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Articles published by Organon & Co.

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Organon’s VTAMA® (tapinarof) cream, 1%, Granted Strong Recommendation in the American Academy of Dermatology Updated 2025 Guidelines for Adult Atopic Dermatitis
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Organon Provides Update on Phase 2 ELENA Proof-of-Concept Study Evaluating OG-6219 in Patients with Endometriosis-Related Pain
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US Food and Drug Administration (FDA) Grants Interchangeability Designation to Samsung Bioepis and Organon HADLIMA™ (adalimumab-bwwd) Injection
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Organon Reports Results for the First Quarter Ended March 31, 2025
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Organon Appoints Ramona A. Sequeira to the Company’s Board of Directors
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Organon To Report First Quarter 2025 Results and Host Conference Call on May 1, 2025
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Organon Acquires TOFIDENCE™ (tocilizumab-bavi), a Commercialized Biosimilar to ACTEMRA® (tocilizumab) Injection, for Intravenous Infusion in the U.S.
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European Medicines Agency (EMA) Validates Henlius and Organon Filing for Perjeta® (pertuzumab) Biosimilar Candidate HLX11
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New Analysis of Organon’s VTAMA® (tapinarof) cream, 1% Phase 3 Data Shows Atopic Dermatitis Disease Activity Remained Low After Treatment-Free Interval in Adults and Children 2 Years of Age and Older
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Organon Reports Results for the Fourth Quarter and Full Year Ended December 31, 2024
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Organon To Report Fourth Quarter and Full Year 2024 Results and Host Conference Call on February 13, 2025
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Organon To Present at the 43rd Annual J.P. Morgan Healthcare Conference
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FDA Approves VTAMA® (tapinarof) cream, 1% for the Treatment of Atopic Dermatitis in Adults and Children 2 Years of Age and Older
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Update on FDA Review of VTAMA® (tapinarof) Cream, 1% for the Treatment of Atopic Dermatitis in Adults and Children 2 Years of Age and Older
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Organon Reports Results for the Third Quarter Ended September 30, 2024
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US FDA Accepts Biologics License Application (BLA) for HLX14, Biosimilar Candidate of PROLIA/XGEVA (denosumab)
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Organon Completes Acquisition of Dermavant, including Innovative Dermatologic Therapy, VTAMA® (tapinarof) Cream, 1%
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Organon to Report Third Quarter 2024 Results and Host Conference Call on October 31, 2024
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Primary Endpoint Met in Phase 3 Comparative Clinical Study of Perjeta® (pertuzumab) Biosimilar Candidate HLX11
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Organon to Acquire Dermavant including its Innovative Dermatologic Therapy, VTAMA® (tapinarof) Cream, 1%
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Organon & Lilly Expand Migraine Commercialization Agreement to 11 Additional Markets
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Organon Reports Results for the Second Quarter Ended June 30, 2024
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Organon To Report Second Quarter 2024 Results and Host Conference Call on August 6, 2024
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European Medicines Agency (EMA) Validates Henlius and Organon Filings for Prolia® and Xgeva® (denosumab) Biosimilar Candidate HLX14
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Organon Announces Pricing of $1.0 Billion Senior Notes Offering
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Organon Announces Proposed $1.0 Billion Senior Notes Offering
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Organon Reports Results for the First Quarter Ended March 31, 2024
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Organon To Report First Quarter 2024 Results and Host Conference Call on May 2, 2024
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Phase 3 Comparative Clinical Study of Prolia® and Xgeva® (denosumab) Biosimilar Candidate HLX14 Met Primary Endpoints
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Organon Announces HADLIMA™ (adalimumab-bwwd) Has Been Exclusively Selected by the US Department of Veterans Affairs (VA), Replacing HUMIRA on Its National Formulary
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