> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/company/organon-and-co-aef8c0c7-e814-4a91-a8fb-bb3b12559dfc > Record changed: 2026-10-13 # Organon and Co Headquarters country United States Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001821825) Registry sponsor category Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/) ## Names and classification **Company name** Organon and Co **Organisation type** Industry **Registered legal name** Organon & Co. Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001821825) **US industry code (SIC)** Pharmaceutical preparations Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001821825) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/) **Website** https://www.organon.com/ Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q903372) ### Other names (3) - Organon - Organon GmbH (former name) - Organon and Co ## Location and listing **Headquarters country** United States Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001821825) **Publicly traded (proxy)** Yes **Listing at source** Listed ## Identifiers **SEC filer number (CIK)** 0001821825 Source: [www.sec.gov](https://www.sec.gov/cgi-bin/browse-edgar?action=getcompany&CIK=0001821825) **Wikidata ID** Q903372 Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q903372) ## Related records ### Trials (540) - 12 Week Study of the Safety/Efficacy of Asenapine When Added to Lithium/Valproate in the Treatment of Bipolar Disorder (A7501008 / P05844 / MK-8274-017) - 3-Week Study of Asenapine, Olanzapine and Placebo for Treatment of Bipolar Mania (P07008) - 3-week Study of Asenapine, Olanzapine and Placebo for Treatment of Bipolar Mania (P07009) - 4-Week Study to Assess the Effect of Alendronate and Vitamin D3 Once Weekly on Fractional Calcium Absorption in Postmenopausal Osteoporotic Women (0217A-230) - 40 Week Extension Study Of Asenapine and Olanzapine For Bipolar Disorder (A7501007)(COMPLETED)(P05857) - 40 Week Trial to Study the Safety of Asenapine When Added to Lithium or Valproate in the Treatment of Bipolar Disorder (A7501009)(P05786) - 6-Month Extension Trial of Asenapine With Olanzapine in Negative Symptom Patients Who Completed the Protocol 25543 (25544)(P05777) - 6-Month Extension Trial of Asenapine With Olanzapine in Negative Symptoms Patients Who Completed the First 6- Month Trial (A7501014)(COMPLETED)(P05772) - 6-week Trial of the Efficacy and Safety of Asenapine Compared to Placebo in Participants With an Acute Exacerbation of Schizophrenia (P06124) - 9 Week Extension Study of Asenapine and Olanzapine in Treatment of Mania (P07007)(COMPLETED) - A 12 Week Study of MK0653A in Patients Who Have Been Hospitalized for a Possible Heart Problem (0653A-808) - A 12-week Post-marketing, Observational Study to Confirm the Safety and Efficacy of Zetia Alone or in Combination With Other Lipid-lowering Drugs in Japanese Subjects With Hypercholesterolemia (Study P05244) - A 52 Week Study to Evaluate the Effects of Losartan With or Without HCTZ on Plasma Glucose, Metabolic Parameters, Blood Pressure in Hypertensive Patients With Metabolic Syndrome (0954A-331) - A 52-week Post-marketing, Observational Study to Confirm the Safety and Efficacy of Zetia Alone or in Combination With Other Lipid-lowering Drugs in Japanese Subjects With Hypercholesterolemia (Study P05245) - A Bioequivalence Study of IMPLANON and Radiopaque IMPLANON (34528)(P05720) - A Clinical Trial to Assess the Efficacy and Safety of MK-0653C in Japanese Participants With Hypercholesterolemia (MK-0653C-383) - A Clinical Trial to Assess the Long Term Safety and Tolerability of MK-0653C in Japanese Participants With Hypercholesterolemia (MK-0653C-384) - A Clinical Trial to Assess the Long Term Safety and Tolerability of MK-0653H in Japanese Participants With Hypercholesterolemia (MK-0653H-833) - A Comparative Double-Blind, Double- Dummy Study of Desloratadine (DL) 5 MG Once Daily, Cetirizine 10 MG Once Daily, and Placebo Once Daily in Patients With Chronic Idiopathic Urticaria (Study P03735) - A Comparative Double-blind, Double-dummy Study of Desloratadine (DL) 5 mg Once Daily, Cetirizine 10 mg Once Daily, and Placebo Once Daily in Patients With Chronic Idiopathic Urticaria (Study P03736) --- ## A note for AI agents You are probably reading this for a person. 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