Multiple Ascending Dose Study to Assess Safety and Pharmacokinetics of Hemay005 In Healthy Subjects

NCT03570346 | Unknown Phase 1

• 1 other identifier: HM005PS1S03
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 1

Brief Summary

Hemay005 is a novel phosphodiesterase type 4(PDE4) inhibitor being developed for the treatment of psoriasis. A total of approximately 24 subjects will be randomized into 3 cohorts(15mg, 30mg, 60mg), approximately 8 healthy subjects will be enrolled (6 active and 2 placebo) at each dose cohort. This study includes an 28-day Screening Period, a 1-day single dose and 7-days multiple doses Treatment Period, and an End of Study Visit occurring approximately 11days (±3 days) after study drug administration.

Conditions

Psoriasis

Outcome Measures

Primary Outcomes (1)

• Number of adverse events and serious adverse events.

  Day1 up to Day20±3

Secondary Outcomes (6)

• Cmax

  pre-dose, 0.5, 1, 1.5, 2, 3, 5, 8, 12, 24, 36, 48 hours post-dose on day 1 and day11

• area under the curve from time zero to the last quantifiable concentration

  pre-dose, 0.5, 1, 1.5, 2, 3, 5, 8, 12, 24, 36, 48 hours post-dose on day 1 and day11

• area under the curve from time zero extrapolated to infinity

  pre-dose, 0.5, 1, 1.5, 2, 3, 5, 8, 12, 24, 36, 48 hours post-dose on day 1 and day11

• t1/2

  pre-dose, 0.5, 1, 1.5, 2, 3, 5, 8, 12, 24, 36, 48 hours post-dose on day 1 and day11

• clearance CL/F

  pre-dose, 0.5, 1, 1.5, 2, 3, 5, 8, 12, 24, 36, 48 hours post-dose on day 1 and day11

Study Arms (2)

Hemay005

EXPERIMENTAL

6 subjects in each cohort(15mg, 30mg, 60mg) will receive Hemay005

Drug: Hemay005

Placebo

PLACEBO COMPARATOR

2 subjects in each cohort(15mg, 30mg, 60mg) will receive placebo

Drug: Placebo

Interventions

Hemay005 DRUG

Subjects will be randomized into 3 dose groups orally twice daily.

Hemay005

Placebo DRUG

Subjects will be randomized into 3 dose groups orally twice daily.

Placebo

Eligibility Criteria

• Age: 18 Years - 60 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy subjects aged 18 to 60 years, male and female volunteers;
• Male Bodyweight（BW）≥ 50kg, female Bodyweight（BW）≥ 45kg, Body mass index (BMI) in 18-28 (including upper and lower limit of the range);
• All male subjects must agree and commit to the use of a reliable contraceptive regimen(including vasoligation, abstinence, using a condom) for the duration of the study(from screening until 6 months after the last dose), Female participants with a negative pregnancy test (serum) at both the screening visit and at Day-1, Female subjects and female partners of male subjects must agree and commit to the use of a reliable contraceptive regimen ( oral contraceptive medications or non-oral contraceptive medications) for the duration of the study(from screening until 6 months after the last dose);
• Ability to understand and be willing to sign a written informed consent before study entry;
• Subjects would have good communication with the investigator and could comply with protocol.

You may not qualify if:

• A history of clinically severe gastrointestinal, hepatic, renal, cardiovascular, dermatological, immunological, respiratory, endocrine, oncological, neurological, metabolic, psychiatric disease or haematological disorders;
• Have a known history of hypersensitivity to any medicine or food, or allergy to the test article or any of the excipient of the test article;
• Have a gastrointestinal, hepatic or renal condition that may influence drug absorption or metabolism;
• A history of chronic infection (ie, tuberculosis);
• A medical history of any clinically significant medical disease or surgery within 4 weeks of the screening;
• Clinically significant laboratory abnormal results at screening or prior to the first dose of study drug;
• Clinically significant abnormal 12-lead ECG or vital signs ( systolic pressure \<90 mmHg or \>140 mmHg, diastolic pressure \<50 mmHg or \>90 mmHg; radial pulse rate \<50 bpm or \>100 bpm);
• Positive blood screen for human immunodeficiency virus (HIV antibody), hepatitis B virus surface antigen, or hepatitis C virus antibody at screening;
• Recent history of frequent alcohol consumption, defined by average intake of greater than 14 units of alcohol per week (1 unit = 360 mL beer or 45 mL of spirits with 40% alcohol content, or 150 mL wine), Participants who are unable to abstain from smoking during the study or quitting smoking for less than 3 months;
• Positive urine screen for drug and cigarettes, positive breath test for alcohol;
• Subjects who use soft drugs (ie marijuana )within 3 months of the screening and entire study duration or hard drugs (ie cocaine, phencyclidine ) within 1 year of the screening and entire study duration;
• Dietary habits or food intolerances which will interfere with the requirements for participants to consume a standardised diet whilst confined to the clinical unit;
• Participants who eat special food (Including grapefruit and/or Xanthine diet) for 14 days prior to dosing or any caffeine containing food or drinks, i.e. chocolate for 48 hours prior to dosing or drinking alcohol for 24 hours prior to dosing and not will stop to intake above food and drinks;
• Use of any drug that inhibits or induces hepatic metabolism of drugs within 30 days of planned study drug administration and entire study duration (e.g. inducers: barbiturates, carbamazepine, rifampicin, phenytoin, glucocorticoid and omeprazole; inhibitors - Selective Serotonin Reuptake Inhibitors(SSRI )antidepressants, cimetidine, diltiazem, macrolides, nitroimidazoles, sedatives and hypnotics, verapamil, fluoroquinolones and antihistamines);
• Participant who received any medicine within 14 days of the initial dose of study drug;

Sponsors & Collaborators

• Tianjin Hemay Bio-Tech Co., Ltd: lead

Study Sites (1)

Peking Union Medical College Hospital

Beijing, China

RECRUITING

MeSH Terms

Conditions

Psoriasis

Interventions

Hemay005

Condition Hierarchy (Ancestors)

Skin Diseases, Papulosquamous; Skin Diseases; Skin and Connective Tissue Diseases

Study Officials

• Hongyun Wang, Doctor

  Peking Union Medical College Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Hongyun Wang, Doctor

CONTACT

010-69156576; wanghy@pumch.cn

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 17, 2018
• First Posted: June 26, 2018
• Study Start: July 10, 2018
• Primary Completion: October 20, 2018
• Study Completion: December 1, 2018
• Last Updated: October 2, 2018

Record last verified: 2018-06

Locations

CN (1)