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Study of the Effects of ITCA 650 on Gastric Emptying and Interaction of ITCA 650 on 4 Commonly Studied Drugs

26. januar 2017 oppdatert av: Intarcia Therapeutics

A Phase 1, Fixed-Sequence, Open-label Study in Healthy Subjects to Estimate the Effects of ITCA 650 on Gastric Emptying and on the Absorption Pharmacokinetics of Each of 4 Commonly Studied Drug/Drug Interaction (DDI) Probe Compounds

A Phase 1, Fixed-Sequence, Open-label Study in Healthy Subjects to Estimate the Effects of ITCA 650 on Gastric Emptying and on the Absorption Pharmacokinetics of Each of 4 Commonly Studied DDI Probe Compounds.

Studieoversikt

Detaljert beskrivelse

Acetaminophen will be use to assess the effect of ITCA 650 on the rate of gastric emptying.

Interactions between ITCA 650 and the medications lisinopril, digoxin, atorvastatin, and warfarin will also be studied.

Studietype

Intervensjonell

Registrering (Faktiske)

33

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Kansas
      • Overland Park, Kansas, Forente stater, 66211
        • Quintiles

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Body mass index (BMI) between 19 to 32 kg/m2.
  • Glycosylated hemoglobin A1c (HbA1c )<6.5%.
  • Normal renal function (eGFR ≥80 mL/min/1.73 m2).
  • Women of child bearing potential - use of an additional adequate method of contraception during the study and until 1 additional menstrual cycle following the end-of-study (EOS) visit. Adequate methods of contraception for women of child bearing potential (WOCBP) include: mechanical products (ie, intrauterine device [IUD]-copper IUD); or barrier methods (eg, diaphragm, condoms, cervical cap) with spermicide.

Exclusion Criteria:

  • History of type 1 or type 2 diabetes.
  • History or evidence of myocardial infarction, coronary revascularization (coronary artery bypass grafting or percutaneous coronary intervention), unstable angina, or cerebrovascular accident or stroke.
  • History of uncontrolled hypertension.
  • History or evidence of acute or chronic pancreatitis.
  • History of liver disease.
  • History of medullary thyroid cancer or a personal or family history of multiple endocrine neoplasia type 2.
  • Poor thyroid, liver, or renal function.
  • Weight loss surgery or requires weight loss medications.
  • History of malignancy (not including basal or squamous cell carcinoma of the skin with past 5 years). (Subjects who have been disease free for 5 years may be included.)
  • History of active alcohol or substance abuse.
  • Weekly consumption of more than 7 alcoholic beverages for females and 14 alcoholic beverages for males.
  • Excessive in xanthine consumption (more than 5 cups of coffee or equivalent per day).
  • Treatment with medications that affect GI motility.
  • Any condition that would affect drug transit time or absorption (eg, gastrointestinal bypass surgery, partial or total gastrectomy, small bowel resection, chronic diarrhea, vagotomy, chronic gastroesophageal reflux disease, malabsorption, colostomy, Crohn's disease, ulcerative colitis, or celiac sprue).
  • History of hypersensitivity to exenatide.
  • Contraindications or warnings according to the specific label(s) for acetaminophen, atorvastatin, lisinopril, digoxin or warfarin therapy.
  • Women that are pregnant, lactating, or planning to become pregnant.
  • Concurrent use of anticoagulants, including daily low dose aspirin (81 mg).
  • History of or positive results on screening tests for hepatitis B and/or hepatitis C and/or human immunodeficiency virus (HIV).
  • Planned in-patient surgery, dental procedure, or hospitalization during the study.
  • Prior or current treatment with any glucagon-like peptide-1 (GLP-1) receptor agonist (eg, Bydureon™, Byetta®, Victoza®, Tanzeum® or exogenous native GLP-1) or prior participation in an ITCA 650 clinical trial.
  • Use or intended use of any drug or other product that inhibits or induces cytochrome P450 (CYP)1A2, CYP2C9, CYP2C19, or CYP3A4 within 14 days prior to the first dose of warfarin or ITCA650 or during the conduct of the study.
  • History of thrombophlebitis, thromboembolic disorders, or deep vein thrombophlebitis.
  • Fasting triglycerides above upper limit of normal at Screening.
  • Any gastrointestinal complaints within 7 days prior to first dosing.
  • Taking drugs or natural herbal supplements (such as albuterol, antacids, and St. John's Wort) with known interactions with atorvastatin, lisinopril, digoxin, or warfarin from within 7 days prior to Day 1 until EOS
  • Consumed or unwilling to refrain from grapefruit, cranberries, grapefruit- or cranberry-containing products, or Seville oranges from within 7 days prior to Day 1 until EOS.
  • Chronic use of analgesics, pain medication, or non-steroidal anti-inflammatory agents.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Experimental Treatment
ITCA 650 20/60 mcg/day Acetaminophen 1000 mg Atorvastatin 40 mg Lisinopril 20 mg Warfarin 25 mg Digoxin 0.5 mg
ITCA 650 osmotic mini pump delivering exenatide 20 mcg/day for 14 days, followed by ITCA 650 osmotic mini pump delivering exenatide 60 mcg/day.
Oral acetaminophen 1000 mg on Day 1 and Day 27
Oral atorvastatin 40 mg on Day 2 and Day 28
Oral lisinopril 20 mg on Day 2 and Day 28
Oral warfarin 25 mg on Day 2 and Day 28
Oral digoxin 0.5 mg on Day 2 and Day 28

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Area under the concentration-time curve from time zero to the last measurable concentration [AUC(0-last)]) of acetaminophen alone and in the presence of ITCA 650.
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Maximum plasma concentration ([Cmax]) of acetaminophen alone and in the presence of ITCA 650
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Area under the concentration-time curve (AUC(0-last)) of atorvastatin, lisinopril, digoxin, R-warfarin, and S-warfarin each alone and in the presence of ITCA 650.
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Cmax of atorvastatin, lisinopril, digoxin, R-warfarin, and S-warfarin each alone and in the presence of ITCA 650.
Tidsramme: time zero to 10 weeks
time zero to 10 weeks

Sekundære resultatmål

Resultatmål
Tidsramme
Time to maximum plasma concentration (tmax) of acetaminophen
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
tmax of atorvastatin, lisinopril, digoxin, R warfarin, and S-warfarin
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
AUC(0-last) of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Cmax of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Maximum effect (Emax)from time zero to the last measurable concentration (AUEC(0-last)) of international normalized ratio (INR) of warfarin.
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Cmax of ITCA 650, 20 mcg/d and 60 mcg/d
Tidsramme: within 8 hours after placement of ITCA 650
within 8 hours after placement of ITCA 650
Treatment-emergent adverse events (TEAEs) including any events local to the placement site, clinical laboratory measurements, ECGs, vital signs and physical examinations.
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Tmax of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Cmin of ITCA 650, 20 mcg/d and 60 mcg/d
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Tmax of ITCA 650, 20 mcg/d and 60 mcg/d
Tidsramme: time zero to 10 weeks
time zero to 10 weeks
Tmin of ITCA 650, 20 mcg/d and 60 mcg/d
Tidsramme: zero to 10 weeks
zero to 10 weeks
Time of maximum effect (tEmax)from time zero to the last measurable concentration (AUEC(0-last)) of international normalized ratio (INR) of warfarin.
Tidsramme: zero to 10 weeks
zero to 10 weeks
Area under the effect-time curve from time zero to the last measurable concentration (AUEC(0-last)) of international normalized ratio (INR) of warfarin.
Tidsramme: zero to 10 weeks
zero to 10 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. desember 2015

Primær fullføring (Faktiske)

1. mars 2016

Studiet fullført (Faktiske)

1. mars 2016

Datoer for studieregistrering

Først innsendt

21. desember 2015

Først innsendt som oppfylte QC-kriteriene

24. desember 2015

Først lagt ut (Anslag)

30. desember 2015

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

27. januar 2017

Siste oppdatering sendt inn som oppfylte QC-kriteriene

26. januar 2017

Sist bekreftet

1. januar 2017

Mer informasjon

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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