Bioequivalence Study to Compare Imeglimin HCl 500 mg Film Coated Tablets Versus Twymeeg Tablets 500 mg

An Open Label, Balanced, Randomized, Single Dose, Two Treatment, Two Sequence, Two Period, Two Way Crossover, Oral Bioequivalence Study of Imeglimin HCl 500 mg Film Coated Tablets and Twymeeg Tablets 500 mg in Healthy, Adult, Human Participants Under Fasting Condition.

An Open Label, Balanced, Randomized, Single dose, Two treatment, Two sequence, Two period, Two way crossover, Oral Bioequivalence Study of Imeglimin HCl 500 mg Film Coated Tablets of Humanis Sağlık A.Ş., Ç.O.S.B. Karaağaç Mahallesi Fatih Bulvarı No:32 Kapaklı/TEKİRDAĞ and Twymeeg Tablets 500 mg of Sumitomo Pharma Co., Ltd. 2-6-8, Dosho-machi, Chuo-Ward, Osaka City, in Healthy, Adult, Human Participants Under Fasting Condition.

Study Overview

• Status: Completed
• Conditions: Type 2 Diabetes
• Intervention / Treatment: Drug: Imeglimin Hydrochloride Film Coated Tablet; Drug: TWYMEEG® Tablets

• Study Type: Interventional
• Enrollment (Actual): 40
• Phase: Phase 1

Contacts and Locations

Study Locations

• India
  • Ahmedabad
    • Gujrāt, Ahmedabad, India, 380 015
      • Veeda Clinical Research Ltd.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Participants aged between 18 to 45 years (both inclusive).
• Participants' weight within normal range according to normal values for Body Mass Index (between 18.5 to 30.0 kg/m2) (both inclusive) with minimum of 45 kg weight.
• Participants with normal health as determined by personal medical history, clinical examination and laboratory examinations within Predefined site Normal range [Annexure III].
• Participants having clinically acceptable 12-lead electrocardiogram (ECG).
• Participants having clinically acceptable chest X-Ray (PA view), if taken.
• Participants having negative urine screen for drugs of abuse (including amphetamines, barbiturates, benzodiazepines, marijuana, cocaine and morphine).
• Participants having negative urine alcohol test / breath alcohol test.
• Non-smoker.
• Participants willing to adhere to the protocol requirements and to provide written informed consent.

• For male Participants:

  1-Participants willing to follow approved birth control methods (a double barrier method) for the duration of the study as judged by the investigator(s), such as (a double barrier method) condom with spermicide, Condom with diaphragm, or abstinence. Participants willing to refrain from donating sperm during the study period

• For Female Participants:

  1. Female of child bearing potential practicing an acceptable method of birth control for the duration of the study as judged by the investigator(s), such as intrauterine device (IUD), abstinence, bilateral tubal ligation or double barrier contraception, i.e., condom + diaphragm, condom + spermicidal or foam
  2. Postmenopausal for at least 1 year, or if less than 1 year, then following acceptable contraceptive measures as mentioned above
• Participants having negative urine pregnancy test at screening and negative serum ƒÒ-hCG pregnancy test on admission day of period 01 (only for female Participants).

Exclusion Criteria:

• Hypersensitivity to Imeglimin or related class of drugs or any of its excipients or heparin.
• History or presence of significant cardiovascular, pulmonary, hepatic, renal, gastrointestinal, endocrine, immunological, dermatological, neurological, urogenital or psychiatric disease or disorder.
• Any treatment which could bring about induction or inhibition of hepatic microsomal enzyme system within 30 days prior to admission in period 01.
• Presence of alcoholism or drug abuse.
• History or presence of asthma, urticaria or other significant allergic reactions.
• History or presence of significant gastric and/or duodenal ulceration.
• History or presence of significant thyroid disease, adrenal dysfunction, organic intracranial lesion such as pituitary tumor.
• History or presence of cancer or basal or squamous cell carcinoma.
• Difficulty with donating blood.
• Difficulty in swallowing solids dosage form like tablets or capsules.
• Use of any prescribed medication or OTC medication including vaccines, vitamins and herbal remedies during last 30 days prior to admission in period 01.
• Major illness within past 3 months.
• Participant who have donated blood (1 unit) or participation in a drug research study within past 90 days prior to the first dose of the study drug.
• Consumption of xanthine-containing products, tobacco containing products or alcohol or any alcohol containing products within 48.00 hours prior to admission in period 01.
• Consumption of grapefruit or grapefruit juice containing products within 72.00 hours prior to admission of period 01.
• Positive screening test for any one or more: HIV, Hepatitis B and Hepatitis C.
• History or presence of significant easy bruising or bleeding.
• History or presence of significant recent trauma.
• Participants who have been on an abnormal diet (for whatever reason) during the four weeks preceding the study.
• Female Participants who are currently breast feeding.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Imeglimin Hydrochloride Film Coated Tablet; Imeglimin Hydrochloride 500 mg Film Coated Tablet	Drug: Imeglimin Hydrochloride Film Coated Tablet; 1 tablet of 500 mg Imeglimin Hydrochloride; Drug: TWYMEEG® Tablets; 1 tablet of 500 mg Imeglimin Hydrochloride
Active Comparator: TWYMEEG® Tablets; TWYMEEG® Tablets (500 mg Imeglimin Hydrochloride)	Drug: Imeglimin Hydrochloride Film Coated Tablet; 1 tablet of 500 mg Imeglimin Hydrochloride; Drug: TWYMEEG® Tablets; 1 tablet of 500 mg Imeglimin Hydrochloride

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Peak Plasma Concentration (Cmax)	Acceptance range for bioequivalence was 80.00%-125.00% for 90% confidence intervals for the geometric least square mean ratio for Cmax.	72.00 hours
Area Under the Curve from time zero to time of last measurable concentration (AUC0-t)	Acceptance range for bioequivalence was 80.00%-125.00% for 90% confidence intervals for the geometric least square mean ratio for AUC0-t.	72.00 hour

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Area Under the Curve from time zero to time infinite (AUC0-∞)	Descriptive Statistic	72.00 hour
Time to reach peak plasma concentration (Tmax)	Descriptive Statistic	72.00 hours
Plasma Elimination Half-Life (t1/2)	Descriptive Statistic	72.00 hours
Kel	Descriptive Statistic	72.00 hours
AUC0-t/ AUC0-∞	Descriptive Statistic	72 hours

Collaborators and Investigators

• Sponsor: Humanis Saglık Anonim Sirketi

Study record dates

Study Major Dates

• Study Start (Actual): February 6, 2026
• Primary Completion (Actual): March 27, 2026
• Study Completion (Actual): May 13, 2026

Study Registration Dates

• First Submitted: July 1, 2026
• First Submitted That Met QC Criteria: July 1, 2026
• First Posted (Actual): July 8, 2026

Study Record Updates

• Last Update Posted (Actual): July 8, 2026
• Last Update Submitted That Met QC Criteria: July 1, 2026
• Last Verified: July 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Endocrine System Diseases; Metabolic Diseases; Glucose Metabolism Disorders; Diabetes Mellitus; Nutritional and Metabolic Diseases; Diabetes Mellitus, Type 2
• Other Study ID Numbers: 25-VIN-0596

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No