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X4 Pharmaceuticals, Inc. Common Stock

X4 Pharmaceuticals Reports First Quarter 2026 Financial Results and Provides Corporate Update

globenewswire.com
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Norgine gibt die Marktzulassung der Europäischen Kommission für XOLREMDI® (Mavorixafor) bekannt, die erste zugelassene Behandlung für Patienten mit WHIM-Syndrom in der Europäischen Union USA - Deutsch USA - English USA - English USA - Français

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XFOR

X4 Pharmaceuticals Announces European Commission Approval of XOLREMDI® (Mavorixafor), the First and Only Authorized Treatment for Patients with WHIM Syndrome in the European Union

globenewswire.com
XFOR

X4 Pharmaceuticals Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

globenewswire.com
XFOR

X4 Pharmaceuticals Reports Fourth Quarter and Full Year 2025 Financial Results and Provides Corporate Update

globenewswire.com
XFOR

X4 Pharmaceuticals to Participate in a Fireside Chat at the Leerink Global Healthcare Conference

globenewswire.com
XFOR

X4 Pharmaceuticals Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

globenewswire.com
XFOR

Norgine welcomes positive CHMP opinion recommending approval of mavorixafor in the European Union for WHIM syndrome USA - English USA - Français USA - español USA - Deutsch USA - English

prnewswire.com
XFOR

Norgine celebra la opinión positiva del CHMP que recomienda la aprobación de mavorixafor USA - español USA - English USA - English USA - Deutsch USA - Français

prnewswire.com
XFOR

Norgine welcomes positive CHMP opinion recommending approval of mavorixafor in the European Union for WHIM syndrome USA - English USA - Français USA - español USA - Deutsch USA - English

prnewswire.com
XFOR