Overview

A Multi-center, Randomized, Double-blind, Parallel-group, Placebo Controlled Phase III Study to Evaluate the Efficacy and Safety of LXI-15028 in Non-erosive Reflux Disease in Chinese Patients for 4 Weeks

Status:
Completed
Trial end date:
2019-11-26
Target enrollment:
0
Participant gender:
All
Summary
This is one multi-center, randomized, double-blind, parallel-group, placebo controlled Phase III clinical study to evaluate the efficacy and safety of LXI-15028 50 mg in treatment of non-erosive reflux disease in Chinese patients for 4 weeks. Screening-eligible subjects will be randomized into LXI-15028 50mg group or placebo group at Visit 2 (Day 0) according to the ratio of 1:1 and receive study treatment for 4 weeks. They will start to take the investigational products in the following morning of Visit 2 (Day 1) and start to complete the subject's diary from the day of study treatment initiation. After 2 weeks of study treatment, subjects will return to the study site and complete Visit 3, after which receive study treatment for another 2 weeks and then complete Visit 4. On the day of Visit 4, subjects will not take any drug. All the subjects will be followed up by phone (Visit 5) at Day 28±3 after the last dose of study medication.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Shandong Luoxin Pharmaceutical Group Stock Co., Ltd.
Criteria
Inclusion Criteria:

- Subject who volunteers to sign the written informed consent form approved by the
independent ethics committee and agrees to participate in this study prior to the
initiation of any study procedures.

- Subject who is able to understand and follow the protocol requirements and agrees to
participate in all the study visits.

- Male or female subjects with age ≥ 18 years.

- Having experienced heartburn (burning or pain behind the breastbone) and regurgitation
(acid taste in the mouth and discomfort movement of materials upwards from the
stomach) symptoms at least three months prior to screening.

- Having experienced heartburn and regurgitation within 7 days prior to screening, with
the frequency and severity in symptom assessment meeting at least one of the following
items:

- Mild heartburn for at least 2 days, with regurgitation;

- Mild regurgitation for at least 2 days, with heartburn;

- Moderate or more severe heartburn for at least 1 day, with regurgitation;

- Moderate or more severe regurgitation for at least 1 day, with heartburn. (Note:
To be determined by using the RDQ [item a, b, e, f] completed by subject.) And
the RDQ symptom assessment before randomization (Visit 2) still meets the above
criteria.

- Within 14 days before study initiation, the subject has been confirmed with no mucosal
damage through upper gastrointestinal endoscopy based on Los Angeles (LA)
classification. And non-erosive reflux disease is clinically diagnosed by the
investigator.

- Subject who agrees to use appropriate medical method for contraception from the
signature of the informed consent form to 28 days after the last dose of study
medication (not including women in medically sterile state):

- Women under medically sterile state can participate in this study, for example,
postmenopausal state (spontaneous amenorrhea at least for 12 months), post
hysterectomy, post bilateral salpingectomy and post bilateral oophorectomy;

- Appropriate medical contraceptive measures include intrauterine device, physical
barrier (male condom, female condom), subcutaneous implant, sustained release
contraceptive injection, bilateral salpingectomy and bilateral vasoligation.
Note: Use of oral contraceptives is not allowed during the course of study, and
dual contraceptive methods are recommended, as to ensure no occurrence of
pregnancy during the course of study.

Exclusion Criteria:

- Subject who had participated in this study previously, or had participated in other
P-CAB drug clinical studies.

- Participation in other clinical study within 3 months prior to screening, except for
the two following circumstances:

- The study which the subject is participating or participated in is a
non-interventional study (e.g. observational study or questionnaire survey) and
is judged by investigators to have no interference with the efficacy and safety
evaluation in the present study;

- Subject had signed the informed consent form and participated in another study
(NC821602) sponsored by this sponsor in the same study site, but had been
withdrawn from that study prior to the start of any treatment.

- Subjects who participate in the plan or conduction of this study (e.g., the sponsor or
staff of the study site).

- Women who are pregnant or lactating.

- Subject who is known to be allergic to the active ingredient or Talcid® of the
investigational product (including esomeprazole).

- Subject who is unable to undertake an upper gastrointestinal endoscopy.

- Subject who is unable to complete the subject's diary by oneself.

- Subject who has history of manic-depression, anxiety disorder, panic disorder,
somatoform disorder, personality disorder or other mental disorder.

- Subject who is diagnosed as erosive esophagitis, acute upper gastrointestinal
bleeding, gastric ulcer or duodenal ulcer within two months prior to screening.

- Subject who has symptoms such as odynophagia, serious dysphagia, bleeding, decreased
body weight, anemia or hematochezia that represent "warning" to presume
gastrointestinal malignant disease, unless the possibility of the malignant disease is
excluded through an endoscopy.

- History of malignant tumor within 5 years prior to screening (if the subject's basal
cell carcinoma or cervical carcinoma in situ has been cured, he/she will be allowed to
participate in this study).

- Subject who is diagnosed as achalasia of the cardia, secondary esophageal motility
disorder, irritable bowel syndrome (IBS), inflammatory bowel disease (IBD),
Zollinger-Ellison syndrome or eosinophilic esophagitis.

- Subject with history of gastrointestinal surgery, except simple fenestration,
appendectomy, cholecystectomy or endoscopic resection of benign tumor.

- Subject who plans to be hospitalized for receiving selective surgery during the study.

- Subject with non-reflux-related esophageal stenosis, hiatus hernia, gastroesophageal
varices, active peptic ulcer, gastric bleeding or malignant tumor that is found in
upper gastrointestinal endoscopy.

- Subject with uncontrolled and unstable hepatic, renal, cardiovascular, respiratory,
endocrine or central nervous system disease as judged by investigators.

- Subject with history of chronic alcohol consumption (more than 14 cups per week, each
cup corresponds to 360 mL beer or 150 mL wine or 45 mL liquor) or drug abuse within 5
years prior to screening.

- Use of any PPI, P-CAB or other drugs related to the treatment of GERD (including
H2-receptor antagonist, prostaglandin or mucosal protective agent), or any other
antiemetic, emetic drugs within two weeks prior to the initiation of study treatment.

- Subject who needs non-steroidal anti-inflammatory drugs (NSAIDs) during the study,
unless the subject had started to use low dose aspirin (≤ 100 mg/day) prior to
screening.

- Use of potent-to-moderate cytochrome metabolism enzyme CYP3A4 inhibitor or inducer
within 4 weeks prior to study treatment, including but not limited to the following
drugs:

- CYP3A4 inhibitors: Ketoconazole, Indinavir, Saquinovir, Atazanavir, Amprenavir,
Fosamprenavir, Nefazodone, Itraconazole, Telithromycin, Fluconazole,
Troleandomycin, Cimetidine, Aprepitant, Fluvoxamine, Amiodarone, Ritonavir,
Erythromycin, Clarithromycin, and Diltiazem;

- CYP3A4 inducers: Barbiturate, Phenytoin, Rifampin, St John's wort, Carbamazepine,
Dexamethasone, Rifabutin, and Phenobarbital etc.

- Subject currently using antipsychotic drug, antidepressant agent or anti-anxiety
agent.

- Any of the following laboratory abnormalities at screening:

- AST≥2 x upper limit of normal (ULN);

- ALT≥2 x ULN;

- ALP≥2 x ULN;

- γ-GT≥2 x ULN;

- Total bilirubin ≥2 x ULN;

- BUN (or urea) ≥1.5 x ULN;

- Creatinine ≥1.5 x ULN.

- Subject with clinically significant abnormality in ECG at screening, including serious
arrhythmia, multifocal premature ventricular contraction (PVC), second degree or above
atrioventricular block, prolonged QT interval (QTc ≥ 450 ms for male, QTc ≥ 470 ms for
female).

- Current infection of human immune deficiency virus (HIV), hepatitis B virus (HBV) or
hepatitis C virus (HCV) confirmed by tests.

- Judged by the investigator, there are other conditions rendering the subject's
illegibility for this study.