- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus 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
Tutkimuksen yleiskatsaus
Tila
Ehdot
Yksityiskohtainen kuvaus
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 1
Yhteystiedot ja paikat
Opiskelupaikat
-
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Texas
-
Austin, Texas, Yhdysvallat, 78744
- PPD Development, LP
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
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.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Jako: Satunnaistettu
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Kaksinkertainen
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
---|---|
Kokeellinen: Plasebo
|
Placebo will be administered once daily for up to 14 days depending on the Part of the study
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Kokeellinen: 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
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
---|---|---|
Adverse Events
Aikaikkuna: Up to 8 months overall
|
Number of participants with adverse events
|
Up to 8 months overall
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
---|---|---|
Concentrations of CC-90001 in plasma
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
|
Yhteistyökumppanit ja tutkijat
Sponsori
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Arvio)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Arvio)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muut tutkimustunnusnumerot
- CC-90001-CP-001
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