CKD-495 emerges as promising therapy for acute and chronic gastritis :- Medznat
EN | RU
EN | RU

Help Support

By clicking the "Submit" button, you accept the terms of the User Agreement, including those related to the processing of your personal data. More about data processing in the Policy.
Back

CKD-495 emerges as promising therapy for acute and chronic gastritis

Acute and chronic gastritis Acute and chronic gastritis
Acute and chronic gastritis Acute and chronic gastritis

What's new?

CKD-495 75 mg significantly improves gastric mucosal healing and symptom improvement in acute and chronic gastritis.

A recent phase II, multi-center, randomized, double-blind study has highlighted the potential of CKD-495, a novel drug derived from Cinnamomum cassia Presl, in effectively treating acute and chronic gastritis.

Gastritis remains a widespread gastrointestinal disorder, and the search for safer, faster-acting therapies continues to gain momentum as clinicians prioritize mucosal healing and symptom relief. CKD-495 has emerged as a promising investigational option with potential anti-inflammatory and mucosal-protective properties. This study by Su Hyun Park et al. aimed to assess the efficacy and safety of CKD-495 in patients with endoscopically confirmed gastritis.

Overall, 250 adults diagnosed with gastric mucosal erosion were randomly assigned to five treatment arms and received either CKD-495 (75 mg or 150 mg), rebamipide (100 mg), Artemisiae argyi folium extract (Stillen, 60 mg), or placebo for a 14-day course. The primary endpoint focused on endoscopic erosion improvement, while secondary endpoints examined erosion healing, symptom resolution, and reductions in edema, redness, and hemorrhagic lesions. Safety profiles and drug-related adverse events were monitored throughout the study.

The results showed that:

  • The 75 mg CKD-495 group achieved the strongest endoscopic improvement among all treatment arms in the full analysis set (FAS) and per-protocol set (PPS), as shown in Table 1:

  • The gastric erosion cure rate was also highest with 75 mg CKD-495.

  • Interestingly, the 150 mg CKD-495 dose showed significant improvement in hemorrhagic erosions, suggesting a dose-dependent effect for specific gastric lesions.

  • CKD-495 was well-tolerated across all doses, with no serious adverse events or drug-related reactions reported.

The researchers concluded that CKD-495 at the 75 mg dose provided meaningful endoscopic and symptomatic improvements in acute and chronic gastritis without compromising safety. The treatment emerged as a well-tolerated and clinically effective option, supporting its potential advancement into larger confirmatory trials.

Source:

Canadian Journal of Gastroenterology and Hepatology

Article:

A Phase 2, Multi-Center, Randomized, Double-Blind, Parallel-Group Trial to Evaluate the Efficacy and Safety of CKD-495 in Patients With Acute and Chronic Gastritis

Authors:

Su Hyun Park et al.

Comments (0)

You want to delete this comment? Please mention comment Invalid Text Content Text Content cannot me more than 1000 Something Went Wrong Cancel Confirm Confirm Delete Hide Replies View Replies View Replies en
Try: