Lenabasum
Preclinical | Phase 1 | Phase 2 | Phase 2b | Phase 3 | |
---|---|---|---|---|---|
Systemic Sclerosis |
Phase 1 Phase complete
|
Phase 2 Phase complete
|
Phase 2b Phase complete
|
Phase 3 Phase in progress
|
|
Cystic Fibrosis |
Phase 1 Phase complete
|
Phase 2 Phase complete
|
Phase 2b Phase in progress
|
Phase 3 Phase not started
|
|
Dermatomyositis |
Phase 1 Phase complete
|
Phase 2 Phase in progress
|
Phase 2b Phase not started
|
Phase 3 Phase not started
|
|
Systemic Lupus Erythematosus |
Phase 1 Phase complete
|
Phase 2 Phase in progress
|
Phase 2b Phase not started
|
Phase 3 Phase not started
|
Lenabasum (formerly known as anabasum) is a synthetic, oral, small-molecule, selective cannabinoid receptor type 2 (CB2) agonist that preferentially binds to CB2 expressed on activated immune cells and fibroblasts. CB2 activation triggers physiologic pathways that resolve inflammation, speed bacterial clearance and halt fibrosis. CB2 activation also induces the production of specialized pro-resolving lipid mediators that activate an endogenous cascade responsible for the resolution of inflammation and fibrosis, while reducing production of multiple inflammatory mediators. Through activation of CB2, lenabasum also is designed to have a direct effect on fibroblasts to halt tissue scarring. Lenabasum has been shown to induce resolution rather than immunosuppression by triggering biological pathways to turn "off" chronic inflammation and fibrotic processes. Lenabasum has demonstrated promising potency in preclinical models of inflammation and fibrosis. Preclinical data and clinical studies have shown lenabasum to have a favorable safety, tolerability and pharmacokinetic profile. Further, the drug has demonstrated clinical benefit and beneficial impact on inflammatory and immunological markers in Phase 2 studies in diffuse cutaneous systemic sclerosis, dermatomyositis and cystic fibrosis.
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