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NCT03196206
Evaluate Pharmacokinetics and Safety of BMS-986177 in Participants With Normal Renal Function and With Moderate or Severe Renal Impairment
Phase 1 trial testing BMS-986177 in Thrombosis in 24 participants. Completed in 4 March 2018.
4 March 2018
Quick facts
| Lead sponsor | Bristol-Myers Squibb |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 24 |
| Start date | 13 July 2017 |
| Primary completion | 4 March 2018 |
| Estimated completion | 4 March 2018 |
| Sites | 3 locations across United States |
Drugs / interventions tested
- BMS-986177 — full drug profile →
Conditions studied
- Thrombosis — all drugs for Thrombosis →
Sponsor
Bristol-Myers Squibb — full company profile →
Who can join
Adults 18 to 70, any sex, with Thrombosis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Assess the pharmacokinetics, safety, and tolerability of a single dose of BMS-986177 in participants with normal renal function and moderate to severe renal impairment.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
Plasma contact factors as therapeutic targets.
Tillman BF, Gruber A, McCarty OJT, Gailani D. · · 2018 · cited 52× · PMID 30075986 · DOI 10.1016/j.blre.2018.04.001 -
Factor XI Inhibition for the Prevention of Venous Thromboembolism: An Update on Current Evidence and Future perspectives.
Poenou G, Dumitru Dumitru T, Lafaie L, Mismetti V, et al · · 2022 · cited 26× · PMID 35707632 · DOI 10.2147/vhrm.s331614 -
Single-Dose Pharmacokinetics of Milvexian in Participants with Normal Renal Function and Participants with Moderate or Severe Renal Impairment.
Perera V, Abelian G, Li D, Wang Z, et al · · 2022 · cited 16× · PMID 35906349 · DOI 10.1007/s40262-022-01150-1 -
Factor XIa Inhibitors as a Novel Anticoagulation Target: Recent Clinical Research Advances.
Xia Y, Hu Y, Tang L. · · 2023 · cited 12× · PMID 37375813 · DOI 10.3390/ph16060866 -
Inhibition of Factor XI: A New Era in the Treatment of Venous Thromboembolism in Cancer Patients?
Poenou G, Heestermans M, Lafaie L, Accassat S, et al · · 2023 · cited 7× · PMID 37833881 · DOI 10.3390/ijms241914433
Verify or expand the search:
- PubMed search for NCT03196206
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of BMS-986177
Trials testing the same drug.
- NCT03939702 — Pharmacokinetic and Metabolism of [14^C] BMS-986177 in Healthy Male Participants · Phase 1 · completed
- NCT03766581 — A Study on BMS-986177 for the Prevention of a Stroke in Patients Receiving Aspirin and Clopidogrel · Phase 2 · completed
- NCT03698513 — A Study to Assess Administration of an Oral Anti-thrombotic With Antiplatelet Therapy in Healthy Subjects · Phase 1 · completed
- NCT02982707 — Single-dose Pharmacokinetics of BMS-986177 in Participants With Hepatic Impairment Compared to Healthy Participants · Phase 1 · completed
- NCT03362437 — Evaluate the Pharmacokinetics of BMS-986177 From Two Formulations in Healthy Participants · Phase 1 · completed
Other recruiting trials for Thrombosis
Currently open trials in the same condition.
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- NCT07358416 — Complications and Antiplatelet and Anticoagulant Therapy in Vascular Surgery. · active not recruiting
- NCT06370273 — Thromboprophylaxis in Lower Limb Immobilisation · Phase 3 · recruiting
Other Bristol-Myers Squibb trials
Trials by the same sponsor.
- NCT07441408 — Long-term Extension Study to Evaluate Safety and Tolerability of Admilparant in Participants With Pulmonary Fibrosis · Phase 3 · not yet recruiting
- NCT07459543 — A Study To Assess the Safety, and Tolerability of Nivolumab + Relatlimab Fixed-Dose Combination (FDC) In Untreated, Unre · Phase 4 · not yet recruiting
- NCT07285798 — A Study of KarXT + KarX-EC for Treatment of Irritability in Children and Adolescents With Autism Spectrum Disorder · Phase 3 · not yet recruiting
- NCT07284745 — A Study of KarXT + KarX-EC for Treatment of Irritability in Children and Adolescents With Autism · Phase 3 · not yet recruiting
- NCT07492680 — A Study of BMS-986504 Monotherapy and in Combination With Other Agents in Participants With Advanced and/or Metastatic S · Phase 2 · not yet recruiting
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 NCT03196206 (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 Bristol-Myers Squibb
- Last refreshed: 10 June 2022
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/NCT03196206.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing