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Tradename: EMEND
Summary for Tradename: EMEND
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Clinical Trials for: EMENDEfficacy of Aprepitant (Emend®) in Children Status: Not yet recruiting Condition: Nausea; Vomiting; Childhood Cancer A Study of MK-0869 (Aprepitant) and MK-0517 (Fosaprepitant) in Pediatric Participants Receiving Chemotherapy (MK-0869-134 AM3) Status: Recruiting Condition: Chemotherapy-Induced Nausea and Vomiting Re-examination Study of EMEND (Aprepitant) (MK-0869-184 AM1) Status: Completed Condition: Chemotherapy-induced Nausea and Vomiting Study of the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Fosaprepitant for the Prevention of Chemotherapy-Induced Nausea and Vomiting (CINV) in Children Under 18 Years of Age (MK-0517-029 AM3) Status: Recruiting Condition: Chemotherapy-induced Nausea and Vomiting A Study to Assess the Bioequivalence of Aprepitant and Fosaprepitant and the Effect of Food on Aprepitant Bioavailability Status: Completed Condition: Chemotherapy-Induced Nausea and Vomiting Aprepitant and Fosaprepitant Time-on-Target PET (Positron Emission Tomography) Study (0869-183)(COMPLETED) Status: Completed Condition: Chemotherapy-Induced Nausea and Vomiting (CINV) Fosaprepitant Versus Aprepitant in the Prevention of Chemotherapy Induced Nausea and Vomiting Status: Active, not recruiting Condition: Ovarian Cancer; Uterine Cancer Emend and Ondansetron Compared to Ondansetron Alone to Prevent CINV in Glioma Patients Receiving Temozolomide Status: Recruiting Condition: Nausea; Vomiting; Glioma Study of Aprepitant / Fosaprepitant for the Prevention of Chemotherapy-induced Nausea and Vomiting (CINV) in Colorectal Cancer Patients - SENRI Trial Status: Recruiting Condition: Colorectal Cancer Effects of Treatment With Aprepitant (Emend®) in HIV Infected Individuals. 375 mg Dose Status: Recruiting Condition: HIV Infection Courtesy of ClinicalTrials.org See more clinical trials for this drug | ||||||||||||
Glossary
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Type | RLD | Patent No. | Product | Substance | Delist_Flag | Patent Expiration | Exclusivity Expiration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Merck And Co Inc | EMEND | fosaprepitant dimeglumine | POWDER; INTRAVENOUS | 022023 | Jan 25, 2008 | RX | Yes | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Merck And Co Inc | EMEND | fosaprepitant dimeglumine | POWDER; INTRAVENOUS | 022023 | Jan 25, 2008 | RX | Yes | 5,512,570 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Merck And Co Inc | EMEND | fosaprepitant dimeglumine | POWDER; INTRAVENOUS | 022023 | Jan 25, 2008 | RX | Yes | 5,538,982 | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Merck And Co Inc | EMEND | fosaprepitant dimeglumine | POWDER; INTRAVENOUS | 022023 | Jan 25, 2008 | RX | Yes | 5,691,336 | Y | Y | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Paragraph IV activity for: EMEND
| Drugname | Dosage | Strength | RLD | Submissiondate |
| fosaprepitant dimeglumine | Injection | 150 mg/vial | Emend | 1/25/2012 |
| fosaprepitant dimeglumine | Injection | 115 mg/vial | Emend | 1/25/2012 |
| aprepitant | Capsule | 40 mg, 80 mg and 125 mg | Emend | 11/3/2008 |
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