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Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously

An Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of GAP-134 Administered Intravenously as 6-Day Continuous Infusions to Healthy Subjects

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00783341
Enrollment
25
Registered
2008-10-31
Start date
2008-11-30
Completion date
2009-02-28
Last updated
2009-07-17

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

Conditions

Healthy Subjects

Brief summary

This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of ascending doses of GAP 134 administered as 6-day continuous IV infusions to healthy subjects.

Interventions

DRUGplacebo

Sponsors

Wyeth is now a wholly owned subsidiary of Pfizer
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion 1. Men or women of non childbearing potential (WONCBP) aged 18 to 50 years inclusive at screening. 2. Body mass index (BMI) in the range of 18.0 to 30.0 kg/m2 and body weight ≥50 kg. 3. Healthy as determined by the investigator on the basis of medical history, physical examination, clinical laboratory test results, vital sign measurements, and 12-lead electrocardiogram (ECG). 4. Serum creatinine level must be less than 1.30 mg/dL. (Normal range: 0.44 to 1.24 mg/dL.) 5. Nonsmoker or smoker of fewer than 10 cigarettes per day as determined by history. Must be able to abstain from smoking during the inpatient stay. Exclusion 1. Presence or history of any disorder that may prevent the successful completion of the study. 2. Any significant cardiovascular, hepatic, renal, respiratory, gastrointestinal, endocrine, immunologic, dermatologic, hematologic, neurologic, or psychiatric disease. 3. Any surgical or medical condition that may interfere with the distribution, metabolism, or excretion of the test article. 4. Acute disease state (eg, nausea, vomiting, fever, or diarrhea) within 7 days before study day 1. 5. Any history of clinically important cardiac arrhythmias. 6. Familial history of long QT syndrome or unexpected cardiac death. 7. History of drug abuse within 1 year before study day 1. 8. History of alcoholism within 1 year before study day 1.

Design outcomes

Primary

MeasureTime frame
Safety as determined by reported adverse events, laboratory test results, and ECGs3 weeks

Secondary

MeasureTime frame
Pharmacokinetic parameters9 days

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026