aprepitant oral / Generic mfg. 
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 156 Diseases   15 Trials   15 Trials   235 News 


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  • ||||||||||  aprepitant oral / Generic mfg.
    Clinical, Journal:  Relative bioavailability of an extemporaneously prepared aprepitant oral suspension in healthy adults. (Pubmed Central) -  Jan 21, 2020   
    With a relative bioavailability of 82.3%, the extemporaneous aprepitant oral suspension was well-absorbed relative to the capsule. Though not bioequivalent to the oral capsule, the clinical use of this aprepitant oral suspension in adult and pediatric patients unable to swallow capsules is likely to be effective and safe.
  • ||||||||||  aprepitant oral / Generic mfg.
    Clinical, Journal:  Aprepitant for Cough Suppression in Advanced Lung Cancer: A Randomized Trial. (Pubmed Central) -  Jan 21, 2020   
    Though not bioequivalent to the oral capsule, the clinical use of this aprepitant oral suspension in adult and pediatric patients unable to swallow capsules is likely to be effective and safe. Aprepitant led to a significant improvement in cough in advanced lung cancer, without increasing severe side-effects.
  • ||||||||||  hydroxyzine hydrochloride / Generic mfg.
    Enrollment open:  APHYPAP: Aprepitant Versus Hydroxyzine in Persistent Aquagenic Pruritus for Patients With Myeloproliferative Neoplasms (clinicaltrials.gov) -  Apr 21, 2019   
    P3,  N=80, Recruiting, 
    Taken together, the present study suggests that inhibition of NK1R using Aprepitant, either alone or in combination with chemotherapeutic drugs, could be a novel therapeutic strategy for the treatment of acute leukemia, especially APL, that may be clinically accessible in the near future. Not yet recruiting --> Recruiting
  • ||||||||||  Emend intravenous (fosaprepitant) / Merck (MSD), Novartis
    Clinical, Journal:  Evaluation of aprepitant and fosaprepitant in pediatric patients. (Pubmed Central) -  Apr 13, 2019   
    Aprepitant and fosaprepitant were safely used and may be equally useful for pediatric patients receiving highly emetogenic chemotherapy. CR rate may be associated with patient age.
  • ||||||||||  pramipexole ER (CTC-413) / Chase Therap
    Enrollment open, Trial initiation date:  A Study to Evaluate in Patients With Parkinsonian Type Disorders (clinicaltrials.gov) -  Apr 11, 2019   
    P2,  N=24, Recruiting, 
    CR rate may be associated with patient age. Not yet recruiting --> Recruiting | Initiation date: Nov 2018 --> Apr 2019
  • ||||||||||  dexamethasone / Generic mfg., mirtazapine / Generic mfg.
    Trial primary completion date:  Adding Mirtazapine to Dexamethasone and Aprepitant for Delayed Emesis (clinicaltrials.gov) -  Feb 16, 2019   
    P3,  N=212, Recruiting, 
    Not yet recruiting --> Recruiting | Initiation date: Nov 2018 --> Apr 2019 Trial primary completion date: Dec 2018 --> Dec 2019
  • ||||||||||  Akynzeo oral (netupitant/palonesteron FDC) / Helsinn, Roche, Otsuka, Mundipharma, Immedica
    New P4 trial, HEOR:  Comparative Effectiveness of AKYNZEO (clinicaltrials.gov) -  Feb 6, 2019   
    P4,  N=426, Recruiting, 
  • ||||||||||  melphalan / Generic mfg., olanzapine / Generic mfg.
    Enrollment open, Trial completion date, Trial initiation date, Trial primary completion date:  Aprepitant- and Olanzapine- Containing Anti-emetic Regimens With High Dose Melphalan (clinicaltrials.gov) -  Jan 28, 2019   
    P3,  N=429, Recruiting, 
    Trial primary completion date: Dec 2018 --> Dec 2019 Not yet recruiting --> Recruiting | Trial completion date: Nov 2018 --> Nov 2020 | Initiation date: Nov 2016 --> Sep 2017 | Trial primary completion date: Nov 2018 --> Nov 2020
  • ||||||||||  Review, Journal, CINV:  Evolving role of neurokinin 1-receptor antagonists for chemotherapy-induced nausea and vomiting. (Pubmed Central) -  Oct 18, 2018   
    To examine pharmacologic and clinical characteristics of neurokinin 1 (NK)-receptor antagonists (RAs) for preventing chemotherapy-induced nausea and vomiting (CINV) following highly or moderately emetogenic chemotherapy, a literature search was performed for clinical studies in patients at risk of CINV with any approved NK RAs in the title or abstract: aprepitant (capsules or oral suspension), HTX019 (intravenous [IV] aprepitant), fosaprepitant (IV aprepitant prodrug), rolapitant (tablets or IV), and fixed-dose tablets combining netupitant or fosnetupi-tant (IV netupitant prodrug) with the 5-hydroxytryptamine type 3 (5HT) RA palonosetron (oral or IV)...Adding an NK RA to 5HT RA and dexamethasone significantly improves CINV control vs the two-drug regimen. Newer NK RAs offer more formulation options, higher acute-phase plasma levels, or improved tolerability, and increase clinicians' opportunities to maximize benefits of this important class of antiemetics.
  • ||||||||||  Januvia (sitagliptin) / Merck (MSD)
    Trial completion date, Trial primary completion date:  Effect of Chronic ACE and DPP4 Inhibition on Blood Pressure (clinicaltrials.gov) -  Sep 26, 2018   
    P=N/A,  N=150, Recruiting, 
    Newer NK RAs offer more formulation options, higher acute-phase plasma levels, or improved tolerability, and increase clinicians' opportunities to maximize benefits of this important class of antiemetics. Trial completion date: Jul 2018 --> Jun 2020 | Trial primary completion date: Jun 2018 --> Mar 2020
  • ||||||||||  dexamethasone / Generic mfg., mirtazapine / Generic mfg.
    Trial primary completion date:  Adding Mirtazapine to Dexamethasone and Aprepitant for Delayed Emesis (clinicaltrials.gov) -  Jan 23, 2018   
    P3,  N=212, Recruiting, 
    Suspended --> Terminated; Study terminated due to no patient population available Trial primary completion date: Dec 2017 --> Dec 2018