- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01270308
Bioequivalence Study of Lansoprazole DR Capsules 30 mg in Fasting Conditions
Open Label, Randomized, Two-treatment, Three-period, Three-sequence, Partial Replicate Oral Bioequivalence Study of Lansoprazole 30 mg DR Capsules of Dr.Reddy's Laboratories Limited, India Comparing With That of PREVACID® (Containing Lansoprazole) 30 mg DR Capsules of TAP Pharmaceuticals Inc. USA, in Healthy, Adult, Human Subjects Under Fasting Conditions.
Studieoversikt
Detaljert beskrivelse
Studietype
Registrering (Faktiske)
Fase
- Fase 1
Kontakter og plasseringer
Studiesteder
-
-
Hyderabad
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Balanagar, Hyderabad, India, 500 037
- Bioserve Clinical Research (P) Ltd
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
i. Provided written informed consent.
ii. Subject who were healthy, adult, human beings within 18 and 45 years of age (both inclusive) weighing at least 50 kg.
iii. Subject having a body mass index between 18.0 and 29.9 (both inclusive), calculated as weight in Kg/height in m2.
iv. Subject having a normal health as determined by medical history, physical examination and laboratory investigation performed within 28 days prior to the commencement of the study. (Laboratory values must be within normal limits or considered by the physician /investigator to be of no clinical significance).
v. Female Subjects 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 condoms, foams, jellies, diaphragm, intrauterine device (IUD), or abstinence.
- postmenopausal for at least 1 year.
- surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy has been performed on the subject)
Exclusion Criteria:
i. Subject who were incapable of understanding the informed consent.
ii. Systolic blood pressure less than 90 mm of Hg or more than 140 mm of Hg.
iii. Diastolic blood pressure less than 60 mm of Hg or more than 90 mm of Hg.
iv. Oral temperature is below 95.0°F or above 98.6°F.
v. Pulse rate below 50/min or above 100/min.
vi. History of hypersensitivity or idiosyncratic reaction to investigational drug product or any other related drugs.
vii. Any evidence of impairment of renal, hepatic, cardiac, lung or gastrointestinal function.
viii. Consumption of grapefruit for the past ten days prior to the check-in, in each period.
ix. Regular smoker who has a habit of smoking more than nine cigarettes per day and has difficulty in abstaining from smoking during sample collection period.
x. Habit of alcoholism and difficulty in abstaining from alcohol during the sample collection period.
xi. Difficulty in abstaining from xanthene containing food or beverages (like tea, coffee, chocolates and cola drinks) during the sample collection period.
xii. Intake of over the counter (OTC) or prescribed medications and enzyme modifying medication or systemic medication for the last 30 days before dosing.
xiii. Clinically significant abnormalities and / or with significant diseases.
xiv. Confirmed positive in alcohol screening.
xv. Confirmed positive in selected drug of abuse.
xvi. Subjects who had participated in any other clinical investigation using experimental drug/donated blood in past 90 days before the date of start of study
xvii. Confirmed positive in urine pregnancy test.
xviii. Female detected to be pregnant, breast feeding or who is likely to become pregnant during the study.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: Lansoprazole DR Capsules 30 mg
Lansoprazole DR Capsules 30 mg of Dr.Reddy's Laboratories Limited
|
Lansoprazole DR Capsules 30 mg
Andre navn:
|
Aktiv komparator: Prevacid 30 mg Capsules
Prevacid 30 mg Capsules of TAP Pharmaceuticals Inc. USA
|
Lansoprazole DR Capsules 30 mg
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Bioekvivalens basert på Cmax og AUC parametere
Tidsramme: 4 måneder
|
4 måneder
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Dr.M.Venkat Jayanth, MBBS, Bioserve Clinical Research (P) Ltd
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- P-699/08
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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