Study of the Effects of ITCA 650 on Gastric Emptying and Interaction of ITCA 650 on 4 Commonly Studied Drugs
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
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Studientyp
Einschreibung (Tatsächlich)
Einschreibung
Phase
Phase
- Phase 1
Kontakte und Standorte
Studienorte
-
-
Kansas
-
Overland Park, Kansas, Vereinigte Staaten, 66211
- Quintiles
-
-
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: 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
|
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
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.
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Maximum plasma concentration ([Cmax]) of acetaminophen alone and in the presence of ITCA 650
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Time to maximum plasma concentration (tmax) of acetaminophen
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
tmax of atorvastatin, lisinopril, digoxin, R warfarin, and S-warfarin
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
AUC(0-last) of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Cmax of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
Zeitfenster: 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.
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Cmax of ITCA 650, 20 mcg/d and 60 mcg/d
Zeitfenster: 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.
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Tmax of orthohydroxy-atorvastatin and parahydroxy-atorvastatin
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Cmin of ITCA 650, 20 mcg/d and 60 mcg/d
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Tmax of ITCA 650, 20 mcg/d and 60 mcg/d
Zeitfenster: time zero to 10 weeks
|
time zero to 10 weeks
|
|
Tmin of ITCA 650, 20 mcg/d and 60 mcg/d
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: zero to 10 weeks
|
zero to 10 weeks
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Studienbeginn
Primärer Abschluss (Tatsächlich)
Primärer Abschluss
Studienabschluss (Tatsächlich)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Hypoglykämische Mittel
- Physiologische Wirkungen von Arzneimitteln
- Molekulare Mechanismen der pharmakologischen Wirkung
- Anti-Arrhythmie-Mittel
- Antihypertensive Mittel
- Agenten des peripheren Nervensystems
- Enzym-Inhibitoren
- Analgetika
- Agenten des sensorischen Systems
- Analgetika, nicht narkotisch
- Antipyretika
- Antimetaboliten
- Hormone
- Hormone, Hormonersatzstoffe und Hormonantagonisten
- Protease-Inhibitoren
- Schutzmittel
- Kardiotonische Mittel
- Anticholesterämische Mittel
- Hypolipidämische Mittel
- Lipidregulierende Mittel
- Hydroxymethylglutaryl-CoA-Reduktase-Inhibitoren
- Antikoagulanzien
- Mittel gegen Fettleibigkeit
- Inkretine
- Angiotensin-Converting-Enzym-Inhibitoren
- Digoxin
- Atorvastatin
- Paracetamol
- Warfarin
- Exenatide
- Lisinopril
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- ITCA 650-CLP-115
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