Ph1 Study of Valortim and Ciprofloxacin in Humans

NCT ID: NCT00964561

Last Updated: 2010-08-10

Basic Information

• Recruitment Status: SUSPENDED
• Clinical Phase: PHASE1
• Total Enrollment: 26 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-08-31
• Study Completion Date: 2010-07-31

Brief Summary

The purpose of this study is to evaluate the safety and tolerability of short-term dosing of IV ciprofloxacin when administered concomitantly with IV Valortim in healthy normal human subjects.

Detailed Description

Valortim (MDX-1303) is a fully human monoclonal antibody (hmAb) with a high affinity for B. anthracis protective antigen (PA). Valortim is designed to target PA, which is one of three plasmid-encoded proteins that together form the toxins released by B. anthracis. Individually, these proteins (protective antigen (PA), lethal factor (LF) and edema factor (EF)) are inactive. Toxic effects require the transport of LF and EF into the host cell, mediated by the activity of PA. Valortim binds to PA and interferes with the activity of the toxins. Based on both non-clinical and clinical data, Valortim may have utility for the pre- and post-exposure prophylaxis of individuals exposed to, or at risk of exposure to, B. anthracis and for the treatment of individuals displaying signs or symptoms of inhalational anthrax. Because the treatment of inhalational anthrax includes the use of antibiotics such as fluoroquinolones, it is necessary to demonstrate that there are no adverse interactions between newer therapeutic interventions and these medications. The purpose of this study is to assess the safety and pharmacokinetics of ciprofloxacin (a commonly used fluoroquinolone for both treatment and post-exposure prophylaxis of anthrax) and Valortim following co-administration, as well as the safety and tolerability of these medications when administered concomitantly. These data are intended to support the use of Valortim as a treatment for inhalational anthrax.

Conditions

Anthrax

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Ciprofloxacin and Valortim

First two subjects to receive treatment arm of Ciprofloxacin and Valortim. Total of sixteen volunteers to be randomized to receive Ciprofloxacin and Valortim.

Group Type: EXPERIMENTAL

Ciprofloxacin and Valortim

Intervention Type: DRUG

Days 1-3 400mg IV Ciprofloxacin BID over 60 minutes. Day 4 20mg/kg Valortim IV over 60 minutes.

Placebo Antibiotic and Valortim

Randomized such that four subjects to receive Placebo Antibiotic and Valortim.

Group Type: EXPERIMENTAL

Placebo Antibiotic and Valortim

Intervention Type: DRUG

Days 1-3 20mg/kg IV Normal Saline BID over 60 minutes. Day 4 20mg/kg Valortim IV over 60 minutes.

Placebo Antibiotic and Placebo Valortim

Randomized such that 4 subjects to receive Placebo Antibiotic and Placebo Valortim.

Group Type: EXPERIMENTAL

Placebo Antibiotic and Placebo Valortim

Intervention Type: OTHER

Days 1-3 200mL IV Normal Saline for Placebo Antibiotic over 60 minutes. Day 4 200mL IV Normal Saline for Placebo Valortim over 60 minutes.

Interventions

Ciprofloxacin and Valortim

Days 1-3 400mg IV Ciprofloxacin BID over 60 minutes. Day 4 20mg/kg Valortim IV over 60 minutes.

Intervention Type: DRUG

Placebo Antibiotic and Valortim

Days 1-3 20mg/kg IV Normal Saline BID over 60 minutes. Day 4 20mg/kg Valortim IV over 60 minutes.

Intervention Type: DRUG

Placebo Antibiotic and Placebo Valortim

Days 1-3 200mL IV Normal Saline for Placebo Antibiotic over 60 minutes. Day 4 200mL IV Normal Saline for Placebo Valortim over 60 minutes.

Intervention Type: OTHER

Other Intervention Names

MDX-1303; MDX-1303; Saline

Eligibility Criteria

Inclusion Criteria

1. Healthy Normal male or female subjects 18 to 59 years of age on Day -1 of the study

2. Subject must have read, understood, and provided written informed consent after the nature of the study has been fully explained and must be willing to comply with all study requirements and procedures

3. In the opinion of the Investigator, subjects should be in generally good health, based upon prestudy medical history, physical examination, ECG and laboratory tests

4. Laboratory screening values (i.e., hematology, clinical chemistries and urinalysis tests) must be within study-defined ranges

5. No detectable antibody to B. anthracis Protective Antigen (PA-IgG) as measured by ELISA testing at study Screening

6. Women of childbearing potential may be enrolled if one of the following criteria applies:

1. Must be using an effective form of contraception (e.g., oral contraceptives, vaginal ring, IUD, injected or implanted hormonal contraception, double barrier method of condom and spermicide, diaphragm with spermicide or sponge with spermicide) for at least one month prior to study entry, must have maintained a normal menstrual pattern for the three months prior to study entry and have a negative pregnancy test at the time of admission to the unit. Women must be willing to continue this contraception throughout the course of the study.

2. Is sexually abstinent

3. Is monogamous with a vasectomized partner (> 3 months prior)

4. Is postmenopausal (i.e., no cycle for at least the previous 12 months, is of menopausal age (> 45 years) and has a negative urine pregnancy test prior to enrollment into the study and a negative serum pregnancy test on Day -1)

5. Is surgically sterilized (confirmed by medical record review)

6. Has had a total hysterectomy a minimum of 3 months prior to dosing on Day 1 (confirmed by medical record review)

7. Sexually active male subjects may be enrolled if one of the following criteria applies:

1. Has had a vasectomy (> 3 months prior to study entry, confirmed by medical record review)

2. Using condoms and whose partner is using an acceptable form of contraception (IUD, oral contraceptives, birth control patch or vaginal ring, injectable or implanted contraceptives, or tubal ligation [surgical sterilization]) for the duration of the study

3. Is sexually abstinent

8. Female subjects must have a negative urine pregnancy test at study Screening and a negative serum pregnancy test on admission to the Phase I unit at Day -1

9. Female subject who are using injectable, transdermal, vaginal ring, oral contraceptives, or an IUD must agree to also use a barrier method (i.e. male condom, female condom, diaphragm, cervical cap) for the duration of their participation in the study.

10. Agreement to not receive any vaccinations from Day -1 through to 31 days post Valortim dosing. Vaccination against B. anthracis is prohibited during the study

11. Body Mass Index (BMI) ≥ 19 and ≤ 30

12. Abstinence from alcohol for 24 hours prior to study drug administration until discharge from the Phase I unit

Exclusion Criteria

1. Prior known or suspected exposure to B. anthracis

2. Prior vaccination for B. anthracis

3. Any participants in the original FTIH study of Valortim.

4. History of drug or alcohol abuse i.e. having been treated either in an in-patient or out-patient facility within 12 months of study Screening

5. Positive drug result and/or positive alcohol result at time of study Screening or at Day -1

6. Smoke more than 10 cigarettes per day for the last 6 months

7. Treatment with an investigational agent within 30 days or 5 half-lives (whichever is longer) of study Screening

8. Use of systemic immunosuppressive agents within 12 months of study Screening. Individuals who have received prednisone or its equivalent in doses of less than 20 mg/day for 14 days or less, as long as it occurred more than 1 month prior to them entering the study and as long as there is no clinical or laboratory evidence of immunosuppression, may be considered for enrollment

9. Use of NSAIDs within 24 hours prior to dosing

10. History of asthma requiring any use of inhaled or oral medication within the previous 5 years

11. History of renal impairment

12. History of central nervous system reactivity to any quinolone

13. Any factor known to increase the risk of tendinitis or tendon rupture when taking a fluoroquinolone, including age older than 59 years; organ transplantation; use of systemic steroids (see number 7)

14. Clinically significant medical or psychiatric condition that, in the opinion of the Investigator, may impair study participation to include ongoing recent illness, new medications prescribed in the previous 6 weeks or use of immunosuppressive agents

15. Electrocardiogram with evidence of clinically significant conduction abnormalities or active ischemia (as determined by the Principal Investigator) at the time of study screening

16. Donation of one or more pints of blood 30 days prior to study Screening visit or donation prior to completion of Day 31 of the study

17. Donation of plasma within 14 days prior to study Screening visit or donation prior to completion of Day 31 of the study

18. Vaccinations within 30 days prior to Day -1 through to 31 days post Valortim dosing on Day 3

19. Prior known serum positivity for human immunodeficiency virus (HIV) antibodies, hepatitis B (surface antigen) or hepatitis C as determined at study Screening

20. Prior known allergy or allergic reaction to ciprofloxacin or any of the group of antibiotics known as quinolones

21. Diagnosis of photosensitivity, including, but not limited to, a history of phototoxic and/or photoallergic reactions to medications

22. Current treatment with, or use of, theophylline, methylxanthines, tizanidine, phenytoin, sulfonylurea glyburide, warfarin, probenecid, methotrexate, metoclopramide, corticosteroids and non-steroidal anti-inflammatory drugs

23. History of seizures, excluding pediatric febrile seizures

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institutes of Health (NIH)

NIH

Sponsor Role: collaborator

Medarex

INDUSTRY

Sponsor Role: collaborator

Quintiles, Inc.

INDUSTRY

Sponsor Role: collaborator

Department of Health and Human Services

FED

Sponsor Role: collaborator

PharmAthene, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

PharmAthene, Inc.

Principal Investigators

Ralph A. Schutz, M.D.

Role: PRINCIPAL_INVESTIGATOR

Quintiles, Inc.

Locations

Quintiles Phase I Services

Overland Park, Kansas, United States

Countries

United States

Related Links

http://www.studyforchange.com

Go to this website for more information about this study.

Other Identifiers

NIAID #08-0053

Identifier Type: -

Identifier Source: secondary_id

#0036-08-05

Identifier Type: -

Identifier Source: org_study_id