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A Drug Interaction Study of SLM0807 and HKB0701 in Healthy Subjects

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HK inno.N

Status and phase

Completed
Phase 1

Conditions

Diabetes Mellitus

Treatments

Drug: Period I : HKB0710 and SLM0807, Period II : SLM0807
Drug: Period I : SLM0807, Period II : HKB0701 and SLM0807

Study type

Interventional

Funder types

Industry

Identifiers

NCT01039896
CJ_VCM_101

Details and patient eligibility

About

The aim of this study is to assess whether HKB0701 alters pharmacokinetics of SLM0807.

Enrollment

24 patients

Sex

All

Ages

20 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers who are in age range of 20-50years and the weight range is not exceed ±20% of ideal weight. Ideal weight = [height -100]*0.9
  • Subjects with no history of any significant chronic disease
  • Judged to be in good health on the basis of their vital sign, ECG, physical exam and routine laboratory data
  • Available for the entire study period
  • Willing to adhere to protocol requirements and sign a informed consent form.

Exclusion criteria

  • Subjects who have taken any drugs to induce or inhibit hepatic enzyme activity within 30days prior to drug administration
  • Subjects who have symptom of an acute illness within 4 weeks prior to drug administration
  • Subjects with a history of clinically significant allergies including drug allergies
  • Subjects whose clinical laboratory test values are outside the accepted normal range(Especially,AST or ALT >1.25 times to normal range or total bilirubin > 1.5times to normal range)
  • Subjects with a history of drug, caffeine or alcohol abuse (caffeine drink >5cups /day, alcohol >30g/day)
  • Heavy smoker ( >10cigarettes/day)
  • Subjects who have had a diet known to interfere with the absorption, distribution, metabolism or excretion of drugs (especially, consumption of grapefruit juice)
  • Subjects who have donated plasma within 60days prior to drug administration
  • Subjects who have participated in a clinical study within 90days prior to drug administration
  • Subjects who have received any drugs that might confound the results of the trial in the opinion of principal investigator (cimetidine within 7days prior to drug administration)
  • Female subjects who are pregnant, breastfeeding or not using medically acceptable birth control

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

24 participants in 2 patient groups

Group1
Experimental group
Description:
SLM0807
Treatment:
Drug: Period I : SLM0807, Period II : HKB0701 and SLM0807
Group2
Experimental group
Description:
SLM0807 and HKB0701
Treatment:
Drug: Period I : HKB0710 and SLM0807, Period II : SLM0807

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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