Pharmacokinetics and Safety Study of Apetrol ES

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LG Life Sciences

Status and phase

Completed
Phase 1

Conditions

Healthy

Treatments

Drug: Apetrol ES / Megace

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02446353
LG-ESCL001

Details and patient eligibility

About

A Randomized, Open Label, Single dose, Cross-over, Phase I Trial to Investigate Safety and Pharmacokinetics of Apetrol ES and Megace® in Healthy Male Volunteers.

Full description

[Part 1] fasting [Part 2] fed

Enrollment

79 patients

Sex

Male

Ages

20 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Is a healty male between 20 and 55 years old.
  • In a ± 20% than ideal body weight. [ideal body weight(kg) = height(cm)-100) x 0.9 (Broca's rule)
  • Subjects who are considered to be suitable in conducting the clinical trial in serum test, hematology test, hemato-chemical test, urine test and 12-ECG result.
  • Is willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
  • Agrees to use an adequate means of contraception during clinical trials
  • Subject who has voluntarily decided to participate in this clinical trial and consented in writing.

Exclusion criteria

  • Is allergic against Megestrol acetate or other drugs (Aspirin, NSAIDs, Antibiotics, etc.) or against foods, or has an clinically serious allergic history.
  • Subjects who have present condition or past history of any disease involving liver, kidney, nervous system, immune system, respiratory system, or endocrine system; hematologic and oncologic disease; cardiovascular disease; or psychiatric disorder (mood disorder, obsessive-compulsive disorder, etc. that may affect ADME of investigational medicinal products.
  • In the vital signs measured in sitting position at the screening visit, subjects who have hypertension desease(a systolic blood pressure of ≥ 150 mmHg or a diastolic blood pressure of ≥ 100 mmHg).
  • Diabetic patients or the patients who are abnormal of impaired glucose tolerance.
  • The patients who have a history of Arterial Embolism.
  • The patients who have a history of adrenal insufficiency like hypotension or nausea or vertigo or asthenia or etc.
  • Subjects who have a history of drug abuse or shown positive reaction to drugs that may be abused from a urine drug screening
  • Subjects who took any specialized drug or an herbal medication within 2 weeks before the date of first administration or took any over the counter (OTC) drug within 1 week (however, they may be included as subjects if appropriate depending on the investigator's discretion)
  • Subjects who had whole blood donation within 2 months or component blood donation within 1 month before the clinical trial.
  • Subjects who have abnormal diets that may affect ADME of investigational medicinal products.
  • Subjects who have been drinking extremely alcohol and caffeine (more than caffeine 5 cups/day, soju 3 cups/day, beer 3 cups/day, liquors 2 cups/day, 10 cigarettes/day) or can't refrain from drinking during the clinical trial period.
  • Subjects who had administration a barbiturates within 1 month before the date of first drug administration
  • Subjects who already participated in other clinical trials within 2 months before this clinical trial.
  • Subjects who are considered to be unsuitable in conducting the clinical trial for other reason at the principal investigator's discretionary judgment

Trial design

79 participants in 4 patient groups

Megace : fed
Experimental group
Description:
Megace / Apetrol ES : comparator / test, fed
Treatment:
Drug: Apetrol ES / Megace
Apetrol ES : fed
Experimental group
Description:
Apetrol ES / Megace : test / comparator, fed, cross-over
Treatment:
Drug: Apetrol ES / Megace
Megace : fasting
Experimental group
Description:
Megace / Apetrol ES : comparator / test, fasting
Treatment:
Drug: Apetrol ES / Megace
Apetrol ES : fasting
Experimental group
Description:
Apetrol ES / Megace : test / comparator, fasting, cross-over
Treatment:
Drug: Apetrol ES / Megace

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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