A Pharmacokinetic Study of MABp1 in Healthy Volunteers
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/2/2017 |
| Start Date: | February 15, 2017 |
| End Date: | March 31, 2017 |
A Phase I Pharmacokinetic Study of MABp1 in Healthy Volunteers
This is an open label study of MABp1 in six healthy volunteers. Participants will receive a
single infusion of MABp1 at the 7.5 mg/kg IV dose. Participants will undergo blood sampling
for pK analysis at 15 times points during the course of 2 weeks (pre-infusion, 0.5 hr, 1 hr,
1.5 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 12 hr, 24 hr, 48 hr, 96 hr, 192 hr, and 336 hr). In
addition to pharmacokinetic data, participants will be monitored for the development of
treatment emergent adverse events.
single infusion of MABp1 at the 7.5 mg/kg IV dose. Participants will undergo blood sampling
for pK analysis at 15 times points during the course of 2 weeks (pre-infusion, 0.5 hr, 1 hr,
1.5 hr, 2 hr, 3 hr, 4 hr, 5 hr, 6 hr, 12 hr, 24 hr, 48 hr, 96 hr, 192 hr, and 336 hr). In
addition to pharmacokinetic data, participants will be monitored for the development of
treatment emergent adverse events.
Inclusion Criteria:
1. Age: ≥18
2. Adequate bone marrow function as defined as:
- absolute neutrophil count (neutrophil and bands) of ≥ 1,500/mm3 (≥ 1.5 x 109/L)
- platelet count > 150,000/mm3
- hemoglobin of ≥ 10 g/dL
3. Adequate renal function, defined by serum creatinine ≤ 1.5 x lab ULN.
4. Adequate hepatic function defined as:
- total bilirubin ≤ 1.5 times lab ULN.
- alanine aminotransferase (ALT) ≤ 2.0 times lab ULN.
5. For WOCBP, a negative pregnancy test at screening. For subjects with reproductive
potential, a willingness to utilize contraception during the study and for at least 3
months after study completion. Sexually active men must use an accepted method of
contraception during the study and for at least 3 months after study completion.
6. Signed and dated Institutional Review Board (IRB) approved informed consent before
any protocol-specific screening procedures are performed.
Exclusion Criteria:
1. Treatment with any biologicals (including intravenous immunoglobulin) or
investigational agents within the last 4 weeks (or 5 half-lives, whichever is
longer).
2. Uncontrolled or significant cardiovascular disease, including:
- A myocardial infarction within the past 6 months.
- Uncontrolled angina within the past 3 months.
- Congestive heart failure within the past 3 months, defined as New York Heart
Association (NYHA) Classes II or higher.
- Uncontrolled hypertension (blood pressure >150 mm Hg systolic and >95 mm Hg
diastolic).
3. Dementia or altered mental status that would prohibit the understanding or rendering
of informed consent.
4. Treatment with immunosuppressant agents, including corticosteroids or cyclosporine
within the last 4 weeks.
5. Serious uncontrolled medical disorders, such as uncontrolled diabetes, active peptic
ulcer disease, recent stroke (within 3 months), ongoing congestive heart failure, and
any other condition, which in the opinion of the investigator, would put the subject
at risk by participation in the protocol.
6. History of severe allergic or anaphylactic reactions to humanized or murine
monoclonal antibodies.
7. Infectious disease:
- CRP >30 mg/L, or infection requiring treatment with antibiotics within 3 weeks
prior to Screening,
- Positive HIV, RPR, Hepatitis C antibody, or IGRA
8. Immunodeficiency by history.
9. Female subjects who are pregnant, planning to become pregnant during the course of
the study, or breast-feeding.
10. Major surgery within 28 days prior to Day 0.
11. WOCBP or men whose sexual partners are WOCBP who are unwilling or unable to use an
acceptable method of contraception for at least 1 month prior to randomization, for
the duration of the study, and for at least 3 months after the last dose of study
medication.
12. History of progressive multifocal leukoencephalopathy or other demyelinating disease.
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