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NCT01442831
Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects
Phase 1 trial testing Human ADME in Healthy in 6 participants. Completed in 22 September 2010.
22 September 2010
Quick facts
| Lead sponsor | Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 6 |
| Start date | 9 September 2010 |
| Primary completion | 22 September 2010 |
| Estimated completion | 22 September 2010 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Human ADME — full drug profile →
Conditions studied
- Healthy — all drugs for Healthy →
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):
-
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
Verify or expand the search:
- PubMed search for NCT01442831
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) trials
Trials by the same sponsor.
- NCT01623401 — A Phase 1, Open-Label, 10 Day Safety Study · Phase 1 · completed
- NCT01577459 — A Phase 1 Crossover Study of Blood Pressure and Heart Rate Response · Phase 1 · completed
- NCT01519778 — A Phase 2 Safety and Exploratory Skin Lesion Measurement of TR-701 FA Study · Phase 2 · completed
- NCT01496677 — Pharmacokinetics, Safety, and Tolerability of TR-701 Free Acid (FA) in Elderly Subjects · Phase 1 · completed
- NCT01461460 — A Thorough QT Study of TR-701free Acid (FA) in Healthy Subjects · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT01442831 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Trius Therapeutics LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
- Last refreshed: 15 November 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01442831.
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