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A Study in Healthy Male Volunteers to Look at How the Test Medicine GLPG1690 is Taken up by the Body When Given by Mouth and Into a Vein as an Injection

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ClinicalTrials.gov Identifier: NCT03787186
Recruitment Status : Completed
First Posted : December 25, 2018
Last Update Posted : February 15, 2019
Sponsor:
Information provided by (Responsible Party):
Galapagos NV

Brief Summary:
The sponsor wants to investigate how well the test medicine is taken up by the body when given orally (by mouth) as a tablet or capsule and as a solution for infusion (into a vein). The capsule and the solution will be radiolabelled. 'Radiolabelled' means that the test medicine has a radioactive component which helps us to track where the test medicine is in the body.

Condition or disease Intervention/treatment Phase
Healthy Drug: GLPG1690 film-coated tablets Drug: [14C]-GLPG1690 solution for infusion Drug: [14C]-GLPG1690 capsules Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 8 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: A Phase 1, Open-label, Single-center Study to Investigate the Pharmacokinetics and Metabolism of GLPG1690 in Healthy Male Subjects Following Single Intravenous GLPG1690 Microtracer and Oral [14C]-GLPG1690 Administrations.
Actual Study Start Date : November 9, 2018
Actual Primary Completion Date : January 17, 2019
Actual Study Completion Date : January 17, 2019

Arm Intervention/treatment
Experimental: GLPG1690 oral and IV
GLPG1690 film-coated tablets followed by [14C]-GLPG1690 solution for infusion
Drug: GLPG1690 film-coated tablets
a single oral dose of GLPG1690

Drug: [14C]-GLPG1690 solution for infusion
a 15-minute IV infusion [14C]-GLPG1690

Experimental: [14C]-GLPG1690 capsules
[14C]-GLPG1690 capsules
Drug: [14C]-GLPG1690 capsules
single oral dose of [14C]-GLPG1690




Primary Outcome Measures :
  1. Change of total radioactivity excreted in urine and feces combined (µg) from baseline at Day 10 (Part 2) [ Time Frame: From Day 1 pre-dose up to Day 10 ]
    To assess the mass balance using [14C]-GLPG1690.

  2. Maximum observed plasma concentration (Cmax) of total radioactivity (Part 2). [ Time Frame: From Day 1 pre-dose up to Day 10 ]
    To assess the pharmacokinetics (PK) of GLPG1690 and its main metabolites in plasma

  3. Maximum observed plasma concentration (Cmax) of GLPG1690 (Part 2). [ Time Frame: From Day 1 pre-dose up to Day 10 ]
    To assess the pharmacokinetics (PK) of GLPG1690 and its main metabolites in plasma

  4. Area under the plasma concentration-time curve (AUC) of total radioactivity (Part 2). [ Time Frame: From Day 1 pre-dose up to Day 10 ]
    To assess the PK of GLPG1690 and its main metabolites in plasma

  5. Area under the plasma concentration-time curve (AUC) of GLPG1690 (Part 2). [ Time Frame: From Day 1 pre-dose up to Day 10 ]
    To assess the PK of GLPG1690 and its main metabolites in plasma

  6. Change in amount of [14C] GLPG1690 excreted in urine and feces combined (µg) from baseline at Day 7 (Part 2). [ Time Frame: From Day 1 pre-dose up to Day 7 ]
    To better characterize the elimination pathways and metabolite profile of GLPG1690


Secondary Outcome Measures :
  1. Intravenous (IV) maximum observed plasma concentration (Cmax) of [14C]-GLPG1690 microtracer (MT) (Part 1). [ Time Frame: From Day 1 pre-dose up to Day 4 ]
    To assess the PK of GLPG1690 and its main metabolites in plasma.

  2. Intravenous (IV) maximum observed plasma concentration (Cmax) of total radioactivity (Part 1). [ Time Frame: From Day 1 pre-dose up to Day 4 ]
    To assess the PK of GLPG1690 and its main metabolites in plasma.

  3. IV Area under the plasma concentration-time curve (AUC) of [14C]-GLPG1690 microtracer (MT) (Part 1). [ Time Frame: From Day 1 pre-dose up to Day 4 ]
    To assess the PK of GLPG1690 and its main metabolites in plasma.

  4. IV Area under the plasma concentration-time curve (AUC) of total radioactivity(Part 1). [ Time Frame: From Day 1 pre-dose up to Day 4 ]
    To assess the PK of GLPG1690 and its main metabolites in plasma.

  5. Safety and tolerability of GLPG1690, assessed by the number of subjects with adverse events (AEs) (Part 1 and Part 2). [ Time Frame: From screening through study completion, an average of 2 months ]
    To evaluate the safety and tolerability of GLPG1690 (in Part 1 and Part 2).



Information from the National Library of Medicine

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Ages Eligible for Study:   30 Years to 64 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Able and willing to comply with the clinical study protocol (CSP) requirements and sign the informed consent form (ICF) as approved by the Independent Ethics Committee (IEC), before any screening evaluations.
  • Male subjects between 30 to 64 years of age (extremes included), on the date of signing the ICF.
  • A body mass index between 18 to 32 kg/m2 (extremes included).
  • Judged to be in good health by the investigator based upon the results of a medical history, physical examination, vital signs, 12-lead ECG, and fasting clinical laboratory safety tests, and not having had any clinically significant illness in the 3 months before first investigational medicinal product (IMP) administration.
  • Having a regular and (at least) daily defecation pattern.
  • Able and willing to comply with restrictions on prior and concomitant medication as described in the protocol.
  • Nonsmoker, defined as an individual who has abstained from smoking (or the use of e-cigarettes or nicotine containing products) from at least 2 months before screening. Having a breath carbon monoxide reading of ≤10 parts per million.
  • Negative urine drug screen (e.g. amphetamines, barbiturates, benzodiazepines, cannabis, cocaine, opiates, methadone, tricyclic antidepressants) and alcohol breath test.
  • Male subjects with female partners of childbearing potential willing to comply with the contraceptive methods described in the protocol from the time of the first IMP administration, during the clinical study, and for at least 90 days after the last IMP administration.

Exclusion Criteria:

  • Known hypersensitivity to IMP ingredients or history of a significant allergic reaction to IMP ingredients as determined by the investigator, such as anaphylaxis requiring hospitalization, and/or known sensitivity to IMP or the excipients (e.g. lactose). Hayfever is allowed unless active.
  • Positive serology for hepatitis B virus surface antigen (HBsAg) or hepatitis C virus (HCV) antibody, or history of hepatitis from any cause with the exception of a history of hepatitis A infection at least 12 weeks before first IMP administration.
  • History of or a current immunosuppressive condition (e.g. human immunodeficiency virus [HIV] infection).
  • Presence or sequelae of gastrointestinal, liver, kidney (creatinine clearance ≤80 mL/min, using the Cockcroft-Gault formula), or other conditions known to interfere with the absorption, distribution, metabolism, and excretion (ADME) properties of drugs. Subjects with documented Gilbert's syndrome are eligible for inclusion in the study.
  • History of malignancy within the past 5 years (except for basal cell carcinoma of the skin that has been treated and with no evidence of recurrence).
  • Hemoglobin level below the lower limit of normal (LLN; 13.0 g/dL). Retesting is allowed once.
  • Significant blood loss (including blood donation [>450 mL]) or transfusion of any blood product within 12 weeks before screening.
  • Active drug abuse (per investigator judgment) or alcohol abuse (more than three glasses of wine, beer, or equivalent/day) within 3 months before first IMP administration.
  • Concurrent participation or participation in a drug, drug/device or biologic investigational research study within 12 weeks or 5 half-lives of the drug, whichever is longer, before first IMP administration.
  • Radiation exposure, including that from the present study, excluding background radiation but including diagnostic Xrays and other medical exposures, exceeding 5 millisievert (mSv) in the last 12 months or 10 mSv in the last 5 years. No occupationally exposed worker, as defined in the Ionising Radiation Regulations 1999, can participate in the study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03787186


Locations
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United Kingdom
Quotient Sciences Limited
Ruddington, United Kingdom, NG11 6JS
Sponsors and Collaborators
Galapagos NV
Investigators
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Study Director: Christopher Brearley, BM. MRCP Galapagos NV

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Responsible Party: Galapagos NV
ClinicalTrials.gov Identifier: NCT03787186     History of Changes
Other Study ID Numbers: GLPG1690-CL-107
First Posted: December 25, 2018    Key Record Dates
Last Update Posted: February 15, 2019
Last Verified: February 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No