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A Study of the Effects of Increasing Doses of a Drug for the Treatment of Nail Fungus

This study has been completed.
Sponsor:
Collaborator:
GlaxoSmithKline
Information provided by (Responsible Party):
GlaxoSmithKline ( Stiefel, a GSK Company )
ClinicalTrials.gov Identifier:
NCT01014962
First received: November 16, 2009
Last updated: June 21, 2012
Last verified: June 2012
  Purpose

The purpose of this study is to determine an upper dose of albaconzole to be administered in a Thorough QTc study.


Condition Intervention Phase
Onychomycosis
Drug: Albaconozole
Drug: Placebo
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Basic Science
Official Title: A Randomized, Double-Blind, Multiple-Dose, Placebo-Controlled Tolerability And Pharmacokinetic Study Of Escalating Doses Of Albaconazole In Healthy Subjects

Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Plasma concentrations of albaconazole in subjects [ Time Frame: During 5 days of dosing and 15 days follow-up ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Electrocardiogram (ECG) QTc values [ Time Frame: During 5 days of dosing and 15 days follow-up ] [ Designated as safety issue: Yes ]

Enrollment: 24
Study Start Date: August 2009
Study Completion Date: January 2010
Primary Completion Date: January 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Albaconazole 400 mg cohort 1
Albaconazole 400 mg
Drug: Albaconozole
Albaconozole 400 mg oral once daily for 5 days
Placebo Comparator: Placebo cohort 1
Placebo once daily
Drug: Placebo
Placebo oral once daily for 5 days
Experimental: Albaconozole 400 mg cohort 2
Albaconozole 400 mg every 12 hours
Drug: Albaconozole
Albaconozole 400 mg every 12 hours for 5 days
Placebo Comparator: Placebo cohort 2
Placebo every 12 hours
Drug: Placebo
Placebo oral every 12 hours for 5 days
Experimental: Albaconozole 400 mg cohort 3
Albaconozole 400 mg every 8 hours
Drug: Albaconozole
Albaconozole 400 mg oral every 8 hours for 5 days
Placebo Comparator: Placebo cohort 3
Placebo every 8 hours
Drug: Placebo
Placebo oral every 8 hours for 5 days

Detailed Description:

This study aims to evaluate the safety and tolerability of 5 days of albaconazole dosing at levels that exceed both the projected therapeutic dose and the projected therapeutic frequency, in order to identify an upper dose for administration in a TQTc study. It also aims to assess the pharmacokinetics of multiple escalating doses of albaconazole, and to assess the effects of multiple and sustained dosing of high doses of albaconazole on ECG parameters.

  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Male or female subjects age 18 to 45
  • A body mass index (BMI) between 18.5 and 30 kg/m2.
  • Good physical and mental health.
  • Vital signs .within the acceptable range.
  • Electrocardiogram (12-lead) after at least 5 minutes in supine position considered as normal or with findings considered as not clinically significant by the investigator. .
  • Non-smoker for at least 6 months before screening.
  • Subject has screening laboratory parameters within the normal ranges unless considered to be not clinically relevant by the principal investigator. .
  • Subject is able to review and understand an informed consent, and must sign the independent ethics committee (IEC)/IRB approved informed consent form before any trial-related procedures are performed.

    • Sexually active females of childbearing potential must have a negative serum pregnancy test result at screening. These subjects must use a medically acceptable method of contraception while receiving protocol-assigned product, and are expected to continue to use this method of contraception for up to 90 days following the last dose of the study medication. A woman of childbearing potential is defined as one who is biologically capable of becoming pregnant; including perimenopausal women who are less than 2 years from their last menses.

Women who are not currently sexually active or lactating must agree to use 2 forms of nonhormonal contraception, should they become sexually active while participating in the study, and for 90 days following the end of participation in the study. Male subjects and/or their partners must use a medically acceptable form of contraception while receiving protocol-assigned product, and up to 90 days following the last dose of the study medication.

  • Subject is willing and able to take the assigned clinical trial medication as directed, comply with clinical trial instructions, and commit to all study visits.

Exclusion Criteria:

  • History of intolerance to any of the ingredients in the study medications, or other related drugs, or history of relevant/clinically significant allergic reactions of any origin.
  • Any disease or physical condition that, in the opinion of the investigator, could impact the PK/pharmacodynamics of the drug or could potentially compromise the safety of the subject.
  • Subject has previously participated in a clinical study of albaconazole.
  • History of drug, prescription medicine, or alcohol abuse within the past 2 years.
  • Positive drug screen.
  • History of psychological or other emotional problems that are likely to invalidate informed consent, or could limit the ability of the subject to comply with the protocol requirements.
  • Any drug treatment taken within 14 days before the first drug intake or within 5 half-lives whichever is longer.
  • Participation in another clinical trial, blood donation, or significant blood loss less than 30 days before the first intake of study drug.
  • Unsuitable veins for repeated venipuncture.
  • Subject has any known liver disease or liver toxicity with other drugs.
  • Subject has a predose ECG before dosing with a QTcB or QTcF interval >450 msec, or abnormal morphology of the ECG, or clinically serious arrhythmia.
  • Subjects who are pregnant, breast-feeding, women of childbearing potential not using adequate contraceptives or planning to conceive, or male subjects who plan to father a child as described in the informed consent.
  • Positive for hepatitis B (HBsAg) or hepatitis C (Ab HCV) or HIV or AIDS.
  • Consumption of any excluded drugs or foodstuff within 72 hours before dosing.
  • Subjects who are employees of a clinical research organization involved in the study, or Stiefel, or an immediate family member.
  • Subjects who have a member of the same household in this study.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01014962

Locations
United States, Wisconsin
Spaulding Clinical Research, LLC
West Bend, Wisconsin, United States, 53095
Sponsors and Collaborators
Stiefel, a GSK Company
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials GlaxoSmithKline
  More Information

No publications provided

Responsible Party: GlaxoSmithKline ( Stiefel, a GSK Company )
ClinicalTrials.gov Identifier: NCT01014962     History of Changes
Other Study ID Numbers: 114555, W0027-107
Study First Received: November 16, 2009
Last Updated: June 21, 2012
Health Authority: United States: Food and Drug Administration

Keywords provided by GlaxoSmithKline:
Pharmacokinetic
tolerability
multiple escalating doses

Additional relevant MeSH terms:
Onychomycosis
Dermatomycoses
Infection
Mycoses
Nail Diseases
Skin Diseases
Skin Diseases, Infectious
Tinea

ClinicalTrials.gov processed this record on November 20, 2014