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Completed

NCT Number: NCT07282054

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

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Nanjing Drum Tower hospital

Nanjing, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female participants, 18 to 75 years of age at informed consent (inclusive).
  • BMI between 18.0 and 30.0 kg/m² (inclusive).
  • T1DM diagnosed ≥6 months per WHO diabetes classification (2019).
  • On insulin therapy ≥6 months prior to screening.
  • 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:
  • 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).
  • Premixed insulin ≥2 times per day.
  • Screening HbA1c between 7.0% and 11.0% (inclusive), measured by the central laboratory.

Exclusion criteria

  • Diabetes other than T1DM.
  • History of pancreatectomy.
  • Prior pancreatic and/or islet cell transplantation.
  • ≥1 episode of Level 3 hypoglycemia within 6 months before screening (requires external assistance).
  • Hepatic or renal impairment at screening (per local laboratory reference ranges):
  • AST or ALT ≥3× ULN; and/or
  • TBL ≥2× ULN (except Gilbert syndrome); and/or
  • Estimated creatinine clearance <45 mL/min (Cockcroft-Gault).
  • Known hypersensitivity/allergy to study insulin products or excipients, or to any component of the standardized test meal.
  • Blood transfusion or major blood loss within 3 months before screening; hemoglobinopathies, moderate-severe anemia, or other conditions that may interfere with HbA1c measurement.
  • 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).
  • 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.
  • Use within 3 months before screening, or current use, of traditional medicines (herbal or proprietary Chinese medicines) with known glucose-lowering effects.

Treatment and study plan

THDB0206

Drug

Subcutaneous THDB0206 three times daily, with individualized dose adjustment.

Insulin Lispro

Drug

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

insulin glargine

Drug

Subcutaneous insulin glargine once daily, with individualized dose adjustment.

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

Sponsors and collaborators

Lead sponsor

Tonghua Dongbao Pharmaceutical Co.,Ltd

Industry

Registry information

Official study title

A Phase 3, Randomized, Open-Label, Multicenter, Active-controlled Trial Comparing Efficacy and Safety of THDB0206 Injection With Insulin Lispro Injection Combined With Insulin Glargine Injection U-100 in Chinese Participants With Type 1 Diabetes

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Dec 15, 2025
Registry last updated
Dec 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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