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NCT01442831

Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects

Completed Phase 1 Last updated 15 November 2019
What this trial tests

Phase 1 trial testing Human ADME in Healthy in 6 participants. Completed in 22 September 2010.

Timeline
9 September 2010
Primary endpoint
22 September 2010
22 September 2010

Quick facts

Lead sponsorTrius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment6
Start date9 September 2010
Primary completion22 September 2010
Estimated completion22 September 2010
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) — full company profile →

Who can join

Adults 18 to 50, male only, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to describe the single dose pharmacokinetics of total radioactivity in plasma and whole blood following PO administration of \[14C\] TR-701 in healthy adult male subjects.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Revolutionizing tuberculosis treatment: Breakthroughs, challenges, and hope on the horizon.
    Kufa M, Finger V, Kovar O, Soukup O, et al · · 2025 · cited 6× · PMID 40370552 · DOI 10.1016/j.apsb.2025.01.023

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Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) trials

Trials by the same sponsor.

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Data sources for this page

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