このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Bioequivalence Study to Compare Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg Extended Release Tablet Versus Trijardy® XR 25 mg/5 mg/1000 mg Extended- Release Tablets

2026年7月1日 更新者:Humanis Saglık Anonim Sirketi

An Open Label, Randomized, Two-period, Two Treatment, Two-sequence, Crossover, Balanced, Single Dose Oral Bioequivalence Study to Compare Empagliflozin/ Linagliptin/ Metformin HCl 25 mg/5 mg/1000 mg Extended Release Tablet Versus Trijardy® XR (Empagliflozin, Linagliptin, and Metformin Hydrochloride Extended-release Tablets) 25 mg/5 mg/1000 mg in Fed Condition.

An open label, randomized, two-period, two treatment, two-sequence, crossover, balanced, single dose oral bioequivalence study to compare Empagliflozin/ Linagliptin/ Metformin HCl 25 mg/5 mg/1000 mg Extended Release Tablet versus Trijardy® XR (Empagliflozin/linagliptin/metformin hydrochloride extended-release tablets 25 mg/5 mg/1000 mg) in healthy subject in fed condition.

調査の概要

研究の種類

介入

入学 (実際)

36

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Sarkhej
      • Ahmedabad、Sarkhej、インド、382210
        • Cliantha Research Limited

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  • Age: 18 to 55 years old, both inclusive.
  • Gender: Male and/or non-pregnant, non-lactating female. A. Female of child-bearing potential had a negative serum beta human chorionic gonadotropin (β-HCG) pregnancy test performed within 28 days of the first dose of study medication. They used an acceptable form of contraception.

For female of child-bearing potential, acceptable forms of contraception included the following:

i. Non hormonal intrauterine device in place for at least 3 months prior to the start of the study and remaining in place during the study period, or ii. Barrier methods containing or used in conjunction with a spermicidal agent, or iii. Surgical sterilization or iv. Practicing sexual abstinence throughout the course of the study.

B. Females were not considered of child-bearing potential if one of the following was reported and documented on the medical history:

i. Postmenopausal with spontaneous amenorrhea for at least 12 consecutive months without other medical explanation, or ii. Bilateral oophorectomy with or without a hysterectomy and an absence of bleeding for at least 6 months, or iii. Total hysterectomy and an absence of bleeding for at least 3 months.

  • 18.5 to 30.0 kg/m2, both inclusive; BMI values were rounded off to one significant digit after decimal point (e.g. 30.04 rounded down to 30.0, while 18.45 rounded up to 18.5).
  • Able to communicate effectively with study personnel.
  • Non-alcoholic, non-smoker and non-tobacco user (i.e. had no past history of drinking alcohol, smoking and tobacco consuming for at least one year prior to study).
  • Normal or clinically non-significant ECG recording during screening.
  • Willing to provide written informed consent to participate in the study.
  • All participants were judged by the principal or sub-investigator or physician as normal and healthy during a pre-study safety assessment performed within 28 days of the first dose of study medication which included: a) A physical examination (clinical examination) with no clinically significant finding.

Exclusion Criteria:

  • History of allergic responses to Empagliflozin, Linagliptin, Metformin or other related drugs, or any of its formulation ingredients.
  • Had significant diseases or clinically significant abnormal findings during screening [medical history, physical examination (clinical examination), laboratory evaluations, ECG recording, gynecological history and examination (including pelvic examination and routine breast examination) (for female participants)].
  • Any disease or condition like diabetes, psychosis or others, which compromised the haemopoietic, gastrointestinal, renal, hepatic, cardiovascular, respiratory, Central nervous system or any other body system.
  • History or presence of bronchial asthma.
  • Used any hormone replacement therapy within 3 months prior to the first dose of study medication.
  • Used any depot injection or implant of any drug within 3 months prior to the first dose of study medication.
  • Used CYP enzyme inhibitors or inducers within 30 days prior to the first dose of study medication (see https://drug-interactions.medicine.iu.edu/MainTable.aspx).
  • History or evidence of drug dependence.
  • History of difficulty with donating blood or difficulty in accessibility of veins.
  • A positive hepatitis screen (included subtypes B & C).
  • A positive test result for HIV antibody.
  • Participant who had received a known investigational drug within seven elimination half-life of the administered drug prior to the first dose of study medication.
  • Participant who had donated blood or loss of blood 50 ml to 100 ml within 30 days or 101 ml to 200 ml within 60 days or >200 ml within 90 days (excluding volume drawn at screening for this study) prior to first dose of study medication, whichever was greater.
  • History of difficulty in swallowing or of any gastrointestinal disease, which affected drug absorption.
  • Intolerance to venipuncture.
  • Any food allergy, intolerance, restriction or special diet that, in the opinion of the principal investigator or sub-investigator, could contraindicate the participant's participation in this study.
  • Institutionalized participant.
  • Used any prescribed medications within 14 days prior to the first dose of study medication.
  • Used any OTC products, vitamin and herbal products, etc., within 7 days prior to the first dose of study medication.
  • Used grapefruit and grapefruit containing products within 7 days prior to the first dose of study medication.
  • Ingested any caffeine or xanthine products (i.e. coffee, tea, chocolate, and caffeinecontaining sodas, colas, etc.), recreational drugs within 48 hours prior to the first dose of study medication.
  • Ingested any unusual diet, for whatever reason (e.g.: low sodium) for three weeks prior to the first dose of study medication.
  • Presence of ketone during urine analysis.
  • History or presence of cardiovascular disorders.
  • Participant with Serum Lactate higher than upper limit of normal range.
  • Participant with Estimated Glomerular Filtration Rate was less than 60 ml/min/1.73 m2 during screening.
  • History or presence of hypoglycemia.
  • Participant with Serum Creatinine higher than upper limit of normal range.
  • History of acute and chronic metabolic acidosis.
  • History or sign and symptoms of pancreatitis.
  • History of genital mycotic infections.
  • History of severe and disabling arthralgia.
  • History of bullous pemphigoid.
  • History of recurrent urinary tract infection

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:他の
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Empagliflozin/Linagliptin/Metformin HCl Extended Release Tablet
Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg Extended Release Tablet
1 extended Release tablet of Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg
1 extended Release tablet of Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg
アクティブコンパレータ:Trijardy® XR extended-release tablets
Trijardy® XR (Empagliflozin/linagliptin/metformin hydrochloride extended-release tablets 25 mg/5 mg/1000 mg)
1 extended Release tablet of Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg
1 extended Release tablet of Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
For Empagliflozin & Linagliptin & Metformin; Maximum concentration obtained (Cmax)
時間枠:Empagliflozin & Metformin; 48 hours, Linagliptin; 72 hours
two-sides 90% CI for the test to reference ratio of the population means is within 80.00-125.00% for each of the Ln-transformed data Cmax
Empagliflozin & Metformin; 48 hours, Linagliptin; 72 hours
For Empagliflozin & Metformin; AUC from time 0 to last collection time (AUC0 - t)
時間枠:Empagliflozin & Metformin: 48 hours
two-sides 90% CI for the test to reference ratio of the population means is within 80.00-125.00% for each of the Ln-transformed data AUC
Empagliflozin & Metformin: 48 hours
For Linagliptin; Area under the plasma concentration-time curve from 0 to 72 hours (AUC72)
時間枠:72 hours
two-sides 90% CI for the test to reference ratio of the population means is within 80.00-125.00% for each of the Ln-transformed data AUC
72 hours

二次結果の測定

結果測定
メジャーの説明
時間枠
For Empagliflozin & Linagliptin & Metformin; Time to reach maximum concentration Cmax (Tmax)
時間枠:Empagliflozin & Metformin: 48 hours, Linagliptin: 72 hours
Descriptive Statistics
Empagliflozin & Metformin: 48 hours, Linagliptin: 72 hours
For Metformin : Area under the plasma concentration versus time curve from the zero time point to the last quantifiable concentration(AUCt)
時間枠:48 hours
Descriptive Statistics
48 hours
For Empagliflozin: Area under the plasma concentration versus time curve from zero to infinity (AUCi)
時間枠:48 hours
Descriptive Statistics
48 hours

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年3月7日

一次修了 (実際)

2026年6月16日

研究の完了 (実際)

2026年7月1日

試験登録日

最初に提出

2026年7月1日

QC基準を満たした最初の提出物

2026年7月1日

最初の投稿 (実際)

2026年7月8日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月8日

QC基準を満たした最後の更新が送信されました

2026年7月1日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する