A Proof of Concept Study of Pradigastat in Patients With Functional Constipation

Completed · Phase 2 · Has a placebo group

Conditions studied: Functional Constipation

In brief

The purpose of this study is to evaluate the efficacy, safety, and tolerability of pradigastat 20 and 40 mg as compared to placebo in patients with Functional Constipation.

Key facts

Study ID

NCT04620161

Run by

Anji Pharma

People needed

181

Starts

2020-09-22

Expected to finish

2022-06-03

Last updated by the study team

2022-08-24

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Written informed consent must be obtained before any assessment is performed.
• Male and female patients aged 18 to 70 years of age, inclusive.
• Patients with FC as defined by the ROME IV diagnostic criteria for FC.
• Diagnostic criteria for FC*:
• Must include 2 or more of the following:
• Straining during more than one-fourth (25%) of defecations
• Lumpy or hard stools (Bristol Stool Form Scale 1 or 2) more than one-fourth (25%) of defecations
• Sensation of incomplete evacuation more than one-fourth (25%) of defecations
• Sensation of anorectal obstruction/blockage more than one-fourth (25%) of defecations
• Manual maneuvers to facilitate more than one-fourth (25%) of defecations (such as digital evacuation, or support of the pelvic floor)
• Fewer than 3 SBMs per week
• Loose stools are rarely present without the use of laxatives
• Insufficient criteria for irritable bowel syndrome (IBS). *Criteria fulfilled for the last 3 months with symptom onset at least 6 months prior to diagnosis.
• Patient has less than 3 SBMs/week within 2 weeks prior to the Screening Visit.
• Patient has completed a colonoscopy with no clinically significant findings which meet other exclusion criteria within 12 months prior to Screening or at the Screening Visit.
• Patient must agree that after the Visit 2 (Run-in Visit) they will discontinue any prohibited medications, laxatives (prescription and over-the-counter), supplemental fibers, or traditional medicine taken for abdominal symptoms or constipation as defined per protocol except the rescue medication, provided by the study site and following the Investigator's instructions for its use. Patient should not take rescue medication (bisacodyl) on the calendar day before and the calendar day of the start of the Treatment Period (Visit 3). If the wash-out criteria are not achieved on Visit 3, the Visit could be postponed once.
• Patient must agree to use and comply with the diet guidance provided in applicable Chronic Constipation Treatment Guideline starting after the Screening Visit and during the study until End of Study.
• Ability of patient to swallow tablets.
• A co-operative attitude and ability to perform all study related procedures and to correctly use the diary.

You may not qualify if…

• Patient with history of surgical resection of stomach, gallbladder, small intestine, large intestine, and bariatric surgery (excluding resection of appendicitis and benign polyp).
• Patient with history or current affection of inflammatory bowel disease (Crohn's disease or ulcerative colitis) and celiac disease.
• Patient with diagnosis of IBS (constipation, diarrhea, or mixed).
• Patient with history or current ischemic colitis.
• Patient currently with infectious enteritis or enterocolitis. Patients with asymptomatic diverticulosis, diagnosed during the colonoscopy can be enrolled, unless previous history of diverticulitis.
• Patient currently with hyperthyroidism or hypothyroidism (unless adequately treated), or patients who have a thyroid-stimulating hormone outside of the laboratory reference range at Visit1.
• Patient with apparent mechanical obstruction (ie, patient with ileus caused by hernia).
• Patient has a structural abnormality of the GI tract or a disease or history of a condition that can affect GI motility.
• Patient has ever had any of the following diseases or conditions that can be associated with constipation: pseudo-obstruction, colonic inertia, megacolon, megarectum, bowel obstruction, descending perineum syndrome, solitary rectal ulcer syndrome, and systemic sclerosis.
• Patient currently affected by constipation due to anorectal disease, affecting the anorectal area such as anal fissure, anorectal fistulas, hemorrhoidal disease Grade III and IV, and bleeding hemorrhoids.
• Patient currently has both unexplained and clinically significant alarm symptoms (lower GI bleeding, rectal bleeding or heme-positive stool, iron-deficiency anemia or any unexplained anemia, or weight loss) or systemic signs of infection or colitis.
• Patient currently affected by drug-induced constipation.
• Patient with constipation due to other organic disease.
• Patient currently affected by active peptic ulcer (ie, disease that is not adequately treated or stable with therapy).
• In the case of a female, the one currently affected by endometriosis or uterine adenomyosis.
• Patient with uncontrolled severe depression, anxiety, or any eating disorder considered by the Investigator to influence drug evaluation.
• Patient has a potential central nervous system cause of constipation (eg, Parkinson's disease, spinal cord injury, and multiple sclerosis.).
• Patients with uncontrolled and unstable diabetes mellitus with reported episodes of hypoglycemia within 1 year prior to Screening or history of diabetic neuropathy.
• Patient with history of abuse of drug or alcohol within 1 year before consent acquisition, or with current abuse.
• Patient with history of or current diagnosis of any cancer (except for nonmelanoma skin cancer which has been removed) diagnosed less than 5 years prior to Screening. Patients with cancer in full remission more than 5 years after diagnosis are acceptable.
• Patient with major surgery or any other condition that may require use of narcotic drugs or general anesthesia within 60 days of Screening and during the study.
• Any clinically significant abnormality identified by physical examination, electrocardiogram (ECG) or laboratory tests, which in the judgment of the Investigator would compromise the patient's safety or successful participation in the clinical study, or any of the following laboratory findings:
• Male hemoglobin < 12 g/dL (< 120 g/L) and female hemoglobin < 10 g/dL (< 100 g/L) at Screening.
• Male serum creatinine ≥ 1.5 mg/dL and female serum creatinine ≥ 1.4 mg/dL, or creatinine clearance ≤ 60 mL/min based on calculation using the Cockcroft-Gault formula: ([140-age in years] × weight in kg)/(72 × [creatinine in mg/dL]). For women, multiply result by 0.85.
• Active liver disease and/or significant abnormal liver function defined as aspartate aminotransferase > 2 × upper limit of the normal (ULN) and/or alanine aminotransferase > 2 × ULN and/or total bilirubin > 1.5 × ULN.

Where it is running

• Advanced Clinical Research-Meridian — Meridian, Idaho, United States
• Evanston Premier Healthcare Research — Evanston, Illinois, United States
• Jubilee Clinical Research — Las Vegas, Nevada, United States
• Long Island Gastrointestinal Research Group LLP — New York, New York, United States
• PMG Research of Charleston — Mt. Pleasant, South Carolina, United States
• Beijing Friendship Hospital, Capital Medical University — Beijing, Beijing Municipality, China
• Quanzhou First Hospital — Quanzhou, Fujian, China
• Southern Medical University Nanfang Hospital — Guangzhou, Guangdong, China
• The Second Hospital of Hebei Medical University — Shijiazhuang, Hebei, China
• People's Hospital of Zhengzhou — Zhengzhou, Henan, China
• Renmin Hospital of Wuhan University — Wuhan, Hubei, China
• The Third Xiangya Hospital of Central South University — Changsha, Hunan, China
• Huai'an First People's Hospital — Huai'an, Jiangsu, China
• Nanjing First Hospital — Nanjing, Jiangsu, China
• Affiliated Hospital of Jiangsu University — Suzhou, Jiangsu, China
• Yangzhou First People's Hospital — Yangzhou, Jiangsu, China
• Pingxiang People's Hospital — Pingxiang, Jiangxi, China
• Siping Central People's Hospital — Siping, Jilin, China
• Huashan Hospital Affiliated to Fudan University — Shanghai, Shanghai Municipality, China
• Shanghai East Hospital — Shanghai, Shanghai Municipality, China
• Ruijin Hopsital — Shanghai, Shanghai Municipality, China
• Sir Run Run Shaw Hospital Affiliated to Medical College of Zhejiang University — Hangzhou, Zhejiang, China
• The Second Affiliated Hospital of Zhejiang University School of Medicine — Hangzhou, Zhejiang, China
• Huzhou Central Hospital — Huzhou, Zhejiang, China
• The First Affiliated Hospital of Wenzhou Medical University — Wenzhou, Zhejiang, China

Full record on ClinicalTrials.gov

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