Evaluation of Meclizine Orodispersible Tablet Pharmacokinetic in Human Volunteers

Overview

The main goal of this study is to develop a new oro-dissolvable/dispersible tablet that will augment the dual rapid absorption of MCZ from the buccal cavity as well as prolonging that from the GIT. A dual function tablet is expected to encompass an outer coat of the drug with special excipients that will rapidly disperse and the drug get dissolve and absorb in the buccal cavity and an inner core that will similarly, disperse to release MCZ coated nanoparticles in the saliva. The latter will be subsequently swallowed without water to be absorbed in a prolonged manner from the GIT. This will be advantageous for geriatric as well as pediatric patients, besides, those suffering from dysphagia. The pharmacokinetics profile of the prepared dual function tablet will be assessed in human volunteers through noncompartmental analysis.

Full Title of Study: “A New Dual Function Oro-Dissolvable/Dispersible Meclizine HCL Tablet to Challenge Patient Inconvenience: In-Vitro Evaluation and In-Vivo Assessment in Human Volunteers”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Sequential Assignment
    • Primary Purpose: Prevention
    • Masking: None (Open Label)
  • Study Primary Completion Date: November 1, 2020

Detailed Description

The oral route is the most advantageous one for delivering drugs due to patient compliance and its convenient administration. Fast disintegrating drug delivery systems are those that disintegrate immediately in the buccal cavity liberating the drug which dissolves or disperses in the saliva without need of water. The European Pharmacopeia adopted oro-dispersible tablets (ODT) for a tablet that disintegrate or disperse in less than 60 sec in the buccal cavity before swallowing. So, the drug dissolution and absorption in addition to onset of clinical influence and drug bioavailability may be considerably better than those detected from conventional tablets and capsules. ODTs were initially industrialized to increase the patient compliance (children, geriatric and bedridden patients). Nanoparticulate delivery systems have been investigated widely in the pharmaceutical industry owing to protection from degradation in GIT, the ability to control release of drugs and improvement of bioavailability. Meclizine HCL, an antihistamine, has been widely used for prophylactic treatment of nausea, vomiting and management of dizziness accompanying motion sickness. MCZ is commonly used due to fewer adverse effects than other antihistaminic drugs but its onset of action is about 1 h and possesses short half-life. MCZ is a poor water soluble drug and associated with slow rate of absorption from oral route, therefore, there is a need to improve its dissolution and so ensure the maximum therapeutic utility. However, many different formulations of MCZ have been investigated to improve its overall solubility in order to enhance its bioavailability, such as; complexation with cyclodextrin, preparation of solid dispersions as oro- dispersible tablets and fast dissolving tablet by sublimation method. Moreover, authors will investigate the ability of floating microspheres to increase the half-life of MCZ

Interventions

  • Drug: Meclizine Hydrochloride
    • A study will be conducted on the three tested orodispersible tablets and the commercial one (control). 6 volunteers are asked to cease any medication 7 days prior to blood sampling at least. Each volunteer will undergo 4 study sessions with one week of washout period in between (cross-overed to receive the other formulation). All volunteers are asked to fast overnight before taking the tablet. The tablet should be kept for 10 min in the mouth before swallowing without water. Just before taking the tablet, three milliliters of venous blood samples will be drown (predose, 0 h) and at 30, 60, 90, 120, 240, 360, 480, 720 min and 24 h postdose and stored in tubes coated with sodium heparin. Separation of plasma from Blood samples will be carried out by centrifuging at 5000 rpm for 10 min, then, it will be frozen at -20┬░C until analysis. By employing high-performance liquid chromatography (HPLC), the plasma concentration of MCZ will be assayed

Arms, Groups and Cohorts

  • Experimental: Volunteers receiving the prepared orodispersible tablets
    • 6 human volunteers will receive the prepared orodispersible tablets plus a commercial one all containing Meclizine HCl in a parallel manner.

Clinical Trial Outcome Measures

Primary Measures

  • measuring the Meclizine HCl plasma concentration
    • Time Frame: over 24 hours after dosing
    • Using high performance liquid chromatography to measure the change in plasma drug concentrationě▓
  • measuring the Meclizine HCl Area under the curve
    • Time Frame: over 24 hours after dosing
    • measuring the Meclizine HCl Area under the curve using high performance liquid chromatography
  • measuring the Meclizine HCl apparent clearance (CL/F)
    • Time Frame: over 24 hours after dosing
    • measuring the Meclizine HCl apparent clearance (CL/F) using high performance liquid chromatography
  • measuring the maximum blood concentration of Meclizine HCl
    • Time Frame: over 24 hours after dosing
    • measuring the maximum blood concentration of Meclizine HCl using high performance liquid chromatography
  • measuring the maximum blood concentration time of Meclizine HCl
    • Time Frame: over 24 hours after dosing
    • measuring the maximum blood concentration time of Meclizine HCl using high performance liquid chromatography

Participating in This Clinical Trial

Inclusion Criteria

  • Male aged between 30 and 40 years. – Body weight range of 75kg-95kg. – Healthy (defined as individuals who are free from significant nasal, cardiac, pulmonary, gastrointestinal, hepatic, renal, haematological, malignancy, endocrine, neurological and psychiatric disease as determined by history, physical examination and screening investigations). – Non-smoking status. This can include ex-smokers who have given up smoking for >1 year. – The subject is able and willing to give written informed consent to take part in the study and is available to complete all study measurements. Exclusion Criteria:

  • As a result of the medical interview, physical examination or screening investigations, the Investigator or appropriately qualified designee considers the subject unfit for the study. – The subject has a history of drug or any other allergy, which, in the opinion of the Investigator or appropriately qualified designee, contraindicates their participation, including known or suspected personal history or family history of adverse reactions or hypersensitivity to anti histamines. – The subject has participated in a study with a new molecular entity during the previous 3 months or any other study during the previous 2 months. – The subject drinks alcohol. – The subject is currently taking regular (or a course of) medication, prescribed (including all anti-allergy medication) or not (including over the counter medication or herbal remedies such as St Johns Wort). Paracetamol is an exception and will be permitted at daily doses of up to 4g following all doses of investigational product. – The subject has tested positive for hepatitis C antibody or hepatitis B surface antigen. – The subject has tested positive for HIV. – The subject has a positive drugs of abuse and alcohol test. – Donation of blood (450 mL or more) within 2 months of screening. – Donation during the study would result in >500mL of blood being donated over a 56 day period – Significant cardiac conduction abnormalities. – Subjects with Perennial Allergic Rhinitis (PAR) and Seasonal Allergic Rhinitis (SAR), unless subjects with SAR are asymptomatic and it is outside of the pollen season – Subjects who are unable to comply with study procedures.

Gender Eligibility: Male

male

Minimum Age: 30 Years

Maximum Age: 40 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Mansoura University
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Alaa Y. Darwesh, Dr, Principal Investigator, Mansoura University
  • Overall Contact(s)
    • Alaa Y. Darwesh, Dr, +201063450461, alyaser_2011@mans.edu.eg

Citations Reporting on Results

Wang K, Li L, Song Y, Ye X, Fu S, Jiang J, Li S. Improvement of pharmacokinetics behavior of apocynin by nitrone derivatization: comparative pharmacokinetics of nitrone-apocynin and its parent apocynin in rats. PLoS One. 2013 Jul 30;8(7):e70189. doi: 10.1371/journal.pone.0070189. Print 2013.

Leach WT, Simpson DT, Val TN, Yu Z, Lim KT, Park EJ, Williams RO 3rd, Johnston KP. Encapsulation of protein nanoparticles into uniform-sized microspheres formed in a spinning oil film. AAPS PharmSciTech. 2005 Dec 6;6(4):E605-17. doi: 10.1208/pt060475.

Aljimaee YH, El-Helw AR, Ahmed OA, El-Say KM. Development and optimization of carvedilol orodispersible tablets: enhancement of pharmacokinetic parameters in rabbits. Drug Des Devel Ther. 2015 Mar 5;9:1379-92. doi: 10.2147/DDDT.S80294. eCollection 2015.

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.