Drug Drug InteractionPhase 1NCT04542252
Drug-Drug Interaction Study of Intravenous Administration of SyB V-1901 and Cyclosporine in Japanese Healthy Subjects
A Phase 1 study testing SyB V-1901 and Cyclosporine in people with Drug Drug Interaction, run by SymBio Pharmaceuticals at 1 site in Japan.
Trial summary
To evaluate the effect of coadministered cyclosporine on the pharmacokinetics of brincidofovir following simultaneous administration of SyB V-1901 with cyclosporine, or coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion in healthy adult subjects 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
- Drug Drug Interaction
- What is being tested?
- SyB V-1901 and Cyclosporine
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 13 participants
- Where
- 1 siteJapan
- Study dates
- 9 Nov 2020to 29 Jan 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
Main Inclusion Criteria:
- Healthy adult male aged between 20 to 55 years at informed consent
- BMI from 18 to 32 kg/m2 with a body weight of ≥ 50 kg
- Creatinine Clearance ≥ 60 mL/min at screening
- Judged to be in good general health, based on the review of medical history and the screening and Pre-Day1 examination
Main Exclusion Criteria:
- Positive for HIV antibody, or HBs antigen, or HCV antibody at the screening or within 6 months prior to the start of screening
- Have a history of infection of SARS-CoV-2, or subjects who have close contact with infected patients of SARS-CoV-2 within 2 weeks prior to screening or visit to epidemic area of SARS-CoV-2 infection in outside of Japan or have close contact with person who visit to epidemic area of SARS-CoV-2 infection within 2 weeks prior to screening
- Positive for SARS-CoV-2 polymerase chain reaction (PCR) in lower respiratory tract specimens, nasopharyngeal swabs or saliva and so on at screening or have a fever ≥ 37.5 °C and respiratory symptoms
- Have a history of drug abuse or alcohol dependence within 2 years prior to the start of screening
- Have a history of gastrointestinal disorders or cholecystectomy etc., which could interfere with the absorption of cyclosporine or could interfere with normal gastrointestinal anatomy or motility, but except for uncomplicated appendectomy.
- Have a history or symptoms of cardiovascular disease, including but not limited to coronary artery disease, hypertension, congestive heart disease, and clinically significant cardiac disorder.
- Have a history of hematological disorders or have a risk of gastrointestinal bleeding
- Have a history of chronic liver disease or hepatic impairment, including but not limited to alcoholic liver disease, chronic viral hepatitis, autoimmune hepatitis, steatosis or hemochromatosis.
- Have increased Alanine aminotransferase (ALT) or Aspartate aminotransferase (AST) greater than ULN at screening or Pre-Day1
- History of Gilbert's syndrome or increased total bilirubin greater than 1.5x the upper limit of the normal range at screening or Pre-Day1
- Have symptoms of infection within 2 weeks prior to Pre-Day1
- Have clinically significant abnormal hemoglobin at the screening or Pre-Day1, or a clinically significant iron deficiency
- Have a history of blood donation or had clinically significant blood loss within 30 days prior to Day 1, or platelet/plasma donation within 7 days prior to Day 1
- Have received any investigational drug, or device within 30 days prior to Day1
- History of tobacco- or nicotine-containing product use within 6 months prior to Day1
Trial locations and contacts
1 site in 1 country.
About this study
Official title: An Open-label, Randomized, Crossover Study to Evaluate the Drug Interaction of Coadministered Cyclosporine on the Pharmacokinetics and Safety of Intravenous Administration of SyB V-1901 in Japanese Healthy Subjects
To evaluate the effect of coadministered cyclosporine on the pharmacokinetics of brincidofovir following simultaneous administration of SyB V-1901 with cyclosporine, or coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion in healthy adult subjects
Read the detailed description
This study is an open-label, randomized and crossover study designed to evaluate the effect of cyclosporine on the pharmacokinetics of SyB V-1901. Healthy adult subjects will receive an IV dose of SyB V-1901 alone, simultaneous administration of SyB V-1901 with cyclosporine, and coadministration of cyclosporine at 2 hours after completion of SyB V-1901 infusion. Eligible subjects will be randomized to one of two groups, to receive the treatment sequence of assigned group.
- Conditions
- Drug Drug Interaction
- Being tested
- SyB V-1901, Cyclosporine
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SyB V-1901Drug
SyB V-1901 10 mg via IV infusion for 2 hours
CyclosporineDrug
200 mg Capsule
| Study group | Role | What they receive |
|---|---|---|
| Group 1 | Experimental | SyB V-1901 alone, Simultaneous administration of SyB V-1901 and cyclosporine, Coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion Receives: Drug: SyB V-1901; Drug: Cyclosporine |
| Group 2 | Experimental | Simultaneous administration of SyB V-1901 and cyclosporine, SyB V-1901 alone, Coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion Receives: Drug: SyB V-1901; Drug: Cyclosporine |
What is being measured
The primary outcome is the main question the study is designed to answer.
Maximum Plasma Concentration (Cmax) of brincidofovir (BCV)
Measured: From initiation of SyB V-1901 administration though 16 days
Area under the plasma concentration versus time curve (AUC) of BCV
Measured: From initiation of SyB V-1901 administration though 16 days
Secondary outcomes (13)
Cmax of cidofovir (CDV)
Measured: From initiation of SyB V-1901 administration though 16 days
AUC of CDV
Measured: From initiation of SyB V-1901 administration though 16 days
Cmax of Intercellular Cidofovir diphosphate (CDV-PP) in Peripheral Blood Mononuclear Cells (PBMCs)
Measured: From initiation of SyB V-1901 administration though 18 days
AUC of Intercellular CDV-PP in PBMCs
Measured: From initiation of SyB V-1901 administration though 18 days
Cmax of cyclosporine in blood
Measured: From initiation of cyclosporine administration though 16 days
AUC of cyclosporine in blood
Measured: From initiation of cyclosporine administration though 16 days
Number of subjects with adverse events (AE)
Measured: Follow up 22 days post dose
Number of subjects with severity of AEs
Measured: Follow up 22 days post dose
Number of subjects with abnormal findings for laboratory parameters
Measured: Follow up 22 days post dose
Number of subjects with abnormal findings for blood pressure
Measured: Follow up 22 days post dose
Number of subjects with abnormal findings for respiratory rate
Measured: Follow up 22 days post dose
Number of subjects with abnormal findings for heart rate
Measured: Follow up 22 days post dose
Number of subjects with abnormal findings for temperature
Measured: Follow up 22 days post dose
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Sep 2020
- Study start9 Nov 2020
- Primary completion22 Dec 2020
- Study completion29 Jan 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Drug Drug InteractionStudies 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
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 13 participants (actual)
Sponsor and investigators
- Lead sponsor
- SymBio Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Takeshi Yoshida, Study director, SymBio Pharmaceuticals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04542252
- Sponsor's protocol ID
- BCV-HV01
- Status last verified
- Apr 2021
- First submitted
- 29 Aug 2020
- Last updated
- 27 Apr 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Apr 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open-label, Randomized, Crossover Study to Evaluate the Drug Interaction of Coadministered Cyclosporine on the Pharmacokinetics and Safety of Intravenous Administration of SyB V-1901 in Japanese Healthy Subjects
- ClinicalTrials.gov ID
- NCT04542252
- Acronym / sponsor ID
- BCV-HV01
- Conditions
- Drug Drug Interaction
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 13 participants (actual)
- Lead sponsor
- SymBio PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- 9 Nov 2020 (actual)
- Primary completion
- 22 Dec 2020 (actual)
- Study completion
- 29 Jan 2021 (actual)
- First posted
- 9 Sep 2020 (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.
To evaluate the effect of coadministered cyclosporine on the pharmacokinetics of brincidofovir following simultaneous administration of SyB V-1901 with cyclosporine, or coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion in healthy adult subjects
Detailed description
This study is an open-label, randomized and crossover study designed to evaluate the effect of cyclosporine on the pharmacokinetics of SyB V-1901. Healthy adult subjects will receive an IV dose of SyB V-1901 alone, simultaneous administration of SyB V-1901 with cyclosporine, and coadministration of cyclosporine at 2 hours after completion of SyB V-1901 infusion. Eligible subjects will be randomized to one of two groups, to receive the treatment sequence of assigned group.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group 1 | Experimental | Drug: SyB V-1901, Drug: CyclosporineSyB V-1901 alone, Simultaneous administration of SyB V-1901 and cyclosporine, Coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion |
| Group 2 | Experimental | Drug: SyB V-1901, Drug: CyclosporineSimultaneous administration of SyB V-1901 and cyclosporine, SyB V-1901 alone, Coadministration of cyclosporine at 2 hours after the completion of SyB V-1901 infusion |
Who may qualify
- Ages
- 20 to 55 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
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 |
|---|---|---|
| SyB V-1901SyB V-1901 10 mg via IV infusion for 2 hours | Drug | Group 1, Group 2 |
| Cyclosporine200 mg Capsule | Drug | Group 1, Group 2 |
Primary outcome
Maximum Plasma Concentration (Cmax) of brincidofovir (BCV)
Time frame: From initiation of SyB V-1901 administration though 16 days
Area under the plasma concentration versus time curve (AUC) of BCV
Time frame: From initiation of SyB V-1901 administration though 16 days
13 secondary outcomes
Cmax of cidofovir (CDV)
Time frame: From initiation of SyB V-1901 administration though 16 days
AUC of CDV
Time frame: From initiation of SyB V-1901 administration though 16 days
Cmax of Intercellular Cidofovir diphosphate (CDV-PP) in Peripheral Blood Mononuclear Cells (PBMCs)
Time frame: From initiation of SyB V-1901 administration though 18 days
AUC of Intercellular CDV-PP in PBMCs
Time frame: From initiation of SyB V-1901 administration though 18 days
Cmax of cyclosporine in blood
Time frame: From initiation of cyclosporine administration though 16 days
AUC of cyclosporine in blood
Time frame: From initiation of cyclosporine administration though 16 days
Number of subjects with adverse events (AE)
Time frame: Follow up 22 days post dose
Number of subjects with severity of AEs
Time frame: Follow up 22 days post dose
Number of subjects with abnormal findings for laboratory parameters
Time frame: Follow up 22 days post dose
Number of subjects with abnormal findings for blood pressure
Time frame: Follow up 22 days post dose
Number of subjects with abnormal findings for respiratory rate
Time frame: Follow up 22 days post dose
Number of subjects with abnormal findings for heart rate
Time frame: Follow up 22 days post dose
Number of subjects with abnormal findings for temperature
Time frame: Follow up 22 days post dose
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 27 Apr 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.
Takeshi Yoshida study director
SymBio Pharmaceuticals
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 SyB V-1901 and Cyclosporine in people with Drug Drug Interaction, run by SymBio Pharmaceuticals at 1 site in Japan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
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 27 Apr 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 Japan. 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?
Maximum Plasma Concentration (Cmax) of brincidofovir (BCV) (time frame: From initiation of SyB V-1901 administration though 16 days). The study lists 2 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 27 Apr 2021.