutrophil, lymphocyte, and eosinophil counts), hemoglobin, hematocrit, and platelets. 10. Abnormal urinalysis -defined as any clinically significant baseline Grade 1 or greater toxicity--evaluating only protein, and RBCs 11. Positive rheumatoid factor 12. IgA deficiency (defined as IgA \< 7 mg/dL) 13. Participation in another research study with receipt of any investigational drug within 5 half-lives or 30 days, whichever is longer, prior to study drug administration (i.e., Day 0) and until completion of the study 14. Participation in any other research study for 30 days after study drug administration 15. Receipt of blood products within 2 months prior to study drug administration (i.e. Day 0) 16. Receipt of any vaccination within 30 days prior to study drug administration (i.e. Day 0) 17. Any acute or chronic condition that, in the opinion of the Investigator, would limit the subject s ability to complete and/or participate in this clinical study

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Having Adverse Events90 daysNumber of participants who experienced an adverse event

Countries

United States

Participant flow

Participants by arm

ArmCount
Cohort 1: 1.0mg/kg
SAB-301 1 mg/kg IV single infusion
2
Cohort 2: 2.5mg/kg
SAB-301 2.5 mg/kg IV single infusion
2
Cohort 3: 5mg/kg
SAB-301 5 mg/kg IV single infusion
4
Cohort 4: 10mg/kg
SAB-301 10 mg/kg IV single infusion
4
Cohort 5: 20mg/kg
SAB-301 20 mg/kg IV single infusion
8
Cohort 6: 50mg/kg
SAB-301 50 mg/kg IV single infusion
8
Placebo
Normal Saline IV single infusion
10
Total38

Baseline characteristics

CharacteristicCohort 1: 1.0mg/kgCohort 2: 2.5mg/kgCohort 3: 5mg/kgCohort 4: 10mg/kgCohort 5: 20mg/kgCohort 6: 50mg/kgPlaceboTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
2 Participants2 Participants4 Participants4 Participants8 Participants8 Participants10 Participants38 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants1 Participants1 Participants1 Participants0 Participants3 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
2 Participants2 Participants4 Participants3 Participants7 Participants7 Participants10 Participants35 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants0 Participants0 Participants1 Participants2 Participants3 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants2 Participants0 Participants2 Participants0 Participants2 Participants6 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants1 Participants0 Participants0 Participants1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants0 Participants2 Participants2 Participants
Race (NIH/OMB)
White
2 Participants2 Participants2 Participants4 Participants5 Participants7 Participants4 Participants26 Participants
Sex: Female, Male
Female
0 Participants2 Participants3 Participants3 Participants4 Participants3 Participants3 Participants18 Participants
Sex: Female, Male
Male
2 Participants0 Participants1 Participants1 Participants4 Participants5 Participants7 Participants20 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
EG004
affected / at risk
EG005
affected / at risk
EG006
affected / at risk
deaths
Total, all-cause mortality
0 / 20 / 20 / 40 / 40 / 80 / 80 / 10
other
Total, other adverse events
1 / 22 / 22 / 44 / 47 / 88 / 810 / 10
serious
Total, serious adverse events
0 / 20 / 20 / 40 / 40 / 81 / 80 / 10

Outcome results

Primary

Number of Participants Having Adverse Events

Number of participants who experienced an adverse event

Time frame: 90 days

Population: Number of participants who completed both treatment and placebo

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Cohort 1: 1.0mg/kgNumber of Participants Having Adverse Events1 Participants
Cohort 2: 2.5mg/kgNumber of Participants Having Adverse Events2 Participants
Cohort 3: 5mg/kgNumber of Participants Having Adverse Events2 Participants
Cohort 4: 10mg/kgNumber of Participants Having Adverse Events4 Participants
Cohort 5: 20mg/kgNumber of Participants Having Adverse Events7 Participants
Cohort 6: 50mg/kgNumber of Participants Having Adverse Events8 Participants
PlaceboNumber of Participants Having Adverse Events10 Participants

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026