- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07691203
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
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.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 1
Kontakter och platser
Studieorter
-
-
Sarkhej
-
Ahmedabad, Sarkhej, Indien, 382210
- Cliantha Research Limited
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Beskrivning
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
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Övrig
- Tilldelning: Randomiserad
- Interventionsmodell: Crossover tilldelning
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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
|
|
Aktiv komparator: 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
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
For Empagliflozin & Linagliptin & Metformin; Maximum concentration obtained (Cmax)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
For Empagliflozin & Linagliptin & Metformin; Time to reach maximum concentration Cmax (Tmax)
Tidsram: 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)
Tidsram: 48 hours
|
Descriptive Statistics
|
48 hours
|
|
For Empagliflozin: Area under the plasma concentration versus time curve from zero to infinity (AUCi)
Tidsram: 48 hours
|
Descriptive Statistics
|
48 hours
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- C1B06324
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