Table 2.
Compound Name | Developer | Target | Inhibitory Class | Phase of Development | Population | Trial Design | Number of Patients | Ref. |
---|---|---|---|---|---|---|---|---|
Abelacimab (MAA868) | Anthos Therapeutics Novartis AG |
FXI and FXIa | Fully human mAb IgG1 | Phase 1 | Healthy volunteers and patents with AF | Randomized, subject-and investigator-blinded, placebo-controlled study |
18 | [22] |
Phase 2 | Patients undergoing total knee arthroplasty | Open-label, parallel-group trial | 412 | [23] | ||||
Osocimab (BAY1213790) |
Bayer Pharmaceuticals |
FXIa | Fully human mAb IgG1 | Phase 1 | Healthy volunteers | Randomized, single-blind, placebo-controlled, dose-escalation study |
81 | [24] |
Phase 2 | Patients undergoing total knee arthroplasty | Randomized, open-label, adjudicator-blinded, noninferiority trial |
813 | [25] | ||||
BAY1831865 | Bayer Pharmaceuticals |
FXI | Humanized mAb IgG1 | Phase 1 | Healthy volunteers | Randomized, single-blind (participant), parallel-group, placebo-controlled, dose-escalation |
70 | [26] |
AB023/ Xisomab 3G3 |
Aronora | FXIa | Fully human monoclonal IgG1 antibody |
Phase 1 | Healthy volunteers | Randomized, double-blind, placebo-controlled, single ascending bolus dose study |
21 | [27] |
Phase 2 | Patients with end stage renal disease on chronic hemodialysis |
Randomized, Double-Blind, Placebo-Controlled Study |
24 | [28] | ||||
Asundexian (BAY 2433334) |
Bayer Pharmaceuticals |
FXIa | Small molecule | Phase 1 | Healthy volunteers | Single-blind, placebo-controlled, dose-escalation study |
70 | [29] |
Phase 2 | Patients with AF | Randomized, double-blind, double-dummy, dose-finding |
755 | [30] | ||||
Phase 2 | Patients with | Randomized, placebo-controlled, double-blind, parallel-group, dose-finding | 1601 | [31] | ||||
Milvexian (BMS-986177 JNJ- 70033093) |
Janssen of Johnson and Johnson and Bristol-Myers Squibb |
FXIa | Small molecule | Phase 1 | Healthy and mild or moderate hepatic impairment | Open-label | 26 | [32] |
Phase 1 | Healthy volunteers | Randomized, double-blind, placebo-controlled, single and multiple ascending doses |
94 | [33] | ||||
Phase 2 | Patients undergoing total knee arthroplasty | Randomized, parallel-group | 1242 | [34] | ||||
Phase 2 | Patients with ischemic stroke | Randomized, double-Blind, placebo-controlled, dose-Ranging Study | 2366 | [35] | ||||
Fesomersen (IONIS-FXI-LRX) | IONIS and Bayer | FXIa | Antisense Oligonucleotide |
Phase 1 | Healthy volunteers | Placebo-controlled, dose escalation study |
36 | [36] |
Phase 1 | End-Stage Renal Disease on Hemodialysis patients | Open-label single-dose and double-blind multiple doses |
49 | [37] | ||||
Phase 2 | Patients with end stage renal disease on chronic hemodialysis |
Double-blind, randomized | 43 | [38] | ||||
Phase 2 | Patients undergoing total knee arthroplasty | open-label, parallel-group | 300 | [39] |
AF: atrial fibrillation; F: factor; Ig: Immunoglobulin.