Mass Balance and Absolute Bioavailability Study of RO7049389 in Healthy Volunteers
Open-Label Study to Investigate the Mass Balance and Absolute Bioavailability of a Single Oral Dose of [14C]-Labeled RO7049389 or RO7049389 and an Intravenous Micro-Dose of [13C]-Labeled RO7049389 in Healthy Volunteers
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
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Nottingham, United Kingdom, NG11 6JS
- Quotient Sciences
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Caucasian (must have Caucasian parents and grandparents) or East Asian (must have Chinese, Korean, or Japanese parents and grandparents)
- Body mass index between 18 to 30 kg/m^2 (inclusive) and a weight range of 50 kg to 100 kg (inclusive) at screening
- For women of childbearing potential: agree to use two methods of contraception, with at least one method considered as highly effective during the study and for at least 90 days after the last dose of study drug
- For men: agree to remain abstinent (refrain from heterosexual intercourse) or agree to use contraceptive measures, and agree to refrain from donating sperm during the treatment period and for at least 90 days after the last dose of study drug
Exclusion Criteria:
- Pregnant or lactating women, and male participants with partners who are pregnant or lactating
- History or symptoms of any clinically significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, oncologic, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; of constituting a risk when taking the study treatment; or of interfering with the interpretation of data
- Personal history or family history of congenital long QT interval (QT) syndrome and/or cardiac sudden death
- History of Gilbert syndrome
- Participants who have had significant acute infection, e.g. influenza, local infection, acute gastrointestinal (GI) symptoms, or any other clinically significant illness within two weeks of dose administration
- Any confirmed significant reactions (urticaria or anaphylaxis) against any drug, or multiple drug allergies
- Any clinically significant concomitant diseases or conditions that could interfere with the conduct of the study, or in the opinion of the Investigator, would pose an unacceptable risk to the participant in this study
- Taking any herbal medications or substances, supplements (including vitamins), traditional Chinese medicines, prescription medicine, or over-the-counter medications within 14 days of first dosing or within 5 times the elimination half-life of the medication prior to first dosing, whichever is longer
- History of having received any systemic anti-neoplastic (including radiation) or immune-modulatory treatment (including systemic oral or inhaled corticosteroids) 6 months prior to the first dose of study drug or the expectation that such treatment will be needed at any time during the study
- Are currently enrolled in or have participated in any other clinical study involving an investigational product or in any other type of medical research within the last 90 days (or within 5 half-lives of the investigational product, whichever is longer)
- Donation or loss of blood or blood products in excess of 500 mL within 3 months of screening
- Evidence of current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection
- Hepatitis A, B, C, D, or E or HIV infection
- History of drug or alcohol abuse in the past 2 years
- Regular alcohol consumption in males > 21 units per week and in females > 14 units per week (1 unit = 1/2 pint of beer, or a 25 mL shot of 40% spirit, 1.5 to 2 units = 125 mL glass of wine, depending on type)
- Use of > 5 cigarettes or equivalent nicotine-containing product per day prior to screening
Exclusion Criteria for Mass Balance Cohorts
- Regular work with ionizing radiation or radioactive material
- Radiation exposure, including that from the present study, excluding background radiation but including diagnostic X-rays and other medical exposures, exceeding 5 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 2017, shall participate in the study
- Exposure to radiation for diagnostic reasons (except dental X-rays and plain X-rays of thorax and bony skeleton [excluding spinal column]), during work, or during participation in a medical trial in the previous year
- History of gastrointestinal (GI) surgery
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
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Experimental: Mass Balance (MB) Cohort
Participants will receive oral [14C] RO7049389 under fasted conditions, followed by intravenous IV [13C] after a two-hour period.
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Participants will receive IV [13C] RO7049389.
Participants will receive an oral suspension of [14C] RO7049389.
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Experimental: Absolute Bioavailability (BA) Cohort
In Periods 1 and 2, participants will receive oral [12C] RO7049389 under fasted conditions, followed by IV [13C] RO7049389.
There is a minimum 7-day washout between periods.
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Participants will receive IV [13C] RO7049389.
Participants will receive oral [12C] RO7049389.
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Percentage of Dose Excreted in Urine - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Percentage of Dose Excreted in Feces - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Percent Total Recovery (Urine + Feces) - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Absolute Oral BA for RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Clearance (CL) of RO7049389 - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Clearance (CL) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Half-Life (T1/2) of RO7049389 - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Half-Life (T1/2) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Maximum Plasma Concentration (Cmax) of RO7049389 - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Maximum Plasma Concentration (Cmax) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Time to Maximum Plasma Concentration (Tmax) of RO7049389 - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Time to Maximum Plasma Concentration (Tmax) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Area Under Concentration-Time Curve From Time Zero to Infinity (AUC0-inf) of RO7049389 - MB Cohort
Time Frame: Up to Day 4
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Up to Day 4
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Area Under Concentration-Time Curve From Time Zero to Infinity (AUC0-inf) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Area Under the Concentration-Time Curve From Time Zero to Last Measurable Concentration (AUClast) of RO7049389 - MB Cohort
Time Frame: Up to Day 17
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Up to Day 17
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Area Under the Concentration-Time Curve From Time Zero to Last Measurable Concentration (AUClast) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Apparent Clearance (CL/F) of RO7049389 - MB Cohort
Time Frame: Up to Day 4
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Up to Day 4
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Apparent Clearance (CL/F) of RO7049389 - BA Cohort
Time Frame: Up to Day 4
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Up to Day 4
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Renal Clearance (CLr) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Amount Excreted in Urine (Ae) of RO7049389 - BA Cohort
Time Frame: Up to Day 4 of Periods 1 and 2
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Up to Day 4 of Periods 1 and 2
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Percentage of Participants With Adverse Events (AEs)
Time Frame: Up to Day 29 (MB Cohort) or up to Day 29 of Period 2 (AB Cohort)
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Up to Day 29 (MB Cohort) or up to Day 29 of Period 2 (AB Cohort)
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Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Director: Clinical Trials, Hoffmann-La Roche
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- BP41811
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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