HealthyPhase 1NCT01130818
First-in-Human Single Ascending Dose of GLPG0492
A Phase 1 study testing GLPG0492 in people with Healthy, run by Lakefront Biotherapeutics NV at 1 site in Belgium.
Trial summary
The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) oral dose of GLPG0492 compared to placebo in healthy subjects. Also, pharmacokinetics (PK) and pharmacodynamics (PD) of GLPG0492 after single oral administration will be evaluated, and, if applicable, the maximum tolerated… Read more about this study
- Who is it for?
- Ages 18 years and older, men onlyHealthy volunteers can take part
- Conditions the study is for
- Healthy
- What is being tested?
- GLPG0492
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 28 participants
- Where
- 1 siteBelgium
- Study dates
- May 2010to Sep 2010
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Men only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- healthy male, age 18-50 years (young subjects) OR ≥60 years (elderly subjects)
- BMI between 18-30 kg/m², inclusive
- non-smoker
Who cannot join
- elevated PSA
- drug or alcohol abuse
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Double Blind Placebo Controlled Dose Ranging Study for the Assessment of Safety, Tolerability and Pharmacokinetics of Single Ascending Oral Doses of GLPG0492 in Healthy Subjects and Open Relative Bioavailability Study of Oral Solution Versus Solid Formulation, Fasted and Fed, in Elderly Subjects
The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) oral dose of GLPG0492 compared to placebo in healthy subjects.
Also, pharmacokinetics (PK) and pharmacodynamics (PD) of GLPG0492 after single oral administration will be evaluated, and, if applicable, the maximum tolerated dose determined. Oral bioavailability (solution vs solid capsule fasting or fed) is evaluated in healthy elderly subjects.
- Conditions
- Healthy
- Being tested
- GLPG0492, placebo
- Keywords
- Safety, Tolerability, Pharmacokinetics, Bioavailability (solid vs solution, fasting vs fed), Young healthy subjects, Elderly healthy subjects
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GLPG0492Drug
single ascending doses, oral solution (25 to max. 120 mg/intake, 10 to 200 mg/mL)
placeboDrug
single dose, oral solution
GLPG0492Drug
single dose, solid formulation, 50 mg (2*25 mg/capsule), fasting
GLPG0492Drug
single dose, solid formulation, 50 mg (2*25 mg/capsule), after high fat breakfast
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | single ascending doses Receives: Drug: GLPG0492 |
| 2 | Placebo comparator | single dose placebo Receives: Drug: placebo |
| 3 | Experimental | single dose, oral solution, 50 mg Receives: Drug: GLPG0492 |
| 4 | Experimental | single dose, capsules (fasting) Receives: Drug: GLPG0492 |
| 5 | Experimental | single dose, capsules (fed) Receives: Drug: GLPG0492 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Safety and tolerability of single ascending doses in healthy young and elderly subjects.
Measured: up to 10 days postdose
Secondary outcomes (3)
Pharmacokinetics of single oral doses (solution) in young and elderly subjects.
Measured: up to 10 days postdose
Determine oral bioavailability of GLPG0492 given to elderly subjects as oral solution or solid dosage form with or without food.
Measured: up to 10 days postdose
Determine the maximum tolerated dose in young subjects.
Measured: Up to 10 days postdose
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2010 (estimated)
- Study startMay 2010
- Primary completionAug 2010
- Study completionSep 2010
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HealthyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 28 participants (actual)
Sponsor and investigators
- Lead sponsor
- Lakefront Biotherapeutics NV
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Florence Namour, PhD, Study director, Lakefront Biotherapeutics NVSofie Mesens, MD, Principal investigator, SGS Stuivenberg
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01130818
- Sponsor's protocol ID
- GLPG0492-CL-101
- Status last verified
- Feb 2024
- First submitted
- 20 May 2010
- Last updated
- 1 Mar 2024
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Mar 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Double Blind Placebo Controlled Dose Ranging Study for the Assessment of Safety, Tolerability and Pharmacokinetics of Single Ascending Oral Doses of GLPG0492 in Healthy Subjects and Open Relative Bioavailability Study of Oral Solution Versus Solid Formulation, Fasted and Fed, in Elderly Subjects
- ClinicalTrials.gov ID
- NCT01130818
- Acronym / sponsor ID
- GLPG0492-CL-101
- Conditions
- Healthy
- Keywords
- Safety, Tolerability, Pharmacokinetics, Bioavailability (solid vs solution, fasting vs fed), Young healthy subjects, Elderly healthy subjects
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 28 participants (actual)
- Lead sponsor
- Lakefront Biotherapeutics NVIndustry (pharma, biotech, devices)
- Study start
- May 2010
- Primary completion
- Aug 2010 (actual)
- Study completion
- Sep 2010 (actual)
- First posted
- 26 May 2010 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) oral dose of GLPG0492 compared to placebo in healthy subjects.
Also, pharmacokinetics (PK) and pharmacodynamics (PD) of GLPG0492 after single oral administration will be evaluated, and, if applicable, the maximum tolerated dose determined. Oral bioavailability (solution vs solid capsule fasting or fed) is evaluated in healthy elderly subjects.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 5
| Arm | Type | Receives |
|---|---|---|
| 1 | Experimental | Drug: GLPG0492single ascending doses |
| 2 | Placebo comparator | Drug: placebosingle dose placebo |
| 3 | Experimental | Drug: GLPG0492single dose, oral solution, 50 mg |
| 4 | Experimental | Drug: GLPG0492single dose, capsules (fasting) |
| 5 | Experimental | Drug: GLPG0492single dose, capsules (fed) |
Who may qualify
- Ages
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- healthy male, age 18-50 years (young subjects) OR ≥60 years (elderly subjects)
- BMI between 18-30 kg/m², inclusive
- non-smoker
Key exclusion criteria (2 listed)
- elevated PSA
- drug or alcohol abuse
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| GLPG0492single ascending doses, oral solution (25 to max. 120 mg/intake, 10 to 200 mg/mL) | Drug | 1, 3 |
| placebosingle dose, oral solution | Drug | 2 |
| GLPG0492single dose, solid formulation, 50 mg (2*25 mg/capsule), fasting | Drug | 4 |
| GLPG0492single dose, solid formulation, 50 mg (2*25 mg/capsule), after high fat breakfast | Drug | 5 |
Primary outcome
Safety and tolerability of single ascending doses in healthy young and elderly subjects.
Time frame: up to 10 days postdose
3 secondary outcomes
Pharmacokinetics of single oral doses (solution) in young and elderly subjects.
Time frame: up to 10 days postdose
Determine oral bioavailability of GLPG0492 given to elderly subjects as oral solution or solid dosage form with or without food.
Time frame: up to 10 days postdose
Determine the maximum tolerated dose in young subjects.
Time frame: Up to 10 days postdose
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Mar 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Florence Namour, PhD study director
Lakefront Biotherapeutics NV
Sofie Mesens, MD principal investigator
SGS Stuivenberg
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing GLPG0492 in people with Healthy, run by Lakefront Biotherapeutics NV at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Mar 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Safety and tolerability of single ascending doses in healthy young and elderly subjects. (time frame: up to 10 days postdose). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Mar 2024.