- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02110420
First-in-human Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of CC-90001
A Phase 1, Randomized, Two-part Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of CC-90001 in Healthy Subjects
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
-
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Texas
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Austin, Texas, États-Unis, 78744
- PPD Development, LP
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
1. Must understand and voluntarily sign a written informed consent prior to any study-related procedures being performed.
2. Must be able to communicate with the investigator, understand and comply with the requirements of the study, and agree to adhere to restrictions and examination schedules.
3. Healthy male or female of any race between 18 to 50 years of age (inclusive) at the time of signing the informed consent, and in good health as determined by a physical examination at screening.
4. For males: Agree to use barrier contraception not made of natural (animal) membrane [for example, latex or polyurethane condoms are acceptable]) when engaging in sexual activity with a female of childbearing potential while on study medication, and for at least 28 days after the last dose of study medication.
For females: Female subjects must have been surgically sterilized (hysterectomy or bilateral oophorectomy; proper documentation required) at least 6 months before screening, or be postmenopausal (defined as 24 months without menses before screening, with an estradiol level of < 30 pg/mL and follicle-stimulating hormone level of > 40 IU/L at screening).
5. Must have a body mass index between 18 and 33 kg/m2 (inclusive). 6. Platelet count, absolute neutrophil count and absolute lymphocyte count must be above the lower limit of normal at the screening visit.
7. Liver function tests must be below the upper limit of normal at screening. 8. All other clinical laboratory tests must be within normal limits or acceptable to the investigator.
9. Subject must be afebrile, with supine systolic blood pressure: 90 to 140 mmHg, supine diastolic blood pressure: 50 to 90 mmHg, and pulse rate: 40 to 110 bpm at screening.
10. Must have a normal or clinically-acceptable 12-lead electrocardiogram at screening. Male subjects must have a QTcF value ≤ 430 msec. Female subjects must have a QTcF value ≤ 450 msec.
Exclusion Criteria:
1. History of any clinically significant and relevant neurological, gastrointestinal, renal, hepatic, cardiovascular, psychological, pulmonary, metabolic, endocrine, hematological, allergic disease, drug allergies, or other major disorders.
2. Any condition which places the subject at unacceptable risk if he or she were to participate in the study, or confounds the ability to interpret data from the study.
3. Exposed to an investigational drug (new chemical entity) within 30 days preceding the first dose administration, or 5 half-lives of that investigational drug, if known (whichever is longer).
4. Used any prescribed systemic or topical medication (including but not limited to analgesics, anesthetics, etc) within 30 days of the first dose administration.
5. Used any non-prescribed systemic or topical medication (including vitamin/mineral supplements, and herbal medicines) within 14 days of the first dose administration.
6. Used cytochrome P450 (CYP)3A inducers and inhibitors (including St. John's Wort) within 30 days of the first dose administration.
7. Has any surgical or medical conditions possibly affecting drug absorption, distribution, metabolism and excretion, for example, bariatric procedure. Appendectomy and cholecystectomy are acceptable.
8. Donated blood or plasma within 8 weeks before the first dose administration to a blood bank or blood donation center.
9. History of drug abuse (as defined by the current version of the Diagnostic and Statistical Manual) within 2 years before dosing, or positive drug screening test reflecting consumption of illicit drugs.
10. History of alcohol abuse (as defined by the current version of the Diagnostic and Statistical Manual) within 2 years before dosing, or positive alcohol screen.
11. Known to have serum hepatitis or known to be a carrier of hepatitis B surface antigen or hepatitis c antibody, or have a positive result to the test for human immunodeficiency virus antibodies at screening.
12. Smoke more than 10 cigarettes per day, or the equivalent in other tobacco products (self reported).
13. History of ulcerative colitis, Crohn's disease, diverticular disease, any polyp(s) along the gastrointestinal tract, or colorectal cancer.
14. History of hemorrhoids, anal fissures, rectal ulcers, minor rectal bleeding (such as red blood on toilet paper after wiping) within 5 years before the first dose administration.
15. History of gastrointestinal bleeding or blood in stool within 5 years before the first dose administration.
16. Any positive fecal occult blood test at screening and/or at any time prior to first dosing.
17. Any history of constipation within 2 years before the first dose administration.
18. Subject does not routinely have a bowel movement, at minimum, every third day.
19. Any subject with a history of Irritable Bowel Syndrome or a history of frequent abdominal cramping, frequent diarrhea, or frequent loose stools (with frequent defined as once per week or greater).
20. Any female subject with menses (natural or artificial). 21. Any subject taking hormonal contraception. 22. Subjects who are part of the clinical staff personnel or family members of the clinical site staff.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Répartition: Randomisé
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Expérimental: Placebo
|
Placebo will be administered once daily for up to 14 days depending on the Part of the study
|
Expérimental: CC-90001 10mg (Single Dose)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 30mg (Single Dose)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 60mg (Single Dose)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 120mg (Single Dose)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 240mg (Single Dose)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 10mg (Multiple Doses)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 30mg (Multiple Doses)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 60mg (Multiple Doses)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 120mg (Multiple Doses)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 240mg (Multiple Doses)
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 480mg (single dose)
CC-90001 480mg will be administered as a single oral dose
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 720mg (single dose)
CC-90001 720mg will be administered as a single oral dose
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Expérimental: CC-90001 480mg (multiple doses)
CC-90001 480mg will be administered daily for 14 days
|
CC-90001 10mg will be administered as a single dose
CC-90001 30mg will be administered as a single dose
CC-90001 60mg will be administered as a single dose
CC-90001 120mg will be administered as a single dose
CC-90001 240mg will be administered as a single dose
CC-90001 10mg will be administered daily for 14 days
CC-90001 30mg will be administered daily for 14 days
CC-90001 60mg will be administered daily for 14 days
CC-90001 120mg will be administered daily for 14 days
CC-90001 240mg will be administered daily for 14 days
CC-90001 480mg will be administered as a single oral dose
CC-90001 720mg will be administered as a single oral dose
CC-90001 480mg will be administered daily for 14 days
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Adverse Events
Délai: Up to 8 months overall
|
Number of participants with adverse events
|
Up to 8 months overall
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Concentrations of CC-90001 in plasma
Délai: Up to 14 days per cohort
|
Blood samples will be collected at pre-specified times to determine levels of CC-90001 in plasma
|
Up to 14 days per cohort
|
Cmax: Maximum observed plasma concentration
Délai: Up to 14 days per cohort
|
Cmax will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
Tmax: Time to Cmax
Délai: Up to 14 days per cohort
|
Tmax will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
AUCinf: Area under the plasma concentration-time curve from time zero extrapolated to infinity
Délai: Up to 14 days per cohort
|
AUCinf will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
AUCt: Area under the plasma concentration-time curve from time zero to the last quantifiable concentration
Délai: Up to 14 days per cohort
|
AUCt will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
AUCtau: Area under the plasma concentration-time curve from time zero to tau, where tau is the dosing interval
Délai: Up to 14 days per cohort
|
AUCtau will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
AUCtau will be estimated for CC-90001 using a non-compartmental approach
Délai: Up to 14 days per cohort
|
t1/2,z will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
CL/F: Apparent total plasma clearance when dosed orally
Délai: Up to 14 days per cohort
|
CL/F will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
Vz/F: Apparent total volume of distribution when dosed orally, based on the terminal phase
Délai: Up to 14 days per cohort
|
Vz/F will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
Ratio of Accumulation based on Day 1 and Day 14 AUCtau
Délai: Up to 14 days per cohort
|
Ratio of accumulation will be estimated for CC-90001 using a non-compartmental approach
|
Up to 14 days per cohort
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- CC-90001-CP-001
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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