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PHARM (PHARM) News

Track canonical SquawkNews coverage tagged to PHARM, PHARM. This hub brings together deduplicated headlines about market instrument, markets catalysts, earnings, analyst actions, and wider market events so traders can review how a developing story changed over time. It contains 17 indexed stories across 8 publication days and is ordered by the same first-publication timeline used by LiveCast.

Symbol PHARM Asset market Sector Markets 90 days 17 Updated Sep 29, 2026, 05:04 AM UTC Open live news feed
L Pharming Announces Fabrice Chouraqui Will Step Down As CEO And Executive Director Effective Immediately Pharming Group N.V. EURONEXT:PHARM NEWS | Sep 29, 2026, 05:04 AM UTC L Pharming Group N.V. (PHARM) CEO Steps Down; CCO/CFO Named Interim Co-CEOs Pharming Group N.V. said CEO and Executive Director Fabrice Chouraqui stepped down effective immediately. CCO Leverne Marsh and CFO Kenneth Lynard were appointed interim co-CEOs while the board begins a search for a perm NEWS | Sep 29, 2026, 05:01 AM UTC L Pharming announces CEO transition Leiden, the Netherlands, September 29, 2026: Pharming (Euronext Amsterdam: PHARM/NASDAQ:PHAR), a global biotechnology company focused on rare immune and genetic diseases, today announced that the Board of Directors and F NEWS | Sep 29, 2026, 05:00 AM UTC L Pharming Announces US FDA Acceptance Of Snda For Lower Doses Of Joenja Pharming Group N.V. EURONEXT:PHARM REGULATION | Sep 25, 2026, 02:36 PM UTC L Pharming Group N.V. (PHARM) Wins FDA Priority Review for Joenja sNDA in Younger Children FDA accepted Pharming’s sNDA for lower Joenja doses in children 4+ weighing 13—27 kg with APDS and granted Priority Review. PDUFA target action date is Jan 30, 2027.Material DetailsContext by AI AnalystThis is a mid-cycl REGULATION | Sep 25, 2026, 02:32 PM UTC L Pharming announces U.S. FDA acceptance and Priority Review of sNDA for lower doses of Joenja® to treat children with APDS Leiden, the Netherlands, September 25, 2026: Pharming (Euronext Amsterdam: PHARM/Nasdaq: PHAR), a global biotechnology company focused on rare immune and genetic diseases, today announced that the U.S. Food and Drug Admi REGULATION | Sep 25, 2026, 02:32 PM UTC M HC Wainwright reiterates Buy on Pharming, lifts $37 target HC Wainwright & Co. reiterated a Buy rating on Pharming with a $37.00 price target, implying upside of 3,736.6% from the Sep 22 close of $0.96. EQUITY | Sep 22, 2026, 04:17 PM UTC M Pharming reports positive Phase II leniolisib topline in PIDs Pharming said it posted positive topline Phase II data for leniolisib in genetically defined PIDs with immune dysregulation, citing a mean 26.4% spleen volume reduction and no new safety signals. Additional data is plann EARNINGS | Sep 22, 2026, 05:01 AM UTC M Pharming posts positive leniolisib Phase II topline data in PIDs Pharming said a late-breaking ESID 2026 abstract will highlight positive Phase II topline data for leniolisib in primary immunodeficiencies with immune dysregulation. EARNINGS | Sep 22, 2026, 05:01 AM UTC H PHARM - Pharming announces positive Phase II topline data for leniolisib in PIDs with immune dysregulation accepted as late-breaking abstract at ESID 2026 PHARM - Pharming announces positive Phase II topline data for leniolisib in PIDs with immune dysregulation accepted as late-breaking abstract at ESID 2026 NEWS | Sep 22, 2026, 05:00 AM UTC H PHARM: Joenja and RUCONEST fuel growth, with pipeline advances and $375—395M revenue projected for 2026 RUCONEST and Joenja drive strong commercial performance, with Joenja expanding into new indications and geographies. Napazimone advances in pivotal trials for mitochondrial disease. Financial guidance projects $375—395M EARNINGS | Sep 15, 2026, 06:37 AM UTC L Pharming Group N.V. Newly Approved Joenja Doses Are Expected To Be Available In October Pharming Group N.V. EURONEXT:PHARM NEWS | Sep 11, 2026, 07:27 PM UTC H FDA approves Pharming’s Joenja for children with APDS Pharming said the FDA approved its supplemental New Drug Application for Joenja® as a first treatment for children with APDS in the U.S. REGULATION | Sep 11, 2026, 06:01 PM UTC M FDA approves Joenja (leniolisib) for APDS in children 4-11 The FDA approved Joenja (leniolisib) as the first treatment for APDS in children aged 4-11. REGULATION | Sep 11, 2026, 04:08 PM UTC L Pharming management to participate in September investor conferences Pharming Group N.V. said management will participate in investor conferences during September. EQUITY | Sep 09, 2026, 06:07 AM UTC H Pharming launches Joenja (leniolisib) commercially in Japan Pharming announces the commercial launch of Joenja (leniolisib) in Japan for adult and pediatric patients with APDS aged 4 and older. EQUITY | Aug 13, 2026, 05:00 AM UTC H PHARM - Pharming reports second quarter and first half 2026 financial results and revises year-end guidance; strong Joenja momentum and near PHARM - Pharming reports second quarter and first half 2026 financial results and revises year-end guidance; strong Joenja momentum and near-term clinical readouts to support broader therapeutic use EQUITY | Jul 30, 2026, 05:00 AM UTC