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OpenTrials
Completed

NCT Number: NCT02532140

Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime

• To evaluate the safety,tolerability and pharmacokinetics of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Quintiles

Overland Park, Kansas, 66211, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male or female, 18-55 years of age (both inclusive).
  • Have a body mass index of 18-30 kg/m2 (both inclusive) calculated as weight (kg)/height (m2).
  • Medical history without any major pathology/surgery in the last 6 months prior to screening.
  • Resting supine blood pressure of 90-139 (systolic)/40-89 (diastolic) mmHg and a resting pulse rate of 40-100 beats per minute.
  • Calculated creatinine clearance ≥80 mL/min
  • Computerized 12-lead ECG recording without signs of clinically significant pathology and showing no clinically significant deviation as judged by the Principal Investigator.
  • Males willing to use double-barrier contraceptive measures and to not donate sperm until 90 days after the follow-up visit.
  • Females should not be pregnant or breast feeding (pregnancy will be confirmed by a urine pregnancy test at screening with confirmation by a serum pregnancy test at admission) or of non-childbearing potential at screening.
  • Females must be either post-menopausal for at least 1 year, surgically sterile (bilateral oophorectomy or hysterectomy), or practicing 1 of the acceptable methods of birth control.

Exclusion criteria

  • History/evidence of clinically relevant pathology.
  • History of clinically significant food or drug allergy, including known hypersensitivity to cefepime or any other related drugs.
  • A positive screen result for drugs of abuse/alcohol at admission to the study center.
  • Use of prescription medications (with the exception of oral contraceptives and hormone replacement therapy) including nonsteroidal anti-inflammatory drugs or sucralfate or herbal preparations.
  • Positive screen result for hepatitis B, hepatitis C, or human immunodeficiency virus at screening.
  • Any strenuous activity within 4 days prior to admission to the study center. Strenuous being defined as any hard labor or exercise outside of a subject's usual behavior.
  • History of blood donation of more than 500 mL in the last 2 months prior to screening.
  • Current use or has used tobacco- or nicotine-containing products.

Treatment and study plan

WCK 5107 250 mg to 2000 mg

Drug

Cefepime 2000 mg

Drug

WCK 5107 1000/2000 mg with Cefepime 2000 mg combination

Drug

Placebo

Drug

Primary outcomes

  1. Safety - number of adverse events .

    Time frame: 14 days

    To evaluate the safety of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

  2. Tolerability-measure of laboratory parameters

    Time frame: 14 days

    To evaluate the tolerability of single intravenous doses of WCK

Secondary outcomes

  1. PK- Cmax

    Time frame: 3 days

    To evaluate the PK of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

  2. PK-AUC

    Time frame: 3 days

    To evaluate the PK of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

  3. PK-time to Cmax

    Time frame: 3 days

    To evaluate the PK of single intravenous doses of WCK 5107 alone and in combination with cefepime in healthy adult human subjects.

Sponsors and collaborators

Lead sponsor

Wockhardt

Industry

Collaborators

  • Quintiles, Inc.

Registry information

Official study title

Phase I Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of WCK 5107 Alone and in Combination With Cefepime Administered as Single IV Doses in Healthy Human Volunteers

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Aug 25, 2015
Registry last updated
May 3, 2016

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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