| Eligibility |
Inclusion Criteria:
Subjects must satisfy the following criteria to be enrolled in the study:
1. Subject is = 18 and = 55 years of age at the time of signing the informed consent form
(ICF).
2. Subject is male.
3. Subject must understand and voluntarily sign an ICF prior to any study-related
assessments/procedures being conducted.
4. Subject is willing and able to adhere to the study visit schedule and other protocol
requirements.
5. Subject is in good health, as determined by the Investigator based on a physical
examination at screening.
6. Subject agrees to abide by the requirements and restrictions outlined in the CC-90009
Pregnancy Prevention Plan for Subjects in Clinical Trials.
7. All subjects must avoid donating semen or sperm and practice complete abstinence (True
abstinence is acceptable when this is in line with the preferred and usual lifestyle
of the subject. Periodic abstinence [eg calendar, ovulation, symptothermal or post
ovulation methods] and withdrawal are not acceptable methods of contraception.) or
condom use during sexual contact with a pregnant female or a female of childbearing
potential (FCBP) while receiving CC-90009 and for at least 28 days after the dose,
even if he has undergone a successful vasectomy. If engaging in sexual contact, inform
their partners who are FCBP to use two methods of reliable contraception, one highly
effective and one additional effective, throughout the entire duration of CC-90009 and
for at least 28 days after their dose of CC-90009. Partners of male subjects who are
females of childbearing potential must use contraception during the same duration as
the male subject to avoid pregnancy. If a pregnancy occurs with your partner, notify
the doctor conducting the study immediately. The following are examples of highly
effective and additional effective methods of contraception:
- Examples of highly effective methods:
- Intrauterine device (IUD)
- Hormonal (birth control pills, injections, implants,
levonorgestrel-releasing intrauterine system [IUS], medroxyprogesterone
acetate depot injections, ovulation inhibitory progesterone-only pills [e.g.
desogestrel])
- Tubal ligation
- Partner's vasectomy
- Examples of additional effective methods:
- Male condom
- Diaphragm
- Cervical Cap
8. Subject has a body mass index (BMI) = 18 and = 33 kg/m2 at screening.
9. Protocol-specified clinical laboratory safety test results should be within the
reference range of the clinical laboratory being used by the study site at screening
and at baseline (Day -1).
10. Subject is afebrile, with supine systolic blood pressure (BP) = 100 and = 140 mmHg,
supine diastolic BP = 50 and = 90 mmHg, and resting pulse rate = 40 and = 110 bpm at
screening and Day -1.
11. Subject has a normal or clinically acceptable 12-lead electrocardiogram (ECG), with a
QTcF value = 430 msec, at screening and Day -1.
Exclusion Criteria:
The presence of any of the following will exclude a subject from enrollment:
1. Subject has any significant medical condition, laboratory abnormality, or psychiatric
illness that would prevent the subject from participating in the study.
2. Subject has any condition including the presence of laboratory abnormalities, which
places the subject or other study participants at unacceptable risk if he were to
participate in the study.
3. Subject has a past or current history of any condition affecting calcium homeostasis
including, but not limited to: hypocalcemia, parathyroid disorders, vitamin D level
lower than 20 ng/mL, disorders of phosphate or magnesium metabolism. The Investigator
should contact the Sponsor for questions on any disorders that may be related to
calcium homeostasis. Subjects with vitamin D levels < 30 ng/mL are not permitted to
serve as sentinel subjects or alternates for the sentinel subjects.
4. Subject has a history of prior infusion reactions, anaphylactic reactions, or
anaphylactoid reactions to any medication regardless of severity.
5. Subject participated in a radiolabeled drug study, where exposures either are known or
unknown to the Investigator, within the previous 12 months prior to Day -1. The total
12-month exposure from this study and a maximum of 2 other previous studies within 4
to 12 months of this study will be within the CFR recommended levels considered safe,
per US Title 21 CFR 361.1: less than 5,000 mrem whole body annual exposure, with
consideration given to the half-lives of the previous radiolabeled study drugs
received.
6. Subject was exposed to significant radiation (eg, serial X-ray or computed tomography
scans, barium meal, current employment in a job requiring radiation exposure
monitoring) within 12 months prior to Day -1. All questions regarding this criterion
should be discussed with the Sponsor.
7. History of less than 1 to 2 bowel movements per day.
8. Subject is unable to take calcium citrate, vitamin D3, Dulcolax®, acetaminophen or
diphenhydramine because of allergy or other intolerance.
9. Subject has any condition that confounds the ability to interpret data from the study.
The Investigator should contact the Sponsor for questions about eligibility based on
this criterion.
10. Subject was exposed to an investigational drug (new chemical entity) within 30 days
prior to dosing, or 5 half-lives of that investigational drug, if known (whichever is
longer).
11. Subject has used any prescribed systemic or topical medication (including but not
limited to analgesics, anesthetics, etc) within 14 days or 5 half-lives of that
medication, whichever is longer, prior to dosing.
12. Subject has used any non-prescribed systemic or topical medication (including
vitamin/mineral supplements and herbal medicines) within 7 days prior to dosing.
13. Subject has used cytochrome P (CYP) 450 inducers and/or inhibitors (including St.
John's Wort) within 30 days prior to dosing. The Indiana University "Cytochrome P450
Drug Interaction Table" should be utilized to determine inducers and/or inhibitors of
CYP (http://medicine.iupui.edu/clinpharm/ddis/table.aspx).
14. Subject has any surgical or medical conditions possibly affecting drug absorption,
distribution, metabolism, and excretion, eg, bariatric procedure. Note: prior
appendectomy is acceptable, but prior cholecystectomy would result in exclusion from
the study.
15. Subject donated blood or plasma within 8 weeks prior to dosing to a blood bank or
blood donation center.
16. Subject has a history of drug abuse (as defined by the current version of the
Diagnostic and Statistical Manual [DSM]) within 2 years prior to dosing, or positive
drug test reflecting consumption of illicit drugs.
17. Subject has a history of alcohol abuse (as defined by the current version of the DSM)
within 2 years prior to dosing, or positive alcohol test.
18. Subject is known to have serum hepatitis or known to be a carrier of hepatitis B
surface antigen (HBsAg) or hepatitis C antibody (HCV Ab), or have a positive result to
the test for human immunodeficiency virus (HIV) antibodies at screening.
a. Note: Subjects who received hepatitis B vaccination and who test positive for
hepatitis B surface antibody and negative for both hepatitis B surface antigen and
hepatitis B core antibody remain eligible for study participation.
19. Subject smokes > 10 cigarettes per day, or equivalent in other tobacco products
including eCigarettes or vapes (self-reported).
20. Subject has received immunization with a live or live attenuated vaccine within 2
months prior to dosing or is planning to receive immunization with a live or live
attenuated vaccine for 2 months following dosing.
21. Subject is part of the study site personnel or a family member of the study site
staff.
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