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Compare Safety and Pharmacokinetic Properties of Surfolase Capsule(Acebrophylline 100mg) and Surfolase CR(200mg)

Information source: Hyundai Pharmaceutical Co., LTD.
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Healthy Male

Intervention: Surfolase capsule (100mg) (Drug); Surfolase CR (200mg, T1) (Drug); Surfolase CR (200mg, T3) (Drug); Surfolase CR (200mg, T4) (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: Hyundai Pharmaceutical Co., LTD.

Official(s) and/or principal investigator(s):
Park, Principal Investigator, Affiliation: Yonsei University Health System, Severance Hospital

Summary

Acebrophylline is metabolized by being separated into Ambroxol and 7-theophylline when orally administered as a salt composed of an acid-base as a compound that was synthesized by and chloride (salifying) the ambroxol to 7-theophylline. Acebrophylline is selectively applied to the bronchial or lung tissue and inhibit the activity of phospholipase bronchoalveolar shows the expectorant action to raise the surface activity of the alveolar, leukotrienes (LTs) and by suppressing the production of prostaglandins (PGs), showed potent anti-inflammatory activity, bronchial was celebrated by reducing the bronchial hyperreactivity to normal state is allowed to recuperate or extended. It was developed to improve compliance improve pharmaceutically Surfolase capsule(Acebrophylline 100mg) that intake twice daily 100mg to Surfolase CR(Acebrophylline 200mg) that intake once daily 200mg

Clinical Details

Study design: Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome:

AUCt of ambroxol

Cmax of ambroxol

Secondary outcome:

AUCinf of ambroxol

Tmax of ambroxol

t1/2 of ambroxol

Eligibility

Minimum age: 20 Years. Maximum age: 55 Years. Gender(s): Male.

Criteria:

Inclusion Criteria: 1. Healthy male subjects between the ages of 20 and 55 years, BMI >18. 5, <25, inclusive *Body mass index (kg/m2) = weight(kg)/height(m)2 2. Subject who don't have congenital or chronic diseases and have no abnormal medical examination results. 3. Subject is healthy (no clinically relevant findings in any of the investigations of the pre-examination) as judged by the investigator 4. Subjects who signed and dated in informed consent form indicating that the subject has decided to participate in the study after being informed of all pertinent aspects of the study Exclusion Criteria: 1. Subject with known for hypersensitivity reaction to acebrophylline, xanthine and food. 2. Patients with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption 3. Subject with serious active cardiovascular, respiratory, hepatologic, renal, hematologic, gastrointestinal, immunologic, dermal, neurologic, or psychological disease or history of such disease 4. Subject with known for history of gastrointestinal disease or gastrointestinal surgery which affect on the absorption drug 5. Subjects with any of the following condition in screening (blood pressure, 12-lead ECG, blood, urinalysis, etc.) 6. Subject with any of the following conditions in laboratory test i. AST(sGOT) or ALT(sGPT) > Upper normal limit × 1. 25 ii. Total bilirubin > Upper normal limit × 1. 5 7. If the estimated GFR < 80mL/min/1. 76m2 using MDRD formula. 8. Systolic blood pressure <=90mmHg or diastolic blood pressure >=150mmHg or a person showing the corresponding figures <=50mmHg or >=100mmHg in vital signs. 9. Who has history of drug abuse (especially hypnotic, central acting analgesics, psychotropic drugs, such as opiates or central nervous system acting drug) or shows positive reactions to drug of abuse in urine drug screening tests. 10. Excessive caffeine and alcohol intake, smoking person(caffeine: > 5cups/day, alcohol: >210g/week, tobacco: > 10 cagarettes/day) 11. Use of any prescription medication within 14 days prior to study medication dosing or use of any medication such as over-the-counter medication including oriental medication within 7 days prior to study medication dosing 12. Participation in any clinical investigation within 60days prior to study medication dosing 13. Subjects with whole blood donation within 60days, component blood donation within 30days 14. Subjects with decision of nonparticipation through investigator's review due to laboratory test results or other excuse such as non-responding to request or instruction by investigator

Locations and Contacts

Additional Information

Starting date: July 2013
Last updated: March 17, 2015

Page last updated: August 23, 2015

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