ABOUT THIS STUDY
1. Healthy or hepatically impaired female subjects of non-child bearing potential and/or male subjects who, at the time of Screening, are between the ages of 18 and 75 years, inclusive.
2. Female subjects of nonchildbearing potential must meet at least 1 of the following criteria:
1. Achieved postmenopausal status, defined as follows: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; with a serum follicle-stimulating hormone (FSH) level confirming the postmenopausal state;
2. Have undergone a documented hysterectomy and/or bilateral oophorectomy;
3. Have medically confirmed ovarian failure. All other female subjects (including females with tubal ligations) are considered to be of childbearing potential.
3. Body mass index (BMI) of 17.5 to 40 kg/m2; and a total body weight >50 kg (110 lb).
4. Evidence of a personally signed and dated informed consent document indicating that the subject (or a legal representative) has been informed of all pertinent aspects of the study.
5. Subjects who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.
Additional Inclusion Criteria for Subjects With Normal Hepatic Function:
Subjects in the normal hepatic function cohort (Cohort 3) must be considered healthy and meet all of the following additional inclusion criteria to be eligible for enrollment into the study:
1. No known or suspected hepatic impairment based on liver function tests, albumin and prothrombin time, defined as the following:
1. ALT and AST <= upper limit of normal (ULN);
2. Total bilirubin <= 1.5 × ULN; subjects with a history of Gilbert's syndrome may have direct bilirubin measured and would be eligible for this study provided the direct bilirubin level is not greater than 0.5 mg/dL;
3. Alkaline phosphatase <= ULN;
4. Albumin within the normal range (local lab ranges);
5. Prothrombin time (PT) within the normal range (local lab ranges).
2. Subjects must fit the demographic-matching criteria, including:
1. A total body weight that is +/- 10 kg of the population median of the pooled hepatic impairment cohorts (Cohorts 1 and 2).
2. An age that is +/- 5 years of the population median of the pooled hepatic impairment cohorts (Cohorts 1 and 2).
3. No known or suspected hepatic impairment.
4. Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, full physical examination, including blood pressure (BP) and pulse rate (PR) measurement, 12 lead ECG or clinical laboratory tests.
Additional Inclusion Criteria for Subjects with Impaired Hepatic Function:
Subjects in the hepatic impairment cohorts (Cohorts 1 and 2) must meet the following additional inclusion criteria to be eligible for enrollment into the trial:
1. Satisfy the criteria for Class B, or C of the modified Child-Pugh Classification.
2. A diagnosis of hepatic dysfunction due to hepatocellular disease (and not secondary to any acute ongoing hepatocellular process) documented by medical history, physical examination, liver biopsy, hepatic ultrasound, computerized tomography (CT) scan, or magnetic resonance imaging (MRI).
3. Known stable hepatic impairment, defined as no evidence of clinically significant change in disease status within the last 30 days, as documented by the subject's recent medical history (eg, no worsening clinical signs of hepatic impairment, or no worsening of total bilirubin or prothrombin time by more than 50%).
4. Stable drug regimen defined as not starting a new drug or changing dosage within seven days or five half-lives (whichever is longer) prior to the dosing of investigational product. History of alcohol abuse is permissible providing that the results of alcohol test are negative at Screening and on Day -1, and the subject is willing and able to abide by the lifestyle guidelines.
1. Any condition possibly affecting drug absorption (eg, gastrectomy).
2. A positive urine drug test. Subjects with hepatic impairment (Cohorts 1 and 2) will be
eligible to participate if their urine drug test is positive with a drug for a
prescribed substance that is not expected to interfere with the PK of glasdegib.
3. Pregnant female subjects; breastfeeding female subjects; fertile male subjects who are
unwilling or unable to use at least one highly effective method of contraception as
outlined in this protocol for the duration of the study and for at least 90 days after
the glasdegib dose and, refrain from sperm donation for the duration of the Study and
for at least 90 days after the glasdegib dose.
4. History of sensitivity to heparin or heparin-induced thrombocytopenia.
5. Blood donation of approximately 1 pint (500 mL) or more within 56 days prior to
6. Unwilling or unable to comply with the Lifestyle Requirements.
7. Subjects who are investigational site staff members directly involved in the conduct
of the study and their family members, site staff members otherwise supervised by the
investigator, or subjects who are Pfizer employees directly involved in the conduct of
8. History of known sensitivity to glasdegib.
9. Treatment with an investigational drug within 30 days (or as determined by the local
requirement) or 5 half-lives preceding the dose of glasdegib (whichever is longer).
10. Subjects with a history of or current positive results for human immunodeficiency
11. Other acute or chronic medical or psychiatric condition including recent (within the
past year) or active suicidal ideation or laboratory abnormality that may increase the
risk associated with study participation or investigational product administration or
may interfere with the interpretation of study results and, in the judgment of the
investigator, would make the subject inappropriate for entry into this study.
Additional Exclusion Criteria for Subjects with Normal Hepatic Function:
In addition, subjects in the normal hepatic function cohort (Cohort 3) presenting with any
of the following will not be included in the trial:
1. Evidence or history of clinically significant hematological, renal, endocrine,
pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or
allergic disease (including drug allergies deemed relevant for participation in this
study, but excluding untreated, asymptomatic, seasonal allergies at the time of
2. History of regular alcohol consumption exceeding 7 drinks/week for females or 14
drinks/week for males (1 drink = 5 ounces (150 mL) of wine or 12 ounces (360 mL) of
beer or 1.5 ounces (45 mL) of hard liquor) within 6 months of Screening.
3. Screening supine BP => 140 mm Hg (systolic) or => 90 mm Hg (diastolic), following at
least 5 minutes of supine rest. If BP is => 140 mm Hg (systolic) or => 90 mm Hg
(diastolic), the BP should be repeated two more times and the average of the three BP
values should be used to determine the subject's eligibility.
4. 12-lead ECG demonstrating QTcF >450 msec or a QRS interval >120 msec at Screening. If
QTcF exceeds 450 msec, or QRS exceeds 120 msec, the ECG should be repeated two more
times and the average of the three QTcF or QRS values should be used to determine the
5. Use of prescription or nonprescription drugs and dietary supplements within 7 days or
5 half-lives (whichever is longer) prior to the first dose of lasdegib. As an
exception, acetaminophen/paracetamol may be used at doses of =<1 g/day. Limited use of
nonprescription medications that are not believed to affect subject safety or the
overall results of the study may be permitted on a case by case basis following
approval by the sponsor. Herbal supplements and hormone replacement therapy must have
been discontinued at least 28 days prior to the dose of investigational product.
6. Subjects with a history of or current positive results for hepatitis B or hepatitis C,
including hepatitis B surface antigen (HepBsAg), hepatitis B core antibody (HepBcAb),
or hepatitis C antibody (HCVAb).
Additional Exclusion Criteria for Subjects With Impaired Hepatic Function:
In addition, subjects in the hepatic impairment cohorts (Cohorts 1 and 2) presenting with
any of the following will not be included in the trial:
1. Other clinically significant disease that contraindicates study drug or that may
affect the PK of glasdegib (stable, chronic, controlled disorders such as hypertension
and diabetes may be acceptable).
2. Hepatic carcinoma and hepatorenal syndrome or life expectancy <1 year.
3. Undergone porta-caval shunt surgery. NOTE: Subjects with a transjugular intrahepatic
portosystemic shunt (TIPS) are permitted provided that they meet the Child-Pugh
4. History of gastrointestinal hemorrhage either due to esophageal varices or peptic
ulcers less than one month prior to study entry.
5. Any clinically significant laboratory abnormality except for those parameters
influenced by hepatic impairment. Due to potential for alteration of hepatic function
in renally impaired patients, subjects must have an estimated glomerular filtration
rate (eGFR) corrected for their body surface area of => 75 mL/min based on the
Modification of Diet in Renal Disease (MDRD) equation, with a single repeat permitted
to assess eligibility, if needed.
6. Presence of clinically active stage 3 or 4 encephalopathy.
7. Severe uncontrolled ascites and/or pleural effusion.
8. Screening blood pressure => 160 mm Hg (systolic) or => 90 mm Hg (diastolic), following
at least 5 minutes of supine rest. If initial BP is => 160 mm Hg (systolic) or => 90
mm Hg (diastolic), the BP should be repeated two more times and the average of the
three BP values should be used to determine the subject's eligibility.
9. Screening supine 12-lead ECG demonstrating QTcF >470 msec or a QRS interval >120 msec.
If initial QTcF exceeds 470 msec, or QRS exceeds 120 msec, the ECG should be repeated
two more times and the average of the three QTcF or QRS values should be used to
determine the subject's eligibility.
10. Use of food, drugs, or dietary supplements that may affect the PK of glasdegib within
7 days or 5 half-lives (whichever is longer) prior to the dose of glasdegib. Use of
medications that are not believed to affect subject safety and are medically necessary
for the treatment and maintenance of hepatic disease and other pre-existing and/or
concurrent stable comorbid conditions are permitted with approval by the sponsor.
Limited use of nonprescription medications that are not believed to affect subject
safety or the overall results of the study may be permitted on a case by case basis
with approval by the sponsor. Herbal supplements and hormone replacement therapy must
have been discontinued at least 28 days prior to the dose of investigational product.
11. Concurrent use of any of the following food or drugs known to inhibit CYP3A4 (consult
the sponsor if in doubt whether a food or a drug falls into any of the above
categories) within 7 days or 5 half-lives (whichever is longer) prior to the dose of
glasdegib, until the completion of the last PK sample collection. Use of strong or
moderate CYP3A4 inhibitors includes but is not limited to: amprenavir, aprepitant,
atazanavir, boceprevir, ciprofloxacin, clarithromycin, conivaptan, darunavir,
delavirdine, diltiazem, erythromycin, fluconazole, fosamprenavir, imatinib, indinavir,
itraconazole, ketoconazole, lopinavir, mibefradil, miconazole, nefazodone, nelfinavir,
posaconazole, ritonavir, saquinavir, telaprevir, telithromycin, troleandomycin,
verapamil, voriconazole, grapefruit juice or grapefruit/grapefruit-related citrus
fruits (eg, Seville oranges, pomelos). The topical use of these medications (if
applicable), such as 2% ketoconazole cream, is allowed. All concomitant medications
must be approved by the sponsor.
12. Concurrent use of any of the following food or drugs known to induce CYP3A4 (consult
the sponsor if in doubt whether a food or a drug falls into any of the above
categories) within 12 days or 5 half-lives (whichever is longer) prior to the dose of
investigational product, until the completion of the last PK sample collection. Strong
or moderate CYP3A4 inducers includes but is not limited to: avasimibe, bosentan,
carbamazepine, efavirenz, etravirine, felbamate, modafinil, nafcillin, nevirapine,
phenobarbital, phenytoin, primidone, rifabutin, rifampin, rifapentin, and St. John's
wort. All concomitant medication must be approved by the sponsor.
13. Subjects with congenital long QT syndrome, medical history of Torsades de Pointes or
clinically significant ventricular arrhythmias.
14. Use of PPIs, including but not limited to esomeprazole, lansoprazole, omeprazole,
pantoprazole, and rabeprazole, within 5 days prior to the day of glasdegib dose (Day
15. Subjects will abstain from taking lactulose or other medications which could result in
diarrhea or have excessive (>2) bowel movements per day within 12 hours prior to
glasdegib dosing and 12 hours post dosing.
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