Phase 1 Dose Escalating Study to Assess Safety, Tolerability, Food Effect and PK of CHR-5154 in Healthy Male Volunteers

NCT01934101 | Terminated Phase 1 DMC

• 1 other identifier: 201302
• Study Type: interventional
• Target: 64
• Locations: 1 country
• Sites: 1

Brief Summary

Primary Objective:

• To determine the safety and tolerability of single and multiple ascending oral doses of CHR-5154 in healthy volunteers. Secondary Objectives:
• To determine the pharmacokinetic profile of CHR-5154 and its metabolite CHR-5426.
• To compare the pharmacokinetic profile of CHR-5154 and CHR-5426 after a single dose of CHR-5154 in the fed and fasted state.

Conditions

Arthritis, Rheumatoid

Outcome Measures

Primary Outcomes (1)

• Number of volunteers with adverse events

  upto 10 days in Single ascending dose phase and 16 days in the Multiple ascending dose phase

Secondary Outcomes (2)

• To determine the pharmacokinetic profile of CHR-5154 and its metabolite CHR-5426.

  upto 48 hrs post dose

• To compare the pharmacokinetic profile of CHR-5154 and CHR-5426 after a single dose of CHR-5154 in the fed and fasted state.

  Upto 48 hours

Study Arms (2)

CHR-5154

EXPERIMENTAL

CHR-5154

Drug: CHR-5154

Placebo

PLACEBO COMPARATOR

Placebo

Drug: Placebo

Interventions

CHR-5154 DRUG

CHR-5154

CHR-5154

Placebo DRUG

Placebo

Placebo

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy male volunteers aged 18-45.
• Non-smokers from at least three months before receiving the first dose of study drug and for the duration of the study.
• Body mass index (BMI) ≥ 18 and ≤ 32 kg/m2.
• Body weight ≥ 50 kg and ≤ 120 kg at screening.
• Able to voluntarily provide written informed consent to participate in the study.
• Must understand the purposes and risks of the study and agree to follow the restrictions and schedule of procedures as defined in the protocol, as confirmed during the informed consent process.
• Sexually active male volunteers must use two highly effective methods of contraception with their partners throughout the study and for 90 days after completion of the study.
• Male volunteers must not donate sperm during the study and for 90 days after completion of the study.
• Must be willing to consent to have data entered into The Over Volunteering Prevention System (TOPS).
• The volunteer's primary care physician must confirm that there is nothing in their medical history that would preclude their enrolment into this clinical study

You may not qualify if:

• Volunteers with history or presence of significant cardiovascular disease, pulmonary, hepatic, gallbladder or biliary tract, renal, haematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, psychiatric disease or current infection.
• Laboratory values at screening or baseline which are deemed to be clinically significant.
• QTcF greater than 450 msec at screening.
• Positive for human immunodeficiency virus (HIV), hepatitis B or hepatitis C.
• Current or history of drug or alcohol abuse or a positive drugs of abuse or alcohol test at screening or check-in.
• Participation in a clinical drug study during the 90 days preceding the initial dose in this study.
• Any clinically significant illness within 30 days prior to study drug administration.
• Donation of blood or blood products within 90 days prior to study drug administration, or at any time during the study, except as required by this protocol.
• Volunteers who have a history or presence of any significant drug allergy.
• Use of any prescription or over-the-counter medication (including vitamins, herbal and mineral supplements) within 30 days prior to study drug administration until the end of the study, with the exception of occasional paracetamol approved by the Investigator.
• Strenuous exercise, as judged by the Investigator, within 72 hours prior to screening, within 72 hours prior to study drug administration and for the duration of the study until after the post-study medical.
• Weekly alcohol intake exceeding the equivalent of 21 units per week.
• Consumption of alcoholic beverages within 24 hours prior to study drug administration and during study confinement.
• Consumption of caffeine or xanthine-containing products within 24 hours prior to confinement and during study confinement.
• Consumption of grapefruit, grapefruit juice, Seville oranges, Seville orange marmalade or other products containing grapefruit or Seville oranges within 7 days prior to confinement and during study confinement.

Sponsors & Collaborators

• GlaxoSmithKline: lead

Study Sites (1)

GSK Investigational Site

Belfast, BT2 7BA, United Kingdom

Location

Related Links

• Results for study 201302 can be found on the GSK Clinical Study Register.

MeSH Terms

Conditions

Arthritis, Rheumatoid

Condition Hierarchy (Ancestors)

Arthritis; Joint Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Connective Tissue Diseases; Skin and Connective Tissue Diseases; Autoimmune Diseases; Immune System Diseases

Study Officials

• GSK Clinical Trials

  GlaxoSmithKline

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 15, 2013
• First Posted: September 4, 2013
• Study Start: August 12, 2013
• Primary Completion: May 28, 2014
• Study Completion: May 28, 2014
• Last Updated: May 15, 2017

Record last verified: 2017-05

Locations

GB (1)