A Single Dose Study of Debio 1450 in Healthy Subjects
- Registration Number
- NCT02162199
- Lead Sponsor
- Debiopharm International SA
- Brief Summary
The sponsor is trying to develop a medicine for infections that are not cured by regular antibiotics. They have an experimental drug called Debio 1450 that may work. They need about 48 healthy adults to volunteer for this study.
This study looks at what the body does to the drug. It measures how the amount of drug in blood and urine changes over time.
From the screening visit through the follow-up visit may be up to 40 days. Volunteers go to the clinic in Baltimore for a screening visit. The study doctor chooses qualified volunteers to participate or serve as alternates. Alternates might not actually complete the study procedures.
The study doctor divides participants into groups of eight. Six receive Debio 1450 and 2 receive Placebo. The drug each participant receives is decided by chance - like flipping a coin.
Eligible volunteers check into the clinic for testing and those chosen to participate remain for a 5-day/ 4-night stay. The clinic serves standard meals, except when fasting is required. Participants must stay at the clinic for the length of the study.
This study is a "dose escalation" study. That means that if no safety concerns come up a new group starts. Each new group of eight participants receives more capsules.
The study product is contained in capsules. Each capsule contains either placebo or 40 mg Debio 1450. After fasting overnight, the first two participants in the group receive their capsules. One gets Debio 1450 and one gets Placebo. If these participants tolerate side effects for 24 hours, the remaining six participants receive their assigned capsules.
The plan is to increase the dose for the next group. The study doctor reviews the measurements collected from each group after three days. He may decide to repeat, increase, or lower the dose or even stop the study. The most any participant receives is 800 mg in 20 capsules.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 48
- Is a healthy adult
- Has met protocol-specified criteria for qualification and use of contraception
- Is willing and able to remain confined in the study unit for the entire duration of the treatment period and comply with restrictions related to food, drink and medications
- Has voluntarily consented to participate and provided written informed consent prior to any protocol-specific procedures
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Has screening laboratory values outside protocol-specified limits
-
Has history of a clinically significant allergic drug reaction
-
Has donated a volume of plasma or whole blood within a time frame not allowed per protocol
-
Has historical or current use not allowed per protocol of:
- over-the-counter medications
- certain foods; dietary, mineral or herbal supplements
- licit or illicit drugs (including experimental drugs, caffeine, nicotine and alcohol)
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Has signs, symptoms or history of any condition that, per protocol or in the opinion of the investigator, might compromise:
- the safety or well-being of the participant or study staff
- the safety or well-being of the participant's offspring (such as through pregnancy or breast-feeding)
- the analysis of results
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo Placebo 0 mg, matching capsules, orally, once in the morning under fasted conditions Debio 1450 Debio 1450 Debio 1450 40 mg, capsules, orally, once in the morning under fasted conditions
- Primary Outcome Measures
Name Time Method Number of participants with at least one treatment emergent adverse event (TEAE) within 10 days post-dose Maximum observed plasma concentration (Cmax) of Debio 1450 within 60 hours post-dose Time of maximum observed plasma concentration (tmax) of Debio 1450 within 60 hours post-dose
- Secondary Outcome Measures
Name Time Method Elimination half-life (t½) of Debio 1450 pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Mean residence time (MRT) of Debio 1450 pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Apparent clearance following oral administration (CL/F) of Debio 1450 pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Percentage of cumulative amount of unchanged Debio 1450 excreted in urine (Ae%) pre-dose and 0-2, 2-6, 6-12, 12-24, 24-48 and 48-60 hours post-dose Renal clearance following oral administration pre-dose and 0-2, 2-6, 6-12, 12-24, 24-48 and 48-60 hours post-dose Area under the plasma concentration-time curve (AUC) of Debio 1450 pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Categorical results will include from time zero to 24 hours post-dose (AUC0-24), from time zero to the last measured concentration (AUC0-t), and from time zero extrapolated to infinity (AUC0-∞).
Percentage of AUC0-∞ that is due to extrapolation beyond the last quantifiable concentration measurement (%AUCex) of Debio 1450 pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Apparent volume of distribution of Debio 1450 during terminal phase (Vz/F) pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Number of participants with clinically significant change from baseline in 12-lead electrocardiogram (ECG) parameters within 48 hours post-dose Number of participants with clinically significant change from baseline in clinical laboratory parameters within 51 hours post-dose Terminal elimination rate constant (λz) of Debio 1450 pre-dose, 15, 30 and 60 minutes post-dose, and 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12, 16, 24, 30, 36, 48 and 60 hours post-dose Cumulative amount of unchanged Debio 1450 excreted in urine (Ae) pre-dose and 0-2, 2-6, 6-12, 12-24, 24-48 and 48-60 hours post-dose Number of participants with clinically significant change from baseline in vital signs within 10 days post-dose
Trial Locations
- Locations (1)
Early Phase Clinical Unit
🇺🇸Baltimore, Maryland, United States