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Organon & Co.
La Commissione Europea (CE) approva POHERDY ® (pertuzumab), messo a punto da Henlius e Organon, il primo biosimilare di PERJETA (pertuzumab) approvato in Europa
businesswire.com
OGN
La Commission européenne (CE) approuve le POHERDY ® (pertuzumab) de Henlius et Organon, premier médicament biosimilaire du PERJETA (pertuzumab) autorisé en Europe
businesswire.com
OGN
La Commission européenne (CE) approuve le POHERDY® (pertuzumab) de Henlius et Organon, premier médicament biosimilaire du PERJETA (pertuzumab) autorisé en Europe
businesswire.com
OGN
Europese Commissie (EC) keurt POHERDY ® (pertuzumab) van Henlius en Organon goed, de eerst goedgekeurde biosimilar voor PERJETA (pertuzumab) in Europa
businesswire.com
OGN
Europese Commissie (EC) keurt POHERDY ® (pertuzumab) van Henlius en Organon goed, de eerst goedgekeurde biosimilar voor PERJETA (pertuzumab) in Europa
businesswire.com
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Form 8-K
sec.gov
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Organon Reports Results for the First Quarter Ended March 31, 2026
businesswire.com
OGN
European Commission (EC) Approves Henlius and Organon's POHERDY® (pertuzumab), the First Approved Biosimilar to PERJETA (pertuzumab) in Europe
prnewswire.com
OGN
Organon Cancels First Quarter Earnings Call
businesswire.com
OGN
European Commission (EC) Approves Henlius and Organon’s POHERDY ® (pertuzumab), the First Approved Biosimilar to PERJETA (pertuzumab) in Europe
businesswire.com
OGN