Quotient Sciences
Nottingham, NG11 6JS, United Kingdom
NCT Number: NCT04729309
The objective of this study is to characterize the mass balance, absolute bioavailability, route and rates of elimination of RO7049839.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 1
Nottingham, NG11 6JS, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Exclusion criteria
for Mass Balance Cohorts
Participants will receive oral [12C] RO7049389.
Participants will receive IV [13C] RO7049389.
Participants will receive an oral suspension of [14C] RO7049389.
Time frame: Up to Day 17
Time frame: Up to Day 17
Time frame: Up to Day 17
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 17
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 17
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 17
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 17
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 4
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 17
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 4
Time frame: Up to Day 4
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 4 of Periods 1 and 2
Time frame: Up to Day 29 (MB Cohort) or up to Day 29 of Period 2 (AB Cohort)
Hoffmann-La Roche
Industry
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
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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