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Completed

NCT Number: NCT00614029

A Study to Evaluate the Pharmacokinetics and Bioequivalence of Sumatriptan Delivered Via the Intraject System

A study to evaluate the pharmacokinetics and bioequivalence of sumatriptan delivered by the Intraject system.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Covance, Inc

Dallas, Texas, 75247, United States

About this study

A single center, randomized, single-dose, open-label, partial-block, four-period, four-way crossover study in 54 healthy adult subjects to evaluate the pharmacokinetics and bioequivalence of sumatriptan delivered by the Intraject system compared to IMITREX STATdose at three injection sites (abdomen, thigh, and arm.)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy subjects
  • Negative serum pregnancy test
  • Female subjects of child-bearing potential must agree to use acceptable birth control 3 weeks prior to and 2 weeks after study dosing.
  • Body Mass Index (BMI) and sufficient subcutaneous thickness, in the opinion of the investigator, for an injection into the abdomen, arm and thigh
  • Non-tobacco user
  • Adequate venous access in the left or right arm to allow collection of a number of blood samples
  • Fluent in the English language
  • Provide written informed consent to participate in the study and be willing to comply with the study procedures

Exclusion criteria

  • History within the previous 2 years of drug or alcohol dependence
  • Evidence of clinically relevant oral, cardiovascular, hematologic, gastrointestinal, hepatic, renal, endocrine, pulmonary, neurologic, psychiatric or skin disorder
  • History of epilepsy or other neurologic disease
  • History of coronary disease, peripheral vascular disease, cerebrovascular accident, transient ischemic attack, uncontrolled hypertension, or signs/symptoms of ischemic heart disease
  • History of allergy, anaphylaxis, or hypersensitivity to sumatriptan or similar drugs including sulphonamides
  • History of scleroderma or any skin condition that may adversely affect the injection or absorption of subcutaneously administered medications
  • Tattoos or birthmarks in the lateral thigh, abdominal area or arm (deltoid) that are large enough to restrict injection site selection and/or evaluation
  • Positive screening test for HIV antibodies, Hepatitis B surface antigen, or Hepatitis C antibody
  • Positive results on illicit drug test at Screening or at Check-in
  • Use of any prescription medication

Treatment and study plan

Sumatriptan (via Intraject System)

Device

0.5 mL of solution with 6 mg of sumatriptan (base) as the succinate salt

Primary outcomes

  1. The area under the plasma concentration-time curve, maximal plasma concentration, time to maximal concentration, terminal elimination half-life, and apparent terminal elimination rate constant of sumatriptan will be determined at each of 3 sites

    Time frame: one week

Sponsors and collaborators

Lead sponsor

Zogenix, Inc.

Industry

Registry information

Official study title

A Randomized, Open-Label, Single-Dose, Four-way Crossover Study to Evaluate the Pharmacokinetics and Bioequivalence of Sumatriptan Delivered Via the Intraject System Versus IMITREX STATdose at Three Injection Sites in Healthy Adults

Important dates

Study start
2006
Primary completion
2006
First posted
Feb 13, 2008
Registry last updated
Nov 10, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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