Table 2.
Type of Drug | Drug Name | Route of Administration | ClinicalTrials.gov Identifier | Clinical Phase and Status | Affected OA Joint |
Primary Measures or Results | References |
---|---|---|---|---|---|---|---|
CGRP antibody | Galcanezumab | S.C. | NCT02192190 | Phase 2, completed | knee | No improvement in WOMAC pain | [60] |
IL-1 receptor antagonist | Anakinra | I.A. | NCT00110916 | Phase 2, completed | Knee | No improvements on OA symptoms | [72] |
TNFα antibody | Adalimumab | S.C. | NCT00686439 | Phase 2, completed | knee | Improvement in WOMAC pain. | [73] |
NGF inhibitor | Tanezumab | I.V. | NCT00394563 | Phase 2, completed | Knee | Reduction in joint pain and improvement in function | [120] |
NGF inhibitor | Fasinumab | S.C. |
NCT02709486, NCT02528188, NCT02697773 |
Phase 3, completed | Knee, hip | Improvement in pain within the first week, and pain and function were improved throughout 24 weeks | [121,122,123] |
S.C. | NCT02447276 | Phase 3, completed | Knee, hip | Improvements in OA pain and function | [124] | ||
S.C. | NCT02683239, NCT03161093, NCT03304379 | Phase 3, completed | Knee, hip | WOMAC pain subscale score | |||
Tanezumab | I.V. |
NCT00863304, NCT00830063, NCT00744471 |
Phase 3, completed | Knee, hip | Improvement of pain, physical function, and patient global assessment of OA | [125,126] | |
TrkA inhibitor | ASP7962 | P.O. | NCT02611466 | Phase 2, completed | Knee | No improvement in WOMAC pain | [127] |
GZ389988A | I.A. | NCT02845271 | Phase 2, completed | Knee | Improvement in WOMAC pain | [128] | |
TNFα antibody | Adalimumab | S.C. | ACTRN12612000791831 | Phase 2, completed | Hand | No improvements on symptoms or bone marrow lesions | [129] |
S.C. | NCT00597623 | Phase 3, completed | Hand | No improvement in WOMAC pain | [130] | ||
CCR2 antagonist | CNTX-6970 | P.O. | NCT05025787 | Phase 2, recruiting | Knee | WOMAC pain | |
NGF/TNF-α bispecific antibody | MEDI7352 | P.O. | NCT04675034 | Phase 2b, recruiting | Knee | NRS | |
IL-1α/β antibody | Lutikizumab | S.C. | NCT02384538 | Phase 2, completed | Hand | No improvement in pain score | [131] |
IL-1R1 antibody | AMG 108 | I.V. | NCT00110942 | Phase 2, completed | Knee | Minimal clinical benefit | [132] |
IL-1α/β antibody | Lutikizumab | S.C. | NCT02087904 | Phase 2, completed | Knee | No improvement in WOMAC pain | [133] |
NLRP3 inhibitor | DVF890 | P.O. | NCT04886258 | Phase 2a, recruiting | Knee | KOOS pain sub-scale | |
Wnt inhibitor | Lorecivivint (SM04690) |
I.A. |
NCT04385303 (NCT03928184 *) |
Phase 3, active, not recruiting | Knee | Improvement in NRS Pain | [134] |
TRPV1 inhibitor | CNTX-4975 | I.A. | NCT03660943, NCT03661996 | Phase 3, completed | Knee | WOMAC | |
NE06860 | P.O. | NCT02712957 | Phase 2, completed | Knee | NRS | ||
TRPA1 antagonist | LY3526318 | P.O. | NCT05080660 | Phase 2, recruiting | Knee | NRS and WOMAC pain | |
SCN9A # antisense drug | OLP1002 | S.C. | NCT05216341 | Phase 2, recruiting | Knee, hip | WOMAC and VAS | |
Central analgesic | Cannabinoid | P.O. | NCT04992962 | Phase 2, recruiting | Knee | NRS and KOOS | |
Tubulin inhibitor | Colchicine | P.O. | NCT03913442 | Phase 4, recruiting | Knee | VAS pain scores | |
Aryl hydrocarbon receptor antagonist | Resvertrol | P.O. | NCT02905799 | Phase 3, recruiting | Knee | NRS | |
Peroxynitrite decomposer | ACP044 | P.O. | NCT05008835 | Phase 2, recruiting | Knee | NRS |
* Terminated due to business reasons by Sponsor; # SCN9A gene encoding Nav1.7sodium ion channel; Abbreviation: Subcutaneous injection, S.C.; Intravenous injection, I.V.; Oral administration, P.O.; Intra-articular injection, I.A.; Numeric rating scale, NRS; Western Ontario and McMaster Universities Osteoarthritis Index, WOMAC; Visual analogue scale, VAS; Knee injury and osteoarthritis outcome score, KOOS.