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Blood Brain Barrier Penetration and Pharmacokinetics of the Elemene in Malignant Patients.

D

Dalian Holley Kingkong Pharmaceutical

Status

Unknown

Conditions

Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT01679847
HSZL201001

Details and patient eligibility

About

The purpose of this study is to elucidate the pharmacokinetics and the blood-brain barrier penetration of the elemene.

Enrollment

8 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • histopathological or cytopathology diagnosis of malignancy
  • heart, liver and renal function is normal
  • Expected survival time is more than 3 months
  • Signed informed consent

Exclusion criteria

  • non cancer patient
  • accepted elemene administration in 1 month
  • Expected survival time is less than 3 months
  • no Signed informed consent
  • heart, liver and renal function is abnormal

Trial contacts and locations

1

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Central trial contact

ZHAN QIONG, MD

Data sourced from clinicaltrials.gov

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