Codeine Phosphate/Guaifenesin ER Tablet 30 mg/600 mg Steady State Clinical Study

• Status: Completed
• Trial end date: 2015-01-01
• Target enrollment: 0
• Participant gender: All

Summary

The objectives of this pivotal study are:

1. to evaluate bioavailability of an extended-release and immediate release Codeine Phosphate/Guaifenesin tablet at steady state following multiple oral administration

2. to assess the safety and tolerability of this Codeine Phosphate/Guaifenesin extended release formulation.

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Nexgen Pharma, Inc
• Collaborator: Pharmaceutical Research Unit, Jordan
• Treatments: Chlorpheniramine, phenylpropanolamine drug combination; Codeine; Guaifenesin; Phenylpropanolamine

Criteria

Inclusion Criteria:

• Healthy non-smoking volunteers (Female volunteers on a stable contraceptive medication regimen (> 3 months) may continue during the course of the study but its use must be documented), 18 to 45 years of age, inclusive; Ethnic Group: Arab & Mediterranean.

• Race: Mixed skin (white & black skin people).

• Body Mass Index (BMI) between 18 and 32 kg/m2, inclusive (minimum of 50 kg weight);

• willing and able to comply with the appropriate instructions necessary to complete the study, and;

• Fully informed of the risks of entering the study and willing to provide written informed consent.

• Subject is available for the whole study period and gave written informed consent

• If female, must be practicing abstinence or using a medically acceptable form of contraception (e.g., intrauterine device, hormonal birth control [continuously used for at least 3 months before first dose], or double barrier method). For the purpose of this study, all females are considered to be of childbearing potential unless they have been post - menopausal, biologically sterile, or surgically sterile (i.e., hysterectomy, bilateral oophorectomy, or tubal ligation) for more than one (1) year

• Normal Physical examination.

• Vital signs within normal ranges.

• All laboratory screening results within the normal range, or being assessed as clinically Non-significant by the attending physician.

• Normal Kidney and Liver functions test.

Exclusion Criteria:

• • Women of childbearing potential who don't use any contraceptive method, pregnant and/or lactating women.

• Ethnic Group (Non- Arab &/ or Non- Mediterranean)

• A significant abnormality in the pre-study physical examination that would place the volunteer at risk during participation in the trial;

• A clinical laboratory test value outside of the accepted reference range that is deemed by the Investigator to be clinically significant;

• Require prescription medication on a regular basis;

• A clinically significant illness during the 28 days prior to Period 1 dosing (as determined by the Investigator);

• History of serious illness that can impact fate of drugs

• History of gastrointestinal obstruction, constipation, inflammatory bowel disease, gallbladder disease, pancreas disorder over last 2 years, or recent (over last 3 years) gastrointestinal tract surgery, including gall bladder resection;

• Known history or presence of cardiac, pulmonary, endocrine, musculoskeletal, neurological, hematological or disease.

• Subjects with acute pulmonary insufficiency, respiratory depression, acute or chronic severe respiratory insufficiency or history of any of these

• History of head injury, seizures over last 4 years deemed by the Investigator to be clinically significant;

• Mental disease

• History of kidney disease or urination problem over last 2 years deemed by the Investigator to be clinically significant

• Subjects with renal and/or hepatic insufficiency should be excluded

• Presence of any significant physical or organ abnormality

• History of low blood pressure is deemed by the Investigator to be clinically significant;

• A positive Hepatitis B surface antigen, Hepatitis C antibody screen, or a reactive HIV antibody screen;

• Known or suspected hypersensitivities, allergies, or other contraindications to Codeine or a related opioid and/or Guaifenesin;

• History of severe allergy or allergic reactions to study drug or related drugs or heparin

• Known history or presence of food allergies, or any condition known to interfere with the absorption, distribution, metabolism or excretion of drugs

• Known or suspected history of drug abuse within lifetime as judged by the Investigator;

• History of alcohol abuse or excessive intake of alcohol within last 5 years as judged by the Investigator;

• Positive screen for drugs of abuse, alcohol, or cotinine (nicotine) at screening or on admission to the unit prior to administration of investigational products;

• Use of drugs that induce or inhibit the hepatic metabolizing cytochrome P450 2D6 enzymes, within 30 days prior to administration of study formulations. Examples of inducers include: piperidins, carbamazepine, dexamethasone, rifampin. Examples of inhibitors include: cimetidine, diphenhydramine, fluvastatine, methadone, and ranitidine;

• Use of prescription medications within 21 days and OTC medications (including vitamins or herbal products) within 7 days (excluding flu vaccination) prior to the first administration of the study medication without Sponsor approval;

• Intake of Alcohol 48 before each study drug administration, and caffeine, or xanthine beverages 24 hrs before each study drug administration.

• Use of any investigational drug within 30 days prior to first dosing;

• Use of any tobacco-containing product within 6 months of first dosing;

• Donated more than 400 mL of blood within 4 weeks before first dosing;

• Participation in another bioequivalence study and/or Clinical trials within 80 days prior to the start of this study Period I

• Exhausting physical exercise in the last 48 hours (e.g. weight lifting) or any recent significant change in dietary or exercise habits.

• Abnormal vital signs

• Abnormal Kidney and Liver functions test.

• In the opinion of the Investigator, unlikely or unable to successfully complete the study;

• Volunteer is vegetarian.

• Vomiting, Diarrhea on admission.