Idiopathic Pulmonary FibrosisPhase 1NCT04888728
To Evaluate Drug-drug Interactions Between DWN12088 and Nebivolol or Paroxetine in Healthy Volunteers
A Phase 1 study testing DWN12088, Nebivolol and Paroxetine in people with Idiopathic Pulmonary Fibrosis, run by Daewoong Pharmaceutical Co. LTD. at 1 site in South Korea.
Trial summary
An open label, 2-part, one-sequence, 3-period study to evaluate drug-drug interactions between DWN12088 and nebivolol or Paroxetine in healthy volunteers Read more about this study
- Who is it for?
- Ages 20 to 55 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Idiopathic Pulmonary Fibrosis
- What is being tested?
- DWN12088, Nebivolol and Paroxetine
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 24 participants
- Where
- 1 siteSouth Korea
- Study dates
- 30 Jun 2021to 27 Jul 2021
- 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 20 to 55 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Healthy male adults aged ≥ 20 and ≤ 55 years at screening
- Subjects who voluntarily decided to participate in the study and provided written consent to follow study compliance requirements after receiving a detailed explanation on this study and fully understanding the information
Who cannot join
- Subjects unable to have the standard meal provided at the study site
- Subjects who took (the day of taking the last dose) another investigational or bioequivalence study product within 180 days prior to the first dose
Trial locations and contacts
1 site in 1 country.
About this study
Official title: An Open Label, 2-part, One-sequence, 3-period Study to Evaluate Drug-drug Interactions Between "DWN12088" and "Nebivolol" or "Paroxetine" in Healthy Male Volunteers
An open label, 2-part, one-sequence, 3-period study to evaluate drug-drug interactions between DWN12088 and nebivolol or Paroxetine in healthy volunteers
- Conditions
- Idiopathic Pulmonary Fibrosis
- Being tested
- DWN12088, Nebivolol, Paroxetine
- Medical subject headings
- Idiopathic Pulmonary Fibrosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DWN12088Drug
Prolyl-tRNA synthetase (PRS) inhibitor
NebivololDrug
Nebivolol
ParoxetineDrug
Paroxetine
| Study group | Role | What they receive |
|---|---|---|
| DWN12088 and Nebivolol | Experimental | Period 1 - Nebivolol A mg, Tablet, oral, once daily, Period 2 - DWN12088 X mg, Tablet, oral, twice daily, Period 3 - 1) Nebivolol A mg, Tablet, oral, once daily \& DWN12088 X mg, Tablet, oral, twice daily, 2) DWN12088 X mg, Tablet, oral, once daily Receives: Drug: DWN12088; Drug: Nebivolol |
| DWN12088 and Paroxetine | Experimental | Period 1 - DWN12088 X mg, Tablet, oral, once daily , Period 2 - Paroxetine B mg, Tablet, oral, once daily, Period 3 - 1) DWN12088 X mg, Tablet, oral, once daily \& Paroxetine B mg, Tablet, oral, once daily, 2) Paroxetine B mg, Tablet, oral, once daily Receives: Drug: DWN12088; Drug: Paroxetine |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cmax of Nebivolol
Cmax of Nebivolol
Measured: Day 1, Day 2, Day 3, Day 6, Day 7, and Day 8
AUCt of Nebivolol
AUCt of Nebivolol
Measured: Day 1, Day 2, Day 3, Day 6, Day 7, and Day 8
Cmax of DWN12088
Cmax of DWN12088
Measured: Day 1, Day 2, Day 3, Day 4, Day 9, Day 10, Day 11, and Day 12
AUCt of DWN12088
AUCt of DWN12088
Measured: Day 1, Day 2, Day 3, Day 4, Day 9, Day 10, Day 11, and Day 12
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 May 2021
- Study start30 Jun 2021
- Primary completion12 Jul 2021
- Study completion27 Jul 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Idiopathic Pulmonary FibrosisStudies of the same condition, open and under way.
- More trials run by Daewoong Pharmaceutical Co. LTD.The sponsor's other registered studies.
- 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
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 24 participants (actual)
Sponsor and investigators
- Lead sponsor
- Daewoong Pharmaceutical Co. LTD.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Jong-Lyul Ghim, Principal investigator, Busan Paik Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04888728
- Sponsor's protocol ID
- DW_DWN12088104
- Status last verified
- Aug 2021
- First submitted
- 28 Apr 2021
- Last updated
- 4 Aug 2021
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Aug 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open Label, 2-part, One-sequence, 3-period Study to Evaluate Drug-drug Interactions Between "DWN12088" and "Nebivolol" or "Paroxetine" in Healthy Male Volunteers
- ClinicalTrials.gov ID
- NCT04888728
- Acronym / sponsor ID
- DW_DWN12088104
- Conditions
- Idiopathic Pulmonary Fibrosis
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 24 participants (actual)
- Lead sponsor
- Daewoong Pharmaceutical Co. LTD.Industry (pharma, biotech, devices)
- Study start
- 30 Jun 2021 (actual)
- Primary completion
- 12 Jul 2021 (actual)
- Study completion
- 27 Jul 2021 (actual)
- First posted
- 17 May 2021 (actual)
- 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.
An open label, 2-part, one-sequence, 3-period study to evaluate drug-drug interactions between DWN12088 and nebivolol or Paroxetine in healthy volunteers
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| DWN12088 and Nebivolol | Experimental | Drug: DWN12088, Drug: NebivololPeriod 1 - Nebivolol A mg, Tablet, oral, once daily, Period 2 - DWN12088 X mg, Tablet, oral, twice daily, Period 3 - 1) Nebivolol A mg, Tablet, oral, once daily \& DWN12088 X mg, Tablet, oral, twice daily, 2) DWN12088 X mg, Tablet, oral, once daily |
| DWN12088 and Paroxetine | Experimental | Drug: DWN12088, Drug: ParoxetinePeriod 1 - DWN12088 X mg, Tablet, oral, once daily , Period 2 - Paroxetine B mg, Tablet, oral, once daily, Period 3 - 1) DWN12088 X mg, Tablet, oral, once daily \& Paroxetine B mg, Tablet, oral, once daily, 2) Paroxetine B mg, Tablet, oral, once daily |
Who may qualify
- Ages
- 20 to 55 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Healthy male adults aged ≥ 20 and ≤ 55 years at screening
- Subjects who voluntarily decided to participate in the study and provided written consent to follow study compliance requirements after receiving a detailed explanation on this study and fully understanding the information
Key exclusion criteria (2 listed)
- Subjects unable to have the standard meal provided at the study site
- Subjects who took (the day of taking the last dose) another investigational or bioequivalence study product within 180 days prior to the first dose
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 |
|---|---|---|
| DWN12088Prolyl-tRNA synthetase (PRS) inhibitor | Drug | DWN12088 and Nebivolol, DWN12088 and Paroxetine |
| NebivololNebivolol | Drug | DWN12088 and Nebivolol |
| ParoxetineParoxetine | Drug | DWN12088 and Paroxetine |
Primary outcome
Cmax of Nebivolol
Time frame: Day 1, Day 2, Day 3, Day 6, Day 7, and Day 8
Cmax of Nebivolol
AUCt of Nebivolol
Time frame: Day 1, Day 2, Day 3, Day 6, Day 7, and Day 8
AUCt of Nebivolol
Cmax of DWN12088
Time frame: Day 1, Day 2, Day 3, Day 4, Day 9, Day 10, Day 11, and Day 12
Cmax of DWN12088
AUCt of DWN12088
Time frame: Day 1, Day 2, Day 3, Day 4, Day 9, Day 10, Day 11, and Day 12
AUCt of DWN12088
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 4 Aug 2021.
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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.
Jong-Lyul Ghim principal investigator
Busan Paik Hospital
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 DWN12088, Nebivolol and Paroxetine in people with Idiopathic Pulmonary Fibrosis, run by Daewoong Pharmaceutical Co. LTD. at 1 site in South Korea.
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 2 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 4 Aug 2021. 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 South Korea. 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. 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?
Cmax of Nebivolol (time frame: Day 1, Day 2, Day 3, Day 6, Day 7, and Day 8). The study lists 4 primary outcomes in all. 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 4 Aug 2021.