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Completed

NCT Number: NCT05694221

Drug Drug Interaction (DDI) Between Supaglutide and Digoxin or Metformin

This is a study of a drug drug interaction between Supaglutide and Digoxin or Metformin.

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Key information

Conditions

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Huashan Hospital, Fudan University

Shanghai, Shanghai Municipality, China

About this study

This is a single-centre, open labeled, fixed-sequence study designed to assess the pharmacokinetic effects of multiple subcutaneous injections of Supalutide on a single oral dose of digoxin or multiple oral doses of metformin. 32 healthy subjects are planned to be enrolled and allocated to 2 parallel trial groups, Digoxin combined with Sulpalutide injection (Group A) and Metformin combined with Sulpalutide injection (Group B), with 16 cases in each group, of which no less than 4 were of a single sex.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy Chinese subjects.
  • Age between 18 and 45 years, inclusive.
  • Body mass index [BMI = weight (kg)/height2 (m2)] of between 20 and 28 kg/m2 (including thresholds), with male subjects weighing no less than 50 kg and female subjects weighing no less than 45 kg.
  • Subjects with no plan of pragnancy within the screening period up to 3 months after the last dose and who are voluntarily using contraception.
  • Subjects who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.

Exclusion criteria

  • Subjects with a previous or existing history of serious cardiac, hepatic, renal, gastrointestinal, neurological, psychiatric abnormalities and metabolic abnormalities.
  • Subjects with a previous or existing disease affecting the absorption, distribution, metabolism or excretion of drugs, such as active peptic ulcers or bleeding, history of ulcers or bleeding, acute and chronic pancreatitis, etc.
  • Subjects with a history or family history of C-cell tumours/carcinoma of the thyroid gland, or a previous history of thyroid insufficiency or thyroid hormone abnormalities
  • Subjects who have undergone major surgery within 4 weeks prior to screening which, in the judgment of the investigator, may affect this trial, such as gastric and duodenal surgery, cholecystectomy, nephrectomy, or removal of malignant tumours (except for previous appendectomy), or those who are scheduled to undergo major surgery during the trial
  • those with existing symptoms of unexplained infection.

Treatment and study plan

Supaglutide injection

Drug

Administered subcutaneously in the Supaglutide arms

Other names: Diabegone

Digoxin

Drug

Oral Administration

Other names: Digoxin Tablets

metformin

Drug

Oral Administration

Other names: Glucophage

Primary outcomes

  1. Group A: Plasma Cmax of digoxin

    Time frame: 39 Days

    when given in combination with supaglutide in healthy volunteers

  2. Group A: Plasma AUC0-last of digoxin

    Time frame: 39 Days

    when given in combination with suplaglutide in healthy volunteers

  3. Group A: Plasma AUC0-inf of digoxin

    Time frame: 39 Days

    when given in combination with supaglutide in healthy volunteers

  4. Group B: Plasma Cmax,ss of Metformin

    Time frame: 34 Days

    when given in combination with supaglutide in healthy volunteers

  5. Group B: Plasma AUC0-tau of Metformin

    Time frame: 34 Days

    when given in combination with suplaglutide in healthy volunteers

Secondary outcomes

  1. Group A: Plasma Tmax of Digoxin

    Time frame: 39 Days

    when given in combination with supaglutide in healthy volunteers

  2. Group A: Plasma t1/2 of digoxin

    Time frame: 39 Days

    when given in combination with supaglutide in healthy volunteers

  3. Group A: Plasma CL/F of digoxin

    Time frame: 39 Days

    when given in combination with suplaglutide in healthy volunteers

  4. Group A: Plasma Vz/F of digoxin

    Time frame: 39 Days

    when given in combination with supaglutide in healthy volunteers

  5. Group B: Plasma Tmax of Metformin

    Time frame: 34 Days

    when given in combination with supaglutide in healthy volunteers

  6. Group B: Plasma Cmin,ss of Metformin

    Time frame: 34 Days

    when given in combination with suplaglutide in healthy volunteers

  7. Group B: Plasma t1/2 of Metformin

    Time frame: 34 Days

    when given in combination with suplaglutide in healthy volunteers

  8. Group B: Plasma CL/F of Metformin

    Time frame: 34 Days

    when given in combination with suplaglutide in healthy volunteers

  9. Group B: Plasma Vz/F of metformin

    Time frame: 34 Days

    when given in combination with suplaglutide in healthy volunteers

Sponsors and collaborators

Lead sponsor

Shanghai Yinnuo Pharmaceutical Technology Co., Ltd.

Other

Collaborators

  • Huashan Hospital

Registry information

Official study title

A Single-centre, Open Labeled, Fixed-sequence Study to Evaluate the Effect of Supaglutide on Digoxin or Metformin Pharmacokinetics

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Jan 23, 2023
Registry last updated
Aug 5, 2024

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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