Current partner codePEPTIDESDE
NCT04504370·Phase 3·INTERVENTIONAL

Safety and Efficacy of Pegylated Exenatine Injection (PB-119) in Drug-naïve T2DM Subjects

Status

Completed

Phase

Phase 3

Enrollment

273

Locations

1

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

A randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of 24 once-weekly subcutaneous doses of PB-119 in Drug-naïve T2DM Subjects.

Full detailed description

The study included a maximum 2-week screening period, a 4-week single-blind introduction period, a 24-week double-blind treatment period, a 28-week open extension treatment period, and a 4-week safety follow-up period. At the end of the single-blind entry period, eligible subjects were randomly assigned to two different administration groups in a 1:1 ratio and received a 24-week double-blind treatment. All subjects who completed the double-blind treatment entered the open extension treatment phase.Open extension treatment with subcutaneous injection of 150μg PB-119 once a week for 28 weeks. Safety follow-up was conducted 4 weeks after the end of treatment/completion of early exit visit in the open extension period.

Interventions

Treatment arms and agents.

DRUG

GLP-1 receptor agonist

PB-119 is an investigational pegylated human glucagon-like peptide-1 (GLP-1) receptor agonist. The dosing regimen is 150μg once every week as subcutaneous administration. Patients in PB-119 group will be administered the active drugs for 52 weeks (24+28).

DRUG

Placebo

PB-119 matched placebo will be used once every week as subcutaneous administration to placebo group for 24 weeks.

Timeline

From registration to results.

  1. First posted

    Aug 7, 2020

  2. Study start

    Apr 27, 2020

  3. Primary completion

    Mar 30, 2022

  4. Study completion

    Nov 28, 2022

  5. Results posted

    Not reported

  6. Registry updated

    Jul 28, 2023

Outcomes

What the study measures.

Primary outcomes

Change in HbA1c

Time frame · week 1, week 25

Change in HbA1c from baseline(week 1) to week 25

Secondary outcomes

HbA1c Below 7.0%

Time frame · week 1, week 25

Percentage of participants with HbA1c below 7.0% was evaluated at week 25.

Change in Body Weight (kg)

Time frame · week 1, week 25

Change from baseline (week 1) in body weight was evaluated at week 25

Change in Fasting Plasma Glucose (FPG)

Time frame · week 1, week 25

Change from baseline (week 1) in FPG was evaluated at week 25

Change in Body Mass Index

Time frame · week 1, week 25

Change from baseline (week 1) in body mass index (BMI) was evaluated at week 25.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
75 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Male or female, aged 18\~75 years old; * Confirmed T2DM patients meet the diagnostic criteria for type 2 diabetes published by WHO1999; * 18.5 kg/m2 \< BMI \< 40.0 kg/m2 at screening; * 7.5% ≤ HbA1c ≤ 11.0% at screening; * 7.0% ≤ HbA1c ≤ 10.5% when the random; * 18.5 kg/m2 \< BMI \< 40.0 kg/m2 during screening and before randomization Exclusion Criteria: * T1DM; * Continuous use of insulin for more than 14 days within 1 year before screening or before randomization; * Treatment with any dipeptidylpeptidase 4 (DPP-4) inhibitor or glucose-dependent insulin-stimulating peptide (GIP) or/and glucagon-like peptide-1 (GLP-1) receptor agonist prior to screening or randomized prior treatment; * Screening for any of the following heart diseases within the first 6 months or before randomization; * Patients whose hypertension was not effectively controlled during screening or before randomization (after resting ≥5 minutes, systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥100mmHg); * Serum amylase or lipase \>3×ULN or those with previous diagnosis of acute/chronic pancreatitis were screened or randomly screened; * Screening for severe trauma or infection that may affect glycemic control within the first month or before randomization; * A history or family history of medullary thyroid carcinoma (MTC) or multiple endocrine adenomatosis type 2 (MEN2); * Known to be allergic or intolerant to the study drug or metformin; * Female subjects during pregnancy or lactation.

Study locations

1 registered sites.

China. Showing up to 24 locations stored in the fast local snapshot.

Central South University The Second Xiangya Hospital

Changsha, Hunan, China

Related trials

More studies on Exenatide.

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