A Clinical Study to Evaluate the Efficacy, Safety and PK/PD Profiles of Anticoagulation of HSK36273 for Injection in Continuous Renal Replacement Therapy Subjects

NCT05602129 | Unknown Phase 2

• 1 other identifier: HSK36273-201
• Study Type: interventional
• Target: 156
• Locations: 1 country
• Sites: 1

Brief Summary

This study is divided into Stage I and Stage II. It is planned to include 156 subjects who need CRRT treatment for more than 48 hours.

Conditions

Renal Replacement Therapy

Keywords

Renal Replacement Therapy; Anticoagulants

Outcome Measures

Primary Outcomes (3)

• Filter life

  the time from the start of administration to the first filter replacement and the average filter using time during the treatment period

  Day1 to Day5

• Times of filter replacement

  the times of filter replacement within 120h after starting administration

  Day1 to Day5

• Coagulation grade of filter and pipeline

  Clotting in the dialyser and the air traps as evaluated by a scale from 0 to 3

  Day1 to Day5

Study Arms (3)

HSK36273 Continuous infusion

EXPERIMENTAL

Drug:HSK36273 Administration mode:Continuous infusion

Drug: HSK36273

HSK36273 Bolus+Continuous infusion

EXPERIMENTAL

Drug:HSK36273 Administration mode:Bolus+Continuous infusion

Drug: HSK36273

Heparin sodium

ACTIVE COMPARATOR

Drug:Heparin sodium Administration mode:Bolus+Continuous infusion

Drug: Heparin sodium

Interventions

HSK36273 DRUG

HSK36273

HSK36273 Bolus+Continuous infusion; HSK36273 Continuous infusion

Heparin sodium DRUG

Heparin sodium

Heparin sodium

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female aged ≥18 and ≤80;
• kg/m2 ≤BMI≤35 kg/m2;
• Those who need CRRT treatment for more than 48 hours and plan to use CVVHDF treatment mode for femoral vein puncture;
• Subjects or their guardians voluntarily sign the informed consent form in writing before any procedure related to the study starts, fully understand the purpose and significance of this trial, and are willing to comply with the trial protocol.

You may not qualify if:

• Those who are known to be allergic to heparin, heparin drugs, investigational drugs or non-active ingredients of study intervention;
• Subjects with severe coagulation dysfunction or bleeding tendency three months before the screening, such as HIT (heparin-induced thrombocytopenia), ITP (idiopathic thrombocytopenia purpura), TTP (thrombocytopenia purpura), persistent systolic blood pressure\>200 mmHg or diastolic blood pressure\>120 mmHg, active gastrointestinal bleeding, intracranial hemorrhage, cerebral aneurysm, severe retinopathy bleeding, hemophilia, hemolytic uremic syndrome, stroke, acute coronary syndrome;
• Those who have undergone major cardiac surgery or craniocerebral surgery within 3 months before screening and who are judged by the study doctor to be at risk of serious bleeding;
• Those whose platelet ≤ 50\*109/L and/or INR\>1.8 and/or aPTT\>55s at screening;
• Those who need to combine other blood purification methods such as blood perfusion or ECMO;
• The time from the point of randomization to the last use of anticoagulants (low-molecular-weight heparin, warfarin, apixaban, bivalirudin, etc.), antiplatelet drugs (clopidogrel, aspirin, etc.), fibrinolytic drugs (urokinase, etc.) is shorter than the 5 half-lives of the drug or the duration of drug efficacy (calculated by the longest time);
• The time of administration is shorter than 1 half-life of low-molecular-weight heparin from the last preventive dose;
• Child-Pugh liver function is grade C in screening period;
• Those with positive hepatitis C antibody or HIV antibody screening;
• Pregnant and lactating women; women or men with fertility are unwilling to use contraception throughout the study period; subjects with pregnancy plans within 6 months after the study (including male subjects);
• Those who have participated in clinical trials of other drugs within 3 months before screening (defined as having received investigational drug or placebo);
• Other conditions that the investigator judges are not suitable for the subject to participate in the clinical trial.

Sponsors & Collaborators

• Haisco Pharmaceutical Group Co., Ltd.: lead

Study Sites (1)

The First Affiliated Hospital of Sun Yat-sen University

Guangzhou, China

Location

MeSH Terms

Interventions

Heparin

Intervention Hierarchy (Ancestors)

Glycosaminoglycans; Polysaccharides; Carbohydrates

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 16, 2022
• First Posted: November 1, 2022
• Study Start: November 1, 2022
• Primary Completion: October 1, 2023
• Study Completion: October 1, 2023
• Last Updated: November 2, 2022

Record last verified: 2022-11

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)