Clinical Trials Logo

Clinical Trial 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 Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT02395913
Study type Interventional
Source Hyundai Pharmaceutical Co., LTD.
Contact
Status Completed
Phase Phase 1
Start date July 2013
Completion date September 2013

See also
  Status Clinical Trial Phase
Completed NCT04135898 - A Study Comparing SIBP-04 and Bevacizumab in Healthy Male Subjects Phase 1
Completed NCT02395926 - To Evaluate Safety and the Pharmacokinetic Characteristics After Oral Administration of HT-003 Compared With Choline Alfoscerate Capsule in Healthy Adult Male Volunteers Phase 1
Recruiting NCT05849311 - Phase I Trial of Envafolimab for Healthy Male Subjects Phase 1
Active, not recruiting NCT06105255 - A Study to Evaluate the Effects of D-1553 on PK of Midazolam, Caffeine, Rosuvastatin, Furosemide, Digoxin, and Itraconazole or Omeprazole on PK of D-1553 Phase 1
Completed NCT01651234 - A Study to Assess Safety, Tolerability, and Pharmacokinetics of Orally Administered GCC4401C in Healthy Volunteers Phase 1
Terminated NCT01359618 - Determining Highest Dose Administration of TC-5214 and Evaluating Effect on the Electrical Activity in the Heart Phase 1
Completed NCT06194500 - A Study of Carbon-14-Labeled [14C]-LY3549492 in Healthy Participants Phase 1
Completed NCT05202912 - Food Effect Study of IDX-1197 in Healthy Subjects Phase 1
Completed NCT04828265 - Study of Aldafermin (NGM282) in Healthy Adult Male Japanese and Non-Japanese Subjects Phase 1