Title

Study of COR388 HCl in Healthy Subjects
A Phase 1 Single Ascending Dose Study of COR388 HCl
  • Phase

    Phase 1
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    COR388 ...
  • Study Participants

    34
The study is a randomized, double-blind, placebo-controlled, dose escalation, first-in-human trial of the safety and tolerability of COR388 HCl in healthy male and female subjects.
Study Started
Dec 11
2017
Primary Completion
Feb 20
2018
Study Completion
Apr 02
2018
Last Update
Apr 18
2018

Drug COR388

Administered as oral capsule

Drug Placebo

Administered as oral capsule

Placebo Placebo Comparator

COR388 TBD mg Active Comparator

Criteria

Major Inclusion Criteria:

Males of reproductive potential must agree to use double-barrier contraceptive measures or avoid intercourse from Day -1 through 28 days after the dose of study drug;
Females of child-bearing potential must be non-lactating, have negative serum pregnancy test results at screening visit and Day 1; agree to use double-barrier contraceptive measures or avoid intercourse from Day -10 through 28 days after the dose of study drug;
Body mass index (BMI) ≥19 to ≤32 kg/m2;
Good health as determined by the absence of clinically significant deviation from normal, by medical history, physical examination, laboratory reports, and 12-lead electrocardiogram (ECG) prior to enrollment;
Non-smoker and non-tobacco user for a minimum of 3 months prior to screening and for the duration of the study;
Able to understand and willing to comply with all study requirements, and follow the study medication regimen.

Major Exclusion Criteria:

History or current evidence of cardiac, hepatic, renal, pulmonary, endocrine, neurologic, gastrointestinal, hematologic, oncologic, infectious, or psychiatric disease as determined by screening history, physical examination, laboratory reports, or 12-lead ECG;
Need for any concomitant medication (with the exception of hormonal contraceptives as allowed for females of child-bearing potential);
Use of any prescription drug within 14 days prior to the first dose of the study (with the exception of hormonal contraceptives for females of childbearing potential);
Use of any non-prescription drug and/or herbal supplements within 7 days prior to the first dose of the study;
History of significant allergic reaction to any drug;
Participation in another investigational new drug research study within the 30 days prior to the first dose of the study;
History of alcohol or drug abuse or dependence within 12 months of screening as determined by the Investigator;
Positive urine screen for prohibited drugs or positive alcohol screen on Day -1.
No Results Posted