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Completed

NCT Number: NCT02280434

Phase 1 Study Accessing the Safety and Tolerability of CBP-307

This study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of CBP-307 following oral single and multiple escalating dose administration in healthy subjects.

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Key information

Age range

18 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Nucleus Network

Melbourne, Victoria, 3004, Australia

About this study

This study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of CBP-307 following oral single and multiple escalating dose administration in healthy subjects. The study will have two parts: Part 1 will assess 5 dose levels of the drug in single dosing; and Part 2 will evaluate 3 dose levels in 28-day repeat dosing. The effect of food will also be evaluated in a single dosing study.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Informed consent must be obtained in writing for all subjects at enrollment into the study
  • Healthy male subjects age between 18 and 55 years, inclusive
  • Body mass index (BMI) between 19 and 30 kg/m2, inclusive
  • No clinically significant findings in the medical history and physical examination, especially with regard to the liver and gastrointestinal systems
  • No clinically significant laboratory values and urinalysis, unless the investigator considers any abnormality to be clinically irrelevant
  • Normal ECG, blood pressure, and heart rate, unless the investigator considers any abnormality to be clinically irrelevant
  • Resting heart rate ≥ 55 bpm

Exclusion criteria

  • Family history of premature CHD (Coronary Heart Disease)
  • Any condition requiring the regular use of any medication
  • Exposure to prescription medications or to drugs known to interfere with metabolism of drugs within 30 days prior to screening
  • Exposure to any other medication, including over-the counter medications, herbal remedies and vitamins 14 days prior to randomization (except paracetamol (see Section 5.2 Prior and concomitant treatments)
  • Participation in another study with any investigational drug in the 2 months preceding the study
  • Treatment in the previous 3 months with any drug known to have a well defined potential for toxicity to a major organ
  • Positive urine cotinine result at screening
  • Be in the exclusion period of any previous study with investigational drugs
  • Symptoms of a clinically significant illness in the 3 months before the study
  • Presence or sequelae of gastrointestinal, liver or kidney disease, or other conditions known to interfere with the absorption, distribution, metabolism, or excretion of drugs
  • Chronic constipation or diarrhea, irritable bowel syndrome, inflammatory bowel disease
  • Hemorrhoids or anal diseases with regular or recent presence of blood in feces
  • History of significant allergic disease (e.g. medications) and acute phase of allergic rhinitis in the previous 2 weeks before randomization or any food allergy
  • Blood or plasma donation of more than 500 ml during the previous 2 month before randomization and/or more than 50 ml in the 2 weeks prior to screening
  • Subjects at risk for tuberculosis (TB), specifically subjects with: Current clinical, radiographic or laboratory evidence of active TB; history of active TB unless there is documentation that the prior anti-TB treatment was appropriate in duration and type;latent TB which has not been successfully treated; a positive quantiFERON® test at screening or within 6 months prior to Day 1
  • Known positive test for HIV
  • Known positive test for hepatitis B (antigens HBs, antibody HBc) or C, unless caused by immunization
  • History of shingles or recurrent episodes of HSV1 or HSV2 infections
  • Current evidence of drug abuse or history of drug abuse within one year before randomization
  • History of alcohol abuse or active alcoholism as defined in Appendix A Definition of alcohol abuse
  • Mental condition rendering the subject incapable to understand the nature, scope, and possible consequences of the study
  • Adults under guardianship and people with restriction of freedom by administrative or legal decisions
  • Unlikely to comply with the clinical study protocol; e.g. uncooperative attitude, inability to return for follow-up visits, and improbability of completing the study
  • Subject is the investigator or any sub-investigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the protocol.
  • Systolic blood pressure less than 95 mmHg or greater than 140 mmHg, or diastolic blood pressure less than or equal to 50 mmHg or greater than or equal to 95 mmHg.
  • Subjects with resting heart rate less than 55 beats per minute or greater than 90 beats per minute.

Treatment and study plan

CBP-307

Drug

Placebo

Drug

Primary outcomes

  1. Number of Participants with Adverse Events as a Measure of Safety and Tolerability

    Time frame: up to 6 weeks

    Safety measurements will include vital signs, hematology, blood chemistry, blood pressure and other readouts.

Secondary outcomes

  1. Plasma Concentrations of Study Drug Over Time and Maximal Plasma Concentration (Cmax)

    Time frame: Up to 6 weeks

  2. Elimination Half-live (T1/2) of Study Drug

    Time frame: Up to 6 weeks

  3. Exposure to Study Drug Measured as Area Under the Curve (AUC)

    Time frame: Up to 6 weeks

  4. Effect of Study Drug on Blood Lymphocyte Counts

    Time frame: Up to 6 weeks

Sponsors and collaborators

Lead sponsor

Connect Biopharm LLC

Industry

Collaborators

  • Nucleus Network Ltd
  • Tigermed Consulting Co., Ltd

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose Escalation Study in Healthy Subjects to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of CBP-307 Following Oral Single and Multiple Escalating Dose Administration

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Oct 31, 2014
Registry last updated
Nov 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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