Status:
RECRUITING
Efficacy and Safety of PJ009 in Patients with Short Bowel Syndrome Requiring Parenteral Nutrition
Lead Sponsor:
Chongqing Peg-Bio Biopharm Co., Ltd.
Conditions:
Short Bowel Syndrome
Eligibility:
All Genders
14+ years
Phase:
PHASE3
Brief Summary
The main aim of this clinical trial is to assess the efficacy and safety of PJ009 in patients aged ≥14 with short bowel syndrome (SBS) requiring parenteral nutrition. The main questions it aims to ans...
Detailed Description
This is a multicenter, randomized, double-blind, placebo-controlled clinical study, aiming to evaluate the efficacy, safety, immunogenicity and pharmacokinetic of PJ009 in patients with short bowel sy...
Eligibility Criteria
Inclusion
- Male and female aged ≥ 14 years;
- SBS patients dependent on PN/IV support for at least 6 consecutive months due to major intestinal resection;
- At least 3 PN/IV support sessions per week are required 1 week before screening or 2 weeks before baseline;
- Be on stable PN/IV support for at least 4 consecutive weeks before administration;
- For subjects with a history of Crohn's disease (CD), clinical assessment of remission for at least 12 weeks prior to administration;
- Be able to understand and provide signed informed consent, for those under 18 years old, the guardian should also sign the informed consent;
- Be able to complete experiments in accordance with the protocol.
Exclusion
- Have used teduglutide in the past or may be allergic to teduglutide or its components;
- Have used natural GLP-2 or its analogs, human growth hormone or its analogs within 6 months before screening;
- Have used glutamine, octreotide, GLP-1 analogs or dipeptidyl peptidase-IV inhibitors within 30 days before screening;
- With active Crohn's disease or those who need to change biological therapy within 6 months before screening;
- With active inflammatory bowel disease (IBD) or IBD patients who have received immunosuppressant therapy changes in the past 3 months;
- With unstable absorption due to cystic fibrosis, untreated megacolon disease or known DNA abnormalities (such as familial adenomatous polyposis, Fanconi syndrome);
- With clinically obvious intestinal obstruction or active stenosis within 6 months before screening;
- Have undergone major gastrointestinal surgical intervention within 3 months before screening, such as continuous transverse enteroplasty or other intestinal lengthening surgery (esophageal intubation or endoscopic surgery is allowed);
- Severe active, uncontrolled, untreated systemic diseases (such as cardiovascular, respiratory, renal, infectious, endocrine, liver or central nervous system diseases, etc.);
- Have malignant tumors within 5 years before screening (except for fully treated cervical carcinoma in situ, basal cell or squamous cell carcinoma of the skin, localized prostate cancer after radical surgery, and breast ductal carcinoma in situ after radical surgery);
- With severe liver function impairment:
- Total bilirubin ≥ 2.0 × upper limit of normal (ULN); for patients with Gilbert's syndrome, direct bilirubin ≥ 2.0 × ULN;
- Aspartate transaminase (AST) ≥ 5.0 × ULN, alanine transaminase (ALT) ≥5.0 × ULN;
- With renal function impairment:
- Serum creatinine ≥2.0 × ULN;
- Creatinine clearance \< 60 ml/min (calculated according to the Cockcroft-Gault formula, see Appendix 3 for details);
- Pancreatic abnormalities:
- Serum amylase ≥ 2.0 × ULN;
- Serum lipase ≥ 2.0 × ULN;
- More than 4 SBS or PN-related hospitalizations (such as catheter sepsis, intestinal obstruction, severe water and electrolyte disorders) within 12 months before screening;
- Unplanned hospitalization within 30 days before screening;
- Pregnant or lactating women, women or men who have fertility plans or do not agree to take effective contraceptive measures during the trial;
- Participated in any clinical trial (excluding antibody treatment-related clinical trials) within 30 days before screening or participated in any antibody treatment-related clinical trials within 3 months before screening;
- Other condition the investigator believes would be unsuitable for participation in this clinical study.
Key Trial Info
Start Date :
September 3 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 27 2026
Estimated Enrollment :
72 Patients enrolled
Trial Details
Trial ID
NCT06512584
Start Date
September 3 2024
End Date
April 27 2026
Last Update
September 19 2024
Active Locations (8)
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1
Beijing Tsinghua Changgung Hospital
Beijing, Beijing Municipality, China, 102218
2
Chongqing General Hospital
Chongqing, Chongqing Municipality, China, 401147
3
The Sixth Affiliated Hospital of Sun Yat-sen University
Guangzhou, Guangdong, China, 510655
4
The Third Xiangya Hospital of Central South University
Changsha, Hu'nan, China, 410013