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RecruitingNCT05870683Updated Jul 11, 2023

Comparison of Two Dual Therapies in the First-line Treatment of Helicobacter Pylori Infection (SHARE2301)

An interventional study of Tegoprazan and Amoxicillin in Helicobacter Pylori Infection, sponsored by Yanqing Li. Recruiting at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-07-11.

Sponsored by Yanqing Li · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
368
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Helicobacter pylori (H. pylori) infection is a common global infectious disease of the gastrointestinal tract. Helicobacter pylori eradication can effectively prevent the development of stomach cancer. Progressive application of dual therapy for the eradication of Helicobacter pylori. Tegoprazan, a Potassium-Competitive Acid Blockers. The efficacy of P-CAB agents represented by vonoprazan in H. pylori eradication therapy has been widely verified.

Read the detailed description

In 1989, it was suggested that amoxicillin combined with PPI could eradicate Hp infection, and in 2015, a prospective, multicenter, randomized controlled study in Taiwan with a large sample showed that the eradication rate of Hp could reach 96.6% with dual therapy for primary treatment of Hp infection, and the results of intention-to-treat analysis were as high as 95.3%. 95.3%. In 2020, a meta-analysis showed that high-dose dual therapy had the same efficacy and fewer side effects than other recommended regimens in first-line treatment. In terms of dosing days, multiple randomized controlled studies and meta-analyses from 2020-2021 have shown that 14 days of high-dose dual therapy is more effective in eradicating H. pylori.

Tegoprazan, a Potassium-Competitive Acid Blockers (P-CAB), is a new type of acid-suppressing drug that compensates for the short half-life of acid-activated traditional acid-suppressing PPI and the low mucosal healing rate due to insufficient acid suppression. The efficacy of P-CAB agents represented by vonoprazan in H. pylori eradication therapy has been widely verified. 2022, tegoprazan was approved by the State Drug Administration for the new indication of eradication of H. pylori infection in adults in combination with appropriate antimicrobial therapy, and its efficacy in clinical application has not yet been verified.

02

Conditions studied

  • Helicobacter Pylori Infection
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Helicobacter pylori infection (either positive for histopathological test, rapid urease test, or C13/C14 urea breath test).
  • Patients who have not previously received helicobacter pylori eradication therapy.

Exclusion criteria

Exclusion Criteria:

  • Serious underlying diseases, such as liver insufficiency, renal insufficiency, immunosuppression, malignant tumor, coronary heart disease (angina pectoris or coronary artery stenosis ≥ 75%).
  • Those who are not willing to take contraceptive measures during pregnancy, lactation or the trial.
  • Active gastrointestinal bleeding.
  • History of drug allergy.
  • History of upper gastrointestinal surgery.
  • Medication history of bismuth, antibiotics and PPI within 4 weeks.
  • Other behaviors that may increase the risk, such as alcohol and drug abuse.
  • Unable or unwilling to provide informed consent.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
368 participants (estimated)

Study arms

  • Experimental
    14-day Tegoprazan-Amoxicillin dual therapy

    14-day Tegoprazan-Amoxicillin dual therapy, Tegoprazan(Luo Xin Pharmaceutical Group Co. LTD)50mg bid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid

    Drug: Tegoprazan · Drug: Amoxicillin

  • Active comparator
    14-day Esomeprazole-Amoxicillin dual therapy

    14-day Esomeprazole-Amoxicillin dual therapy, Esomeprazole(Astrazeneca Pharmaceutical Co., LTD.) 20mg qid, Amoxicillin (Amoxicillin, United Laboratories Co. LTD) 750mg qid

    Drug: Amoxicillin · Drug: Esomeprazole

Interventions

  • DrugTegoprazan

    Included in dual eradication medication.

  • DrugAmoxicillin

    Included in dual eradication medication.

  • DrugEsomeprazole

    Included in dual eradication medication.

05

What researchers measure

Primary outcomes

  1. Eradication rate

    Both intention to treat (ITT) and per-protocol (PP) analyses will be used for the assessment of the eradication rates of Helicobacter pylori infections in two groups. The ITT analysis includes all randomly assigned patients who take at least one dose of the study medications. The PP analysis is limited to patients who take over 80% of the study medications and complete follow-up.

    Time frame: Immediately after follow-up check

Secondary outcomes

  1. Rate of adverse reactions

    Rate of adverse reactions

    Time frame: Immediately after follow-up check

  2. Patient compliance

    good compliance is defined as the actual dosage is within the range of 80%-100% of the dosage that should be taken

    Time frame: Immediately after follow-up check

06

Study locations

1 of 1 sites recruiting
  • Department of Gastroenterology, Qilu Hospital, Shandong University
    Jinan, Shandong 250012, China
    Recruiting
07

References and documents

Publications

  • Malfertheiner P, Megraud F, O'Morain CA, Gisbert JP, Kuipers EJ, Axon AT, Bazzoli F, Gasbarrini A, Atherton J, Graham DY, Hunt R, Moayyedi P, Rokkas T, Rugge M, Selgrad M, Suerbaum S, Sugano K, El-Omar EM; European Helicobacter and Microbiota Study Group and Consensus panel. Management of Helicobacter pylori infection-the Maastricht V/Florence Consensus Report. Gut. 2017 Jan;66(1):6-30. doi: 10.1136/gutjnl-2016-312288. Epub 2016 Oct 5. PubMed 27707777 ↗

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT05870683
Lead sponsor
Yanqing Li
Collaborators
Linyi People's Hospital, Weifang Medical University, Zhengzhou Central Hospital, Yuncheng Traditional Chinese Medicine Hospital, The Affiliated Hospital of Qingdao University, The People's Hospital of Jimo, Shandong University of Traditional Chinese Medicine
Responsible party
Yanqing Li (Vice-President, Shandong University) — Sponsor-investigator
First posted
May 23, 2023
Start date
May 24, 2023
Primary completion
Oct 1, 2023 (estimated)
Completion
Dec 30, 2023 (estimated)
Last update
Jul 11, 2023

Study contacts

Yanqing Li, MD
Contact
qlxhkqz@163.com
18560086667
Yanqing Li
study chair · Qilu Hospital of Shandong University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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