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CompletedNCT07282054Updated Dec 15, 2025

Efficacy and Safety of THDB0206 Compared to Insulin Lispro Injection in Participants With Type 1 Diabetes

A Phase 3 interventional study of THDB0206 and Insulin Lispro in Type 1 Diabetes, sponsored by Tonghua Dongbao Pharmaceutical Co.,Ltd. Completed at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-12-15.

Sponsored by Tonghua Dongbao Pharmaceutical Co.,Ltd · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 7 months after the study started (first participant enrolled Apr 2022, registered Dec 2025).
Phase
Phase 3
Study type
Interventional
Enrollment
550
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is a 26-week randomized, open-label, multicenter, active-controlled parallel group trial. The purpose of this study is to compare efficacy and safety of THDB0206 injection with insulin lispro injection combined with insulin glargine injection U-100 in Chinese participants with T1DM.

02

Conditions studied

  • Type 1 Diabetes
03

In context

Diabetes Mellitus, Type 1

3,523 studies on the registry are indexed under Diabetes Mellitus, Type 1; 577 are open to participants now.

This study's enrollment of 550 is above the median of 40 across 2,650 interventional studies indexed under Diabetes Mellitus, Type 1.

Browse Diabetes Mellitus, Type 1 studies →

Lead sponsor

Tonghua Dongbao Pharmaceutical Co.,Ltd is the lead sponsor of 10 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Male or female participants, 18 to 75 years of age at informed consent (inclusive).
  2. BMI between 18.0 and 30.0 kg/m² (inclusive).
  3. T1DM diagnosed ≥6 months per WHO diabetes classification (2019).
  4. On insulin therapy ≥6 months prior to screening.
  5. Stable insulin regimen ≥3 months prior to screening (no change in insulin class), with or without metformin or alpha-glucosidase inhibitors; willing to follow multiple daily injections:

    1. Intermediate/long-acting insulin once or twice daily (e.g., NPH, glargine, detemir, degludec); plus prandial insulin 1\~3 times daily (or as per usual diet) (e.g., regular human insulin, lispro, aspart, glulisine).
    2. Premixed insulin ≥2 times per day.
  6. Screening HbA1c between 7.0% and 11.0% (inclusive), measured by the central laboratory.

Exclusion criteria

Exclusion Criteria:

  1. Diabetes other than T1DM.
  2. History of pancreatectomy.
  3. Prior pancreatic and/or islet cell transplantation.
  4. ≥1 episode of Level 3 hypoglycemia within 6 months before screening (requires external assistance).
  5. Hepatic or renal impairment at screening (per local laboratory reference ranges):

    1. AST or ALT ≥3× ULN; and/or
    2. TBL ≥2× ULN (except Gilbert syndrome); and/or
    3. Estimated creatinine clearance \<45 mL/min (Cockcroft-Gault).
  6. Known hypersensitivity/allergy to study insulin products or excipients, or to any component of the standardized test meal.
  7. Blood transfusion or major blood loss within 3 months before screening; hemoglobinopathies, moderate-severe anemia, or other conditions that may interfere with HbA1c measurement.
  8. Use of oral antihyperglycemics within 3 months before screening (except metformin and alpha-glucosidase inhibitors), or use of non-insulin injectables (e.g., GLP-1 receptor agonists).
  9. Systemic corticosteroid therapy for ≥14 consecutive days within 3 months prior to screening (including IV, IM, SC, or oral routes; excluding topical, intraocular, intranasal, intra-articular, and inhaled use), or systemic corticosteroid therapy within 8 weeks prior to screening (except physiologic replacement for adrenal insufficiency), or anticipated need for prolonged systemic corticosteroid therapy during the study.
  10. Use within 3 months before screening, or current use, of traditional medicines (herbal or proprietary Chinese medicines) with known glucose-lowering effects.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
550 participants (actual)

Study arms

  • Experimental
    THDB0206 Injection

    Drug: THDB0206 · Drug: Insulin Glargine

  • Active comparator
    Insulin Lispro Injection

    Drug: Insulin Lispro · Drug: Insulin Glargine

Interventions

  • DrugTHDB0206

    Subcutaneous THDB0206 three times daily, with individualized dose adjustment.

  • DrugInsulin Lispro

    Subcutaneous insulin lispro three times daily, with individualized dose adjustment.

  • DrugInsulin Glargine

    Subcutaneous insulin glargine once daily, with individualized dose adjustment.

06

What researchers measure

Primary outcomes

  1. Change from Baseline in HbA1c at Week 26

    Time frame: Week 26

Secondary outcomes

  1. Change from Baseline in 1-hour Postprandial Glucose (PPG) Excursion at Week 26

    Time frame: Week 26

  2. Change from Baseline in 2-hour Postprandial Glucose (PPG) Excursion at Week 26

    Time frame: Week 26

07

Study locations

1 site
  • Nanjing Drum Tower hospital
    Nanjing, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 15, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07282054
Lead sponsor
Tonghua Dongbao Pharmaceutical Co.,Ltd
Responsible party
Sponsor
First posted
Dec 15, 2025
Start date
Apr 13, 2022
Primary completion
Jan 23, 2025
Completion
Jan 24, 2025
Last update
Dec 15, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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