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Kiniksa Announces Issuance of U.S. Patent for Treatment of Recurrent Pericarditis
June 08, 2021 16:01 ET | Kiniksa Pharmaceuticals, Ltd.
HAMILTON, Bermuda, June 08, 2021 (GLOBE NEWSWIRE) -- Kiniksa Pharmaceuticals, Ltd. (Nasdaq: KNSA) (“Kiniksa”), a biopharmaceutical company with a portfolio of assets designed to modulate...
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Kiniksa Outlines Next Steps for the Development of Mavrilimumab
June 08, 2021 07:30 ET | Kiniksa Pharmaceuticals, Ltd.
- Defined regulatory pathway for Phase 3 clinical development of mavrilimumab in multiple indications - - Continued development in COVID-19-related ARDS represents fastest path to potential...
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Kiniksa Pharmaceuticals to Present at Goldman Sachs 42nd Annual Global Healthcare Conference
June 01, 2021 16:01 ET | Kiniksa Pharmaceuticals, Ltd.
HAMILTON, Bermuda, June 01, 2021 (GLOBE NEWSWIRE) -- Kiniksa Pharmaceuticals, Ltd. (Nasdaq: KNSA) announced today that it will present at the Goldman Sachs 42nd Annual Global Healthcare...
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Kiniksa Reports First Quarter 2021 Financial Results and Recent Corporate and Portfolio Activity
May 04, 2021 08:00 ET | Kiniksa Pharmaceuticals, Ltd.
- ARCALYST® (rilonacept) launched as the first and only FDA-approved therapy for recurrent pericarditis -- Mavrilimumab Phase 2 severe COVID-19 data demonstrated a reduction in mechanical ventilation...
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Kiniksa Announces Positive Final Data from Phase 1 Trial of KPL-404
May 04, 2021 07:59 ET | Kiniksa Pharmaceuticals, Ltd.
- Highest dose cohorts confirm and extend previously-reported 3 mg/kg IV cohort data -- 10 mg/kg IV dose provides full receptor occupancy through Day 71 and complete suppression of TDAR after KLH...
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Kiniksa Announces Positive Results for Mavrilimumab Phase 2 Trial in Non-Mechanically Ventilated Severe COVID-19 Patients
April 12, 2021 07:30 ET | Kiniksa Pharmaceuticals, Ltd.
– Primary endpoint achieved: the proportion of patients alive and free of mechanical ventilation at Day 29 was 12.3 percentage points higher with mavrilimumab versus placebo (p=0.1224 met predefined...
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Kiniksa Announces Commercial Availability of ARCALYST ® (rilonacept) for Recurrent Pericarditis
April 01, 2021 08:00 ET | Kiniksa Pharmaceuticals, Ltd.
- ARCALYST is the first and only FDA-approved therapy for recurrent pericarditis –- ARCALYST now available on prescription basis in the U.S. –- Kiniksa One Connect™ program provides ongoing patient...
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Kiniksa Announces FDA Approval of ARCALYST ® (rilonacept) for Recurrent Pericarditis
March 18, 2021 16:30 ET | Kiniksa Pharmaceuticals, Ltd.
- ARCALYST is the first and only FDA-approved therapy for recurrent pericarditis -- Commercial launch expected in April 2021 -- Kiniksa launches Kiniksa One Connect™ patient support program --...
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Kiniksa Launches Patient Registry (RESONANCE) for Recurrent Pericarditis
March 02, 2021 08:00 ET | Kiniksa Pharmaceuticals, Ltd.
HAMILTON, Bermuda, March 02, 2021 (GLOBE NEWSWIRE) -- Kiniksa Pharmaceuticals, Ltd. (Nasdaq: KNSA) (“Kiniksa”), a biopharmaceutical company with a pipeline of assets designed to modulate...
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Kiniksa Reports Fourth Quarter and Full-Year 2020 Financial Results and Corporate and Pipeline Activity
February 23, 2021 08:00 ET | Kiniksa Pharmaceuticals, Ltd.
- Strong execution across pipeline of immune-modulating assets throughout 2020 enables multiple milestones in 2021 -- Rilonacept in recurrent pericarditis granted priority review, with PDUFA goal date...