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NCT Number: NCT02245828

A First in Human Study to Assess the Safety, Tolerability and Pharmacokinetics of Single and Multiple Ascending Doses of QCC374

This is a double blind, randomized, placebo controlled, single and multiple ascending dose study in healthy subjects. Safety evaluation will include (serious) adverse events, vital signs, body weight and lung function tests. Blood samples for Pharmacokinetics will also be drawn at specified timepoints.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Novartis Investigative Site

Mid Glamorgan, Wales, CF484DR, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Written informed consent must be obtained before any assessment is performed.
  • Healthy male and female subjects age 18 to 55 years of age included, and in good health as determined by past medical history, physical examination, vital signs, electrocardiogram, and laboratory tests at screening.
  • Weight of at least 50 kg and body mass index (BMI) within the range of 18 - 32 kg/m2. BMI = Body weight (kg) / [Height (m)]2.
  • Oxygen saturation (O2) at screening must be ≥ 95% on room air.
  • FEV1 ≥ 90% predicted.

Exclusion criteria

  • 1. A history of clinically significant ECG abnormalities and/or orthostatic vital signs at screening.
  • History of asthma or reactive airway diseases.
  • Smokers or anyone who smoked within 5 years of screening. Urine cotinine levels ≥ 500 ng/mL.
  • History of malignancy of any organ system other than localized basal cell carcinoma of the skin, treated or untreated within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.
  • Women of child-bearing potential

Treatment and study plan

QCC374

Drug

Single and multiple ascending doses of QCC374

Placebo

Drug

Placebo comparator

Primary outcomes

  1. Safety and tolerability

    Time frame: 39 days

    Number of Participants with Adverse Events

Secondary outcomes

  1. AUCinf

    Time frame: 39 days

    Area under the plasma concentration-time curve from time zero to infinity

  2. AUClast

    Time frame: 39 days

    The area under the plasma concentration-time curve from time zero to the time of the last quantifiable concentration

  3. AUCtau

    Time frame: 39 days

    The area under the plasma concentration-time curve from time zero to the end of the dosing interval tau

  4. Cav

    Time frame: 39 days

    The average steady state plasma concentration during multiple dosing

  5. Cmax

    Time frame: 39 days

    The observed maximum plasma concentration following drug administration

  6. T1/2

    Time frame: 39 days

    The terminal elimination half life

  7. Tmax

    Time frame: 39 days

    The time to reach the maximum concentration after drug administration

Sponsors and collaborators

Lead sponsor

Novartis Pharmaceuticals

Industry

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled First-in-human Study to Assess the Safety, Tolerability and Pharmacokinetics of Single and Multiple Ascending Doses of QCC374 in Healthy Subjects

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Sep 22, 2014
Registry last updated
Mar 22, 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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