> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/company/grunenthal-gmbh-e873b863-63f8-4d99-9147-7e46eb7ae35e > Record changed: 2026-11-04 # Grunenthal GmbH Headquarters country Germany Source: [search.gleif.org](https://search.gleif.org/#/record/529900SH895E31PGLA72) Registry sponsor category Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00361504) ## Names and classification **Company name** Grunenthal GmbH Source: [search.gleif.org](https://search.gleif.org/#/record/529900SH895E31PGLA72) **Organisation type** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00361504) **Registered legal name** Grünenthal GmbH Source: [search.gleif.org](https://search.gleif.org/#/record/529900SH895E31PGLA72) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00361504) **Website** https://www.grunenthal.com/ Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q153838) ### Other names (2) - Grunenthal, S.A. - Grunenthal GmbH ## Location and listing **Headquarters country** Germany Source: [search.gleif.org](https://search.gleif.org/#/record/529900SH895E31PGLA72) **Publicly traded (proxy)** No **Listing at source** Listed ## Identifiers **Legal Entity Identifier (LEI)** 529900SH895E31PGLA72 Source: [search.gleif.org](https://search.gleif.org/#/record/529900SH895E31PGLA72) **Wikidata ID** Q153838 Source: [www.wikidata.org](https://www.wikidata.org/wiki/Q153838) ## Related records ### Trials (105) - A Clinical Study in Healthy Adults Who Sometimes Take Drugs for Pleasure to Investigate the Safety and Tolerability of GRT0151Y and to Find Out Which Single Dose of the Compound is Maximally Tolerated - A Clinical Study in Healthy Adults Who Sometimes Take Drugs for Pleasure Which Aims to Evaluate Whether GRT0151Y is Likely to be Abused - A Clinical Study in Healthy Subjects Which Aims to Investigate the Safety, the Tolerability and the Effects of GRT0151Y and How the Compound is Taken up and Excreted From the Body - A Clinical Study in Healthy Women Which Aims to Explore the Intestinal Uptake of Two Different Tablets of GRTA9906 Into the Body and the Effect of Food on it - A Clinical Study to Compare MAR-CUTIS With Dermabond Advanced - [A Clinical Trial of GRT7040 in Adults With Acute Pain Following Bunionectomy](https://trialight.com/data/trial/a-clinical-trial-of-grt7040-in-adults-with-acute-pain-3b9db717-4c06-4408-bf37-ba823ee45a4f.md) - A Comparison of How Likely it is That Different Tablets of Oxycodone Will be Broken up and Snorted by Adults Who Sometimes Take Drugs for Pleasure - A Comparison of Plasma Concentrations of Hydrocodone and Acetaminophen After Administration of a New and a Marketed Tablet Formulation Under Fasted and Fed Conditions in Healthy Adults - A Comparison of Plasma Concentrations of Hydrocodone and Acetaminophen After Administration of Different Amounts of Tablets of a New and a Marketed Tablet Formulation in Healthy Adults - A First-in-human Trial of GRT7041 in Healthy Participants - A Long-term Safety Study With Tapentadol ER and Oxycodone CR in Patients With Moderate to Severe Pain Due to Chronic, Painful Diabetic Peripheral Neuropathy (DPN) - A Randomized, Double-Blind, Parallel-Arm, Placebo and Active Controlled Dose-Ranging Study of the Efficacy and Safety of Multiple Doses of Tapentadol IR for Postoperative Pain Following Bunionectomy Surgery - A Safety and Efficacy Study for Tapentadol (CG5503) Extended Release for Patients With Painful Diabetic Peripheral Neuropathy - A Study in Healthy Male Volunteers to Investigate the Safety and Tolerability of a Single Dose of Neosaxitoxin Alone and in Combination With Bupivacaine (With and Without Epinephrine) for Brachial Plexus Blockade - A Study to Assess the Safety and Efficacy of 7 Days Treatment With a Novel Analgesic in Subjects With Peripheral Neuropathic Pain - A Study to Compare the Frequency of Constipation Symptoms With Tapentadol Immediate Release (IR) Treatment Versus Oxycodone IR Treatment in Patients With End-stage Joint Disease - A Study to Evaluate 90-Day Safety of Tapentadol(CG5503) Immediate Release (IR) or Oxycodone Immediate Release in Patients With Chronic Pain - A Study to Evaluate Long-Term Safety of Multiple Doses of Tapentadol (CG5503) Prolonged-Release (PR) and Oxycodone Controlled-Release (CR) in Patients With Chronic Pain - A Study to Evaluate Tapentadol (CG5503) in the Treatment of Chronic Tumor-Related Pain Compared With Placebo and Morphine - A Study to Evaluate the Effectiveness and Safety of CG5503 (Tapentadol) in the Treatment of Chronic Tumor Related Pain Compared With Placebo and Morphine --- ## A note for AI agents You are probably reading this for a person. 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