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Kiniksa Pharmaceuticals
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U.S.A
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Kiniksa Pharmaceuticals Corp. 100 Hayden Avenue Lexington, MA 02421 USA
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Telephone
(781) 431-9100
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KPL-404 (abiprubart) is an investigational humanized anti-CD40 monoclonal antibody designed to inhibit CD40-CD154 (CD40 ligand) interaction. It is being evaluated for the treatment of Sjogren’s Disease.


Lead Product(s): Abiprubart

Therapeutic Area: Immunology Product Name: KPL-404

Highest Development Status: Phase IProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 02, 2024

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KPL-716 (vixarelimab) is an investigational fully human monoclonal antibody that targets oncostatin M receptor beta (OSMRβ), which mediates signaling of interleukin-31 (IL-31) and oncostatin M (OSM), two key cytokines implicated in pruritus, inflammation, and fibrosis.


Lead Product(s): Vixarelimab

Therapeutic Area: Dermatology Product Name: KPL-716

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Genentech

Deal Size: $700.0 million Upfront Cash: $100.0 million

Deal Type: Licensing Agreement September 12, 2022

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Genentech will focus on development of KPL-716 (vixarelimab) in fibrosis, where oncostatin M (OSM)-mediated pathogenesis is thought to be an important pathway for intervention in multiple fibrotic indications.


Lead Product(s): Vixarelimab

Therapeutic Area: Trauma (Emergency, Injury, Surgery) Product Name: KPL-716

Highest Development Status: PreclinicalProduct Type: Large molecule

Partner/Sponsor/Collaborator: Genentech

Deal Size: $700.0 million Upfront Cash: $100.0 million

Deal Type: Licensing Agreement August 03, 2022

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Ongoing Phase 3 study of mavrilimumab in COVID-19-related ARDS represents the fastest path to potential registration for the asset, and there remains a significant unmet need in these patients.


Lead Product(s): Mavrilimumab

Therapeutic Area: Infections and Infectious Diseases Product Name: KPL-301

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 08, 2021

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The US FDA has approved Kiniksa Pharmaceuticals’ interleukin-1 alpha (IL-1α) and interleukin-1 beta (IL-1β) inhibitor Arcalyst (rilonacept) for the treatment of recurrent pericarditis and reduction in risk of recurrence in adults and children 12 years and older.


Lead Product(s): Rilonacept

Therapeutic Area: Cardiology/Vascular Diseases Product Name: Arcalyst

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 18, 2021

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Data showed an early signal of efficacy, with trends toward clinical improvement as well as lower mortality and shorter duration of mechanical ventilation in patients treated with mavrilimumab on top of corticosteroids, including dexamethasone, and/or remdesivir.


Lead Product(s): Mavrilimumab

Therapeutic Area: Infections and Infectious Diseases Product Name: KPL-301

Highest Development Status: Phase II/ Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 22, 2020

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Vixarelimab is a fully-human monoclonal antibody that targets oncostatin M receptor beta. The Phase 2b trial is designed to investigate the efficacy, safety, and pharmacokinetics of vixarelimab in patients with prurigo nodularis.


Lead Product(s): Vixarelimab

Therapeutic Area: Dermatology Product Name: KPL-716

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 15, 2020

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Kiniksa expects to initiate a Phase 2b clinical trial of vixarelimab in prurigo nodularis, evaluating a range of once-monthly dose regimens, by the end of the year.


Lead Product(s): Vixarelimab

Therapeutic Area: Dermatology Product Name: KPL-716

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 16, 2020

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Mavrilimumab was well-tolerated; there were no drug-related serious adverse events, and the rates of drug-related treatment-emergent adverse events between mavrilimumab recipients and placebo recipients were similar.


Lead Product(s): Mavrilimumab

Therapeutic Area: Immunology Product Name: KPL-301

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 09, 2020

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The Phase 2a trial met its primary efficacy endpoint: there was a statistically significant reduction in weekly-average Worst-Itch Numeric Rating Scale (WI-NRS) from baseline at Week 8 in vixarelimab recipients compared to placebo recipients.


Lead Product(s): Vixarelimab

Therapeutic Area: Dermatology Product Name: KPL-716

Highest Development Status: Phase IIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 29, 2020

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